green tea - manuscript text1

Upload: wulan-ambar-waty

Post on 04-Jun-2018

213 views

Category:

Documents


0 download

TRANSCRIPT

  • 8/14/2019 Green Tea - Manuscript Text1

    1/9

    JOURNAL OF CONTEMPORARY DENTAL SCIENCES VOLUME 1 ISSUE 1

    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.

  • 8/14/2019 Green Tea - Manuscript Text1

    2/9

    JOURNAL OF CONTEMPORARY DENTAL SCIENCES VOLUME 1 ISSUE 1

    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

  • 8/14/2019 Green Tea - Manuscript Text1

    3/9

    JOURNAL OF CONTEMPORARY DENTAL SCIENCES VOLUME 1 ISSUE 1

    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

  • 8/14/2019 Green Tea - Manuscript Text1

    4/9

    JOURNAL OF CONTEMPORARY DENTAL SCIENCES VOLUME 1 ISSUE 1

    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

  • 8/14/2019 Green Tea - Manuscript Text1

    5/9

    JOURNAL OF CONTEMPORARY DENTAL SCIENCES VOLUME 1 ISSUE 1

    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:

    [email protected]

    REFERENCES

    1. Bun SS, Bun H, Guedon D, et al. Effect of green

    tea extracts on liver functions in Wistar rats.

    Food Chem Toxicol 2006; 44(7): 1108-13.

    2. Cabrera C, Artacho R, Gimnez R: Beneficial

    effects of green tea: a review. J Am Coll Nutr

    2006, 25:79-99.

    3. Rice-Evans CA, Miller NJ, Bolwell PG, Bramley

    PM, Pridham JB. The relative antioxidant

    activities of plant-derived polyphenolic

    flavonoids. Free Radic Res 1995;22:37583.

    4. McKay DL, Blumberg JB: The role of tea in

    human health: An update. J Am Coll Nutr

    2002;21:113.

    5. Wu CD, Wei GX: Tea as a functional food for

    oral health. Nutrition2002; 18:443444.

    6. Zuo Y, Chen H, Deng Y: Simultaneous

    determination of catechins, caffeine and gallic

    acids in green, Oolong, black and Pu-erh teas

    using HPLC with a photodiode array detector.

    Talanta2002; 57:307316.

    7. FDA. Veregen [online]. Available from URL:

    http://www.

    fda.gov/cder/foi/label/2006/021902lbl.pdf

    [Accessed 2007Oct 23]

    mailto:[email protected]:[email protected]
  • 8/14/2019 Green Tea - Manuscript Text1

    6/9

    JOURNAL OF CONTEMPORARY DENTAL SCIENCES VOLUME 1 ISSUE 1

    8. Graham H. Green tea composition, consumption

    and polyphenol chemistry.Preventive

    Medicine1992;21:334350.

    9. Balentine DA, Wiseman SA, Bouwens LC. The

    chemistry of tea flavonoids. Crit Rev Food Sci

    Nutr 1997;37: 693-704.

    10. Manach C, Scalbert A, Morand C, Remesy C,

    Jimenez L: Polyphenols: food sources and

    bioavailability. Am J Clin Nutr2004; 79: 727

    747.

    11. Okushio K, Matsumoto N, Kohri T, Suzuki M,

    Nanjo F, Hara Y: Absorption of tea catechins into

    rat portal vein. Biol Pharm Bull1996; 19:326

    329.

    12. Lee MJ, Malialal P. Chen L, Meng X, Bondoc

    FY, Prabhu S, Lambert G, Mohr S, Yang CS.

    Pharmacokinetics of tea catechins after ingestion

    of green tea and epigallocatechin-3-gallate by

    humans: Formation of different metabolites and

    individual variability. Cancer epidemiology,

    Biomarkers and Prevention2002; 11:1025-1032.

    13. Williamson G, Manach C. Bioavailability and

    bioefficacy of polyphenols in humans. II. Review

    of 93 intervention studies. Am J Clin Nutr

    2005;81:243-255.

    14. Leenen R, Roodenburg A, Tijburg L, Wiseman S:

    A single dose of tea with or without milk

    increases plasma antioxidant activity in humans.

    Eur J Clin Nutr2000; 54:879.

    15. Van het Hof K, Kivits G, Weststrate J, Tijburg L:

    Bioavailability of catechins from tea: The effect

    of milk. Eur J Clin Nutr1998; 52:356359.

    16. Hollman PC, Van Het Hof K, Tijburg L, Katan

    MB: Addition of milk does not affect the

    absorption of flavonols from tea in man. Free

    Radic Res2001; 34:297300.

    17. Xu JZ, Yeung SY, Chang Q, Huang Y, Chen ZY:

    Comparison of antioxidant activity and

    bioavailability of tea epicatechins with their

    epimers. Br J Nutr2004; 91:873881.

    18. Ramsey AC, et al. Fluoride intakes and caries

    increments in relation to tea consumption by

    British children. Caries Res1975; 9:312.

    19. Wei SHY, et al (1989) Concentration of fluoride

    and selected other elements in tea. Nutrition1989;

    5: 237-40.

    20. Chan JT, et al (1996) Fluoride content in

    caffeinated, decaffeinated and herbal teas. Caries

    Research1996; 30:88-92

    21. Hayacibara MF, et al. Fluoride and aluminium in

    teas and tea-based beverages. Rev Saude

    Publica2004 ;38: 100-5.

    22. Wu CD, Wei, GX. Tea as a functional food for

    oral health. Nutrition2002; 18:443-444.

    23. Ooshima T, Minami T, Aono W, Tamura Y,

    Hamada S. Reduction of dental plaque deposition in

    humans by oolong tea extract. Caries Res. 1994;28(3):146-

    9.

  • 8/14/2019 Green Tea - Manuscript Text1

    7/9

    JOURNAL OF CONTEMPORARY DENTAL SCIENCES VOLUME 1 ISSUE 1

    24. Liu T, Chi Y. Experimental study on polyphenol

    anti-plaque effect in human. Zhonghua Kou Qiang Yi Xue

    Za Zhi. 2000;35(5):383-4.

    25. Hirasawa M, Takada K, Otake S. Inhibition of

    acid production in dental plaque bacteria by green teacatechins. Caries Res. 2006;40(3):265-70.

    26. Lodhia P; Yaegaki K, Khakbazhejad A, Imai T,

    Sato T, Tanaka T, Murata T, Kamada T. Effect of green tea

    on volatile sulfur compounds in mouth air. J Nutr Sci

    Vitaminol, 2008;84:89-94.

    27. Yang C. S., Maliakal P., Meng X. (2002)

    Inhibition of carcinogenesis by tea. Annu. Rev. Pharmacol.

    Toxicol.2002; 42:25-54.

    28. Halder A, et al. Black tea (Camellia sinensis) as a

    chemopreventive agent in oral

    precancerous lesions. J Envir Path Toxicol Oncol 2005;

    24:141-4.

    29. Schwartz JL, et al (2005) Molecular and cellular

    effects of green tea on oral cells of smokers: a pilot study.

    Mol Nutr Food Res2005; 49: 43-51.

    30. Chapple ILC: Reactive oxygen species and

    antioxidants in inflammatory diseases. J Clin Periodontol

    1997; 24: 287-296.

    31. Makimura M, Hirasawa M, Kobayashi K, Indo

    J, Sakanaka S, Teguchi T and Otake S. Inhibitory effect of

    Tea Catechins on collegenase activities. J Periodontol

    1993; 64: 630-636.

    32. M, Ghiselli A, FerroLuzzi A. In vivo antioxidant

    effect of green and black tea in man. European Journal of

    Clinical Nutrition 1996;50(1):28-32.

    33. VanhetHof KH, deBoer HSM, Wiseman SA, Lien

    N, Weststrate JA, Tijburg LBM. Consumption of green or

    black tea does not increase resistance of low-density

    lipoprotein to oxidation in humans. American Journal of

    Clinical Nutrition 1997;66(5):1125-1132.

    34. Benzie IFF, Szeto YT, Strain JJ, Tomlinson B.

    Consumption of green tea causes rapid increase in plasma

    antioxidant power in humans. Nutrition and Cancer- An

    International Journal 1999;34(1):83-87.

    35. Higdon JV, Frei B. Tea Catechins and

    Polyphenols: Health Effects, Metabolism, and Antioxidant

    Functions. Critical Reviews in Food Science and

    Nutrition,2003; 43(1):89 143.

    36. Cherubini A, Beal MF, Frei B. Black tea increases

    the resistance of human plasma to lipid peroxidation in

    vitro, but not ex vivo. Free Radical Biology and Medicine

    1999;27(3-4):381- 387.

    37. Leung LK, Su YL, Chen RY, Zhang ZH, Huang

    Y, Chen ZY. Theaflavins Theaflavins in Black tea and

    catechins in green tea are equally effective antioxidants.

    Journal of Nutrition 2001;131(9):2248-2251.

    38. Zhu QY, Huang Y, Tsang D, Chen ZY.

    Regeneration of alpha-tocopherol in human low-density

    lipoprotein by green tea catechin. Journal of Agricultural

    and Food

    Chemistry 1999;47(5):2020-2025.

    39. Takayuki Maruyama, Takaaki Tomofuji,

    Yasumasa Endo, Koichiro Irie, Tetsuji Azuma et al.

    Supplementation of green tea catechins in dentifrices

    suppresses gingival oxidative stress and periodontal

    inflammation. Archives of oral biology2011; 56: 4 8 53

    40. Sugita- Konishi Y, Hara-Kudo Y, Amano F, et al.

    Epigallocatechin gallate and Gallocatechin gallate in green

    tea catechins inhibit extracellular release of Vero toxin

  • 8/14/2019 Green Tea - Manuscript Text1

    8/9

    JOURNAL OF CONTEMPORARY DENTAL SCIENCES VOLUME 1 ISSUE 1

    from entero hemorrhagic Escherichia coli O157:H7.

    Biophys Acta 1999: 1472: 42-50.

    41. Mabe K, Yamada M, Oguni I, Takahashi T. In

    vitro and in vivo activities of tea Catechin against

    Helicobacter pylori. Antimicrob Agents Chemother1999;43:1788- 1791.

    42. Zhao WH, Hu ZQ, Okubo S, Hara Y, Shimamura

    T. Mechanism of synergy between epigallocatechin gallate

    and beta-lactams against methicillin-resistant

    Staphylococus.Antimicrob Agents Chemother

    2001;45:1737-1742.

    43. Yasuda H, Arakawa T. Deodorizing mechanism

    of ()-epigallocatechin against Methyl mercaptan.

    Bioscience, Biotechnology and Biochemistry

    1995;59:12321236.

    44. Makinnira M. Hirasawa M. Kobaytishi K.

    Inhibitory effect of tea catechins on collagenase activity. J

    Periodontol 1993; 64:630-636.

    45. Sakanaka S, Aizawa M, Kim M, Yamamoto T.

    Inhibitory effects of green tea polyphenols on growth and

    cellular adherence of an oral bacterium, Porphyromonas

    gingivalis. Bioscience, Biotechnology and Biochemistry

    1996;60:745749.

    46. Isemura M, Saeki K, Minami T et al. Inhibition

    of matrix metalloproteinases by tea catechins and related

    polyphenols. Ann N Y Acad Sci 1999;878:629631.

    47. Okamoto M, Sugimoto A, Leuing K-P,

    Nakayama K, Kamaguchi A, Maeda N.

    Inhibitory effect of green tea catechins on cysteine

    proteinases in Porphyromonas gingivalis. Oral

    Microbiology and Immunology 2004;19:118120.

    48. Mitoshi Kushiyama, Yoshihiro Shimazaki,

    Masatoshi Murakami, and Yoshihisa Yamashita.

    Relationship between the intake of green tea and

    periodontal disease. J Periodontol 2009;80:372-377.

    49. J. Prabhakar, MDS, M. Senthilkumar, PhD, M.S.

    Priya, MDS, K. Mahalakshmi, MSc,P.K. Sehgal, PhD, and

    V.G. Sukumaran, MDS. Evaluation of Antimicrobial

    Efficacy of Herbal Alternatives (Triphala and Green Tea

    Polyphenols), MTAD, and 5% Sodium Hypochlorite

    against Enterococcus faecalis Biofilm Formed on Tooth

    Substrate: An In Vitro Study. J Endod 2010;36:8386.

    50. Nakagawa H, Wachi M, Woo JT et al. Fenton

    reaction is primarily involved in a

    Mechanism of ()-epigallocatechin-3-gallate to induce

    osteoclastic cell death. Biochem

    Biophys Res Commun 2002;288: 142150.

    51. Yun J-H, Pang E-K, Kim C-S, Yoo Y-J, Cho K-S,

    Chai J-K, Kim C-K, Choi S-H.Inhibitor effects of green tea

    polyphenol ()-epigallocatechin gallate on the expression

    of matrix metalloproteinase-9 and on the formation of

    osteoclasts. J Periodont Res 2004; 39; 300307.

    52. Yun JH, Kim CS, Cho KS, Chai JK, Kim CK,

    Choi SH. (-)-Epigallocatechin gallate induces apoptosis, via

    caspase activation, in osteoclasts differentiated from RAW

    264.7 cells. J Periodontal Res 2007;42:212- 218.

    53. Costa LM, Gouveia ST, Nobrega JA:

    Comparison of heating extraction procedures for Al, Ca,

    Mg and Mn in tea samples. Ann Sci 2002, 18:313-318.

    54. Hamdaoui MH, Chabchob S, Heidhili A: Iron

    bioavailability and weight gains to iron- deficient rats fed a

    commonly consumed Tunisian meal bean seeds ragout

    with or without beef and with green or black tea decoction.

    J Trace Elem Med Biol 2003, 17:159-164.

  • 8/14/2019 Green Tea - Manuscript Text1

    9/9

    JOURNAL OF CONTEMPORARY DENTAL SCIENCES VOLUME 1 ISSUE 1