ArticlePDF AvailableLiterature Review

Rhodiola rosea L. and Alzheimer's Disease: From Farm to Pharmacy

  • Gazi University, Faculty of Pharmacy

Abstract and Figures

Rhodiola rosea L. (roseroot) is a common member of the family Crassulaceae, known as one of the most important popular medicinal plants in the northern region of Europe. The roots of R. rosea possess a wide range of pharmacological activities such as antioxidant, antiinflammatory, anticancer, cardioprotective, and neuroprotective effects that are because of the presence of different phytochemicals such as phenols and flavonoids. In addition, the presence of salidroside, rosavins, and p-tyrosol are responsible for its beneficial effects for the treatment of on depression, fatigue, and cognitive dysfunction. A plethora of studies report that R. rosea has potent neuroprotective effects through the suppression of oxidative stress, neuroinflammation, and excitotoxicity in brain tissues and antagonism of oncogenic p21-activated kinase. However, to our knowledge, no review articles have been published addressing the neuroprotective effects of R. rosea. Therefore, the present article aims at critically reviewing the available literature on the beneficial effects of R. rosea on as a therapeutic strategy for the treatment of Alzheimer's disease and other neurodegenerative diseases where oxidative stress plays a major role in disease development and progression. We also discuss the cultivation, phytochemistry, clinical impacts, and adverse effects of R. rosea to provide a broader insight on the therapeutic potential for this plant.
Content may be subject to copyright.
Rhodiola rosea L. and Alzheimers Disease: From
Farm to Pharmacy
Seyed Fazel Nabavi,
Nady Braidy,
*Ilkay Erdogan Orhan,
Arash Badiee,
Maria Daglia
Seyed Mohammad Nabavi
Applied Biotechnology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran
Centre for Healthy Brain Ageing, School of Psychiatry, University of New South Wales, Sydney, Australia
Department of Pharmacognosy, Faculty of Pharmacy, Gazi University, Ankara, Turkey
Deputy of Food and Drug, Mazandaran University of Medical Sciences, Sari, Iran
Department of Drug Sciences, Medicinal Chemistry and Pharmaceutical Technology Section, University of Pavia, Italy
Rhodiola rosea L. (roseroot) is a common member of the family Crassulaceae, known as one of the most impor-
tant popular medicinal plants in the northern region of Europe. The roots of R. rosea possess a wide range of
pharmacological activities such as antioxidant, antiinflammatory, anticancer, cardioprotective, and neuroprotec-
tive effects that are because of the presence of different phytochemicals such as phenols and flavonoids. In ad-
dition, the presence of salidroside, rosavins, and p-tyrosol are responsible for its beneficial effects for the
treatment of on depression, fatigue, and cognitive dysfunction. A plethora of studies report that R. rosea has po-
tent neuroprotective effects through the suppression of oxidative stress, neuroinflammation, and excitotoxicity in
brain tissues and antagonism of oncogenic p21-activated kinase. However, to our knowledge, no review articles
have been published addressing the neuroprotective effects of R. rosea. Therefore, the present article aims at
critically reviewing the available literature on the beneficial effects of R. rosea on as a therapeutic strategy for
the treatment of Alzheimers disease and other neurodegenerative diseases where oxidative stress plays a major
role in disease development and progression. We also discuss the cultivation, phytochemistry, clinical impacts,
and adverse effects of R. rosea to provide a broader insight on the therapeutic potential for this plant. Copyright
© 2016 John Wiley & Sons, Ltd.
Keywords: Neurodegeneration; Neuroinflammation; Neurotoxicity; Oxidative stress; Rhodiola rosea.
Alzheimers disease (AD) is one of the most common
debilitating age-related neurodegenerative disorders,
which causes dementia in the elderly. It is associated
with progressive cognitive impairment and dementia,
eventually leading to complete incapacity and death
(Birks, 2006; Reitz et al., 2011). Ageing represents the
main risk factor for developing AD (Lindsay et al.,
2002). However, cardiovascular diseases, obesity, diabe-
tes, traumatic brain injury, cigarette smoking, and alcohol
abuse are other important risk factors of major concern.
AD was first reported in a 51-year-old woman who suf-
fered from progressive dementia, by the German psychi-
atrist and neuropathologist, Alois Alzheimer, in 1907
(Berchtold and Cotman, 1998). Since then, while exten-
sive progress has been made in AD research, the exact
etiology and pathogenesis of the disease remain unclear.
Although AD remains untreatable, it has been reported
that mental stimulation and exercise training can delay
cognitive impairment in patients who suffer from AD.
Histopathologically, AD is characterized by the pres-
ence of extracellular amyloid plaques containing aggre-
gated amyloid beta (Aβ) peptides and intracellular
neurofibrillary tangles containing hyperphosphorylated
tau protein. A wealth of evidence has shown that
marked increases in oxidative stress are present in the
AD brain in addition to the well-established pathology.
Increased production of reactive oxygen species (ROS)
and reactive nitrogen species (RNS) induces oxidative
stress and cell death in neural tissues of the brain.
ROS and RNS are well known to induce oxidative dam-
age to biological macromolecules, including proteins
and lipids resulting in the cross-linking of cytoskeletal
biological macromolecules (Yu, 1994; Stadtman and
Berlett, 1997; Toyokuni, 1999; Patel et al., 2000). In
addition, accelerated production of ROS and RNS leads
to oxidative injuries to RNA and DNA leading to a
variety of mutations and cell death. With respect to the
high metabolic activity as well as high levels of polyun-
saturated fatty acids and low levels of antioxidant
enzymes and non-enzymatic antioxidants, the brain is
highly susceptible to oxidative stress. Because of
regional differences in total brain antioxidant activity,
it is likely that selective regional susceptibilities for oxi-
dative stress exist in the brain.
Pathological evidence has shown that oxidative stress
plays a crucial role in both the initiation and progression
of AD. It has been reported that in AD, cholinergic neu-
rons in the forebrain are highly vulnerable to oxidative
* Correspondence to: Nady Braidy, Centre for Healthy Brain Ageing,
School of Psychiatry, University of New South Wales, Sydney, Australia;
Seyed Mohammad Nabavi, Applied Biotechnology Research Center,
Baqiyatallah University of Medical Sciences, Tehran, Iran, P.O. Box
E-mail: (Nady Braidy);
(Seyed Mohammad Nabavi)
Phytother. Res. 30: 532539 (2016)
Published online 11 January 2016 in Wiley Online Library
( DOI: 10.1002/ptr.5569
Copyright © 2016 John Wiley & Sons, Ltd.
Received 05 October 2015
Revised 07 December 2015
Accepted 12 December 2015
stress (Yankner, 1996; Gibbs and Aggarwal, 1998). In
addition, increased levels of F
-isoprostanes, a marker
for lipid peroxidation in the neuronal tissues, have been
reported in multiple regions of the brain and cerebrospi-
nal fluid of patients with AD (Praticò et al., 1998;
Montine et al., 2005). Furthermore, in the neural tissues,
oxidative stress is associated with increasing in the level
of protein carbonyls that can induce DNA damage. The
levels of protein carbonyls and 3-nitrotyrosine and
markers of oxidative damage to DNA and RNA, such
as 8-hydroxydeoxyguanosine, are higher in AD brains
compared with age-matched controls (Butterfield and
Kanski, 2001). As well, the activities of several endoge-
nous antioxidant enzymes such as superoxide dismutase
(SOD) and catalase have been observed in both the cen-
tral nervous system and peripheral nervous system tissues
of AD patients (Pratico and Sung, 2004). Elevations in
oxidative stress markers have also been reported in mild
cognitive impairment, an intermediate state between nor-
mal ageing and dementia (Ansari and Scheff, 2010). This
suggests that oxidative damage in AD may commence
prior to the onset of the disease. Therefore, oxidative
stress may represent an early alteration during the devel-
opment of the disease.
Neuroinflammation also appears to play a prominent
role in the pathogenesis of AD. Microglial cells, the resi-
dent immune cells of the brain, have been shown to be re-
cruited to AD-associated Aβplaques and in close
proximity to neurofibrillary tangles (Rogers et al., 1988;
Griffin et al., 1989). Increased levels of several inflamma-
tory molecules have been reported, including complement
compounds, cytokines, macrophage colony-stimulating
factor, transforming growth factor-α, C-reactive protein,
S100β, and arachidonic acid (Hensley, 2010). These
inflammatory markers are capable of producing ROS
and RNS, which are elevated in the AD brain and amply
evidenced. Despite this, the exact role of the primacy
and consequences of neuroinflammation as an initiator
or accelerator of AD remains unclear. Current research
suggests that neuroinflammation represents an early and
continuous feature in AD that is amenable to pharmaco-
logical exploitation.
Glutamate neurotoxicity has also been thought to
play critical roles in the pathophysiology of AD and
other neurodegenerative disorders, including hypoxic-
ischemic brain injury, epileptic seizures, and Parkinsons
disease. L-glutamate (L-glu) is the most abundant excit-
atory neurotransmitter in the central nervous system
(CNS). It plays a crucial role in the neurological pro-
cesses including cognition, learning, and memory
(Collingridge and Lester, 1989). However, hyperactiva-
tion of glutaminergic receptors, under pathophysiologi-
cal conditions, induces neuronal damage and cell death
via apoptosis and energy restriction, known as
excitotoxicity (Olney et al., 1971). Therapeutic strate-
gies that attenuate L-glu-induced excitotoxicity are
potential candidates for the treatment of AD.
Dendritic spine defects are a common feature in AD
and human developmental mental retardation syn-
dromes (Fiala et al., 2002). While it is likely that
dendritic spine defects occur secondarily to upstream
deficits in mental retardation, the exact significance of
dendritic spine defects in AD pathology was strength-
ened by the recent finding that the genes associated with
mental retardation are linked to the X chromosome
(Ramakers, 2002). These studies identified a clustering
of proteins in the postsynaptic pathways modulating
spine actin assembly and disassembly and spine mor-
phogenesis (Kichina et al., 2010). Most important are
p21-activated kinases (PAKs), which represent a down-
stream signaling effector of the Rho/Rac family of small
GTPases (Kichina et al., 2010). PAKs have been shown
to be involved in multiple signal transduction pathways
in mammalian cells (Maruta, 2014). For instance,
PAK1 has been shown to be decreased in the hippocam-
pus from postmortem AD brain, accompanied by
relocalization of activated PAKs to the membrano-
cytoskeletal fractions (Zhao et al., 2006). A recent study
showed that a dominant-negative form of PAK1 sensi-
tizes, while the wild-type form ameliorated toxicity
induced by cytotoxic Aβoligomers in cultured primary
neurons (Zhao et al., 2006). Dominant-negative PAK1
has been shown to antagonize other PAK isoforms,
following expression in mouse forebrain-affected
synapse morphology and consolidation of long-term
memory (Hayashi et al., 2004).
In respect to this, much attention has been paid to an-
tioxidants as a therapeutic strategy for the treatment of
AD (Choi et al., 2012; Feng and Wang, 2012; Galasko
et al., 2012; Mecocci and Polidori, 2012). Plants and
plant products are rich sources of natural polyphenolic
antioxidants such as flavonoids, which can scavenge free
radicals while demonstrating potent antiinflammatory
properties and low adverse effects (Nabavi et al.,
2012b; Nabavi et al., 2013b; Nabavi et al., 2014; Nabavi
et al., 2015c). At present, there are numerous scientific
evidences regarding the beneficial effects of natural
products in human diseases (Nabavi et al., 2012a;
Nabavi et al., 2013a; Nabavi et al., 2015a; Nabavi et al.,
2015b; Nabavi et al., 2015d). Rhodiola rosea L. is an
important plant species from the genus Rhodiola.Itis
most abundant in Eastern Europe and Asia where it is
used as a traditional medicine for a variety of different
ailments (Brown et al., 2002; Panossian et al., 2010).
The aim of this paper is to critically review the scientific
evidence regarding the beneficial effects of R.rosea in
AD and lay foundation for its future research.
Rhodiola rosea L. (roseroot, golden root, or Arctic root)
is a genus of herbaceous perennial plants that belongs to
the family Crassulaceae (Rohloff, 2002; Ming et al.,
2005). Rhodiola species grow wild in high-altitude areas
as well as other cold parts of continental Asia, Europe,
and America (Brown et al., 2002; De Bock et al.,
2004). In continental Asia, the genus Rhodiola is abun-
dant in the Altai Mountains located between Mongolia
and Siberia regions (Furmanowa et al., 1995; Galambosi,
2006). In the continental Europe, it is widely distributed
in Iceland and the British Isles between Scandinavia and
several mountains such as Pyrenees, Alps, Carpathian
as well as other mountains in the Balkan area (Brown
et al., 2002; Wiedenfeld et al., 2007; Panossian et al.,
2010). In addition, some varieties of Rhodiola have
been found in different high-altitude regions of Alaska,
Canada as well as other mountains of the North American
continent (Brown et al., 2002). It is an herbaceous
perennial flowering member of the genus Rhodiola that
has a wide range of medicinal effects in the traditional
Copyright © 2016 John Wiley & Sons, Ltd. Phytother. Res. 30: 532539 (2016)
medicine. It is widely distributed in the Arctic and moun-
tainous area of the Europe and Asia and traditionally
used for treatment of human diseases especially mental
diseases (Adaptogen, 2001; Brown et al., 2002). In addi-
tion to R.rosea, there are over 200 species from the genus
Rhodiola (Platikanov and Evstatieva, 2008) of which at
least 20 species (such as Rhodiola alterna S.H. Fu,
Rhodiola brevipetiolata (Fröd.) S.H. Fu, Rhodiola
crenulata (Hook.f. & Thomson) H.Ohba, Rhodiola
kirilowii (Regel) Maxim., Rhodiola quadrifida (Pall.)
Fisch. & C.A.Mey, Rhodiola sachalinensis Boriss., and
Rhodiola sacra (Prain ex Raym.-Hamet) S.H. Fu) are
known to have different medicinal effects in traditional
medicine (Adaptogen, 2001; Brown et al., 2002; Goldstein
et al., 2008; Li et al., 2009).
Up till now, cultivation experiments have been
performed in Russia, Sweden, Poland, Finland, and
Germany (Galambosi, 2006; Platikanov and Evstatieva,
2008; Galambosi et al., 2009; Kylin, 2010; Adamczak
et al., 2014) that show that R.rosea can be successfully
cultivated in cool and moist climates with precipitation
(Galambosi, 2006; Platikanov and Evstatieva, 2008;
Galambosi et al., 2009; Kylin, 2010; Adamczak et al.,
2014). However, it does not prefer shaded areas
(Kucinskaite et al., 2006). It is well grown in deep soil
in which it can easily penetrate (Galambosi, 2006).
Moreover, R.rosea prefers moderately rich and well-
drained slightly acidic soils (pH 67) (Galambosi, 2006;
Platikanov and Evstatieva, 2008). It can also grow in
sandy loam soils and even rocks (Alm, 2004; Galambosi,
2006). There are negligible reports regarding the benefi-
cial effects of fertilizers for the cultivation of Rhodiola
(Galambosi, 2006; Platikanov and Evstatieva, 2008;
Galambosi et al., 2009; Kylin, 2010; Adamczak et al.,
2014). However, it has been reported that the root size
of Rhodiola in weak soils is significantly lower than that
occurring in the cultivation that is because of insufficient
nutrients required for Rhodiola (Galambosi, 2006;
Platikanov and Evstatieva, 2008; Galambosi et al.,
2009; Kylin, 2010; Adamczak et al., 2014). It has also
been reported that R.rosea can be propagated by seed-
lings, root division as well as seed germination
(Furmanowa et al., 1995; Galambosi, 2006). The propa-
gation of seedlings is the most effective method for
larger scale cultivation of R.rosea (Galambosi, 2006;
Platikanov and Evstatieva, 2008).
Rhodiola rosea has a rich variety of phytochemical con-
tent including cinnamoyl glycosides (phenylethanoids),
flavonoids, phenylpropanoids, essential oil (monoter-
penes), phenolic acids, cyanogenic glucosides as well as
polysaccharides and oligomeric proanthocyanidins (Zhou
et al., 2014) (Fig. 1). Flavonoids appear to be the main con-
stituents in R.rosea asmainly,i.e.herbacetin,
gossypetin, and kaempferol derivatives. Early studies
originating from the 1980s indicated that the plant
contains a number of flavonoids such as tricin (4,5,7-
trihydroxy-3,5-dimethoxyflavone) and its 7- and 5-O
glucosides, herbacetin (3,4,5,7,8-pentahydroxyflavone),
and its derivatives; rhodionin (herbacetin 7-O-α-
rhamnopyranoside), rhodiosin (herbacetin 7-O-3-O-β-
D-glucopyranosyl-α-L-rhamnopyranoside), rhodiolin (a
flavonolignan), rhodionidin (herbacetin-7-O-α-L-
rhamnopyranose-8-O-β-D-glucopyranoside), rhodiolgin
(gossypetin-7-O-α-L-rhamnopyranoside), rhodiolgidin (go
side), rhodalin (herbacetin-8-O-β-D-xylopyranoside), rho
dalidin (herbacetin-8-O-β-D-xylopyranose-3-O-β-D-gluco
pyranoside), the flavonoid glycosides; gossypetin-7-O-L-
rhamnopyranoside and rhodioflavonoside, rhodioflavo
noside, kaempferol-3-O-β-d-glucopyranosyl-7-O-α-l-
rhamn-opyranoside, kaempferol 3-O-β-d-glucopyrano
side-(2 1)-β-d-xylopyranoside 3, and herbacetin-8-O-
Figure 1. Main chemical classes present in Rhodiola rosea L.
Copyright © 2016 John Wiley & Sons, Ltd. Phytother. Res. 30: 532539 (2016)
β-d-glucopyranoside. In addition, Tolonen and Uusitalo
(Tolonen and Uusitalo, 2004) detected several flavonoid
derivatives in the flowers of R.rosea identified as
rhodiolgidin, rhodiolgin, rhodionin as well as some
unidentified flavonol-glucoside mixtures using a fast and
simple LC-MS method. Isolation of the common flavonoid
derivatives apigenin, luteolin, kaempferol, quercetin,
cosmosiin, astragalin, linocinamarin, rutin, and nicotiflorin
was reported by Jeong et al. (Jeong et al., 2009) as well as
kaempferol-7-O-alpha-L-rhamnopyranoside, herbacetin-
7-O-alpha-L-rhamnopyr-anoside, herbace-tin-7-0-(3-O-
and 5,7,3,5-tetrahydroxy-flavanone.
Phenylpropanoids and cinnamyl alcohol glycosides
(or phenyl ethanoids) constitute a large quantity in R.
rosea. Thesalidroside (rhodioloside) [β-D-glucopyranoside
of β-(p-hydroxyphenyl)ethanol] (Fig. 2) is the first
cinnamyl glycoside reportedly isolated from this species
in 1967 (Troshchenko and Kutikova, 1967). Kurkin et al.
(Kurkin et al., 1991) successfully isolated 11
phenylpropanoid and cinnamyl glycosidic compounds
from the callus culture of the plant, some of which
were identified as p-coumaric acid 4-glucoside and
1-glucoside, caffeic acid 3-glucoside, triandrin,
lariciresinol 4-glucoside, vimalin, rosarin, and rosin
(Fig. 2). Later, cinnamyl-(6-O-β-xylopyranosyl)-O-β-
glucopyranoside and 4-methoxy-cinnamyl-(6-O-α-arabino
pyranosyl-O-β-glucopyranoside were obtained from R.
rosea as new phenylpropanoid derivatives, in addition to
picein and benzyl-O-beta-glucopyranoside (Tolonen et al.,
2003). Rosarin, rosin, and rosavin were also quantified in
the roots of the plant using high-performance thin layer
chromatography and reverse-phase HPLC methods
(Fig. 2). Among these derivatives, salidroside needs a spe-
cial mention as it possesses many potent biological activi-
ties. Although its presence was earlier reported from a
number of plant genera such as Salix species, Rhodo-
dendron ponticum,Comus sp., Forsythia sp., Strychnos
nux-vomica,Rehmannia glutinosa,Linaria japonica,
Penstemon acuminatus, etc., it is most common in
Rhodiola species and occasionally serves as a chemo-
taxonomic marker. Salidroside is the main substance
in R.rosea, which is responsible for many pharmaco-
logical activities reported by the plant as well as the
reference compound in quality assessment of
preparations containing roseroot extracts. R.rosea
roots also yielded rhodiolosides AE, identified as five
new monoterpene glycosides. Their corresponding
chemical structures were elucidated as (2E,6E,4R)-
4,8-dihydroxy-3,7-dimethyl-2,6-octadienyl β-D-gluco
pyranoside (rhodioloside A), (2E,4R)-4-hydroxy-3,7-
dimethyl-2,6-octadienyl α-D-glucopyranosyl(1 6)-β-
D-glucopyranoside (rhodioloside B), (2E,4R)-4-hy-
droxy-3,7-dimethyl-2,6-octadienyl β-D-glucopyranosyl
(1 3)-b-D-glucopyranoside (rhodioloside C), (2E,4R)-
4,7-dihydroxy-3,7-dimethyl-2-octenyl β-D-glucopyranoside
(rhodioloside D), and (2E)-7-hydroxy-3,7-dimethyl-2-
octenyl α-L-arabinopyranosyl(1 6)-β-D-glucopyranoside
(rhodioloside E) (Ma et al., 2006).
Moreover, a few studies have shown that the plant
contains essential oils. For instance, the sample of R.rosea
was found to contain myrtenol (36.9%), trans-pinocarveol
(16.1%), geraniol (12.7%), and dihydrocumin alcohol
(12.1%) as the major components. In another study, the
essential oils obtained from three samples of R.rosea
from Bulgaria, China, and India were analyzed, and
geraniol was determined as the chief compound in
Bulgarian and Chinese samples, whereas phenylethyl
alcohol was the major oil in the Indian sample. Other
chemicals found in R.rosea were reported as lotaustralin
(a cyanogenic glucoside) (Fig. 2), β-sitosterol, and
oligomeric proanthocyanidins composed of ()-epigallo-
catechin and its 3-O-gallate esters, polysaccharides, and
lignins. Rosiridol, the oxygenated derivative of geraniol,
was identified as the aglycon of rosiridin, suggested to be
an important bioactive compound for R.rosea (Fig. 2)
(Van Diermen et al., 2009).
Rhodiola rosea has been used in traditional medicine
from ancient times till current times for the treatment
of diarrhea, hysteria, hernias, headaches as well as cog-
nitive dysfunctions. Additionally, it has been widely
used as an astringent in traditional herbal medicine. It
has also been reported that Rhodiola infusion possesses
a beneficial effects on mouth pain and kidney stones,
swellings, back pain, as well as mood disorders
(Panossian et al., 2010; ; Cropley et al., 2015). In addition
to these beneficial effects, it has been reported that
Rhodiola infusion has significant effects on hair growth
(Panossian et al., 2010; Zhu et al., 2014). In traditional
medicine, its roots are also used for mitigation of differ-
ent skin diseases (Mamedov et al., 2005). According to
Grasnytjar, dried roots of Rhodiola have beneficial ef-
fects on freckles, scurvy, as well as physical and mental
weakness. It has also been reported that Rhodiola has
a stimulant effect as well as vasoconstrictive and hemo-
static activity on hemorrhoids (Sandberg and Bohlin,
1993; Linné, 2005). It has also been reported that R.
rosea can be used for the treatment of different mental
diseases such as schizophrenia. R.rosea is currently
Figure 2. Main compounds found in Rhodiola rosea L.
Copyright © 2016 John Wiley & Sons, Ltd. Phytother. Res. 30: 532539 (2016)
known as an adaptogen for treatment of fatigue and
weakness in the traditional herbal medicine (Panossian,
2003; Ishaque et al., 2012).
A search in with keywords
Rhodiola rosea,Roserootand Golden root(6 October
2014) demonstrated that there are only three clinical
trials on the beneficial effects of R.rosea. The first clin-
ical trial is aimed at evaluating the beneficial role of R.
rosea in comparison with placebo on shift work nurses.
The second clinical trial evaluates the antidepressant
effect of R.rosea in comparison with the antidepres-
sant, sertraline, in patients who suffered from major
depressive disorder. The last clinical trial examines
the beneficial effects of R.rosea in comparison with
ginseng and placebo in patients who suffered from mild
depression. Details of clinical trials on R.rosea are pre-
sented in Table 1.
At present, scientific reports regarding the adverse
effects of R.rosea are negligible (Adaptogen, 2001;
Ming et al., 2005). However, it has been reported
that the median lethal dose (LD
)forR.rosea ex-
tract is 3360 mg/kg body weight in rat (Khanum
et al., 2005). Therefore, it can be concluded that
equivalent dosage in a 70-kg man is about 235.2 g,
which represents a very high amount of extract.
The safety of daily consumption of R.rosea in
humans (at doses 200 to 600 mg per day) remains
negligible (Udintsev and Schakhov, 1991). It has
also been reported that the consumption of R.rosea
may be associated with hyperactivity, jittery, and/or
agitation (Uyeturk et al., 2013). Consumption of R.
rosea in the first weeks can interfere with sleep
and/or induce extra-vivid dreams in consumers
(Hartwich, 2010). Additionally, R.rosea should not
be consumed in patients who suffer from bipolar
disorder, because of its potent antidepressant activ-
ity that can trigger a manic episode (Gerbarg
et al., 2014).
Oxidative stress
Rhodiola rosea is composed of large tuberous roots
composed of several active compounds including pheno-
lics, flavonoids, and phenylpropanoids (Devasagayam
et al., 2004). The oligomeric proanthocyanidin
(OPCRR), a kind of phenolics, have demonstrated po-
tent antioxidant activity (Hernández-Santana et al.,
2014). One study evaluated the effects of OPCRR on
the antioxidant enzymes activity and lipid peroxide con-
tent in vivo. In particular, three biochemical biomarkers
were evaluated, including SOD, glutathione peroxidase
(GSH-Px), and malondialdehyde (MDA) in serum,
heart, liver, and brain tissues in mice. The data showed
that OPCRR significantly increased SOD and GSH-Px
activities,while reducing the MDA content inmice (Zhou
et al., 2014). The data suggests indicated that OPCRR is a
potent natural antioxidant because of its considerable an-
tioxidant activities both in vitro and in vivo.
The activation of microglia is a major feature in the patho-
genesis of AD (McGeer and McGeer, 1999). Several stud-
ies have demonstrated that activated microglia can
produce significant quantities of inflammatory mediators
capable of releasing large amounts of ROS, nitric oxide
(NO), and proinflammatory cytokines such as TNF-α,
interleukin-1β(IL-1β), and interleukin-6 (IL-6), culminat-
ing in neuronal cell death (Gonzalez-Scarano and Baltuch,
1999). Therefore, drugs with antiinflammatory properties
represent a promising therapeutic strategy for the treat-
ment of AD. NO is the main mediator of neuroinflamma-
tion. Lee et al. (2013) investigated the neuroprotective
effect of R.rosea constituents on the NO production after
the activation of murine microglial BV2 cells by lipopoly-
saccharides. The study showed that the R.rosea constitu-
ents, rosarin, and salidroside suppressed the generation of
NO in activated microglia in a dose-dependent manner.
The expression of inducible nitric oxide synthase (iNOS)
was heavily increased by LPS leading to increased pro-
duction of TNF-α. The study also showed that rosarian
and salidroside can inhibit LPS-induced iNOS expression
and decreased the production of TNF-α,IL-1β, and IL-6
that are induced by LPS in BV2 microglia cells in a
Table 1. Details of our search in with keywords Rhodiola rosea,Roserootand Golden root
NCT number Study start Study type Condition Title
NCT01278992 January 2011 Interventional Fatigue Rhodiola rosea for Mental and Physical Fatigue
NCT01098318 June 2010 Interventional Depression Rhodiola rosea Therapy of Major Depressive Disorder
NCT01006460 November 2009 Interventional Depression, stress A Study With Arctic Root Compared With the Extract When
Combined With Schizandra and Russian Root (Adapt 232),
Standardized Ginseng Extract and Placebo Regarding Impact
on the Level of Energy, Ability to Work Under Stress, Quality
of Life and Wellbeing, in Middleaged Women Who Are Still
Copyright © 2016 John Wiley & Sons, Ltd. Phytother. Res. 30: 532539 (2016)
dose-dependent manner (Lee et al., 2013). TNF-α,which
potentiates damage to neuronal cell, is a costimulator that
is thought to be mediated in the regulation of iNOS gene,
via the mitogen-activated protein kinase (MAPK) and
NF-κB signaling pathway (Gautron et al., 2002). The
study further showed that oral administration of R.rosea
extract significantly decreased iNOS and proinflamma-
tory cytokine expression in the kidney and prefrontal cor-
tex of the brain (Lee et al., 2013). This suggests that R.
rosea constituents can cross the bloodbrain barrier and
enter the brain to suppress inflammation in the CNS.
R.rosea constituents have been shown to suppress L-Glu-
induced excitotoxicity in vitro in primary cortical neurons
in vitro. More specifically, rosin and salidroside prevented
neuronal toxicity following 18-h exposure with L-glu at
pathophysiological concentrations as evidenced by the
lactate dehydrogenase assay (Lee et al., 2013).
Effect on oncogenic kinase PAK1
Salidroside, one of the major ingredients in R.rosea,has
beenshowntoactivate5AMP-activated protein
kinase (AMPK) (Li et al., 2008). Similarly, R.rosea
extract (1025 μg/ml) has been shown to promote life
span in Caenorhabditis elegans by activating FOXO.
This longevity transcription factor can activate the heat
shock protein, HSP16. As AMPK is necessary for
activation of FOXO, the life extension properties of R.
rosea extract are most likely attributed to salidroside
(Wiegant et al., 2009). Moreover, salidroside has also been
shown to attenuate tumor-induced angiogenesis, which is
dependent on both PAK1 and AMPK. It is well
established that activation AMPK alone cannot amelio-
rate angiogenesis (Skopińska-Rózewska et al., 2008).
Taken together, these studies suggest that salidroside
can exert neuroprotection by inhibiting PAK1 and
activating AMPK.
Other effects against neurodegeneration
In AD brain, a strong correlation association between
neurotoxicity and MAPK activation, has been reported
in dystrophic neurons and astroglial cells (Webster
et al., 2006). MAPK cascades, which are involved in the
apoptotic signal transduction, are induced by neurotox-
icity. It is thought that activation of JNK and p38 MAPK
is closely associated with cytotoxic insult, whereas the
activation of extracellular signal-regulated kinase
(ERK) is associated with cell proliferation and acts as
an anti-apoptotic signal (Junttila et al., 2008). One study
showed that the R.rosea constituents, rosarin, and
salidroside can inhibit L-glu-induced JNK and p38
MAPK but not ERK phosphorylation (Lee et al., 2013).
In this paper, we critically reviewed the available litera-
tures regarding the neuroprotective effects of the medic-
inal plant R.rosea L., against oxidative stress,
neuroinflammation, PAK1, and AD. Taken together,
current research using R.rosea has been shown to pos-
sess both preventive and/or protective effects in AD
Figure 3. Schematic representation of the neuroprotective effects of Rhodiola rosea L. Current research using R.rosea has been shown to
possess both preventive and/or protective effects in AD through the suppression of oxidative and nitrosative stress, reduction of
excitotoxicity, altered intracellular signaling, antiinflammatory effects, and upregulation of endogenous antioxidant enzymes in neuronal
Copyright © 2016 John Wiley & Sons, Ltd. Phytother. Res. 30: 532539 (2016)
through the suppression of oxidative and nitrosative
stress in neuronal tissues (Fig. 3). In addition, we
showed that R.rosea is a non-toxic medicinal plant even
at high doses with limited interaction with other drugs.
Henceforth, R.rosea can be suggested as a potential
candidate for future clinical trials aimed at examining
the beneficial role of R.rosea in AD patients. R.rosea
can easily be cultivated in some European countries
and propagates by seedling propagation. However,
there are few clinical trials on the beneficial role of R.
rosea in humans, and therefore, it can be difficult to
make a clear decision about its most effective clinical
doses. Respect to negligible adverse effects of R.rosea,
it can be recommended that future studies should aim to
(1) ascertain the best method for large-scale cultivation
of R.rosea, (2) elucidate the exact molecular mechanisms
of neuroprotective effects of R.rosea, (3) identify the
neuroprotective constituents of R.rosea using new phyto-
chemical analysis techniques, (4) ascertain the most effec-
tive clinical doses of R.rosea, and (5) examine the
neuroprotective activities of R.rosea through clinical
Conflict of Interest
The authors disclose no conflict of interest.
Adamczak A, Gryszczyńska A, Buchwald W. 2014. Biometric and
phytochemical variability of roseroot (Rhodiola rosea L.) from
field cultivation. Herba Pol. 60:717.
Adaptogen APP. 2001. Rhodiola rosea: a possible plant adaptogen.
Altern Med Rev 6: 293302.
Alm T. 2004. Ethnobotany of Rhodiola rosea (Crassulaceae) in
Norway. SIDA, Contrib. Bot. 321344.
Ansari MA, Scheff SW. 2010. Oxidative stress in the progression
of Alzheimer disease in the frontal cortex. J Neuropath Exp
Neur 69: 155167.
Berchtold NC, Cotman CW. 1998. Evolution in the conceptualiza-
tion of dementia and Alzheimers disease: Greco-Roman period
to the 1960s. Neurobiol Aging 19: 173189.
Birks J. 2006. Cholinesterase inhibitors for Alzheimers disease
(review). Cochrane Database Syst Rev 1: CD005593.
Brown RP, Gerbarg PL, Ramazanov Z. 2002. Rhodiola rosea:a
phytomedicinal overview. Herbalgram 56:4052.
Butterfield DA, Kanski J. 2001. Brain protein oxidation in age-
related neurodegenerative disorders that are associated with
aggregated proteins. Mech Ageing Dev 122: 945962.
Choi DY, Lee YJ, Hong JT, Lee HJ. 2012. Antioxidant properties of
natural polyphenols and their therapeutic potentials for
Alzheimers disease. Brain Res Bull 87: 144153.
Collingridge GL, Lester RA. 1989. Excitatory amino acid recep-
tors in the vertebrate central nervous system. Pharmacol
Rev 41:143210.
Cropley M, Banks AP, Boyle J. 2015. The effects of Rhodiola rosea
L. extract on anxiety, stress, cognition and other mood symp-
toms. Phytother Res. DOI:10.1002/ptr.5486.
De Bock K, Eijnde BO, Ramaekers M, Hespel P. 2004. Acute
Rhodiola rosea intake can improve endurance exercise perfor-
mance. Int J Sport Nutr Exerc Metab 14: 298307.
Devasagayam TP, Tilak JC, Boloor KK, Sane KS, Ghaskadbi SS,
Lele RD. 2004. Free radicals and antioxidants in human health:
current status and future prospects. J Assoc Physicians India
52: 794804.
Feng Y, Wang X. 2012. Antioxidant therapies for Alzheimers dis-
ease. Oxid Med Cell Longev 2012: 472932.
Fiala JC, Spacek J, Harris KM. 2002. Dendritic spine pathology:
cause or consequence of neurological disorders? Brain Res
Brain Res Rev 39:2954.
Furmanowa M, Oledzka H, Michalska M, Sokolnicka I, Radomska
D. 1995. Rhodiola rosea L.(Roseroot): In vitro regeneration
and the biological activity of roots. In Medicinal and Aromatic
Plants VIII. Springer: Berlin, Germany; 412426.
Galambosi B. 2006. Demand and availability of Rhodiola rosea raw
material. Frontis 17: 223236.
Galambosi B, Galambosi Z, Uusitalo M, Heinonen A. 2009. Effects
of plant sex on the biomass production and secondary metab-
olites in roseroot (Rhodiola rosea L.) from the aspect of cultiva-
tion. Z Arznei-Gewurzpfla 14:114121.
Galasko DR, Peskind E, Clark CM, et al. 2012. Antioxidants for
Alzheimer disease: a randomized clinical trial with cerebrospi-
nal fluid biomarker measures. Arch Neurol 69: 836841.
Gautron L, Lafon P,Chaigniau M, Tramu G, LayeS. 2002. Spatiotem-
poral analysis of signal transducer and activator of transcription
3 activation in rat brain astrocytes and pituitaryfollowing periph-
eral immune challenge. Neuroscience 112:717729.
Gerbarg PL, Illig PA, Brown RP. 2014. Rhodiola rosea 10 in Psychi-
atric and Medical Practice. Rhodiola rosea. CRC Press: Boca
Raton, USA; 225.
Gibbs RB, Aggarwal P. 1998. Estrogen and basal forebrain cholin-
ergic neurons: implications for brain aging and Alzheimers
disease-related cognitive decline. Horm Behav 34:98111.
Goldstein MS, Chen CW, Mammone T, Gan DC. 2008. Cosmetic
compositions and methods comprising Rhodiola rosea. Google
Gonzalez-Scarano F, Baltuch G. 1999. Microglia as mediators of in-
flammatory and degenerative diseases. Ann Rev Neurosci 22:
Griffin WST, Stanley LC, Ling C, et al. 1989. Brain Interleukin-1 and
S-100 immunoreactivity are elevated in down syndrome and
Alzheimer-disease. Proc Natl Acad Sci U S A 86: 76117615.
Hartwich M. 2010. The importance of immunological studies on
Rhodiola rosea in the new effective and safe herbal drug dis-
covery. Centr Eur J Immunol 35: 263266.
Hayashi ML, Choi SY, Rao BS, Jung HY, Lee HK, Zhang D. 2004.
Altered cortical synaptic morphology and impaired memory
consolidation in forebrain-specific dominant-negative PAK
transgenic mice. Neuron 42: 773787.
Hensley K. 2010. Neuroinflammation in Alzheimers disease:
mechanisms, pathologic consequences, and potential for ther-
apeutic manipulation. J Alzheimers Dis 21:114.
Hernández-Santana A, Pérez-López V, Zubeldia JM, Jiménez-del-Rio
M. 2014. A Rhodiola rosea root extract protects skeletal muscle
cells against chemically induced oxidative stress by modulating
heat shock protein 70 (HSP70) expression. Phytother Res
Ishaque S, Shamseer L, Bukutu C, Vohra S. 2012. Rhodiola rosea
for physical and mental fatigue: a systematic review. BMC
Complement Altern Med 12: 70.
Jeong HJ, Ryu YB, Park SJ, et al. 2009. Neuraminidase inhibitory
activities of flavonols isolated from Rhodiola rosea roots and
their in vitro anti-influenza viral activities. Bioorg Med Chem
17: 68166823.
Junttila MR, Li SP, Westermarck J. 2008. Phosphatase-mediated
crosstalk between MAPK signalling pathways in the regulation
of cell survival. FASEB J 22: 954965.
Khanum F, Bawa AS, Singh B. 2005. Rhodiola rosea: a versatile
adaptogen. Compr Rev Food Sci Food Saf 4:5562.
Kichina JV, Goc A, Al-HuseinB, Somanath PR, Kandel ES. 2010. PAK1
as a therapeutic target. Expert Opin Ther Targets 14: 703725.
Kucinskaite A, Pobłocka-Olech L, Krauze-Baranowska M,
Sznitowska M, Savickas A, Briedis V. 2006. Evaluation of bio-
logically active compounds in roots and rhizomes of Rhodiola
rosea L. cultivated in Lithuania. Medicina 43: 487494.
Kurkin V, Zapesochnaya G, Dubichev A, Vorontsov E,
Aleksandrova I, Panova R. 1991. Phenylpropanoids of a callus
culture of Rhodiola rosea.Chem Nat Comp 27: 419425.
Kylin M 2010. Genetic diversity of roseroot (Rhodiola rosea L.)
from Sweden, Greenland and Faroe Islands.
Copyright © 2016 John Wiley & Sons, Ltd. Phytother. Res. 30: 532539 (2016)
Lee Y, Jung JC, Jang S, et al. 2013. Anti-inflammatory and neuro-
protective effects of constituents isolated from Rhodiola
rosea. Evid Based Compl Alt 2013: 514049.
Li HB, Ge YK, Zheng XX, Zhang L. 2008. Salidroside stimulated
glucose uptake in skeletal muscle cells by activating AMP-
activated protein kinase. Eur J Pharmacol 588: 165169.
Li H, Sze S, Tong Y, Ng T. 2009. Production of Th1-and Th2-
dependent cytokines induced by the Chinese medicine herb,
Rhodiola algida, on human peripheral blood monocytes. J
Ethnopharmacol 123: 257266.
Lindsay J et al. 2002. Risk factors for Alzheimers disease: a
prospective analysis from the Canadian Study of Health and
Aging. Am J Epidemiol 156: 445453.
Linné CV. 2005. 1749. Materia Medica. Liber I. de Plantis.:
Stockholm: Laurentius Salvius; 168.
Ma G, Li W, Dou D, et al. 2006. Rhodiolosides AE, monoterpene gly-
cosides from Rhodiola rosea.Chem Pharm Bull 54: 12291233.
Mamedov N, Gardner Z, Craker LE. 2005. Medicinal plants used in
Russia and Central Asia for the treatment of selected skin con-
ditions. J Herbs Spices Med Plants 11: 191222.
Maruta H. 2014. Herbal therapeutics that block the oncogenic ki-
nase PAK1: a practical approach towards PAK1-dependent
diseases and longevity. Phytother Res 28: 656672.
McGeer EG, McGeer PL. 1999. Brain inflammation in Alzheimer
disease and the therapeutic implications. Curr Pharm Des 5:
Mecocci P, Polidori MC. 2012. Antioxidant clinical trials in mild
cognitive impairment and Alzheimers disease. Biochim
Biophys Acta 1822: 631638.
Ming DS, Hillhouse BJ, Guns ES, et al. 2005. Bioactive compounds
from Rhodiola rosea (Crassulaceae). Phytother Res 19:740743.
Montine TJ, Montine KS, McMahan W, Markesbery WR, Quinn JF,
Morrow JD. 2005. F2-isoprostanes in Alzheimer and other neu-
rodegenerative diseases. Antioxid Redox Signal 7:269275.
Nabavi SF, Nabavi SM, Mirzaei M, Moghaddam AH. 2012a. Protec-
tive effect of quercetin against sodium fluoride induced oxida-
tive stress in rats heart. Food Funct 3: 437441.
Nabavi SF, Nabavi SM, Moghaddam AH, Naqinezhad A, Bigdellou
R, Mohammadzadeh S. 2012b. Protective effects of Allium
paradoxum against gentamicin-induced nephrotoxicity in
mice. Food Funct 3:2829.
Nabavi SF, Nabavi SM, Ebrahimzadeh MA, Jafari N, Yazdanpanah
S. 2013a. Biological activities of freshwater algae, Spirogyra
singularis Nordstedt. J Aquat Food Prod Technol 22:5865.
Nabavi SF et al. 2013b. Hepatoprotective effect of gallic acid iso-
lated from Peltiphyllum peltatum against sodium fluoride-
induced oxidative stress. Ind Crops Prod 44:5055.
Nabavi SF, Daglia M, Moghaddam AH, Habtemariam S, Nabavi
SM. 2014. Curcumin and liver disease: from chemistry to
medicine. Compr Rev Food Sci Food Safe 13:6277.
Nabavi SF, Dean O, Turner A, Sureda A, Daglia M, Nabavi S. 2015a.
Oxidative stress and post-stroke depression: possible therapeu-
tic role of polyphe nols? Curr Med Chem 22(3): 343351.
Nabavi SF, Habtemariam S, Daglia M, Shafighi N, Barber A, Nabavi
S. 2015b. Anthocyanins as a potential therapy for diabetic ret-
inopathy. Curr Med Chem 22(1): 5158.
Nabavi SM, Marchese A, Izadi M, Curti V, Daglia M, Nabavi SF.
2015c. Plants belonging to the genus Thymus as antibacterial
agents: From farm to pharmacy. Food Chem 173: 339347.
Nabavi SF, Russo GL, Daglia M, Nabavi SM. 2015d. Role of quer-
cetin as an alternative for obesity treatment: you are what
you eat!. Food Chem 179: 305310.
Olney JW, Ho OL, Rhee V. 1971. Cytotoxic effects of acidic and
sulphur containing amino acids on the infant mouse central
nervous system. Exp Brain Res 14:6176.
Panossian AG. 2003. Adaptogens: tonic herbs for fatigue and
stress. Altern Complement Ther 9: 327331.
Panossian A, Wikman G, Sarris J. 2010. Rosenroot (Rhodiola
rosea): traditional use, chemical composition, pharmacology
and clinical efficacy. Phytomedicine 17: 481493.
Patel RP, Moellering D, Murphy-Ullrich J, Jo H, Beckman JS,
Darley-Usmar VM. 2000. Cell signaling by reactive nitrogen
and oxygen species in atherosclerosis. Free Radic Biol Med
28: 17801794.
Platikanov S, Evstatieva L. 2008. Introduction of wild golden root
(Rhodiola rosea L.) as a potential economic crop in Bulgaria.
Econ Bot 62: 621627.
Pratico D, Sung S. 2004. Lipid peroxidation and oxidative imbal-
ance: early functional events in Alzheimers disease. J
Alzheimers Dis 6: 171175.
Praticò D, Lee VMY, Trojanowski JQ, Rokach J, Fitzgerald GA.
1998. Increased F2-isoprostanes in Alzheimers disease: evi-
dence for enhanced lipid peroxidation in vivo. FASEB J 12:
Ramakers GJ. 2002. Rho proteins, mental retardation and the cel-
lular basis of cognition. Trends Neurosci 25: 191199.
Reitz C, Brayne C, Mayeux R. 2011. Epidemiology of Alzheimer
disease. Nat Rev Neurol 7: 137152.
Rogers J, Lubernarod J, Styren SD, Civin WH. 1988. Expression of
immune system-associated antigens by cells of the human
central nervous-systemrelationship to the pathology of
alzheimers-disease. Neurobiol Aging 9: 339349.
Rohloff J. 2002. Volatiles from rhizomes of Rhodiola rosea L. Phy-
tochemistry 59: 655661.
Sandberg F, Bohlin L. 1993. Fytoterapi: växtbaserade läkemedel.
Hälsokostrådet: Stockholm.
Skopińska-Rózewska E, Malinowski M, Wasiutyński A. 2008. The
influence of Rhodiola quadrifida 50% hydro-alcoholic extract
and salidroside on tumor-induced angiogenesis in mice. Pol J
Vet Sci 11:97104.
Stadtman ER, Berlett BS. 1997. Reactive oxygen-mediated protein
oxidation in aging and disease. Chem Res Toxicol 10:485494.
Tolonen A, Uusitalo J. 2004. Fast screening method for the analy-
sis of total flavonoid content in plants and foodstuffs by high-
performance liquid chromatography/electrospray ionization
time-of-flight mass spectrometry with polarity switching.
Rapid Commun Mass Spectrom 18:31133122.
Tolonen A, Pakonen M, Hohtola A, Jalonen J. 2003. Phenylpropanoid
glycosides from Rhodiola rosea.Chem Pharm Bull 51: 467470.
Toyokuni S. 1999. Reactive oxygen species-induced molecular dam-
age and its application in pathology. Pathol Int 49:91102.
Troshchenko A, Kutikova G. 1967. Rhodioloside from Rhodiola
rosea and Rh.quadrifida.I.Chem Nat Comp 3: 204207.
Udintsev SN, Schakhov VP. 1991. Decrease of cyclophosphamide
haematotoxicity by Rhodiola rosea root extract in mice with
Ehrlich and Lewis transplantable tumours. Eur J Cancer Clin
Oncol 27: 1182.
Uyeturk U, Terzi EH, Gucuk A, Kemahli E, Ozturk H, Tosun M.
2013. Prevention of torsion-induced testicular injury by
Rhodiola rosea.Urology 82: 254. e251254. e256.
Van Diermen D, Marston A, Bravo J, Reist M, Carrupt PA,
Hostettmann K. 2009. Monoamine oxidase inhibition by
Rhodiola rosea L. roots. J Ethnopharmacol 122: 397401.
Webster B et al. 2006. Astroglial activation of extracellular-
regulated kinase in early stages of Alzheimer disease. J
Neuropath Exp Neur 65: 142151.
Wiedenfeld H, Dumaa M, Malinowski M, Furmanowa M,
Narantuya S. 2007. Phytochemical and analytical studies of
extracts from Rhodiola rosea and Rhodiola quadrifida.
Pharmazie 62: 308311.
Wiegant FA, Surinova S, Ytsma E. 2009. Plant adaptogens in-
crease lifespan and stress resistance in C.elegans.
Biogerontology 10:2742.
Yankner BA. 1996. Mechanisms of neuronal degeneration in
Alzheimers disease. Neuron 16: 921932.
Yu BP. 1994. Cellular defenses against damage from reactive oxy-
gen species. Physiol Rev 74: 139162.
Zhao L, Ma QL, Calon F, Harris-White ME, Yang F, Lim GP. 2006.
Role of p21-activated kinase pathway defects in the cognitive
deficits of Alzheimer disease. Nat Neurosci 9: 234242.
Zhou Q, Yin ZP, Ma L, Zhao W, Hao HW, Li HL. 2014. Free radical-
scavenging activities of oligomeric proanthocyanidin from
Rhodiola rosea L. and its antioxidant effects in vivo. Nat Prod
Res 28: 23012303.
Zhu C, Guan F, Wang C, Jin LH. 2014. The protective effects of
Rhodiola crenulata extracts on Drosophila melanogaster gut
immunity induced by bacteria and SDS toxicity. Phytother
Res 28: 18611866.
Copyright © 2016 John Wiley & Sons, Ltd. Phytother. Res. 30: 532539 (2016)
... Rhodiola rosea (also named "roseroot" or "golden root"), primarily growing in the sandy soil in high-altitude regions of Asia, Europe and Northern Hemisphere, such as Altai Mountains, Iceland, British Isles, has been widely used [11]. In addition to R. rosea, there are over 95 species in the genus Rhodiola and 20 of them have been reported to produce the medicinal effects [12]. ...
... R. rosea improves the physiological functionalities of the central nervous system, cardiovascular system, endocrine system, and reproductive system [13]. Of note, R. rosea relieves fatigue and weakness subsequent to intense physical and psychological stress, enhances learning and memory function, cognition, endurance performance, athletic ability, as well as mood disorders and mental fatigue [11,13]. Also eminent is that R. rosea can produce immune-enhancing, anti-oxidant, and anti-inflammatory effects and suppress the proliferation of cancer cells [14]. ...
Full-text available
Among the vast resources of traditional Chinese medicine (TCM) herbal species, only a handful of Chinese herbs are growing in frigid regions or extreme environment but they have a unique property. The most recognizable TCM herb falling in this category is Panax ginseng, which is widely considered the representative tonic herb with oceans of beneficial effects on human health. In this article, we will introduce several typical Chinese herbal medicines with beneficial effects aiming to arouse broader attention from the scientific community to expand the exploration and exploitation on this for their potential applications to meet the increasingly demanding medical needs.
... Schizophrenia is represented by a series of hallucinations, usually triggered by acoustic stimuli as voices or noises, and patients have thinking, talking and social issues, uncapable of decision making (Dominguez et al, 2013). The Alzheimer's disease is a neurodegenerative disorder with unknown aetiology, where first symptoms observed at people younger than 65-70 years old are correlated with dementia-like family history (Nabavi et al, 2016). ...
... Thymus vulgaris essential oils involves phenols like thymols, carvacrol, cinnamon, and pinene, that could have inhibitory activity on acetylcholinesterase and, therefore, prevent Alzheimer's disease. Garlic, Hypericum perforatum, and rosemary are also known for their neuroprotective actions (Nabavi et al, 2016). ...
Full-text available
Background. Nowadays' society becomes increasingly interested in plant-based alternatives in order to treat various diseases. Humans worldwide are diagnosed with neuropsychiatric disorders like epilepsy, autism, Alzheimer's disease, Parkinson's disease, or ADHD (attention deficit hyperactivity disorder) and, consequently, research has been done in order to analyse different plant extracts' effects in their treatment, considering the various side effects conventional drugs could have. Judging by the neuroanatomical similarities to the human body and due to the advantages it has as experimental purpose animal, zebrafish (Danio rerio) has been preferred throughout the past years in the detriment of mammalian animal models. Objectives. This study aims to analyse the specialized literature regarding the benefits of phytotherapy in neuropsychiatric disorders treatment, using the zebrafish as animal model. Methods. This systematic analysis involved search engines like PubMed, Zfin, Semantic Scholar, Microsoft Academic, Scite and BASE (Bielefeld Academic Search Engine). Publications from 1960-2021 were used only, and reviews, conference articles or video/audio information were not selected in order to avoid redundancy, while journal articles were preferred. Different key words combinations were used to collect the articles related to the subject of interest. Results. Analysing the collected data, it can be concluded that zebrafish is increasingly used in behavioural, toxicological, or genetical research as descriptive or experimental model. Also, there is an expanding interest in using this species to investigate phytotherapy's benefits in neuropsychiatric disorders treatment.
... Natural products are a rich source of chemical substances for human beings, especially plants with good medicinal value that have been utilized since ancient times. Rhodiola rosea is a high altitude plant with a wide range of antioxidant, anti-fatigue, and anti-aging activities [2,21]. SAL is a unique chemical constituent of Rhodiola rosea that exerts a plethora of pharmacological effects, particularly on neurological disorders including depression, Parkinson's disease, and Alzheimer's disease [1,3,22,23]. ...
Full-text available
Objective Salidroside (SAL) is a marker glycoside of Rhodiola rosea with significant antioxidant, anti-inflammatory, and other health benefits. In this study, we determined its neuroprotective effects against Cd-induced toxicity in cultured cells and mice. Materials and methods GL261 cell and Cd-intoxicated mouse model were used. ICP-MS and MWM were performed to measure Cd content and Cd-induced cognitive impairment in mice, respectively. Results SAL attenuated Cd toxicity in GL261 cells as well as protected mice from substantial organic damage and cognitive deficits. SAL treatment alleviated Cd-induced oxidative stress, glial cell activation, and elevation of pro-inflammatory factors including TNF-α, IL-1β, and IL-6. Cd-induced cognitive deficits observed in the Morris water maze in mice were rescued by SAL. At the mechanistic level, SAL maintained the activity of antioxidant enzymes such as SOD and GSH-Px in the serum and brain, and scavenged the peroxidation product MDA, thereby restoring redox homeostasis in vivo, attenuating neuronal damage, and ultimately antagonized Cd-induced toxicity. Furthermore, Cd activated the RIP1-driven inflammatory signaling pathway and Notch/HES-1 signaling axis in the brain, leading to inflammation and neuronal loss, which could be attenuated by SAL. Conclusion SAL is a natural product with good anti-Cd effects, indicating that Rhodiola rosea is promising plant that is worthy of cultivation for health and economic benefits.
... Nonetheless, in vitro and in vivo studies are limited, with most data deriving from observational studies. These plants include Commiphora wightii, Tinospora cordifolia, Hypericum perforatum, Rhodiola rosea, Moringa oleifera, Convolvolus pluricaulis, Hericium erinaceus, Camellia sinensis, and others [174][175][176][177][178][179]. Similarly, there are also neuroprotective natural products that could be obtained from food. ...
Full-text available
Alzheimer’s disease (AD) is an age-related, progressive neurodegenerative disorder characterized by impaired cognition, memory loss, and altered personality. Many of the available pharmaceutical treatments do not alter the onset of disease progression. Recently, alternatives to developed drug candidates have been explored including medicinal plants and herbal treatments for the treatment of AD. This article examines the role of herbal plant extracts and the neuroprotective effects as alternative modes of intervention for AD progression. These extracts contain key metabolites that culminate alterations in AD progression. The traditional plant extracts explored in this article induce a variety of beneficial properties, including antioxidants, anti-inflammatory, and enhanced cognition, while also inducing activity on AD drug targets such as Aβ degradation. While these neuroprotective aspects for AD are relatively recent, there is great potential in the drug discovery aspect of these plant extracts for future use in AD treatment.
... Glycosylation is one of the most common modifications in natural product biosynthesis, influencing the chemical properties and bioactivities of natural products (McArthur and Chen, 2016;Vasudevan and Lee, 2020). Cinnamyl alcohol mono-and diglycosides known as rosavins (rosin, rosavin and rosarin) are the characteristic ingredients of Rhodiola rosea L., an important medicinal plant widely used throughout Europe, Asia, and North America, which has been recognized as a botanical adaptogen and documented by European Medicines Agency (Nabavi et al., 2016;Tao et al., 2019). Clinical trials of R. rosea extract have reported positive efficacy on fatigue, depression, mountain sickness, and cardiovascular disease (Hung et al., 2011;Dimpfel et al., 2018;Tao et al., 2019). ...
Phytochemicals are rich resources for pharmaceutical and nutraceutical agents. A key challenge of accessing these precious compounds can present significant bottlenecks for development. The cinnamyl alcohol disaccharides also known as rosavins are the major bioactive ingredients of the notable medicinal plant Rhodiola rosea L. Cinnamyl-(6′-O-β-xylopyranosyl)-O-β-glucopyranoside (rosavin E) is a natural rosavin analogue with the arabinopyranose unit being replaced by its diastereomer xylose, which was only isolated in minute quantity from R. rosea. Herein, we described the de novo production of rosavin E in Escherichia coli. The 1,6-glucosyltransferase CaUGT3 was engineered into a xylosyltransferase converting cinnamyl alcohol monoglucoside (rosin) into rosavin E by replacing the residue T145 with valine. The enzyme activity was further elevated 2.9 times by adding the mutation N375Q. The synthesis of rosavin E from glucose was achieved with a titer of 92.9 mg/L by combining the variant CaUGT3T145V/N375Q, the UDP-xylose synthase from Sinorhizobium meliloti 1021 (SmUXS) and enzymes for rosin biosynthesis into a phenylalanine overproducing E. coli strain. The production of rosavin E was further elevated by co-overexpressing UDP-xylose synthase from Arabidopsis thaliana (AtUXS3) and SmUXS, and the titer in a 5 L bioreactor with fed-batch fermentation reached 782.0 mg/L. This work represents an excellent example of producing a natural product with a disaccharide chain by glycosyltransferase engineering and artificial pathway construction.
COVID-19 infection causes complications, even in people who have had a mild course of the disease. The most dangerous seem to be neurological ailments: anxiety, depression, mixed anxiety–depressive (MAD) syndromes, and irreversible dementia. These conditions can negatively affect the respiratory system, circulatory system, and heart functioning. We believe that phytotherapy can be helpful in all of these conditions. Clinical trials confirm this possibility. The work presents plant materials (Valeriana officinalis, Melissa officinalis, Passiflora incarnata, Piper methysticum, Humulus lupulus, Ballota nigra, Hypericum perforatum, Rhodiola rosea, Lavandula officinalis, Paullinia cupana, Ginkgo biloba, Murraya koenigii, Crataegus monogyna and oxyacantha, Hedera helix, Polygala senega, Pelargonium sidoides, Lichen islandicus, Plantago lanceolata) and their dominant compounds (valeranon, valtrat, apigenin, citronellal, isovitexin, isoorientin, methysticin, humulone, farnesene, acteoside, hypericin, hyperforin, biapigenin, rosavidin, salidroside, linalool acetate, linalool, caffeine, ginkgolide, bilobalide, mihanimbine, epicatechin, hederacoside C,α-hederine, presegenin, umkaline, 6,7,8-trixydroxybenzopyranone disulfate, fumaroprotocetric acid, protolichesteric acid, aucubin, acteoside) responsible for their activity. It also shows the possibility of reducing post-COVID-19 neurological, respiratory, and cardiovascular complications, which can affect the functioning of the nervous system.
Medicinal plants have always been prescribed around the world with therapeutic purposes for various diseases and disorders related to their profile of biologically active substances and health-promoting effects. Meantime, Rhodiola rosea has been of particular importance among physicians, researchers and the general public. Accordingly, the present perspective aimed to explore the beneficial effects of this plant by focusing on in vitro and in vivo studies, and nutritional effects. The current work also provides a comprehensive analysis of the Rhodiola rosea studies in the literature throughout a quantitative literature research analysis approach. The literature search was carried out by means of the Scopus database to retrieve Rhodiola rosea-related publications. VOSviewer software (v.1.6.16, 2020) was used to extract and elaborate bibliometric data. 958 publications ranging from 1966 to 2021 were given by the literature search. Technological prospecting for patents was also assessed.
Pharmacological treatment of Parkinson’s disease consists of a combined chemotherapy that mostly relies on levodopa (L-DOPA) administration together with inhibitors of dopa-decarboxylase (DDC), monoamine oxidase (MAO) and catechol-methyltransferase (COMT). Identification of inhibitors specifically targeting these enzymes is still a significative part of the development of new alternative antiparkinsonian drugs. Most of the available methods use measurement of enzymatic reactions through radioactive labeling, antibody-recognized products or coupled enzymatic assays. Mass spectrometry (MS) represents an interesting alternative approach as it allows direct and specific detection and quantification of enzymatic reactions. We describe the development of a simple, reliable, label-free assay based on high-resolution mass spectrometry (HRMS) for the detection and relative quantification of three different enzymatic reactions using non-isolated enzymes. The assay was applied both to reference drugs and plant crude extracts. This method can be used to detect hits in extracts libraries as well as determine relative IC50 of inhibitors.
In the past few years, emerging evidence established persistent oxidative stress to be a key player in the pathogenesis of polycystic ovary syndrome (PCOS). Particularly, it damages the function of granulosa cells, and thus hinders the development of follicles. The present study aimed to explore and establish the protective effects of salidroside on dihydrotestosterone (DHT)‐induced Granulosa‐like tumor cell line (KGN), mediated via antioxidant mechanisms. The study assessed the positive effects of salidroside on DHT‐induced apoptosis, reactive oxygen species (ROS) accumulation, damage of antioxidant capacity, and mitochondrial membrane potential depolarization. Interestingly, salidroside partly reversed DHT mediated effects, via stimulation of nuclear factor erythroid 2‐related factor 2 (Nrf2) signaling pathway and the downstream antioxidant proteins heme oxygenase‐1(HO‐1) and quinine oxidoreductase 1(NQO1). Additionally, the knockdown of Nrf2 partly moderated the antioxidant and anti-apoptosis effects of salidroside in DHT-treated KGN cells. Mechanistically, AMP‐activated protein kinase (AMPK) was identified to be the upstream signaling involved in salidroside‐induced Nrf2 activation, as silencing of AMPK partly prevented the upregulation of Nrf2 and the downstream proteins HO‐1 and NQO1. Altogether, the present study is the first to effectively demonstrate the inhibitory effect of salidroside on DHT‐stimulated oxidative stress and apoptosis in KGN cells, which was dependent on Nrf2 activation that involved AMPK.
Methodological approaches to the analysis of biologically active compounds in rhizomes and roots of Rhodiola rosea L. are substantiated. An HPLC method for quantitative determination of rosavin and salidroside, the predominant and diagnostically significant biologically active compounds in raw material of this plant, was developed. The content of rosavin in rhizomes and roots of R. rosea varied from 1.17 ± 0.04% to 1.41 ± 0.06%; of salidroside, from 1.63 ± 0.05% to 2.88 ± 0.12%, respectively. Statistical processing of the results indicated that the relative error of the mean content of rosavin and salidroside was less than ±5.0% with confidence probability 95%.
Full-text available
This trial evaluated the impact of a Rhodiola rosea L. extract on self-reported anxiety, stress, cognition, and other mood symptoms. Eighty mildly anxious participants were randomized into two different groups of either Rhodiola rosea L (2 × 200 mg dose Vitano®, 1 tablet taken before breakfast and 1tablet before lunch) or a control condition (no treatment). Self-report measures and cognitive tests were completed at four testing sessions over a period of 14 days. Relative to the controls, the experimental group demonstrated a significant reduction in self-reported, anxiety, stress, anger, confusion and depression at 14 days and a significant improvements in total mood. No relevant differences in cognitive performance between the groups were observed. Rhodiola rosea L (Vitano®) presented a favourable safety tolerability profile. Although this was a non-placebo controlled trial, it is unlikely that the findings were the result of placebo effects as changes appeared gradual and were specific to certain psychological measures. However, we cannot determine a causal relationship; further investigations are recommended to support the effects of Rhodiola rosea L. extract on stress related symptoms. Copyright © 2015 John Wiley & Sons, Ltd.
Full-text available
Roseroot (Rhodiola rosea L.) is a dioecious perennial, but little is known about the differences between the sexes. The objectives of this field experiment were to study the variations of growth parameters and concentrations of the main pharmacological metabolites between male and female plants in generatively propagated populations. In addition, we evaluated 12-year-old mother plants. Field experiments were carried out in Mikkeli, Finland (61°44'N, 27°18' E), during 1997-2007. The plants were propagated from seed and grown in black plastic mulch. Ten male and ten female plants were chosen randomly from five accessions at the age of four years. Root length, weight, rhizome diameter and weight were measured. The contents of salidroside, cinnamyl alcohol, rosavin, rosavin isomers and tyrosol were analysed from the rhizomes. The 12-year-old mother plants were evaluated similarly. The male plants had better vegetative features: they were larger and heavier, and the roots were longer than those of the female plants. The total fresh root weights of the male plants ranged from 677 g to 992 g, those of the female plants were 18-20% less. The salidroside content of the rhizomes ranged from 0.239% to 0.749% and the total content of rosavins from : 0.932% to 1.629%, with no significant differences being detected between male and female plants. The average total fresh root weight of the 12-year old plants was 2.314 kg/plant. The rhizomes of the old plants contained a significant proportion of dead tissue of lower quality. No dead tissue was observed in the rhizomes of the four-year: old plants. According to the results, the contents of the active metabolites are at quite similar levels in males and females and the seed-propagated population can produce j raw material of high quality.
Altered dendritic spines are characteristic of traumatized or diseased brain. Two general categories of spine pathology can be distinguished: pathologies of distribution and pathologies of ultrastructure. Pathologies of spine distribution affect many spines along the dendrites of a neuron and include altered spine numbers, distorted spine shapes, and abnormal loci of spine origin on the neuron. Pathologies of spine ultrastructure involve distortion of subcellular organelles within dendritic spines. Spine distributions are altered on mature neurons following traumatic lesions, and in progressive neurodegeneration involving substantial neuronal loss such as in Alzheimer's disease and in Creutzfeldt-Jakob disease. Similarly, spine distributions are altered in the developing brain following malnutrition, alcohol or toxin exposure, infection, and in a large number of genetic disorders that result in mental retardation, such as Down's and fragile-X syndromes. An important question is whether altered dendritic spines are the intrinsic cause of the accompanying neurological disturbances. The data suggest that many categories of spine pathology may result not from intrinsic pathologies of the spiny neurons, but from a compensatory response of these neurons to the loss of excitatory input to dendritic spines. More detailed studies are needed to determine the cause of spine pathology in most disorders and relationship between spine pathology and cognitive deficits.
Rhodiola rosea L. Sp. Pl. 1035 (1753), [synonym: Sedum roseum (L.) Scop., Sedum rhodiola DC., incl. R. arctica Boriss. and R. iremelica Boriss.] belongs to the family Crassulaceae, subfamily Sedoideae (Engler 1964). It is a perennial with a thick rhizome, fragrant when cut, bearing persistent flowering stems with alternate leaves and flowers in terminal cymes. Petals are free, with eight stamens, four carpels, follicles are reddish, 2n = 22. It is distributed in Europe and in most mountains of central Europe, southwards to the Pyrenees, central Italy, and Bulgaria. In Flora Europea (Webb 1964), besides Rhodiola rosea L., a second species, Rhodiola quadrifida (Pallas) Fischer a.C.A. Meyer, Enum. Pl. Nov. 1: 69(1851), growing in NE Russia and N Asia, is described.
Rhodiola rosea is a widespread species in Norway. It is well known in Norwegian folk tradition, with a variety of vernacular names, of which many reflect its traditional uses. Past use as a cure for scurvy in cattle may explain names with the prefix kalv- ("calf"). Its widespread use as a hair wash is also reflected in vernacular names. In the past, Rhodiola was planted on turf roofs to protect them from fire, i.e. as an apotropaic (supposedly averting evil forces); this tradition is documented as early as the 13th century.
Rhodiola rosea (roseroot, golden root) is the best known alpine-arctic medicinal plant species of the Family Crassulaceae, growing in Asia, Europe and North America. The rhizomes of this plant contain tonic, phytoadaptogen, antidepressant, anti-inflammatory, antitumor, anticancer, antiviral, anti-AD agents and are recommended to apply in many complementary therapies. Rhodiola rosea is used in the traditional folk incl. Chinese medicine (known as Hongjingtian) and further studied in the Institute of Traditional Chinese Medicine at the China Academy of Traditional Chinese Medicine (Beijing, China). Many actually "excellent- advertised!?" commercial dietary supplements consisting of R. rosea pulverized rhizomes/extracts/constituents are to order and buy via Internet and also in many drugstories world-wide. The genetic diversity of the roseroot (great number of clones) demonstrated directly in the unstable quantitative production of the biologically active compounds, and potentially therefore also with dose-dependent differences in the immunological responses between aqueous and dried hydroalcoholic extracts of R. rosea or in the comparison of R. rosea with other Rhodiola sp. rhizomes have been shown and discussed in this review. The studies suggest to inform and warn the European Medicines Agency and the all self-medicated patients, especially with serious illnesses e.g. cancer, about the risks and danger for the health, and life by the use of any R. rosea products. The standardized, effective, and safe, pesticides-/contaminates-/microorganisms-free EU-/EMA-controlled R. rosea drug/drugs should be elaborated and sale only in drugstories. In my opinion, the sale of the R. rosea/potential all "pseudo-herbal" dietary supplements in Internet should be officially prohibited by EMA as soon as possible.
In the present study, the possible protective effects of gallic acid isolated from Peltiphyllum peltatum against sodium fluoride (NaF)-induced hepatotoxicity and oxidative stress were evaluated. Rats were intoxicated with 600. ppm NaF through drinking water for one week. Gallic acid (10 and 20. mg/kg) and the positive control, silymarin (10. mg/kg) were administrated for seven days prior to NaF intoxication. 24. h after the treatment period, superoxide dismutase and catalase activities, lipid peroxidation and reduced glutathione levels were measured in the liver. Serum biochemical markers including: alanine transaminase, aspartate aminotransferase, alkaline phosphatase, lipase and α-amylase activities and triglyceride, cholesterol, glucose, total bilirubin, direct bilirubin, total protein and albumin levels were determined. The results demonstrated that pretreatment with gallic acid normalized the sodium fluoride-induced alterations in serum parameters and oxidative stress in hepatic tissue. Fluoride intoxication resulted in an increased level of thiobarbituric acid reactive substances (TBARS) (53.05 ± 2.23. nmol MDA equiv./g tissue) in the liver homogenates in comparison with control group (25.03 ± 1.27. nmol MDA equiv./g tissue). Pretreatment with gallic acid at 20. mg/kg demonstrated significant mitigation in TBARS level (33.95 ± 2.51. nmol MDA equiv./g tissues). Fluoride intoxication did also suppress the superoxide dismutase and catalase activity of hepatic tissue homogenates by 33.87% and 66.87%, respectively. Treatment with gallic acid resulted in a dose-dependent mitigation of the fluoride-mediated suppression of antioxidant enzymes. In conclusion, gallic acid prevented the NaF-induced abnormalities in the serum and hepatic biochemical markers.