ArticlePDF Available

Curcumin, an Active Component of Turmeric (Curcuma longa), and Its Effects on Health

Taylor & Francis
Critical Reviews In Food Science and Nutrition
Authors:
  • Erzurum Technical University

Abstract and Figures

Turmeric (Curcuma Longa) is a type of herb belonging to ginger family, which is widely grown in southern and south western tropical Asia region. Turmeric, which has an importance place in the cuisines of Iran, Malesia, India, China, Polynesia and Thailand, is often used as spice and has an effect on the nature, color and taste of foods. Turmeric is also known to have been used for centuries in India and China for the medical treatments of such illnesses as dermatologic diseases, infection, stress and depression. Turmeric's effects on health generally are centered upon an orange-yellow colored, lipophilic polyphenol substance called 'curcumin', which is acquired from the rhizomes of the herb. Curcumin is known recently to have antioxidant, anti-inflammatory, anti-cancer effects and, thanks to these effects, to have an important role in prevention and treatment of various illnesses ranging notably from cancer to autoimmune, neurological, cardiovascular diseases and diabetic. Furthermore, it is aimed to increase the biological activity and physiological effects of the curcumin on the body by synthesizing curcumin analogues. This paper reviews the history, chemical and physical features, analogues, metabolites, mechanisms of its physiological activities and effects on health of curcumin.
Content may be subject to copyright.
Full Terms & Conditions of access and use can be found at
http://www.tandfonline.com/action/journalInformation?journalCode=bfsn20
Critical Reviews in Food Science and Nutrition
ISSN: 1040-8398 (Print) 1549-7852 (Online) Journal homepage: http://www.tandfonline.com/loi/bfsn20
Curcumin, an active component of turmeric
(Curcuma longa), and its effects on health
Betül Kocaadam & Nevin Şanlier
To cite this article: Betül Kocaadam & Nevin Şanlier (2017) Curcumin, an active component of
turmeric (Curcuma longa), and its effects on health, Critical Reviews in Food Science and Nutrition,
57:13, 2889-2895, DOI: 10.1080/10408398.2015.1077195
To link to this article: https://doi.org/10.1080/10408398.2015.1077195
Accepted author version posted online: 03
Nov 2015.
Published online: 03 Nov 2015.
Submit your article to this journal
Article views: 2124
View related articles
View Crossmark data
Citing articles: 15 View citing articles
Curcumin, an active component of turmeric (Curcuma longa), and its effects on health
Bet
ul Kocaadam and Nevin ¸Sanlier
Faculty of Health Sciences, Nutrition and Dietetics Department, Gazi University, Ankara, Turkey
ABSTRACT
Turmeric (Curcuma longa) is a type of herb belonging to ginger family, which is widely grown in southern
and south western tropical Asia region. Turmeric, which has an importance place in the cuisines of Iran,
Malesia, India, China, Polynesia, and Thailand, is often used as spice and has an effect on the nature, color,
and taste of foods. Turmeric is also known to have been used for centuries in India and China for the
medical treatments of illnesses such as dermatologic diseases, infection, stress, and depression. Turmerics
effects on health are generally centered upon an orange-yellow colored, lipophilic polyphenol substance
called curcumin,which is acquired from the rhizomes of the herb. Curcumin is known recently to have
antioxidant, anti-inammatory, anticancer effects and, thanks to these effects, to have an important role in
prevention and treatment of various illnesses ranging notably from cancer to autoimmune, neurological,
cardiovascular diseases, and diabetic. Furthermore, it is aimed to increase the biological activity and
physiological effects of the curcumin on the body by synthesizing curcumin analogues. This article reviews
the history, chemical and physical features, analogues, metabolites, mechanisms of its physiological
activities, and effects on health of curcumin.
KEYWORDS
Turmeric; curcumin; health;
safety
Introduction
Turmeric is acquired from Curcuma long L., a tuberous herba-
ceous perennial plant with yellow owers and wide leaves,
which is a member of ginger family and grows in tropical cli-
mate (Akpolat et al., 2010; Prasad et al., 2014). Unlike cinna-
mon, turmeric has not any different kinds. On the other hand,
geographical conditions of the region where it grows and the
features of its soil may affect the growth, nutrition composition,
and quality of this plant (Hossain and Ishimine, 2005; Haya-
kawa et al., 2011). While this plant is rather an important spice
in Iran, it is also an important component of curries to which it
gives the yellow color in Malesia, India, China, Polynesia, and
Thailand, and the mustard and sauces in the West (Gupta
et al., 2013a). Turmeric is also used to add avor and color to
rice, pasta, meat and vegetable dishes, and salads.
It is stated that turmeric has been widely used for medical
treatments of various diseases for at least 2500 years in Asian
countries mostly (Gupta et al., 2013a) and it has many benets
for prevention and treatment of many diseases in Ayurveda
and traditional Chinese medicine (Deogade and Ghate, 2015).
The importance of turmeric in medical treatment primarily
stems from orange-yellow colored curcumin, the most active
component. Curcumin is a lipophilic polyphenol substance
(Jurenka, 2009), which constitutes the 25% of turmeric
powder (Deogade and Ghate, 2015).
With the studies about curcumin, it has been determined
that the chemical structure of this polyphenol substance shows
antioxidant, antimicrobial, anti-inammatory, antiangiogenic,
antimutagenic, and antiplatelet aggregation properties (Patil
et al., 2009; Shehzad et al., 2013; Prasad et al., 2014; Deogade
and Ghate, 2015). It is stated that, thanks to this properties,
curcumin has a protective and preventive effect against various
diseases such as cancer, autoimmune, neurological, metabolic,
lung, liver, and cardiovascular diseases (CVDs) (Gupta et al.,
2013b; Prasad et al., 2014).
Recently, substantial importance has been put on polyphe-
nol substances due to their effects on various degenerative dis-
eases, especially cancer (Sohrab et al., 2013). Examination of
the effects of curcumin on health, which is also a polyphenol
substance, is highly signicant.
Curcumin and its historical process
Curcumin was dened as substance that gives the yellow
colorby Vogel and Pelletier about 200 years ago. In 1842, it
was purely acquired by Vogel Jr. In the mid-1900, curcumin
was stated to be a biologically active component, to have
antibacterial property, and therefore, to be effective against
Staphylococcus aureus, Salmonella paratyphi, Mycobacterium
tuberculosis, and Trichophyton gypseum types. In 1953,
Srinivasan determined the existence of other components called
curcuminoids as well as curcumin with the analysis of turmeric
through chromatography (Patil et al., 2009; Prasad et al., 2014;
Deogade and Ghate, 2015).
Later, curcumin was said to have a cholesterol-lowering,
antidiabetic, anti-inammatory, and antioxidant properties and
CONTACT Nevin ¸Sanlier, Professor nevintekgul@gmail.com Gazi University, Faculty of Health Sciences, Nutrition and Dietetics Department, Emniyet Mahallesi,
Muammer Ya¸s ar BostancıCaddesi, No:16, 06500 Be¸sevler/Ankara, Turkey.
Color versions of one or more of the gures in the article can be found online at www.tandfonline.com/bfsn.
© 2017 Taylor & Francis Group, LLC
CRITICAL REVIEWS IN FOOD SCIENCE AND NUTRITION
2017, VOL. 57, NO. 13, 28892895
http://dx.doi.org/10.1080/10408398.2015.1077195
to have an anticancer activity in both in vitro and in vivo mod-
els. Then, with the clinical studies conducted with humans, it
was determined that curcumin was safe and effective. Food and
Drug Administration (FDA) conrmed curcumin as a com-
pound generally recognized as safe(Patil et al., 2009; Prasad
et al., 2014).
Chemical and physical characteristic of curcumin
The compound of turmeric contains carbohydrate (69.4%),
protein (6.3%), fat (5.1%), mineral (3.5%), and moisture
(13.1%) (Prasad et al., 2014). The essence of turmeric roots,
pulverized by drying, also contains curcuminoids consisting of
curcumin components. Curcuminoids consist of curcumin
(77%), demethoxycurcumin (DMC; 17%), and bidemethoxy-
curcumin (BDMC; 3%) (Goel et al., 2008). It is stated that even
if studies focus on curcumin, other curcuminoid components
also have biological activities (Shehzad et al., 2010).
Chemical denotation of curcumin is 1,7-bis-(4-hydroxy-3-
methoxyphenyl)-hepta-1,6-diene-3,5-dione or dipheruloylme-
thane; while its chemical formula is C
21
H
20
O
6
(Fig. 1) (Deogade
and Ghate, 2015; Pubchem Open Chemistry Data Base, 2015).
Curcumin is not soluble in water at acidic and neutral pH.
However, it is soluble in acetone, methanol, and ethanol (Goel
et al., 2008; Jurenka, 2009). It is stated that curcumin is sensi-
tive to light and, therefore, it is recommended that biological
samples containing curcumin are to be protected from light
(Prasad et al., 2014).
Curcumins natural, synthetic analogues and
metabolites
Due to its insufcient absorption by the body, high metabolism
speed, and high elimination from the body, curcumin has a
limited bioavailability in the body. The low bioavailability of
curcumin limits signicantly the therapeutics effects of this
component (Devassy et al., 2015). Now, new methods have
been developed to increase the bioavailability of curcumin. One
of these methods is to use piperine with curcumin. It has been
shown that piperine increases the bioavailability of curcumin
on humans and rats by decreasing glucuronidation of curcumin
(Aggarwal and Harikumar, 2009). Use of liposomal curcumin,
curcumin nanoparticles, and phospholipid complexes are
among other methods. Besides, it is stated that use of structural
analogues of curcumin also increases bioavailability (Shehzad
et al., 2010; Devassy et al., 2015).
It is stated that DMC and BDMC, natural analogues of cur-
cumin, have biological activity like curcumin. A study has
found that inammatory transcription factor nuclear factor
kappaB (NF-kB) suppression of curcumin is much more effec-
tive than others (curcumin >DMC >BDMC). It is thought
that this result may stem from the important role of methoxy
groups on the phenyl ring of curcumin (Sandur et al., 2007).
DMC and BDMC have been determined to suppress Inos
and COX-2, which are NF-kB onset inammatory molecules
(Guo et al., 2008). Curcumin and DMC have been shown to be
effective for decreasing AGEs-originated reactive oxygen types
(ROS) in mesangial cells curcumin and DMC have also been
determined to increase signicantly the advanced glycosylation
end products (AGEs) decreasing superoxide dismutase activity
and malondialdehyde component in the surface of cell culture.
It is also stated that these two components provide protection
against AGEs-originated apoptosis, and due to these effects,
they may provide protection against diabetic neuropathy (Liu
et al., 2012).
There are many metabolites of curcumin such as dihydro-
curcumin, tetrahydrocurcumin (THC), octahydrocurcumin
(OHC), hexahydrocurcumin (HHC), curcumin glucuronide,
and curcumin sulfate (Prasad et al., 2014). After many
researches on curcumin metabolites, it has been determined
that THC shows antioxidant (Murugan and Pari, 2006), anti-
inammatory (Lai et al., 2011), and anticancer (Wu et al.,
2011) effects; that HHC has anticancer (Srimuangwong et al.,
2012), antioxidant and anti-inammatory (Li et al., 2012), and
platelet aggregation epistasis (Dong et al., 2012) properties; that
OHC has anti-inammatory and antioxidant effects (Somparn
et al., 2007; Prasad et al., 2014).
Furthermore, synthetic derivatives of curcumin can be
acquired with such chemical modications as phenolic
hydroxyl groups, acylation, alkylation, glycosylation, and
amino acylation (Prasad et al., 2014).
Biological activities and molecular targets of curcumin
and related diseases
In ancient times, curcumin appeared in the Ayurveda medical
treatment methods applied in India, used in treatment of inju-
ries, skin diseases, eye infections, ambustions, and acne
(Hatcher et al., 2008). Curcumin is also an important compo-
nent of traditional treatment methods called Jiawei-Xiaoyao in
China, and it has been used for the treatment of various dis-
eases like dyspepsia, stress, and depression for thousands of
years (Qin et al., 2009). In the last 30 years, curcumin was
shown to have a therapeutic effect against cancer, autoimmune
diseases, metabolic diseases, neurological diseases, CVDs, lung
diseases, liver diseases, and a variety of other inammatory dis-
eases (Aggarwal and Harikumar, 2009; Kannappan et al., 2011).
Curcumin is thought to be effective on pathogenesis of
molecular targets with the purpose of prevention and treatment
of diseases. It is stated that the modulation of these molecular
targets that have a role in the formation process of the disease
can be achieved. It has been proven, for instance, that tumor
development can be suppressed by suppressing cancer cell sig-
nal pathway (Devassy et al., 2015). Curcumin, with its polyphe-
nol structure, is shown to be able to effectively modulate
Figure 1. Chemical structure of curcumin.
2890 B. KOCAADAM AND N. ¸SANLIER
molecular targets that have a role in the pathogenesis of many
diseases (Fig. 2). Curcumin has been determined to play an
important role regulating cytokines, kinases, enzymes, tran-
scription factors, growth factors, receptors, metastatic, and apo-
ptotic molecules in almost all phases of the development of
many diseases (Shehzad and Lee, 2010; Baliga et al., 2012; Pra-
sad et al., 2014). The fact that its structure is inclined to high-
level methoxylation and low-level hydrogenation and gives cur-
cumin a property that increases free radicals scavenging activ-
ity. It is stated that this structure probably enables curcumin to
have an anticancer, anti-inammatory, and antioxidant effect
(Devassy et al., 2015)(Fig. 2).
Anticancer effect
Even curcumin has already been shown to have a positive effect
against many diseases; its effect against cancer is the most
under-researched topic (Devassy et al., 2015). Curcumin has
been found to be effective in many phases of cancer develop-
ment, to suppress transformation, beginning, development and
invasion of tumor, angiogenesis, and metastasis. Curcumin has
been determined to suppress the growth of tumor cells via cell
proliferation pathway (cyclin D1, c-myc), cell survival pathway
(Bcl-2, Bcl-xL, cFLIP, XIAP, and cIAP1), caspase activation
pathway (caspase ¡8, ¡3, and ¡9), tumor suppressor pathway
(p53, p21), death receptor pathway (DR4, DR5), and many cell
signal pathways that contain protein kinase pathway (c-Jun
N-terminal kinases (JNK), protein kinase B (PKB), also known
as Akt, and 50adenosine monophosphate-activated protein
kinase (AMPK)) (Ravindran et al., 2009). It is stated that,
thanks to these effects of curcumin, it is effective for decreasing
or preventing various cancer types including multiple myeloma
and colon, pancreas, breast, prostates, and lung cancers (Anand
et al., 2008; Devassy et al., 2015). It is also stated that curcumin
increases the effectiveness of radiotherapy and thus, it may
open a quicker path to treatment (Akpolat et al., 2010).
In a study dealing with monocarbonyl analogue of B63
acquired through some chemical modications of curcumins
structure, this component has been shown to have a higher
antiproliferative effect than curcumin on colon cancer cells. At
the same time, with the use of less B63 (50 mg/kg B63, 100 mg/
kg curcumin), suppression of tumor growth has been achieved
like curcumin (Zheng et al., 2014).
Anti-inammatory and antioxidant effects
Curcumin has been determined to be an anti-inammatory and
antioxidant agent (Deogade and Ghate, 2015). It is thought that
curcumin has these properties due to hydroxyl and methoxy
groups (Rahman and Biswas, 2009). Curcumin enables negative
regulation of proinammatory interleukins (IL-1, ¡2, ¡6, ¡8,
and ¡12), cytokines (tumor necrosis factor-alpha (TNF-a),
monocyte chemoattractant protein-1) by causing down-regula-
tion of janus kinase and signal transducer and activator of tran-
scription (JAK/STAT) signaling pathway. It is also stated that
curcumin regulates the inammatory response by down-regu-
lating enzymes of inducible nitric oxide synthase (iNOS), cyclo-
oxygenase-2 (COX-2), lipoxygenase, and xanthine oxidase
activity; and thus, it may cause to suppress activation of NF-kB
(Rahman and Biswas, 2009).
Curcumin is stated to show its effectiveness by inhibiting
inammatory cell proliferation, metastasis, and angiogenesis
through various molecular targets (Shehzad et al., 2013). Large-
scale studies have shown that inammation changes the signal
pathways; and thus it is related to the increase of inammatory
biomarkers, lipid peroxides, and free radicals. Acute and chron-
ical inammation is an important risk factor for cardiovascular,
neurodegenerative, and metabolic diseases, obesity, type 2
Figure 2. Related molecular targets and diseases of curcumin.
CRITICAL REVIEWS IN FOOD SCIENCE AND NUTRITION 2891
diabetes, and some cancer types (Dantzer et al., 2008; Medzhi-
tov, 2008). Curcumin is stated to be effective for the treatment
of various inammatory diseases such as obesity, diabetes,
CVDs, neurological diseases, and inammatory bowel disease
(IBD) (Shehzad et al., 2013; Prasad et al., 2014; Deogade and
Ghate, 2015).
Curcumin exhibits strong antioxidant effect through free-
radical-scavenging activity (Deogade and Ghate, 2015). Even
though curcumin shows antioxidant effect, in order to increase
its antioxidant capacity, analogues of curcumin are focused on.
Dolai et al. (2011) showed that the synthetic sugar analogue of
curcumin is a stronger antioxidant. It has been determined that
while curcumin suppresses tau peptides aggregation and amy-
loid-bat micromolar concentrations, sugar-curcumin conju-
gate shows suppressing effect for this aggregation even in
nanomolar levels.
Cardiovascular diseases
Inammation has been determined to play a great role in devel-
opment of cardiovascular diseases (CVD). Curcumin treatment
is stated to have an anti-inammatory effect against CVD, by
means of various mechanisms. Curcumin is stated to enable
HO-1 expression by actuating Nrf2-dependent antioxidant
response element. It is also stated that curcumin suppress
TNF-ain vascular and aortic smooth muscle cells; and that it
increases p21 expression through HO-1 (Pae et al., 2007;
Wongcharoen and Phrommintikul, 2009). Curcumin treatment
on animals has been determined to decrease ischemia through
activation of JAK2/STAT3 signal pathway (Duan et al., 2012).
In a study done on rats, it has been proven that applying
50 mg/kg curcumin to rats with salt-sensitivity and hyperten-
sive heart disease develops systolic function and prevents coro-
nary failure (Morimoto et al., 2008). In a study on the
effectiveness of curcumin on cardiovascular risk factors in indi-
viduals with coronary artery disease, it has been determined
that serum triglyceride, LDL and VLDL cholesterol levels
decrease considerably in the group of individuals taking curcu-
min. Even though effects of curcumin on blood lipid prole
have been proven, no considerable effect has been determined
on inammatory markers (Mirzabeigia et al., 2015). In a study
conducted in Turkey, the consumption prevalence of plant-
based alternative treatments and supplementary foods of indi-
viduals with CVDs was researched; and it was found out that
turmeric is one of the most popular herbal foods. Also, hyper-
tension and hyperlipidemia are found to be the most important
reasons for patients to use alternative products (
_
Ipek et al.,
2013).
Diabetes mellitus
Diabetes mellitus is a health problem affecting liver, heart,
brain, and kidneys. It has been determined that inammation
is the primary cause of type II diabetes development and that
various inammatory cytokines, transcription factors, and
enzymes have an important role in the outset and progression
of diabetes (Choudhary et al., 2011; Shehzad et al., 2013).
Ghorbani et al. (2014) pointed out that curcumin has proper-
ties such as decreasing hepatic glucose production, suppressing
inammatory response stemming from hyperglycemia, increas-
ing GLUT2, GLUT3, and GLUT4 gene expression, increasing
glucose intake of cells, and activating AMPK; and thus, that it
may decrease blood glucose decreasing insulin resistance. They
also stated that, for these reasons, curcumin has an increasing
effect on antihyperglycemic and insulin sensitivity.
One study conducted on type 2 diabetic KK-Ay mice found
that curcumin suppresses the increase in blood glucose level via
peroxisome proliferator-activated receptor-gamma (PPAR-g)
activation (Kuroda et al., 2005). Studies have been conducted
on derivatives of curcumin with the aim of increasing the anti-
diabetic effect of curcumin. For instance, as a result of a study
researching whether a new curcumin derivative (NCD),
acquired by covalent modication of curcumin molecule,
shows hypoglycemic effect on diabetic rats, it has been proven
that NCD decreases plasma glucose level at the rate of 27.5%,
and that it increases plasma insulin up to 66.67%. It is stated
that NCD shows this effect by inducing HO-1 gene (Aziz et al.,
2012; Aziz et al., 2013).
Obesity
Curcumin has been shown to suppress mitogen-activated
protein kinase (MAPK, extracellular signal-regulated kinases
(ERK), JNK, and p38), which is associated with differentiation
of 3T3-L1 cells into adipocytes and activates Wnt/b-catenin
signaling in differentiated adipocytes., which are closely related
to obesity (Ahn et al., 2010). It is stated that curcumin decreases
the macrophage inltration, leptin, and leptin receptor level
(Ob-R) in the white adipose tissue; that it increases the adipo-
nectin expression in inammation-related obesity. It is pointed
out that the adiponectin production, which increases due to
effect of curcumin, may have a positive effect against obesity by
decreasing NF-kB activity (Shehzad et al., 2011).
Inammatory bowel disease
IBD is an immune impairment including Crohn disease and
ulcerative colitis, commonly characterized with digestion sys-
tem chronical inammation (Shehzad et al., 2013). Studies
indicate that curcumin is useful in prevention and treatment of
IBD (Holt et al., 2005; Ali et al., 2012). Curcumin inhibit the
activity of activated protein-1 (AP-1), STAT proteins, PPAR-g,
b-catenin, COX-2, 5-LOX, and iNOS expression which play a
key role in inammation (Taylor and Leonard, 2011). There-
fore, it can reduce colitis. It has been proven that curcumin, at
the same time, suppress TLR4-based NF-kB activation; and
thus, it may be effective for recovery of bowel inammation
(Lubbad et al., 2009; Ali et al., 2012; Baliga et al., 2012).
A pilot study done with Crohn or ulcerative patients by Sus-
kind et al. (2013) indicated that recovery in disease symptoms
is achieved as a result of using curcumin as 500 mg capsules
twice a day during three weeks. Researchers have suggested
that using curcumin as an adjunctive therapy for the individu-
als seeking combination of traditional and alternative treat-
ment. Likewise, Taylor and Leonard (2011) have stated that
curcumin becomes more effective when used with traditional
medicines for the treatment of IBD; and that this combination
is a cheaper alternative method.
Neurodegenerative diseases
Aging is a signicant risk factor for neurodegenerative diseases.
It is considered that curcumin may be effective on aging
2892 B. KOCAADAM AND N. ¸SANLIER
mechanisms; thus, it may prevent the changes in the cell pro-
teins which occur due to aging. Therefore, it is indicated that
curcumin may help to maintain protein homeostasis and it
may be effective for prevention of aging-associated diseases
(Monroy et al., 2013). Besides, curcumin has scavenge oxygen
derived free-radical property; and thus, curcumin is stated to
be a potential neuroprotective agent (Nabiuni et al., 2011).
In neurodegenerative diseases such as Alzheimer character-
ized with inammation and oxidative injury, abnormal protein
development causes such gene mutations as human amyloid
precursor protein or presenile 1 or 2 (Smith et al., 2007). In
Alzheimer disease, curcumin as an antioxidant, anti-inamma-
tory properties can improve the cognitive functions, and also it
is stated to bring various therapeutic benets through decreased
b-amyloid plaques and microglia formation, delayed deteriora-
tion of neurons in patients. (Mishra and Palanivelu, 2008).
Parkinsons disease (PD), one of the most common neuro-
degenerative diseases, is characterized by loss of dopaminergic
neurons in the substantia nigra. The most important biological
effect of curcumin, related to neuroprotection, is its antioxidant
function (Mythri and Srinivas Bharath, 2012). Thus, it protects
substantia nigra neurons, ameliorates dopamine levels in the 6-
OHDA rat model of PD. It is pointed out that curcumin pro-
tects many tyrosine hydroxylase-positive cells in substantia
nigra; and that it maintains the dopamine levels in striatum
probably because of this effect (Zbarsky et al., 2005).
Multiple sclerosis (MS) is a chronic inammatory autoim-
mune disease, characterized with oligodendrocyte in central
nervous system and degradation of myelin sheath. Curcumin
has been shown to inhibit autoimmune diseases by regulating
inammatory cytokines and associated JAK-STAT, AP-1, and
NF-kB signaling pathways (Bright, 2007; Tegenge et al., 2014).
Th17 cells are important factor for the pathophysiological pro-
cess of MS. Curcumin suppresses the differentiation and devel-
opment of Th17 cells through the down-regulation of IL-6,
TGF-b,IL-1b, IL-23, and STAT3-phosphorylation (Xie et al.,
2011). Furthermore, it has been determined that curcumin
inhibits channel Kv1.3, which is mainly effective on T(EM)
cells; and at the same time it suppress the cytokine secretion
and proliferation of T(EM) cells which are isolated from MS
patients (Lian et al., 2013).
Skin diseases
The use of curcumin for treatment of skin diseases dates back
to ancient times. Due to its role in treatment of skin diseases in
India, turmeric is used in production of cream and soap in
Ayurveda, the ancient Indian medical system, turmeric is
widely used as an easy treatment method for eye infections,
treat bites, burns, and acne (Hatcher et al., 2008; Akpolat et al.,
2010).
Now, it is indicated that curcumin may be effective against
various skin diseases such as dermatitis, psoriasis, and sclero-
derma. It is pointed out that psoriasis, a chronical skin disease,
which is characterized with hyperproliferation and abnormal
differentiation of keratinocyte, can be treated by curcumin
(Prasad et al., 2014). Curcumin can protect skin by scavenging
free radicals and reducing inammation through nuclear fac-
tor-kB inhibition and cytokines (Thangapazham et al., 2007). A
study conducted on mice indicates that curcumin diminished
psoriasis-like inammation by reducing cytokines such as IL-
1band IL-6 (Sun et al., 2013).
Allergy and asthma
Allergy and asthma are proinammatory diseases, stemming
from inammatory cytokines (Shehzad et al., 2013). Turmeric
rhizomes have been long used for treatment of allergy and
asthma in Asia, especially in India; for treatment of itching and
other skin diseases in Thailand (Tewtrakul and Subhadhirasa-
kul, 2007; Viswanath and Christy, 2008). Yano et al. (2000)
have indicated that turmeric exhibits antiallergic activity by
suppressing the 48/80-induced histamine release from mast
cells. The hydroxyl groups of curcumin are indicated to
decrease the allergic reactions and to have a positive effect
against asthma by broadening the narrowed air pathway and
increasing the antioxidant capacity (Viswanath and Christy,
2008; Shehzad et al., 2013). Curcumin has been determined to
cause Th2 response down-regulation by decreasing the produc-
tion of IgE antibodies and cytokine, and enabling the formation
of less inammatory response (Viswanath and Christy, 2008).
The safe dosage and toxicology of curcumin
Curcumin has been conrmed as a generally recognized as
safecompound by FDA, and it is stated not to have any toxic
effect. According to Joint FAO/WHO Expert Committee on
Food Additives (JECFA) and European Food Safety Authority
(EFSA) reports, adequate daily intake (ADI) value of curcumin
is 03 mg/kg (JECFA, 2004; EFSA, 2014) Lao et al. (2006)
applied 50012,000 mg curcumin to healthy individuals so as
to examine the maximum tolerance dosage and safety of curcu-
min. As a result, up to 12 g/day intake of curcumin has been
shown to have no harmful effects on individuals. There are
some concerns about the relationship between inhibition of
some enzymes working in drug metabolism, potential DNA
impairment, iron chelation, and curcumin intake. However,
more studies need to be conducted to examine these relation-
ships (Devassy et al., 2015).
Conclusion and suggestions
In conclusion, the effects of curcumin on health are rather
complex as in many other natural products. The results of clini-
cal studies on in vitro, in vivo, and human indicate that curcu-
min may be effective in prevention and treatment of many
diseases, particularly cancer, by affecting various molecular tar-
gets. Safety, active ingredients, interactions, and dosage of the
medicine are highly important in treatment of diseases. For this
reason, the fact that curcumin is a safe natural product and its
cost is lower than drugs may give rise to the thought that curcu-
min can be used in treatment and prevention of diseases.
Because it prevents formation and progression of various dis-
eases, and has positive effects on health, a healthy individual
with a 70 kg body weight can consume 410 g turmeric powder
in accordance with JECFA and EFSAs suggestion that curcu-
mins ADI value should be 03 mg/kg. Oral intake of curcumin
exhibits poor bioavailability, so it limits signicantly the thera-
peutic effects of this component. Other structural analogues of
curcumin are more bioavailable and effective, and they could
CRITICAL REVIEWS IN FOOD SCIENCE AND NUTRITION 2893
be designed as to be combined with large and well-controlled
clinical trials. It will be good to conduct more studies in order
to determine the effectiveness of curcumin, its analogues and
metabolites, interaction of drug-food and drug-nutrient more
rmly; to clarify the other possible biological activities; to
develop suggestions; to provide evidence about its relations
with other diseases.
References
Aggarwal, B. B. and Harikumar, K. B. (2009). Potential therapeutic effects
of curcumin, the anti-inammatory agent, against neurodegenerative,
cardiovascular, pulmonary, metabolic, autoimmune, and neoplastic
diseases. Int J Biochem Cell Biol. 41:4059.
Ahn, J., Lee, H., Kim, S. and Ha, T. (2010). Curcumin-induced suppression
of adipogenic differentiation is accompanied by activation of Wnt/
beta-catenin signaling. Am. J. Physiol. Cell. Physiol. 298:15101516.
Akpolat, M., Tarlada¸calı¸sır, Y., Uz, Y., Metin, M. and Kızılay, G. (2010).
Kanser tedavisinde curcuminin yeri. Yeni Tıp Dergisi 27:142147.
Ali, T., Shakir, F. and Morton, J. (2012). Curcumin and inammatory
bowel disease: Biological mechanisms and clinical implication. Diges-
tion 85:249255.
Anand, P., Sundaram, C., Jhurani, S., Kunnumakkara, A. B. and Aggarwal,
B. B. (2008). Curcumin and cancer: An old-agedisease with an age-
oldsolution. Cancer Lett. 267:133164.
Aziz, M. T., El-Asmar, M. F., El-Ibrashy, I. N., Rezq, A., Al-Malki, A., Was-
sef, M. A., Fouad, H. H., et al. (2012). Effect of novel water soluble cur-
cumin derivative on experimental type-1 diabetes mellitus (short term
study). Diabetology Metab. Synd. 4:30.
Aziz, M. T., El Ibrashy, I. N., Mikhailidis, D. P., Rezq, A. M., Wassef, M. A.,
Fouad, H. H., Ahmet, H. H., et al. (2013). Signaling mechanisms of a
water soluble curcumin derivative in experimental type 1 diabetes with
cardiomyopathy. Diabetol Metab Syndr. 5:13.
Baliga, M. S., Joseph, N., Venkataranganna, M. V., Saxena, A., Ponemone,
V. and Fayad, R. (2012). Curcumin, an active component of turmeric
in the prevention and treatment of ulcerative colitis: Preclinical and
clinical observations. Food Funct 3:11091117.
Bright, J. (2007). Curcumin and autoimmune disease. Adv Exp Med Biol.
595:425451.
Choudhary,S.,Sinha,S.,Zhao,Y.,Banerjee,S.,Sathyanarayana,P.,Shahani,
S., et al. (2011). NF-kB-inducing kinase (NIK) mediates skeletal muscle
insulin resistance: Blockade by adiponectin. Endocrinol. 152:36223627.
Dantzer, R., OConnor, J. C., Freund, G., Johnson, W. and Kelley, W.
(2008). From inammation to sickness and depression: When the
immune system subjugates the brain. Nat. Rev. Neurosci. 9:4656.
Devassy, J., Nwachukwu, I. and Jones, P. (2015). Curcumin and cancer:
Barriers to obtaining a health claim. Nutr. Rev. 73(3):155165.
Deogade, S. and Ghate, S. (2015). Curcumın: Therapeutıc applıcatıons in
systemıc and oral health. Int. J. Biol. Pharm. Res. 6(4):281290.
Dolai, S, Shi, W, Corbo, C, Sun, C, Averick, S, Obeysekera, D, et al. (2011).
Clickedsugar-curcumin conjugate: Modulator of amyloid-beta and
tau peptide aggregation at ultralow concentrations. ACS Chem Neuro-
sci. 2:694699.
Dong, H. P., Yang, R. C., Chunag, I. C., Huang, L. J., Li, H. T., Chen, H. L.
and Chen, C. Y. (2012). Inhibitory effect of hexahydrocurcumin on
human platelet aggregation. Nat. Prod. Commun. 7(7):883884.
Duan, W., Yang, Y., Yan, J., Yu, S., Liu, J., Zhou, J., et al. (2012). The effects
of curcumin post-treatment against myocardial ischemia and reperfu-
sion by activation of the JAK2/STAT3 signaling pathway. Basic Res
Cardiol. 107:263
European Food Safety Authority. (2014). Rened exposure assessment for
curcumin (E 100). EFSA J. 12(10):3876
Ghorbani, Z., Hekmatdoost, A. and Mirmiran, P. (2014). Antihyperglyce-
mic and insulin sensitizer effects of turmeric and its principle constitu-
ent curcumin. Int J Endocrinol Metab. 12(4):e18081.
Guo, L. Y., Cai, X. F., Lee, J. J., Kang, S. S., Shin, E. M., Zhou, H. Y., et al.
(2008). Comparison of suppressive effects of demethoxycurcumin and
bisdemethoxycurcumin on expressions of inammatory mediators in
vitro and in vivo. Arch Pharm Res 31:490496.
Gupta, S. C., Sung, B., Kim, J. H., Prasad, S., Li, S. and Aggarwal, B. B.
(2013a). Multitargeting by turmeric, the golden spice: From kitchen to
clinic. Mol Nutr Food Res. 57(9):15101528.
Gupta, S. C., Kismali, G. and Aggarwal, B. B. (2013b). Curcumin, a compo-
nent of turmeric: From farm to pharmacy. Biofactors. 39(1):213.
Goel, A., Kunnumakkara, A. B. and Aggarwal, B. B. (2008). Curcumin as
curecumin: From kitchen to clinic. Biochem Pharmacol. 75:787809.
Hatcher, H., Planalp, R., Cho, J., Torti, F. M. and Torti, S. V. (2008). Cur-
cumin: From ancient medicine to current clinical trials. Cell Mol Life
Sci. 65:16311652.
Hayakawa, H., Kobayashi, T., Minamiya, Y., Ito, K., Miyazaki, A., Fukuda,
T. and Yamamoto, Y. (2011). Development of a molecular marker to
identify a candidate line of turmeric (Curcuma longa L.) with a high
curcumin content. Am. J. Plant Sci. 2(1):526.
Holt, P., Katz, S. and Kirshoff, R. (2005). Curcumin therapy in inamma-
tory bowel disease: A pilot study. Digest. Dis. Sci. 50(11):21912193.
Hossain, A. and Ishimine, Y. (2005). Growth, yield, and quality of turmeric
(Curcuma longa L.) cultivated on dark-red soil, gray soil, and red soil in
Okinawa, Japan. Plant. Prod. Sci. 8(4):482486.
_
Ipek, E., G
uray, Y., Demirkan, B., G
uray, (., Kafes, H. and Ba¸syi
git, F.
(2013). Kardiyoloji poliklini
gine ba¸svuran hastalarda bitkisel k
okenli
alternatif tedavilerin ve tamamlayıcıbesin (r
unlerinin T
uketim preva-
lansı.Arch Turk Soc Cardiol. 41(3):218224.
JECFA. (2004). Curcumin. (Prepared by Ivan Stankovic). Chemical and
Technical Assessment Compendıum Addendum 11/Fnp 52 Add.11/29;
Monographs 1 Vol.1/417.
Jurenka, J. S. (2009). Anti-inammatory properties of curcumin, a maj
or
constituent of Curcuma longa: A review of preclinical and clinical
research. Altern Med Rev. 14(2):141153.
Kannappan, R., Gupta, S. C., Kim, J. H., Reuter, S. and Aggarwal, B. B.
(2011). Neuroprotection by spice-derived nutraceuticals: You are what
you eat! Mol Neurobiol. 44:142159.
Kuroda, M., Mimaki, Y., Nishiyama, T., Mae, T., Kishida, H., Tsukagawa,
M., Takahashi, K., Kawada, T., Nakagawa, K. and Kitahara, M. (2005).
Hypoglycemic effects of turmeric (Curcuma longa L. rhizomes) on
genetically diabetic KK-Ay mice. Biol Pharm Bull. 28(5):937939.
Lai, C. S., Wu, J. C., Yu, S. F., Badmaev, V., Nagabhushanam, K., Ho, C. T.
and Pan, M. H. (2011). Tetrahydrocurcumin is more effective than cur-
cumin in preventing azoxymethane-induced colon carcinogenesis. Mol
Nutr Food Res. 55:18191828.
Lao, C. D., Rufn, M. T., Normolle, D., Heath, D. D., Murray, S. I., et al.
(2006). Dose escalation of a curcuminoid formulation. BMC. Complem.
Altern. Med. 6:10.
Li, F., Nitteranon, V., Tang, X., Liang, J., Zhang, G., Parkin, K. L. and Hu,
Q. (2012). In vitro antioxidant and anti-inammatory activities of 1-
dehydro-[6]-gingerdione, 6-shogaol, 6-dehydroshogaol and hexahy-
drocurcumin. Food Chem. 135:332337.
Lian, Y. T., Yang, X. F., Wang, Z. H., Yang, Y., Yang, Y., Shu, Y. W., Cheng,
L. X. and Liu, K. (2013). Curcumin serves as a human kv1.3 blocker to
inhibit effector memory T lymphocyte activities. Phytother Res.
27:13211327.
Liu, J. P., Feng, L., Zhu, M. M., Wang, R. S., Zhang, M. H., Hu, S. Y., et al.
(2012). The in vitro protective effects of curcumin and demethoxycur-
cumin in Curcuma longa extract on advanced glycation end products-
induced mesangial cell apoptosis and oxidative stress. Planta Med.
78:17571760.
Lubbad, A., Oriowo, A. and Khan, I. (2009). Curcumin attenuates inam-
mation through inhibition of TLR-4 receptor in experimental colitis.
Mol. Cell. Biochem. 322:127135.
Medzhitov, R. (2008). Origin and physiological roles of inammation.
Nature 454:428435.
Mirzabeigia, P., Mohammadpour, A. H., Salarifar, M., Gholami, K., Mojta-
hedzadeh, M. and Javadi, M. R. (2015). The effect of curcumin on
some of traditional and nontraditional cardiovascular risk factors: A
pilot randomized, double-blind, placebo-controlled trial. Iran. J.
Pharm. Res. 14(2):479486.
Mishra, S. and Palanivelu, K. (2008). The effect of curcumin (turmeric) on
Alzheimers disease: An overview. Ann Indian Acad Neurol. 11(1):1319.
2894 B. KOCAADAM AND N. ¸SANLIER
Morimoto, T., Sunagawa, Y., Kawamura, T., Takaya, T., Wada, H., Naga-
sawa, A., et al. (2008). The dietary compound curcumin inhibits p300
histone acetyltransferase activity and prevents heart failure in rats. J.
Clin. Invest. 118:868878.
Monroy, A., Lithgow, G. J. and Alavez, S. (2013). Curcumin and neurode-
generative diseases. Biofactors. 39(1):122132.
Murugan, P. and Pari, L. (2006). Antioxidant effect of tetrahydrocurcumin
in streptozotocinnicotinamide induced diabetic rats. Life Sciences. 79
(18):17201728.
Mythri, R. B. and Srinivas Bharath, M. M. (2012). Curcumin: A potential
neuroprotective agent in Parkinsonsdisease.Curr. Pharm. Des. 18:9199.
Nabiuni, M., Nazari, Z., Abdolhamid Angaji, S. and Nejad, S. (2011). Neuro-
protective effects of curcumin. Aust.J.BasicAppl.Sci.5(9):22242240.
Pae, O., Jeong, S., Jeong, O., Kim, S., Kim, A., et al. (2007). Roles of heme
oxygenase-1 in curcumin-induced growth inhibition in rat smooth
muscle cells. Exp. Mol. Med. 39:267277.
Patil, P., Jayaprakasha, G. K., Chidambara Murthy, K. N. and Vıkram, A.
(2009). Bioactive compounds: Historical perspectives, opportunities,
and challenges. J. Agric. Food Chem. 57:81428160.
Pubchem Open Chemistry Data Base, Curcumin. (2015). Access Date:
22.07.2015 http://pubchem.ncbi.nlm.nih.gov/compound/curcumin#
sectionDTop
Prasad, S., Gupta, S., Tyagi, A. and Aggarwal, B. (2014). Curcumin, a com-
ponent of golden spice: From bedside to bench and back. Biotechnol.
Adv. 32:10531064.
Qin, F., Huang, X., Zhang, H. M. and Ren, P. (2009). Pharmacokinetic
comparison of puerarin after oral administration of Jiawei-Xiaoyao-
San to healthy volunteers and patients with functional dyspepsia: Inu-
ence of disease state. J. Pharm. Pharmacol. 61:125129.
Rahman, I. and Biswas, S. K. (2009). In Regulation of Inammation, Redox,
and Glucocorticoid Signaling by Dietary Polyphenols, Surh, Y. J., Dong,
Z., Cadenas, E., Packer, L. (Eds.), Boca Raton: CRC Press
Ravindran, J., Prasad, S. and Aggarwal, B. B. (2009). Curcumin and cancer cells:
How many ways can curry kill tumor cells selectively? AAPS J. 11:495510.
Sandur, S. K., Pandey, M. K., Sung, B., Ahn, K. S., Murakami, A., Sethi, G.,
et al. (2007). Curcumin, demethoxycurcumin, bisdemethoxycurcumin,
tetrahydrocurcumin, and turmerones differentially regulate anti-
inammatory and antiproliferative responses through a ROS indepen-
dent mechanism. Carcinogen. 28:17651773.
Shehzad, A., Ha, T., Subhan, F. and Lee, S. (2011). New mechanism and
anti-inammatory role of curcumin in obesity and obesity related met-
abolic disease. Eur. J. Nutr. 50:151161.
Shehzad, A., Khan, S., Shehzad, O. and Lee, Y. S. (2010). Curcumin thera-
peutic promises and bioavailability in colorectal cancer. Drugs Today
46(7):523532.
Shehzad, A. and Lee, Y. S. (2010). Curcumin: Multiple molecular targets medi-
ate multiple pharmacological actions Areview.Drugs Fut. 35:113119.
Shehzad, A., Rehman, G. and Lee, Y. (2013). Curcumin in inammatory
diseases. Int. Union Biochem. Mol. Biology, Inc. 39(1):6977.
Smith, G., Cappai, R. and Barnham, J. (2007). The redox chemistry of the
Alzheimers disease amyloid beta peptide. Biochim. Biophys. Acta.
1768:19761790.
Srimuangwong, K., Tocharus, C., Yoysungnoen Chintana, P., Suksamrarn,
A. and Tocharus, J. (2012). Hexahydrocurcumin enhances inhibitory
effect of 5-uorouracil on HT-29 human colon cancer cells. World J
Gastroenterol. 18:23832389.
Sohrab, G., Hosseinpour-Niazi, S., Hejazi, J., Yuzbashian, E., Mirmiran, P.
and Azizi, F. (2013). Dietary polyphenols and metabolic syndrome
among Iranian adults. Int J Food Sci Nutr. 64(6):661667.
Somparn, P, Phisalaphong, C, Nakornchai, S., Unchern, S. and Morales, N.
P. (2007). Comparative antioxidant activities of curcumin and
its demethoxy and hydrogenated derivatives. Biol Pharm Bull. 30:
7478.
Sun, J., Zhao, Y. and Hu, J. (2013). Curcumin inhibits imiquimod-induced
psoriasis-like inammation by inhibiting IL-1beta and IL-6 production
in mice. PLoS One. 8:e67078.
Suskind, D. L., Wahbeh, G., Burpee, T., Cohen, M., Christie, D. and Weber,
W. (2013). Tolerability of curcumin in pediatric inammatory bowel
disease: A forced-dose titration study. J Pediatr Gastroenterol Nutr.
56:277279.
Taylor, R. A. and Leonard, M. C. (2011). Curcumin for inammatory
bowel disease: A review of human studies. Altern Med Rev. 16:152156.
Tegenge, M. A., Rajbhandari, L., Shrestha, S., Mithal, A., Hosmane, S. and
Venkatesan, A. (2014). Curcumin protects axons from degeneration in
the setting of local neuroinammation. Exp Neurol. 253C:102110.
Tewtrakul, S. and Subhadhirasakul, S. (2007). Antiallergic activity of some
selected plants in the Zingiberaceae family. J. Ethnopharmacol.
109:535538.
Thangapazham, R. L., Sharma, A. and Maheshwari, R. K. (2007). Benecial
role of curcumin in skin diseases. Adv Exp Med Biol. 595:343357.
Viswanath, P. K. and Christy, S. B. (2008). Immunomodulatory effects of
curcumin in allergy. Mol. Nutr. Food Res. 52:10311039.
Wongcharoen, W. and Phrommintikul, A. (2009). The protective role of
curcumin in cardiovascular diseases. Int. J. Cardiol. 133:145151.
Wu, J. C., Lai, C. S., Badmaev, V., Nagabhushanam, K., Ho, C. T. and Pan,
M. H. (2011). Tetrahydrocurcumin, a major metabolite of curcumin,
induced autophagic cell death through coordinative modulation of
PI3K/Akt-mTOR and MAPK signaling pathways in human leukemia
HL-60 cells. Mol Nutr Food Res. 55:16461654.
Xie, L., Li, A X. and Takahara, S. (2011). Curcumin has bright prospects
for the treatment of multiple sclerosis. Int. Immunopharmaco. 11:
323330.
Yano, S., Terai, M., Shimizu, K. L., Futagami, Y., Sekine, T., et al. (2000).
Antiallergic activity of Curcuma longa (II). Features of inhibitory
actions on histamine release from mast cells. Nat. Medicines.
54:325329.
Zbarsky, V., Datla, K. P., Parkar, S., Rai, D. K., Aruoma, O. I. and Dexter,
D. T. (2005). Neuroprotective properties of the natural phenolic antiox-
idants curcumin and naringenin but not quercetin and setin in a 6-
OHDA model of Parkinsons disease. Free Radic Res. 39(10):1119
1125.
Zheng, A, Li, H., Wang, X., Feng, Z., Xu, J. and Cao, K., et al. (2014).
Anticancer effect of a curcumin derivative B63: ROS production and
mitochondrial dysfunction. Current Cancer Drug Targets 14:156166.
CRITICAL REVIEWS IN FOOD SCIENCE AND NUTRITION 2895
... More than a half of them were published in 2014 or later which indicates growing scientific interest in this subject. However, even though curcumin is the most extensively investigated active ingredient of turmeric and is considered as the most potent one, the other curcuminoids also reveal pharmacological activities [21,25,26]. The rhizome also contains other compounds of potential biological importance, including mostly mono-and sesquiterpenoids of volatile oil responsible for the taste and scent of turmeric [27]. ...
... Since then, the numbe focusing on curcumin has increased significantly, and in 2019, the number of m deposited in the Web of Science database was about 18,000 [24]. More than a h were published in 2014 or later which indicates growing scientific interest in However, even though curcumin is the most extensively investigated active in turmeric and is considered as the most potent one, the other curcuminoids pharmacological activities [21,25,26]. The rhizome also contains other compo tential biological importance, including mostly mono-and sesquiterpenoids oil responsible for the taste and scent of turmeric [27]. ...
... As turmeric and its constituents reveal numerous pharmacological activities combined with low toxicity, they have been also extensively investigated as medicinal agents potentially useful in stomatology and in the treatment of conditions localized in mouth. It is noteworthy that according to USA Food and Drug Administration classification, curcumin falls into "generally recognized as safe" (GRAS) category [25]. Because of its centuries-long history as a spice and natural medicine supported with recent findings, it is well-recognized for its antioxidant, anti-inflammatory and chemoprevention potential combined with antimicrobial properties. ...
Article
Full-text available
Turmeric has been known for centuries as a spice and an important element of traditional medicine. Nowadays, plant-derived compounds are still an object of extensive scientific investigations aiming at the development of novel drugs and dosage forms. Turmeric and its most important component, curcumin, reveal numerous interesting biological properties, including antioxidant, anti-inflammatory and antimicrobial activity. Numerous scientific studies focusing on various aspects of the activity of turmeric-derived compounds show that curcuminoids display an enormous potential as active pharmaceutical ingredients useful in a wide spectrum of medical conditions. Oral diseases comprising both mild inflammations and severe life-threatening conditions are classified as the most common ones, affecting an enormous part of the global population. In this review, the current research regarding turmeric and its constituents in oral diseases is summarized and discussed, with special attention paid to novel findings and future directions regarding scientific exploration of curcuminoids.
... The previous studies mentioned that turmeric had long been known for its various medicinal properties, such as antiseptic, antibacterial, and anti-inflammatory, as well as its use in the treatment of digestive disorders, gastric upset, and liver and kidney disease. It stimulates bile production, improving digestion and eliminating toxins from the liver (34,(65)(66)(67)(68). The anti-inflammatory properties of turmeric lowered the production of inflammation-inducing histamine, extending the action of the natural anti-inflammatory adrenal hormone cortisol and finally improving circulation by flushing toxins out of small joints where cellular wastes and inflammatory compounds were trapped. ...
... Turmeric's hepatoprotective properties were primarily due to its antioxidative properties and ability to reduce the formation of proinflammatory cytokines. Turmeric, C. longa, and curcumin were used to treat biliary hyperplasia, fatty changes, and necrosis (30, 34,67). Pomegranate is high in carbohydrates, minerals, crude fiber, and various biologically active compounds such as vitamin C and phenolic compounds such as punicalagin and ellagic acid, known as natural antioxidants (69). ...
Article
Full-text available
Introduction Curcuma longa extract and pomegranate peel extract as homeotherapy have numerous therapeutic uses, mainly for anti-inflammatory, immunomodulatory, and hepatoprotective efficacy. The current study compared ORNIPURAL ® (as a commercial hepatoprotective drug) and a herbal mixture of Curcuma longa extract and pomegranate peel extract [as homeotherapy] in dogs with dexamethasone-induced hepatopathy throughout a 42-day long-term study. Methods The study was conducted on mongrel dogs ( n = 30) throughout three phases of the experiment: an acclimatization phase (14 days), a steroidal-induced hepatopathy phase (14 days), and a treatment phase (14 days, i.e., either with ORNIPURAL® or with herbal mixtures). The investigated dogs undergoing complete clinical and ultrasonographic examinations as well as hematological analysis and serum hepatorenal biomarkers that were estimated in days 0 (control group), 7 (hepatopathy group), 14 (hepatopathy group), 21 (treatment group), and 28 (treatment group). Histopathology of the liver was conducted for some dogs on days 0, 14, and 28 after the euthanization of these animals. Results and conclusion The present study reported the most remarkable efficacy of both ORNIPURAL ® and a herbal mixture of Curcuma longa extract and pomegranate peel extract as hepatoprotective medicaments in the therapy of dexamethasone-induced fatty liver in dogs. Therefore, a 14-day treatment with either a herbal mixture or ORNIPURAL ® in treated dogs (treatment groups) induced an unmistakable improvement in their clinical status, blood pictures, and serum hepatorenal parameters as well as characteristic sonographic and histopathological findings compared with those in dexamethasone-induced hepatic lipidosis (hepatopathy groups). Compared to dogs treated with ORNIPURAL ® , this clinical improvement was more evident in dogs treated with an herbal mixture. Moreover, no significant alterations in blood pictures and serum hepatorenal indices were demonstrated between ORNIPURAL ® and herbal-treated dogs. Overall, the herbal mix of Curcuma longa extract and pomegranate peel extract had higher efficacy and greater potency than conventional therapy that uses ORNIPURAL® in treating dogs with hepatopathy. The study also recommended the parallel use of this herbal mixture as well as ORNIPURAL® in long-term therapeutic strategies in dogs with dexamethasone-induced fatty liver as both minimized dexamethasone side effects. Ultrasonography alone was not enough to evaluate hepatobiliary disorders in canines.
... Historical texts such as the Bencao Gangmu highlight its ability to prevent liver damage, reduce blood pressure and lipid levels, and alleviate pain, showcasing its significant therapeutic potential. Curcumin, the primary active compound in turmeric, is a natural polyphenol known for its effectiveness in treating various ailments (Kocaadam and Şanlier, 2017). Research demonstrates that curcumin can significantly inhibit angiotensin II-induced myocardial fibrosis, both in vivo and in vitro, through the upregulation of PPAR-γ. ...
Article
Full-text available
Cardiovascular disease poses a significant risk to human health and remains the leading cause of illness and death globally, with its incidence continuing to rise. The intricate pathophysiological mechanisms of CVDs include inflammation, oxidative stress, autophagy, and myocardial fibrosis. In light of these underlying mechanisms, traditional Chinese medicine (TCM) and its constituents have demonstrated distinct advantages in managing CVDs. By exerting synergistic effects across multiple components and targets, traditional Chinese medicine can modulate the inflammatory response, mitigate oxidative stress, regulate excessive autophagy, and enhance myocardial fibrosis repair. This article reviews the latest advancements in understanding how TCM compounds regulate signaling pathways involved in the treatment of CVDs.
... Turmeric is a yellow spice derived from the rhizomes of the Curcuma longa L. plant, traditionally utilized in Asian cuisine (Kocaadam and Şanlier 2017). The diverse applications of turmeric involve its utilization in the food industry as a natural coloring agent, flavor enhancer, and spice (Serpa Guerra et al. 2020). ...
Article
Full-text available
Phenolic antioxidants and curcuminoids are biologically important molecules playing a crucial role in combating reactive species under oxidative stress conditions. In this study, microwave‐assisted extraction (MAE) and ultrasound‐assisted extraction (UAE) processes for the extraction of phenolic antioxidants and curcumin from turmeric using an ethanol‐water mixture were optimized and modeled with the face‐centered composite design of the response surface methodology. Under optimal conditions, CUPRAC total antioxidant capacity (TAC), curcumin content (CC), DPPH free radical scavenging capacity, ABTS radical scavenging capacity, and total phenolic contents (TPC) of the extracts obtained using MAE, UAE, and automated soxhlet‐assisted extraction were determined to distinguish the water ratio of the ethanolic solvent as the most important operational factor affecting TAC and CC responses. The highest TAC and CC yields were obtained at a 200 μm particle size, 100°C temperature, 30 min time, and 20% water in ethanol conditions for MAE. The highest TAC and CC yields were obtained at a 200 μm particle size, 48 min time, G = 600 W ultrasonic power, and 26% water in ethanol conditions for UAE. In addition, the red lentil (R.L.) soup was selected as a model food system and was enriched with extracts obtained by the UAE process. The effects of curcumin addition to a protein‐rich food matrix, spontaneous protein‐curcumin interaction, and the existence of olive oil as an oil/water emulsion delivery system in the prepared soup samples were investigated in association with simulated gastrointestinal digestion. The (R.L + water + 5% turmeric extract) sample was shown to have a higher TPC value than analogous mixtures after in vitro digestion. TPC values of enriched soup samples with olive oil were higher than those enriched without olive oil due to the potential ability of olive oil to provide solubility and stability of curcuminoids together with its potential as a phenolic source. The solubility, oil–water interfacial absorption, and stability of curcuminoids were important in the measured TAC response before and after simulated digestion. Curcumin addition to protein‐rich foods may be recommended considering the health‐promoting effects of functional foods. The proposed extraction processes show a potential to recover bioactive compounds with high efficiency through green chemistry to design new functional foods.
... 4 Curcumin is a bioactive compound primarily extracted from the root of the turmeric plant (Curcuma longa), which belongs to the ginger family. 5 Historically, curcumin has been utilized extensively in traditional medicine systems such as Ayurveda in India and traditional Chinese medicine. In these practices, it is revered for its potent anti-inflammatory, antibacterial and healing properties. ...
Article
Full-text available
Curcumin (diferuloylmethane), the active constituent of turmeric, has been used as a treatment fora wide variety of inflammatory conditions. Extensive research over the past two decades has shown that curcumin mediates its effects through the inhibition of transcription factors (NF-κB, AP-1), enzymes (COX-1, COX-2, LOX), cytokines (TNF, IL-1, IL-6) and downregulation of antiapoptotic genes (BCL2, BCL2L1). Curcumin has been widely used for the treatment of several chronic diseases, including various cancers, Alzheimer's disease, cardiovascular diseases, diabetes, arthritis, alcohol-induced liver injury, multiple sclerosis and inflammatory eye conditions. In addition, curcumin enhances wound healing and blocks HIV replication. Studies have also shown that curcumin has no effect on normal cells and kills only tumor cells. Various pharmacological aspects of curcumin are discussed with regard to different types of chronic diseases. Copyright © 2010 Prous Science, S.A.U. or its licensors. All rights reserved.
Article
Full-text available
Numerous interventional studies in clinical and preclinical setting stated that intake of curcumin may provide protection against cardiovascular disease. The aim of this trial was investigation of curcumin efficiency on some cardiovascular risk factors in patients with coronary artery disease (CAD). A total of 33 patients with CAD who fulfilled inclusion and exclusion criteria were entered the study. Patients were randomly assigned to receive curcumin or placebo, 500 mg capsules, four times daily for 8 weeks. Lipid profile, blood glucose and high sensitive C-reactive protein (hs-CRP) levels were analyzed at baseline and two months after treatment. Serum levels of triglycerides (P=0.01), LDL-cholesterol (P=0.03) and VLDL-cholesterol (P=0.04) significantly decreased in the curcumin group compared to baseline, without significant changes in total cholesterol, HDL-cholesterol, blood glucose and hs-CRP levels. In all mentioned laboratory parameters, significant difference was not detected between curcumin and placebo. Although curcumin improved some of lipid profile components, it did not show appreciable effect on inflammatory markers in patients with CAD. Therefore, more detailed assessment of metabolic effects or anti-inflammatory activities of curcumin need to perform by extensive human study.
Article
Full-text available
Curcumin is a highly pleiotropic molecule found in the rhizomes of Curcuma longa (turmeric). It is responsible for the yellow color of turmeric and has been shown to inhibit the proliferation of cancer cells and to be of use in preventing or treating a number of diseases. Curcumin has been shown to modulate multiple cell-signaling pathways simultaneously, thereby mitigating or preventing many different types of cancers, including multiple myeloma and colorectal, pancreatic, breast, prostate, lung, head, and neck cancers, in both animal models and humans. Current therapeutic approaches using a single cancer drug for a single target can be expensive, have serious side effects, or both. Consequently, new approaches to the treatment and prevention of cancer, including the integration of curcumin as a viable treatment strategy where dysregulation of many pathways is involved, are warranted. A methodical review of the evidence was performed to evaluate the effects of curcumin in support of a health claim, as established through the regulatory framework of Health Canada, for a relationship between the consumption of curcumin and the prevention and treatment of cancer. © The Author(s) 2015. Published by Oxford University Press on behalf of the International Life Sciences Institute. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.
Article
Full-text available
Turmeric is obtained from the plant Curcuma longa L; its major constituent, curcumin, is a polyphenol with multiple effects which can modulate some signaling pathways. Insulin resistance is a major risk factor for chronic diseases such as type 2 diabetes, atherosclerotic, metabolic syndrome and cardiovascular disease. In addition, Insulin resistance in peripheral tissue is one of the most important reasons of hyperglycemia which can cause global or systemic effects. The present study reviewed studies published in PubMed from 1998 to 2013, indicating the role of curcumin in attenuation of many pathophysiological processes involved in development and progression of hyperglycemia and insulin resistance. Curcumin can reduce blood glucose level by reducing the hepatic glucose production, suppression of hyperglycemia-induced inflammatory state, stimulation of glucose uptake by up-regulation of GLUT4, GLUT2 and GLUT3 genes expressions, activation of AMP kinase, promoting the PPAR ligand-binding activity, stimulation of insulin secretion from pancreatic tissues, improvement in pancreatic cell function, and reduction of insulin resistance. Curcumin has antihyperglycemic and insulin sensitizer effects. Thereby, more studies evaluating the effects of curcumin on hyperglycemic state and insulin resistance in related disorders such as diabetes are recommended.
Article
Full-text available
Axon degeneration is a hallmark of several central nervous system (CNS) disorders, including multiple sclerosis (MS), Alzheimer’s disease (AD) and Parkinson’s disease (PD). Previous neuroprotective approaches have mainly focused on reversal or prevention of neuronal cell body degeneration or death. However, experimental evidence suggests that mechanisms of axon degeneration may differ from cell death mechanisms, and that therapeutic agents that protect cell bodies may not protect axons. Moreover, axon degeneration underlies neurologic disability and may, in some cases, represent an important initial step that leads to neuronal death. Here, we develop a novel quantitative microfluidic-based methodology to assess mechanisms of axon degeneration caused by local neuroinflammation. We find that LPS-stimulated microglia release soluble factors that, when applied locally to axons, result in axon degeneration. This local axon degeneration is mediated by microglial MyD88/p38 MAPK signaling and concomitant production of nitric oxide (NO). Intra-axonal mechanisms of degeneration involve JNK phosphorylation. Curcumin, a compound with both anti-oxidant and JNK inhibitory properties, specifically protects axons, but not neuronal cell bodies, from NO-mediated degeneration. Overall, our platform provides mechanistic insights into local axon degeneration, identifies curcumin as a novel axon protectant in the setting of neuroinflammation, and allows for ready screening of axon protective drugs.
Article
An Ethyl acetate (AcOEt) extract from the rhizome of Curcuma longa L. has preventive activities in experimental models of allergy types I and IV. The purpose of the present study is to clarify the features of inhibitory actions of the AcOEt extract on the histamine release from rat mast cells (allergy type I) and to compare the effect with that of curcumin. At a concentration of 50 μg/ml, both the AcOEt extract and curcumin inhibited the histamine release induced by concanavalin A, and also suppressed the histamine release induced by compound 48/80, in the absence or presence of Ca2+ and that induced by A23187. In the experiment of two stage models, they markedly reduced the histamine release when administered prior to and posterior to the addition of concanavalin A. The effect of the AcOEt extract on the inhibition of histamine release was somewhat stronger than that of curcumin. These findings suggest that 1) the AcOEt extract potently suppresses the histamine release probably through the blockage of the degranulation process following a rise in intracellular Ca2+ levels induced by the three types of histamine releasers, and 2) the features of the actions of the AcOEt extract are similar to those of curcumin.
Article
Turmeric, derived from the plant Curcuma longa, is a gold-colored Spice that has been used as a traditional medicine. Curcumin (CUR), the principal curcuminoid of turmeric, which gives the yellow color to turmeric, is now recognized as being responsible for most of the therapeutic effects. It has been shown to exhibit antioxidant, anti-inflammatory, antiviral, antibacterial and antifungal as well as anticancer activities. The loss of functional neurons and synapses lead to neurodegenerative diseases. Current treatments for most of these diseases had not succeeded adequate until now. Both of oxidative damage and inflammation have been proved as having roles in age-related neurodegenerative diseases. Antioxidants have been demonstrated to protect neurons against a variety of experimental neurodegenerative conditions. A number of experimental studies indicate that CUR, as an antioxidant protects the brain against various oxidative stressors. CUR is a powerful scavenger of superoxide anions, and it has both neuroprotective and anti-aging effects. CUR can cross the blood-brain barrier (BBB) and reach the brain. Accumulating cell culture and animal model data show that dietary CUR is a strong candidate for use in the prevention or treatment of Neurodegenerative diseases includes Alzheimer's disease, Parkinson's disease and multiple sclerosis. Also CUR showed protection against Ischemic cerebral stroke, epilepsy and depression.