green tea - manuscript text1
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REVIEW ARTICLE
BENIFICIAL EFFECTS OF POLYPHENOLIC BEVERAGE ON ORAL AND
PERIODONTAL HEALTH
SWETA SONI,MDS*,PRAMOD JAIN,MDS**, VIJAY KUMAR CHAUDHARY,MDS***
*SENIOR LECTURER, DEPARTMENT OF PERIODONTICS, VYAS DENTAL COLLEGE & HOSPITAL, JODHPUR, INDIA
** MEDICAL OFFICER,SMS HOSPITAL, JAIPUR, INDIA
***MEDICAL OFFICER, AMER, JAIPUR, INDIA
ABSTRACT
Periodontal diseases, if left unchecked, can lead to major health problems. There are a number of traditional
herbal remedies for the treatment and management of diseases related to periodontium and oral hygiene. Green tea has
long been used in much of the world as a popular beverage and a respected medicinal agent. Early Chinese medical
literature lists green tea as an antibacterial, astringent, antioxidant, anticaries, anti-inflammatory, circulatory-stimulant,
haemostatic, anti-halitosis. In recent years, there has been a significant upsurge in research on the characterization and
verification of the potential health benefits associated with the use of green tea. The use of green tea in promoting
gastrointestinal and cardiovascular health, use in prevention of cancer and neurodegenerative diseases and other
infectious conditions like periodontal disease. This review appraises the available evidence for and against the health
claims associated with green tea and its use as preventive and therapeutic products for periodontal disease. However,
considerable work is still needed to confirm these potential health benefits.
Key words: Green tea, Green tea catechins, Polyphenol, Periodontal disease, oral health.
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Introduction
Tea is considered the second most consumed
beverage in the world, next only to water and consumed in
different parts of the world as green, black, or Oolong tea.
Among all of these, however, the most significant effectson human health have been observed with the consumption
of green tea(1,2). Compared with black tea and Oolong tea
green tea is a non-oxidized and non-fermented product that
contains several polyphenolic components, also called
catechins, including epigallocatechin-3 gallate, epicatechin-
3 gallate, epicatechin, and epigallocatechin. Green tea
catechins have been shown to possess potent antioxidant
activity several times higher than that of vitamin C and
vitamin E(3).
McKay and Blumberg, 2002(4) reported a per capitamean consumption of tea in the world of 120 mL/ day.
Approximately 7678% of the tea produced and consumed
is black tea, 2022% is green tea and less than 2% is
oolong tea(5). Black tea is consumed principally in Europe,
North America and North Africa while green tea is widely
drunk in China, Japan, Korea and Morocco; oolong tea is
popular in China and Taiwan(5,6).
Green tea is used in several forms: consumed as
dilute infusion or concentrated supple or applied topically.
Commercial preparation use various extraction techniques
and manufacturing procedures and are not uniform. 2
Recently, the FDA approved a topical ointment con-
taining green tea extract as a prescription drug for the
treatment of genital warts(7).
Historical Context:
The tea plant, source of the most popular beverage
in the world, is believed to have originated in the landmass
encompassing Tibet, western China, and northern India.
According to ancient Chinese legend, tea was discovered
by the Chinese emperor Shen-Nung in 2737 B.C., when
leaves from a wild tea bush accidentally fell into a pot of
water he was boiling. The first recorded mention of tea
appears in a contract for slaves known as "Tan Yuch,"
written by Wang Pao, poet laureate to Emperor Husan, in
59B.C(8).
The word tea has been used to describe the shrub
Camellia sinensis . Tea plants produce abundant foliage, a
camellia-like flower, and a berry, but only the smallest and
youngest leaves are picked for tea-the two leaves and bud
at the top of each young shoot. The growth of new shoots,
called a flush(8).
Biochemistry of Green Tea:
Green tea chemical composition is complex:
proteins (15 20% dry weight) whose enzymes constitute
an important fraction; aminoacids (14% dry weight) such
as teanine or 5- N ethylglutamine, glutamic acid,
tryptophan, glycine, serine, aspartic acid, tyrosine, valine,
leucine, threonine, arginine, lysine; carbohydrates (57%
dry weight) such as cellulose, pectins, glucose, fructose,
sucrose; lipids as linoleic and linolenic acids; sterols as
stigmasterol; vitamins (B, C, E); xanthic bases such as
caffeine and theophylline, pigments such as chlorophyll
and carotenoids; volatile compounds as aldehydes,
alcohols, esters, lactones, hydrocarbons, etc.; minerals and
trace elements (5% dry weight) such as Ca, Mg, Cr, Mn,
Fe, Cu, Zn, Mo, Se, Na, P, Co, Sr, Ni, K, F and Al(8).
Green tea prepared in such a way as to preclude
the oxidation of green leaf polyphenols. The beneficial
effects generally associated with green tea have been
attributed to its polyphenol content, particularly to
catechins. Catechins are a group of very active flavonoids
that include (+)catechin, (+)gallocatechin, ()epicatechin
(EC) and ()epigallocatechin (EGC), and the galloyl
catechins such as ()epicatechin gallate (ECg),
()epigallocatechin gallate (EGCg), ()catechin gallate
(Cg) and ()gallocatechin gallate(GCg). EGCg is the most
abundant of these, comprising about 50% of the catechin
pool; EGC accounts for around 20%, ECg 13% and EC 6%.
Catechins are colourless, water-soluble compounds that
contribute to the bitterness and astringency of green tea. A
typical green tea serving contains approximately 90mg
catechins(9).
Bioavailability of Green Tea Catechins
The potential health effects of catechins depend not
only on the amount consumed but on their bioavailability
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which appears to be very variable. In order to know the
catechin bioavailability and metabolism, it is necessary to
evaluate their biological activity within target tissues. 10
Following oral administration of tea catechins to rats, the
four principal catechins (EC, ECG, EGC, and EGCG) have
been identified in the portal vein, indicating that tea
catechins are absorbed intestinally(11). Green tea catechins
have been shown to be bioavailable in human, with EGCG
showing lower bioavailability than EGC and EC(12). Only
a small percentage of the ingested catechins appear in the
blood. In a study by Lee et al,2002(12), at the time point
tmax ( the time reach maximum concentration), 0.16,0.58,
and 1.1% of the ingested doses of EGCG, EGC and EC
from green tea administration were present in the
circulating plasma. According to different studies on
catechin pharmacokinetics, EGCG are mostly present in the
free form in the plasma, whereas EGC and EC are
predominantly found as glucuronic acid and sulphate
conjugates in plasma and urine. There is evidence that
EGCG is only present in trace or non-detectable amounts
in the urine and is excreted in to bile(12,13).
Further research results are largely consistent in
demonstrating that the addition of milk to tea does not
interfere with catechin absorption(14-16), but milk may
affect the antioxidant potential of tea, depending upon milk
fat content, milk volume added, and the method used to
assess this parameter(14-16). Xu et al .(17) observed that
the epimerization reaction occurring in manufacturing
canned and bottled tea drinks would not significantly affect
antioxidant activity and bioavailability of total tea
polyphenols.
Oral Health and Green Tea:
Earlier epidemiological studies reported that
populations who drink tea on a regular basis have a reduced
number of carious teeth(18). The tea plant extracts fluoride
from the soil, which then accumulates in its leaves. For this
reason tea is a very rich natural source of fluoride; dry tea
leaves may contain 4-400ppm fluoride, the brewed tea
0.34-6ppm resulting in one cup of tea containing between
0.3mg and 0.5mg of fluoride(19-21). Several mechanisms
have been proposed for the observed anticariogenic
properties of tea and its polyphenols. This includes
inhibitory effect on bacterial growth and bacterial viability,
inhibition of glucosyl transferase which limits the
biosynthesis of sticky glucan (glucan synthesis allows the
bacteria to firmly attach to the tooth surface), and inhibition
of salivary -amylase activities and the consequent
inhibition of starch hydrolysis(22). In a few human trials,
catechins (without added sugar) have been shown to inhibit
plaque deposition(23) reduce plaque and gingival index(24)
and inhibit acid production in dental plaque bacteria(25).
Also, it has been shown that green tea was very effective in
reducing oral malodour temporarily because of its
disinfectant and deodorant activities(26).
It has been suggested that tea may play a role in the
prevention of oral cancer(27). One double-blind,randomised intervention trial suggested that treating
patients with a mixture of black and green tea components
could improve the clinical manifestations of precancerous
oral lesions(28). A pilot study showed that heavy smokers
who consumed 5 cups of green tea a day for four weeks
reduced the number of damaged cells in the mouth. The
authors concluded that these results warrant a large scale
intervention trial to further verify the role of green tea in
the prevention of oral cancer in smokers(29).
Green Tea as a Preventive and Therapeutic Product in
Periodontal Disease:
Oxidative stress plays an important role in the
pathogenesis of periodontal disease, as well as many other
disorders(30). Antioxidants such as polyphenols in green
tea can neutralize free radicals and may reduce or even help
prevent some of the damage they cause. Makimura M,
1993(31) investigated the effect of various tea polyphenol
and caffeine on induction of NO synthetase (NOS) in
thioglycollate elicited and lipopolysaccharide(LPS)-activated peritoneal macrophages. EGC and EGCg found to
be inhibit inducible NOS protein (iNOS) in activated
macrophages, and reduction could occur through
prevention of the binding of nuclear factor kappa-B to the
iNOS promoter, thereby inhibiting the induction of iNOS
transcription. Moreover, there is consistent evidence that
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green tea consumption produces a significant increase in
the overall plasma antioxidant capacity in humans(32-34).
Green tea extracts and catechins are known to have strong
antioxidant properties in vitro(34). In various in-vitro
tests, catechins are able to protect biological molecules e.g.
endogenous antioxidants, lipids, and proteins, against the
adverse effects of reactive oxygen and reactive nitrogen
species(35-38). It has been reported that a dentifrice
containing green tea catechins was effective in inhibiting
gingival oxidative stress in periodontal lesions(39). Topical
green tea catechins may also be an effective therapeutic
agent, acting to suppress periodontal inflammation with
decreasing gingival oxidative stress(39).
There have been reports showing that the (-)-
epigallocatechin gallate ( EGCg), which is a predominant
component of Japanese green tea catechins, exhibited a
number of inhibitory effects on bacteria, tumor cells, and
the hosts immune systems. The bactericidal effects of tea
catechins on pathogenic bacteria, such as Escherichia
coli(40), Helicobacter pyroli(41), and methicillin-resistant
Staphylococcus aureus(42), were demonstrated by their
ability -
to damage the bacterial lipid bilayer, to inhibit bacterial enzymatic activities,
and
to bind directly to peptidoglycan, as
observed with beta lactams.
Mouth rinsing with a dilute catechin solution
reduced the mouth odour (halitosis) associated with
periodontal disease; it was subsequently established that tea
catechins deodorized methyl mercaptan, the main cause of
halitosis(43).
Green tea catechins, such as (-)-epigallocatechin
gallate (EGCg), inhibit periodontal pathogens and inhibited
the collagenase activity at optimal concentration of teacatechin (50 to 100 mg/ ml)(44). Green tea poly phenol
such as catechin gallates, especially EGCg (active at 250
500 g/ml), inhibited growth and adherence to buccal
epithelial cells of P. gingivalis(45).
Green tea catechins and related polyphenols
inhibited the activity and expression of collagenase of
gelatinase (MMP-2 and MMP-9) further it has been
reported that EGCg and its derivatives inhibit protein-
tyrosine phosphatase activity in prevotella intermedia(46).
The green tea catechins produced bactericidal activity at 1
mg/ml concentration against species of Prevotella and P.
gingivalis , and reduction in markers of gingivitis after the
use of a slow-release buccal delivery system applied over a
period of 8 weeks(25). More recently, the effects of the
EGCg and its derivatives from Japanese green tea on the
activities of Rgp and Kgp in P.gingivalis investigated, and
the findings suggest that green tea catechins may have the
potential to reduce periodontal breakdown resulting from
the potent proteinase activity of P.gingivalis. 47 EGCg and
epicatechin gallate inhibited lactate dehydrogenase and
effective in reducing acid production in dental plaque and
mutans streptococci(25).
Recently, Mitoshi Kushiyama, 2009(48)
investigate the relationship between the intake of green tea
and periodontal disease. In multivariate linear regression
models, every one cup/day increment in green tea intake
was associated with decrease in the mean probing depth,
decrease in the mean clinical attachment level and decrease
in bleeding on probing Further more J. Prabhakar, 2010(49)
investigate the antimicrobial efficacy of Triphala, green tea
polyphenols, MTAD(a mixture of doxycycline, citric acid,
and Tween-80 detergent), and 5% sodium hypochlorite
against E. faecalis biofilm formed on tooth substrate. 5%
sodium hypochlorite showed maximum antibacterial
activity against E. Faecalis biofilm formed on tooth
substrate. Triphala, green tea polyphenols and MTAD
showed statistically significant antibacterial activity.
Alveolar bone resorption is a characteristic
feature of periodontal diseases and involves the removal of
both the mineral and organic constituents of the bone
matrix, which is caused by multinucleated osteoclast cells.
It has been reported that (-)-epigallocatechin gallate could
induce the apoptotic cell death of osteoclast(50). Yun J-
H,et al 2007(51) has been found that EGCG inhibited the
osteoclast formation induced by 1-alpha,25(OH)2D3 ,
investigation based on TRAP staining in the co-culture
system. Finding suggest that EGCG remar kably reduced
the number of TRAP-positive multinucleated cells at a
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concentration of 20 uM. Yun J-H,et al 2007(52) further
suggest that (-)-epigallocatechin gallate might prevent
alveolar bone resorption by inhibiting osteoclast survival
through the caspase-mediated apoptosis.
Harmful Effects of Green Tea:
Although green tea has several beneficial effects on
health, the effects of green tea and its constituents may be
beneficial up to a certain dose yet higher doses may cause
some harmful effects. Harmful effects of tea over-
consumption are due to three main factors: its caffeine
content, the presence of aluminum, and the effects of tea
polyphenols on iron bioavailability. Green tea should not
be taken by patients suffering from heart conditions or
major cardiovascular problems. Pregnant and breastfeeding
women should drink no more than one or two cups per day,
because caffeine can cause an increase in heart rhythm. It is
also important to control the concomitant consumption of
green tea and some drugs, due to caffeines diuretic
effects(53). Some studies revealed the capacity of tea plants
to accumulate high levels of aluminum. This aspect is
important for patients with renal failure because aluminum
can be accumulated by the body, resulting in neurological
diseases; it is therefore necessary to control the intake of
food with high amounts of this metal. Likewise, green tea
catechins may have an affinity for iron, and green tea
infusions can cause a significant decrease of the iron
bioavailability from the diet(55).
Conclusion:
Various studies suggest that there is a modest
association between daily intake of green tea and its
preventive role. Drinking green tea at meals is a relatively
easy habit to maintain a healthy periodontium. Definitive
conclusions concerning the protective effect of green tea
have to come from well-designed observational
epidemiological studies and intervention trials. The
development of biomarkers for green tea consumption, as
well as molecular markers for its biological effects, will
facilitate future research in this area.
Corresponding author: Dr. Sweta Soni, Senior Lecturer,
Department of Periodontics, Vyas Dental College and
Hospital, Jodhpur, India. Phone: +91 9414915087, Email:
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