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1
REVIEW ARTICLE
Rooibos Tea and Health: A Systemac Review of the Evidence from the Last
Two Decades
Timothy Bond J1, and Emma Derbyshire J2*
1Tea Advisory Panel; Tea and Herbal Soluons, Bedford, United Kingdom
2Nutrional Insight, Epsom, Surrey, United Kingdom
Received: 08 May, 2020 | Accepted: 29 May, 2020 | Published: 05 Jun, 2020
Volume 6 - Issue 1
e health properties of rooibos tea have been ascribed to it being
caeine free and its abundant phenolic composition [9,10]. Rooibos
tea has a divergent polyphenol prole and is a rare dietary source of
dihydrochalcones-aspalathin and nothofagin which possess potent
antioxidant actions [11-13]. Aspalathin and nothofagin are the
main avonoids in Rooibos tea and have a particularly strong anti-
oxidative activity, though aspalathin tends to be lower in fermented
than unfermented foods [10,12,14]. is is relevant to health as the
antioxidants present in rooibos may help to protect against oxidative
stress which is known to induce inammation and other health
conditions [10,15].
Rooibos tea is naturally slightly sweet with caramel, oral, honey
and woody undertones [16]. It has been used both as a tisane, as
well as consumed traditionally for medicinal purposes and has been
popular in South Africa for generations [5,11]. Traditionally, rooibos
has been used for its medicinal properties in South Africa to help
alleviate allergies, asthma, dermatological conditions and infantile
colic [17]. Both the leaves and ne stems can be used as herbal tea,
predominantly in the traditional ‘fermented’ (oxidised/aerated) red-
brown form but also in its ‘unfermented’ (unoxidized/aerated) green
form [18]. Rooibos tea can also be extracted and dried, spray-dried/
freeze-dried to form powdered rooibos tea extract (RTE) which is also
abundant in polyphenols [5]. Traditionally fermented beverages such
as Kombucha have been produced eectively using rooibos leaves [19].
*Corresponding author: Emma Derbyshire J, Nutrional Insight, Epsom, Surrey, United Kingdom, E-mail: emma@nutrional-insight.co.uk
Citaon: Bond TJ, Derbyshire EJ (2020) Rooibos Tea and Health: A Systemac Review of the Evidence from the Last Two Decades. Nutr Food
Technol Open Access 6(1): dx.doi.org/10.16966/2470-6086.166
Copyright: © 2020 Bond TJ, et al. This is an open-access arcle distributed under the terms of the Creave Commons Aribuon License,
which permits unrestricted use, distribuon, and reproducon in any medium, provided the original author and source are credited.
Abstract
An expanse of research has invesgated the eects of black and green teas in relaon to aspects of health. Rooibos tea, also known as Red bush is
derived from the South African Cape fynbos plant, Aspalathus linearis, and is caeine free, naturally sweet and abundant in polyphenols. Evidence
related to the health aspects of drinking Rooibos tea is advancing, but does not appear to have been collated. Therefore, we aimed to examine the
health eects of Rooibos tea through a systemac review of the literature. A PUBMED search was undertaken (2000 up to June 2020) for human and
laboratory studies invesgang the ecacy of Rooibos in relaon to health. Seven human studies and 49 laboratory studies were idened. Overall
Rooibos tea consumpon seems to benet the lipid and redox proles of those at risk of cardiovascular disease. It also appears to possess other
promising ‘general’ eects on glycaemic control, bone, liver, cognive and respiratory health. Ongoing research using standardised intervenons is
now needed to help formulate congruent conclusions that are relevant to public health.
Keywords: Rooibos tea; Poly phenols; Health; Evidence-base
Introduction
e pattern of health and disease is changing-continued shis in
longevity mean that multimorbidity and ‘disease clusters’ are now
on the rise [1]. It is well appreciated that lifestyle e.g. alterations in
diet, physical activity and avoiding smoking can improve outcomes
for medical conditions such as cardiovascular disease [2]. ere is
already an extensive body of evidence showing that drinking two
to three cups of tea daily could be benecial for health, including
reduced risk of cardiac death, coronary artery disease, stroke, type 2
diabetes mellitus and total mortality [3]. Benecial inter-relationships
have also been observed for several cancers, cognitive, skeletal and
maternal health [3]. Most of this research has focused on green, black
and oolong tea [4].
“Rooibos” is Afrikaans for “red bush” [5]. It is prepared from
unfermented and fermented plant material from the Cape fynbos
plant, Aspalathus linearis [6,7]. In South Africa, the proportion of
black tea drinkers has declined between 2011 and 2015, from 58.6%
to 51.5% whilst the percentage of Rooibos consumers has risen from
29.4% in 2011 to 30.9% in 2015.8 e demand for Rooibos tea is also
extending further aeld with South Africa exporting Rooibos tea to
more than 30 countries [8].
Such shis in consumption habits are being attributed to rising
awareness and interest in the health properties of Rooibos tea [8].
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Citaon: Bond TJ, Derbyshire EJ (2020) Rooibos Tea and Health: A Systemac Review of the Evidence from the Last Two Decades.
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provided six cups of fermented, traditional Rooibos daily (one tea bag
in 200ml with an infusion time of 5 minutes) for 6 weeks [21].
ree studies reported positive ndings in relation to aspects of
health [21,22,25]. One study used ex vivo samples from atopic adults
showing that extracts prepared from both fermented and unfermented
Rooibos inhibited basophil activation, an eect that was stronger using
the extract of fermented Rooibos [22]. ese ndings are aligned with
that from earlier laboratory models [26] and indicate that Rooibos
appears to possess anti-allergic eects by inhibiting antigen- and
calcium ionophore-stimulated degranulation. One of the largest trials
conducted on 40 participants observed signicant increases in plasma
total polyphenol levels, reductions in markers of lipid peroxidation,
improvements in lipid proles (low-density lipoprotein declined and
high-density lipoprotein increased) and redox status [21]. Eects were
observed aer drinking six cups of fermented (traditional) Rooibos
tea daily for 6 weeks [21]. Another trial looking into underpinning
mechanisms showed that freshly prepared Rooibos tea (made with 10g
tea in 400ml boiled water for 10min using a tea filter) signicantly
inhibited angiotensin-converting enzyme (ACE) activity, 30 and 60
minutes aer ingestion, indicating possible cardiovascular eects via
the inhibition of ACE activity [25].
Two human studies focused on aspects of metabolite absorption
and bioavailability [14,20]. In a human crossover study where 500 ml
unfermented Rooibos tea was ingested aspalathin (a dihydrochalcone
C-glucoside) was found to be particularly bioavailable [20]. An earlier
bioavailability trial comprised of 10 adults drinking a similar quantity
of Rooibos tea also showed that most metabolites were absorbed either
via the small or large intestine [14]. In two trials involving Rooibos
tea ingestion, one did not show any signicant eects on renal stone
formation [23] and the other showed that rooibos tea and plain water
similarly rehydrated 23 athletes [24].
Laboratory Studies
A wealth of research has studied the health eects and potential
mechanisms of Rooibos tea and its associated avonoids. Forty-nine
laboratory/mechanistic studies were identied and published over
the last two decades. Of these, eleven focused on aspects of oxidative
stress and antioxidant activity [10,12,27-35]. Four studies observed
improvements in dimensions of sperm function [36-39]. is included
enhanced sperm velocity, vitality, acrosome structure and membrane
integrity [36 38]. ese eects were attributed to high levels of
antioxidants found in Rooibos, sequestering reactive oxygen species
and lipid peroxidation [38,39].
Other research has focused on aspects of metabolic health. Some
work has found associations between unfermented/green Rooibos
extract and improvements in fasting blood glucose levels using type
2 diabetic mice [40]. Similarly, In vitro work showed that Rooibos
extract high in aspalathin had a sustained glucose lowering eect [41].
Other work indicated that aspalathin or nothofagin avonoids inhibit
glucose-mediated vascular hyperpermeability and inammation [42].
A further seven studies showed that Rooibos could improve insulin
resistance and have antidiabetic potential [43-49].
With regard to potential mechanisms aspalathin found in Rooibos
stimulated glucose uptake in muscle tissues and insulin secretion from
pancreatic beta-cells in a type 2 diabetes mouse model [48]. Work
by Ulicna O, et al. (2006) found that the antioxidant compounds in
Rooibos tea prevented oxidative stress concluding that it could be a
suitable adjunctive therapy for diabetic vascular conditions [49]. One
study using a cell model found that a fermented Rooibos infusion
prepared at ‘cup-of-tea’ strength and the soluble matter of the infusion
Increasingly, rooibos has been studied in human populations,
mainly for its antioxidant and cardio protective properties [14,20,21].
Alongside this, over the years a growing body of laboratory and
mechanistic studies have investigated how rooibos tea could impact
on health. Given the gaining popularity of rooibos tea, the current
publication collates evidence from human and laboratory studies,
published over the last two decades. Such a review does not appear
to have been undertaken previously. e present review focuses
on rooibos tea which has been gaining popularity both in its native
province the Western Cape of South Africa and worldwide in recent
years [8].
Methods
e National Centre for Biotechnology Information (NCBI) search
engine (PubMed) was used to extract relevant publications. Two
search phases were undertaken. In Phase 1 English-language human
studies published between January 2000 (month start) and June 2020
(month start) were screened. Publications were included if they used
Rooibos tea or RTE and studied a named health outcome. Studies were
excluded if they were conducted with children due to potential ethical
issues, focused on chemical proling, used a multi-intervention or did
not specify a distinctive health outcome. External health conditions
such as skin healing were also excluded.
e search terms “Rooibos”, “Red bush” or “Aspalathus linearis”
were used. ED and TB identied the scientic publications. In Phase
1 the database search was restricted to human studies. In Phase 2 the
search was restricted to laboratory studies the same search terms were
applied. Data extracted from each human study included: (1) Study
(author, year, location and reference number), (2) Subjects (age,
gender, number), (3) Study design (type), (4) Tea intervention (type)
(5) Intervention type (dosage) and (6) Main ndings. Data extracted
from each laboratory/mechanistic study included: (1) Study (author,
year and reference number), (2) Study Design, (3) Intervention (type),
(4) Main outcome and (5) Main ndings.
Results
In Phase 1 using the applied search terms 47 human studies were
identied. Of these, three were review papers, three had methods that
were unclear or not fully reported, ve were laboratory studies and 29
irrelevant as they did not investigate health outcomes. Subsequently,
aer these exclusions seven human studies were included in the nal
review. Of the human studies three were conducted in South Africa
[21-23], one in the USA [24], one in Italy [14], one in Sweden [25] and
one in Germany [20].
In Phase 2 91 laboratory studies were rst identied. Two of these
were excluded due to them being multi-interventions, two focused
on external (skin) conditions, four were review papers, seven had
methods that were unclear or not fully reported and 27 were irrelevant
as they did not measure health outcomes. is resulted in 49 laboratory
studies being included in the main paper. e algorithm of qualifying
papers is shown in gure 1.
Human Studies
Seven human studies were identied using Rooibos tea preparations
(Table 1) [14,20-25]. Sample sizes ranged from eight to 40 subjects.
Interventions also varied between studies. Most studies used Rooibos
infusions that had been seeped for approximately 10 minutes in hot
water infusions [20,23,25]. One study provided Rooibos tea (two 125
ml cups each made with two tea bags, low mineral content water and
a brewing time of 5 min at 90oC) for 30 days [23]. Other research
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Citaon: Bond TJ, Derbyshire EJ (2020) Rooibos Tea and Health: A Systemac Review of the Evidence from the Last Two Decades.
Nutr Food Technol Open Access 6(1): dx.doi.org/10.16966/2470-6086.166 3
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PubMed and Reference Search. “Rooibos” or “Red
bush” or “Aspalathus linearis” (2000-2020)
47 Human Studies
91 Laboratory Studies
40 papers excluded due to:
A review-3
Laboratory study-5
Methods not fully reported or unclear-3
Other (irrelevant)-29
42 papers excluded due to:
A review-4
External health conditions-2
Methods not fully reported or unclear-7
Multi-intervention-2
Other (irrelevant)-27
7 studies included
(Table 1)
49 studies included
(Table 2)
Figure 1: Algorithm for database search results.
inhibited adipogenesis, also implying a potential role in obesity
prevention [50]. ese ndings imply a potential role in glycaemic
regulation.
Other research suggests benecial eects on aspects of bone health
[51,52], hepatoprotection [31,43,44,53], allergic response [26] and
immune function [54,55]. Rooibos tea has been found to improve
osteoblast activity [52] while fermented Rooibos was found to inhibit
osteoclasts and associated gene expression [51]. Some work has
discovered that Rooibos tea could help to stabilise the liver from injury
[12]. In another study Rooibos extract eased induced liver injury by
suppressing oxidative stress and the formation of pro-inammatory
cytokines [31]. A laboratory model showed that Rooibos tea acted as a
‘hepatoprotector’ showing histological regression of liver cirrhosis and
steatosis in an experimental model of liver cirrhosis [53].
Alongside these ndings, other evidence from laboratory
models suggests inter-relationships between Rooibos ingestion
and improvements in spatial memory, [56] reduced brain oedema
and neuronal apoptosis, [57] reductions in esophageal papilloma
size, [58] antispasmodic eects, [59,60] bronchodilation, [60] and
chemoprotection [61,62].
Discussion
Overall there appears to be a growing body of evidence relating to
Rooibos tea and various biological health outcomes. e largest body
of evidence is currently derived from laboratory and mechanistic
studies although human research is emerging. Research focusing on
cardiovascular health looks particularly promising. e trial conducted
by Marnewick JL, et al. (2011) [21] was well conducted showing that
drinking six cups of fermented, traditional rooibos daily signicantly
improved the lipid prole and redox status which is relevant to adults
at risk for developing cardiovascular disease. Elsewhere other review
ndings also conclude that Rooibos appears to have preventative and
complementary therapeutic benets in the context of cardiovascular
disease [63].
e antioxidant properties of Rooibos tea and its ability to sequester
oxidative stress are also prominent in the research [27,34,49,64]. e
polyphenols aspalathin (present at >5 mg/l) and nothofagin (present
at <1 mg/L) found in Rooibos tea have been attributed to some of its
health benets [65,66]. Antioxidants such as these suppress oxidative
stress in the body which has been implicated in the pathophysiology of
certain diseases including Alzheimer’s disease [67]. Several laboratory
studies concentrated on aspects of sperm function [36-39]. Fermented
Rooibos, in particular, was found to improve several dimensions
including sperm concentration, viability and motility [38]. ese
ndings imply that Rooibos consumption could have a role to play
in supporting male fertility, namely by sequestering oxidative damage
by improving antioxidant defence mechanisms and subsequently
improving the sperm quality and function [39]. Human randomised
controlled trials are now needed to explore this.
Fermented Rooibos extracts have been found to inhibit human
basophil activation [22] a nding that supports earlier laboratory
research showing that Rooibos has allergen-dependent inhibitory
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Citaon: Bond TJ, Derbyshire EJ (2020) Rooibos Tea and Health: A Systemac Review of the Evidence from the Last Two Decades.
Nutr Food Technol Open Access 6(1): dx.doi.org/10.16966/2470-6086.166 4
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Study (Author- Year-
Locaon- Reference
Number)
Subjects (age-
gender- number) Study design Tea Intervenon
(type) Tea Intervenon (dosage)
Main ndings (with any
reported signicant
p-values)
Pedre s- et al. (2020)
[22] South Africa n=9 atopic adults
Used ex vivo
samples from
atopic paents
Fermented and
unfermented
Rooibos extracts
Three opmised decreasing
concentraons of unfermented
(0.1- 0.03 or 0.01mg/ml) or
fermented Rooibos extracts
(0.05- 0.017 or 0.005mg/
ml) were used during the
experiments
Rooibos extracts inhibited
basophil acvaon in a
dose-dependent non-
allergen specic manner.
The inhibitory eect was
stronger using fermented
versus unfermented extract.
Rodgers A- et al. (2016)
[23] South Africa
n=8 calcium
oxalate (CaOx)
renal stone
formers
30-day trial
Green tea from
Japan or Rooibos
from South Africa
Samples were prepared for
analysis by adding 250 ml of
boiling water to each teabag.
These were removed aer
brewing mes of 5 and 10 min.
Ingeson of Rooibos tea
does not reduce the risk
factors for CaOx stone
formaon in humans-
Breiter T- et al. (2011)
[20] Germany
n=12 healthy
males.
24-hr crossover
trial.
Dierent Rooibos
drinksfrom
unfermented
Rooibos or a
placebo
10g Rooibos extracted with
500ml boiling water seeped from
10 minutes
On average a total of
0.76nmol of avonoids were
detected during their peak
concentraon aer intake of
the Rooibos tea- accounng
for 0.26% compared to the
total amount of avonoids
ingested.
Marnewick JL- et al.
(2011) [21] South
Africa
n=40 volunteers 6-week trial Fermented/
tradional Rooibos
Six 200 ml cups daily (one tea
bag per cup; 5 minute infusion
me).
Consumpon of fermented-
tradional Rooibos
signicantly improved the
lipid prole as well as redox
status- both relevant to
heart disease- in adults
at risk for developing
cardiovascular disease.
Persson IA- et al.
(2010) [25] Sweden
n=17 healthy
volunteers.
Three phase
randomized-
three-phase-
crossover study.
Green tea- black
tea or Rooibos tea
(South Africa)
10g tea in 400ml 10 min infusion
freshly prepared and cooled so
the parcipants could drink it
within approximately 2min.
Oral intake of a single dose
of Rooibos tea signicantly
inhibited ACE acvity aer
30 min (p< 0.01) and aer
60 min (p< 0.05).Rooibos
tea may have cardiovascular
eects through inhibion of
ACE acvity.
Uer AC- et al. (2010)
[24] USA n=23 athletes
Randomized-
cross-over design
with three
dierent study
arms.
Rooibos tea-
carbohydrate
beverage or boled
water (placebo)
NR (restricted access paper)
Rooibos tea was no more
eecve in promong
rehydraon than plain
water.
Stalmach A- et al.
(2009) [14] Italy n=10 volunteers Bioavailability
trial
Fermented or
unfermented
Rooibos tea
500ml
The overall metabolite
levels excreted were 82
and 352 nmol- accounng
for 0.09 and 0.22% of the
avonoids in the fermented
and unfermented drinks-
respecvely. Most of the
aspalathin metabolites
were excreted within 5 h of
tea consumpon- implying
absorpon in the small
intesne.
Table 1: Rooibos Tea & Health: Evidence from Human Trials.
Key: ACE- Angiotensin-Converng Enzyme; NR- Not Reported.
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Citaon: Bond TJ, Derbyshire EJ (2020) Rooibos Tea and Health: A Systemac Review of the Evidence from the Last Two Decades.
Nutr Food Technol Open Access 6(1): dx.doi.org/10.16966/2470-6086.166 5
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Study (Author-
Year- Reference
Number)
Laboratory/
Mechanisc study
Rooibos tea Intervenon
(type) Main outcomes Main ndings
Lawal AO- et al.
(2019) [27]
In vitro anoxidant
capacity
Aqueous extracts of
fermented Rooibos- green
Rooibos and Honey bush.
Oxidave stress
Herbal extracts oered protecon against diesel
exhaust parcles that induced oxidave stress and
inammatory response.
Mazibuko-Mbejeet
SE- al. (2019) [43]
In vitro- using liver
cells Aspalathin treatment Hepac insulin
resistance
Aspalathin improved insulin signalling and
mitochondrial bioenergecs.
Mazibuko-Mbeje
SE- et al. (2019)
[44]
In vitro- using rats Aspalathin-enriched green
Rooibos extract
Hepac insulin
resistance
Green Rooibos extract showed potenal in
ameliorang hepac insulin resistance by improving
insulin sensivity via PI3K/AKT- FOXO1 and AMPK-
mediated pathways.
Morishita Y- et al.
(2019) [26]
Rat basophilic
leukaemia cells
Quercen- luteolin and
chrysoeriol were mixed
in the rao that occurs in
Rooibos tea extract
Allergic response
The mixture inhibited angen- and calcium
ionophore-smulated degranulaon to the same
degree as whole Rooibos tea extract. Flavonoids
underly the degranulaon inhibitory acvity of
rooibos tea.
Orlando P- et al.
(2019) [28]
Diabec and non-
diabec vervet
monkeys
90 mg/kg of aspalathin-rich
green Rooibos extract for 28
days.
Oxidave stress- LDL
cholesterol
Green Rooibos extract could counteract hyperglycemia-
oxidave stress and dyslipidemia- lowering
cardiovascular risk factors linked to diabetes.
Pyrzanowska J- et
al. (2019) [56]
Sprague-Dawley
male rats
Infusions- prepared using
1- 2 and 4 g of ‘fermented’
Rooibos leaves for 100 ml of
hot water.
Spaal memory
All treated rats showed improvement of long-
term spaal memory. Striatal dopamine and
3-methoxytyramine levels were increased in treated
rats.
Uličná O- et al.
(2019) [12]
Rats with carbon
tetrachloride-
induced liver
damage
Rooibos tea administraon Anoxidant acvity-
liver damage
Improved histological features support the view of
anoxidant and membrane-stabilizing acvity of
Rooibos tea. This may play a role in the protecon of
the liver from injury caused by known toxins.
Dludla PV- et al.
(2018) [45] Diabec mice Aspalathin intervenon Glycaemic control
Meormin and a high dose (130 mg/kg) of
aspalathin ameliorated diabec symptoms i.e.
abnormally raised fasng plasma glucose levels.
Moosa S- et al.
(2018) [51] Murine study Rooibos tea extract Bone health
Fermented Rooibos had a more potent inhibitory
eect on osteoclasts and associated gene expression
than unfermented Rooibos extract.
Yang S- et al. (2018)
[71] Murine study Aspalathin and nothofagin
from green Rooibos Sepsis Aspalathin and nothofagin appear to protect mice
against sepsis-triggered renal injury.
Akinrinmade 0- et
al. (2017) [57]
Adult male Wistar
rats
Fermented Rooibos herbal
tea
Brain oedema-
neuronal apoptosis
Long-term consumpon of fermented Rooibos tea
signicantly reduced brain oedema and neuronal
apoptosis.
Dludla PV- et al.
(2017) [46] Diabec mice Aspalathin intervenon Glycaemic control
Aspalathin maintained cellular homeostasis and
protected the myocardium against hyperglycemia-
induced oxidave stress by acvang Nrf2 and its
downstream target genes.
Johnson R- et al.
(2017) [72] In vitro Aspalathin intervenon Cardioprotecon Aspalathin co-treatment could protect the
myocardium from Dox-induced cardiotoxicity.
Johnson R- et al.
(2017) [73]
Cardiomyocyte
model Aspalathin intervenon Cardioprotecon
Aspalathin acvated Adipoq and modulated the
expression of Pparγ and Srebf1/2- decreasing
inammaon via Il6/Jak2 pathway- which increased
expression of Bcl2 prevenng myocardium apoptosis.
Table 2: Rooibos Tea and Health: Evidence from Laboratory Studies.
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Citaon: Bond TJ, Derbyshire EJ (2020) Rooibos Tea and Health: A Systemac Review of the Evidence from the Last Two Decades.
Nutr Food Technol Open Access 6(1): dx.doi.org/10.16966/2470-6086.166 6
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Ros-Santaella JL- et
al. (2017) [36] Boar semen
Four concentraons both of
fermented and unfermented
Rooibos extracts
Sperm funcon
Rooibos extract enhanced sperm velocity- protected
acrosome structure- and preserved membrane
integrity during semen storage.
Johnson R- et al.
(2017) [74] In vitro Aspalathin intervenon Cardioprotecon
Aspalathin increased glucose oxidaon and
modulated fay acid ulizaon and induced a
favourable substrate shi in H9c2 cardiomyocytes
exposed to high glucose.
Nash LA- et al
(2016) [52] Saos2 cells
Rooibos- green and black tea
-normalized to 1 or 10 μg /
mL gallic acid equivalents.
Bone health Green- black and Rooibos tea improved osteoblast
acvity at a low level.
Kamakura R- et al.
(2015) [40]
Obese diabec
mice Green Rooibos extract Blood glucose-
andiabec potenal
Green Rooibos extract suppressed the increase in
fasng blood glucose levels in type 2 diabec model
mice.
Ku SK- et al. (2015)
[42]
Human umbilical
vein endothelial
cells and mice
Aspalathin and nothofagin
from green Rooibos
High glucose-induced
inammaon
Treatment of aspalathin or nothofagin inhibited
high glucose-mediated vascular hyperpermeability-
adhesion of monocytes toward human umbilical vein
endothelial cells- and expression of cell adhesion
molecules.
Lee W- et al. (2015)
[65]
Human umbilical
vein endothelial
cells and mice
Aspalathin and nothofagin
from green Rooibos
An-inammatory
funcons
Aspalathin and nothofagin possess an-inammatory
funcons are could be a useful therapy for vascular
inammatory diseases.
Mazibuko SE- et al.
(2015) [47]
In vitro- using
cultured
adipocytes
Treated with green Rooibos
extract or aspalathin
Glucose and lipid
metabolism
At a protein level green rooibos extract and
aspalathin suppressed markers of insulin resistance
i.e. insulin receptor substrate one.
van der Merwe JD-
et al. (2015) [29] Male Fischer rats Aspalathin-enriched green
Rooibos extract Anoxidant acvity
Glutathione reductase acvity signicantly (p<0.05)
increased aer 28 days- while glutathione content
was decreased aer 90 days- suggesng an altered
glutathione redox cycle.
Waisundara & Hoon
(2015) [30]
In vitro models
of diabetes and
cancer
Rooibos tea Oxidave stress-
diabetes- cancer
The Rooibos tea extract was observed to have
increased the CAT and SOD acvies in two in vitro
disease models.
Ajuwon OR- et al.
(2014) [31] Male Wistar rats Fermented Rooibos extract Hepatoprotecon-
Oxidave stress
Aqueous Rooibos extract aenuated LPS-induced
liver injury possibly by modulang oxidave stress
and suppressing pro-inammatory cytokines
formaon.
Ayeleso AO- et al.
(2014) [37] Diabec rats Aqueous Rooibos tea extract
(2%) for 7 weeks. Sperm funcon
Signicant (p<0.05) elevated levels of wobble and
sperm linearity were observed following Rooibos tea
extract treatment
Canda BD- et al.
(2014) [32]
Forty male Wistar
rats
Fermented Rooibos-
unfermented rooibos- a
rooibos-derived commercial
supplement- or water.
Oxidave stress-
Anoxidant acvity
Fermented Rooibos caused a decrease (p< 0.05) in
superoxide dismutase acvity.
Dludla PV- et al.
(2014) [33] Diabec rats Aqueous extract of
fermented Rooibos Oxidave stress
Aqueous extract of fermented Rooibos protected
cardiomyocytes- derived from diabec rats- against
experimentally induced oxidave stress and
ischemia.
Hong IS- et al.
(2014) [34] Laboratory model Rooibos tea Oxidave stress
Rooibos tea appears to (i) reverse the increase
in stress-related metabolites (ii) prevent lipid
peroxidaon- (iii) restore stress-induced protein
degradaon- (iv) regulate glutathione metabolism
and (v) modulate changes in the acvies of
anoxidant enzymes.
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Opuwari CS- et al.
(2014) [38] Male rats Fermented Rooibos Sperm funcon
Fermented Rooibos signicantly improved sperm
vitality (p<0.01)- but caused a signicant increase in
spontaneous acrosome reacon (p< 0.05)- whereas
unfermented did not.
Sanderson M- et al.
(2014) [50] In vitro Fermented Rooibos Obesity prevenon
Hot water soluble solids from fermented Rooibos
inhibited adipogenesis- suggesng its potenal in
prevenng obesity.
Schloms L- et al.
(2014) [75] Rats Rooibos Inammaon
In vivo studies demonstrate that Rooibos signicantly
decreased glucocorcoid levels in rats and steroid
metabolite raos linked to metabolic disorders.
Mazibuko SE- et al.
(2013) [76]
In vitro using
skeletal muscle
cells
Treated with aspalathin-
enriched green
(unfermented) Rooibos
extract
Insulin resistance Rooibos aenuated palmitate-induced insulin
resistance in C₂C₁₂ skeletal muscle cells.
Awoniyi DO- et al.
(2012) [39] Male Wistar rats
Fermented Rooibos- 'green'
Rooibos- Chinese green tea-
Rooibos supplement- green
tea supplement or water.
Sperm funcon
Both Rooibos extracts oered a measure of
protecon against induced oxidave damage by
increasing the anoxidant defence mechanisms
improving the sperm quality and funcon.
Muller CJ- et al.
(2012) [41] In vitro Rooibos extract high in
aspalathin content
Hypoglycaemic
potenal
In vivo the extract sustained a glucose lowering
eect comparable to meormin over a 6h period
aer administraon (25mg/kg body weight (BW)) to
STZ-induced diabec rats.
Pantsi WG- et al.
(2011) [77] Male Wistar rats Aqueous Rooibos and green
tea Cardioprotecon
Results demonstrate the cardio-protecve properes
of aqueous Rooibos extracts via the inhibion
of apoptosis which can possibly be related to its
avonol content.
Sissing O- et al.
(2011) [58] Male rats Rooibos- Honeybush and
Camellia sinensis teas
Esophageal
papillomas
The mean total papilloma size was reduced by
unfermented Rooibos (87%).
Hendricks R- et al.
(2010) [54]
Whole blood
culture assays
Rooibos tea and Camellia
sinensis Immune funcon
Rooibos and black tea modulate immune funcon in
vitro. Rooibos tea smulated whole blood cultures
induced higher Interleukin-6- lower Interleukin-10-
and had no eect on Interferon gamma secreon
Baba H- et al.
(2009) [10]
Seven-week-old
Wister rats Rooibos tea and water. Oxidave stress-
Anoxidant acvity
Serum SOD levels were signicantly higher in the
Rooibos group compared to the controls (p< 0.05).
Kawano A- et al.
(2009) [48]
Type 2 diabetes
model mice in vivo
Aspalathin- a green Rooibos
tea component
Andiabec
potenal
Aspalathin appears to have benecial eects
on glucose homeostasis in type 2 diabetes by
smulang glucose uptake in muscle ssues and
insulin secreon from pancreac beta-cells.
Marnewick JL- et al.
(2009) [61] Rat liver Unfermented and fermented
Rooibos Chemo protecon
Unfermented rooibos signicantly (p<0.05) to
marginally (p<0.1) reduced the total number of foci
(>10microm). Fermentaon seems to reduce the
protecve eect of the herbal teas.
Gilani AH- et al.
(2006) [59]
Isolated ssue
preparaons
Aqueous extract of Rooibos
tea
Anspasmodic
eects
Rooibos tea possessed a combinaon of dominant K
(ATP) channel acvaon and weak Ca(++) antagonist
mechanisms jusfying its use in hyperacve
gastrointesnal disorders.
Khan AU- et al.
(2006) [60]
Isolated ssue
preparaons
Aqueous extract of Rooibos
tea
Bronchodilator-
anspasmodic
The bronchodilator- anspasmodic and blood
pressure lowering eects of Rooibos tea appear to
be mediated predominantly through K (ATP) channel
acvaon with the selecve bronchodilatory eect.
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eects [26]. is research suggests promise for conditions such
as allergic rhinitis [22] but further investigations are needed.
Additionally, its eects on bone health [51,52], cognitive health
[56,57] and potential hepatoprotective eects [12,31,53] warrant
further exploration in the form of human trials. Recently, a review of
experimental evidence [68] concluded that blood glucose levels were
signicantly lower in diabetic rodent models treated with rooibos
extracts providing phenolic compounds. Other work suggests that
Rooibos extracts and its constituent C-glucosyl avonoids, and Z-2-
(β-D-glucopyranosyloxy)-3-phenylpropenoic acid may elicit positive
eects on cellular oxidative stress, inammation and transcription
factors that control genes regulating glucose and lipid metabolism
helping to attenuate features of metabolic disease [69].
In the present review human subjects tended to drink Rooibos
beverages aer they had been infused for approximately 10 minutes
[20,23,25]. Recently, from a consumer stance the ideal ‘optimal cup’
of Rooibos tea has been dened as one that had been seeped for 10
minutes or longer [70]. Unfortunately, recent research shows that
only 15.9% of respondents consumed an ‘optimal cup’ of Rooibos in
an amount that enables its potential cardioprotective health benets
to be provided (dened as a minimum of 4 to 6 cups per day) [70].
Interestingly, compared with cold and regular-brewed Rooibos
infusions of unfermented/green and red Rooibos prepared by boiling
have the highest antioxidant capacities and total polyphenol proles
[9]. Such ndings suggest that more information needs to be imparted
to consumers’ regarding preparation methods and the potential health
benets that drinking Rooibos tea could bring.
With regard to limitations and future research directions greater
uniformity is needed in forthcoming studies. For example, some
studies used fermented and others unfermented Rooibos extracts or
infusions the fermented form appeared to have stronger impact on
some health eects [38,51]. Others used Rooibos tea and Rooibos
‘extracts’ or unfermented/green Rooibos. Production seasons and
grade quality could also alter the phenolic proles and antioxidant
capacity of Rooibos samples and should be considered [66]. Future
trials should also better encompass how ndings could be translated
into public health messages. For example, Marnewick JL, et al. (2011)
[21] asked volunteers to drinks six cups Rooibos tea daily for 6-weeks
to study its cardiovascular eects. Similar studies are now needed for
other health outcomes such as bone health, liver or brain (cognitive)
function.
Considering such evidence Rooibos tea, like teas from Camellia
sinensis (e.g. black, green and oolong tea) could be regarded as a
‘general health’ tea, potentially providing an array of benets to human
health and wellbeing [56] Rooibos tea is naturally slightly sweet [16]
thus does not require the addition of extra sugar or articial sweeteners.
It is also caeine free with a favourable phenolic composition [9,10].
(Table 2)
Ulicná O- et al.
(2006) [49]
Streptozotocin-
induced diabec
rats
Aqueous and alkaline
extracts of Rooibos tea
Andiabec
potenal
Anoxidant compounds in rooibos tea parally
prevent oxidave stress and they are eecve in
both hydrophobic and hydrophilic biological systems.
van der Merwe JD-
et al. (2006) [78]
Comparave- in
vitro
Rooibos and honey bush tea
compared with black- oolong
and green teas
Anmutagenic
Anmutagenic acvity of the South African herbal
teas was mutagen-specic- aected by fermentaon.
Unfermented Rooibos was less eecve than
fermented Rooibos
Lee EJ- et al. (2004)
[79]
DNA strand
scission Rooibos tea Anoxidant acvity
Result suggests that total soluble phenolics- specially
avonoid- of Rooibos tea are responsible for several
kinds of anoxidant acvies and prevenve acvity
on peroxyl radical induced DNA strand scission.
Kucharská J- et al.
(2004) [35]
Rat model
of carbon
tetrachloride-
induced liver
damage
Rooibos tea Oxidave stress
Rooibos tea restored liver concentraons of CoQ9H2
and alpha-tocopherol and inhibited the formaon of
MDA.
Marnewick JL- et al.
(2004) [62] Male Fischer rats
Unprocessed (not oxidized)-
processed (oxidized) rooibos-
honey bush- green and black
teas
Mutagenic response
The mutagenic response of aatoxin B1 against
Salmonella strain TA 100 was signicantly (p<0.05)
inhibited by cytosolic fracons from rats treated with
processed and unprocessed herbal teas.
Ulicná O- et al.
(2003) [53]
Rat model of liver
injury Rooibos tea Hepatoprotecon
Rooibos tea showed histological regression of
steatosis and cirrhosis in the liver ssue with a
signicant inhibion of the increase of liver ssue
concentraons of malondialdehyde- triacylglycerols
and cholesterol.
Kunishiro K- at al.
(2001) [55] In vitro and in vivo. Rooibos tea extract Immune funcon
Rooibos tea extract may facilitate the angen-
specic anbody producon through selecve
augmentaon of IL-2 generaon both in vitro and in
vivo.
Key: ATP-Adenosine Triphosphate; CAT-Chloramphenicol Acetyltransferase; DNA-Deoxyribonucleic Acid; IL-Interleukin; LDL-Low-Density Lipoprotein;
LPS-Lipopolysaccharide; MDA- Malondialdehyde; ROS- Reacve Oxygen Species- SOD-Superoxide Dismutase; STZ- Streptozotocin.
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Citaon: Bond TJ, Derbyshire EJ (2020) Rooibos Tea and Health: A Systemac Review of the Evidence from the Last Two Decades.
Nutr Food Technol Open Access 6(1): dx.doi.org/10.16966/2470-6086.166 9
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Conclusions
In conclusion previous health research has tended to focus on
black or green tea. Rooibos is widely consumed in South Africa but
is gaining popularity globally. is has been attributed to the fact that
it is caeine free, naturally sweet and abundant in polyphenols with
potent antioxidant properties. Now, a growing body of evidence from
7 human studies and 49 laboratory studies suggests that Rooibos could
be regarded as a ‘general’ health tea. Evidence for cardioprotective
eects (especially lipid prole) looks promising, particularly as a
potential adjunctive therapy. It is suggested that future research now
builds on the other potential aspects of health including glycaemic,
bone, liver and cognitive wellness enhancing eects that also appear
to be emerging.
Disclosure
e views expressed are those of the authors alone and personnel
from the UK TEA & INFUSIONS ASSOCIATION (UKTIA) had no
role in writing this review.
Conicts of Interest
e authors declare no conicts of interest.
Acknowledgements
e authors received funding provided by the Tea Advisory
Panel which is supported by an unrestricted educational grant from
the UK TEA & INFUSIONS ASSOCIATION (UKTIA), the trade
association for the UK tea industry. UKTIA plays no role in producing
the outputs of the panel. Independent panel members include
nutritionists, biochemists, dietitians, dentist and doctors. See www.
teaadvisorypanel.com
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