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. 2016 May 11;10:166–173. doi: 10.2174/1874210601610010166

Green Tea (Camellia Sinensis): Chemistry and Oral Health

Zohaib Khurshid 1, Muhammad S Zafar 2,*, Sana Zohaib 3, Shariq Najeeb 4, Mustafa Naseem 5
PMCID: PMC4911733  PMID: 27386001

Abstract

Green tea is a widely consumed beverage worldwide. Numerous studies have suggested about the beneficial effects of green tea on oral conditions such as dental caries, periodontal diseases and halitosis. However, to date there have not been many review articles published that focus on beneficial effects of green tea on oral disease. The aim of this publication is to summarize the research conducted on the effects of green tea on oral cavity. Green tea might help reduce the bacterial activity in the oral cavity that in turn, can reduce the aforementioned oral afflictions. Furthermore, the antioxidant effect of the tea may reduce the chances of oral cancer. However, more clinical data is required to ascertain the possible benefits of green tea consumption on oral health.

Keywords: Antimicrobial, caries, dental care, periodontitis, tobacco

INTRODUCTION

Before the development of pharmaceutical industry, herbal products were used for curing various conditions. The concept of using natural and herbal products is very old. Humans have used these products for curing various diseases and become popular accordingly. In terms of oral care, most commonly used herbal product is “Miswak” that become popular in several communities as an effective, cheap and efficient way of maintaining oral hygiene [1-4]. Similarly, beneficial effects of using various types of tea leaves have been a common topic of discussion in general public and professionals. According to Chinese legend, tea has a known history of over 4000 years ago which was discovered accidentally by an emperor, while according to other sources the Chinese have been drinking tea since 3000 B.C. and over millions of acres are devoted to its cultivation. Currently, it is being used in almost every country around the world and is now been grown in India, Sri Lanka, Iran, Java and Japan [5].

Green tea (botanical name of tea plant is Camellia Sinensis) belonging to the family Theaceae (Table 1) has been explored in the recent years for its beneficial effects on oral health. It can be available as a shrub or evergreen tree. Its leaves may vary from exstipulate, lanceolate to obovate up to 30 cm long, 2–5 cm broad, pubescent, sometimes becoming glabrous, serrate, acute or acuminate [6].

Table 1.

Classification of green tea plant.

Kingdom Plantae
Subkingdom Tracheobionta
Super-division Spermatophyte
Division Magnoliophyta
Class Magnoliopsida
Sub-class Dillenidea
Order Theales
Family Theaceae
Genus Camellia L.
Species Camellia Sinensis

According to an estimate, daily consumption of tea is more than 3 billion cups; almost 75 percent consumption by China [7]. The standard method defined in Chinese culture is illustrated Fig. (1). Tea leaves are available in a variety of forms depending on processing techniques illustrated in Fig. (2) [8]. Dissimilarity between green tea and black tea is due to processing methods adopted during manufacturing. As a consequence of fermentation of black tea, chemical substance known as catechins (i.e. polyphenols with molecular weight less than 450Da) are oxidized and condensed while these are present in green tea. A third type of tea, known as oolong, contains mixture of monomeric and oligomeric catechins and is in semi fermented form [9].

Fig. (1).

Fig. (1)

Standard method to make green tea in chinese history.

Fig. (2).

Fig. (2)

Different kinds of tea according to their processing.

Distinctive composition of green is listed in Table 2 [10, 11]. It is reported that one third part of bioactive compounds in green tea is contributed by polyphenols that is the most interesting constituent [12]. The main type of polyphenols are called catechins (flavan-3-ols) also known as tannins serve as astringency constituent. Dr. Michiyo Tsujimura extracted the catechins from tea leaves in 1929 and studied their functions (Fig. 3) for the first time during his work at The Institute of Physical and Chemical Research, Japan.

Table 2.

Chemical composition of green tea plant.

Protein Peptides and enzymes
Carbohydrates Fructose, sucrose, cellulose, pectin and glucose
Vitamins Vitamins (B, C, and E)
Xanthic bases Caffeine, Theophylline
Pigments Chlorophyll, Carotenoids
Minerals and trace elements Calcium, Magnesium, Sodium, Chromium, Manganese, Copper, Cobalt, Nickel, Iron, Molybdenum, Selenium, Phosphorus, Potassium, Fluoride, Zinc, Aluminum

Fig. (3).

Fig. (3)

Functions of catechins in human body.

Most important kind of catechins include epigallocatechin-3-gallate (EGCG; 59%), epigallocatechin (EGC; 19%), epicatechin-3-gallate (ECG; 13.6%) and epicatechin (EC; 6.4%) including EGCG and EGC are reported for their presence in green tea. Both the types along with ECG exhibit antimicrobial activity [13]. ECG reviles the possibility of protection against urinary tract infections (UTI) as it is reported to be excreted by kidney while it is also extracted in bile along with EGCG. Large variations can be observed in the chemical structures of catechins due to dissimilar composition (Fig. 4). Green tea also serves as a great source of anti-oxidants.

Fig. (4).

Fig. (4)

Chemical structures of catechin and its family.

Numerous therapeutic effects of green tea are reported after human clinica trials [13, 14] . It contributes to improved oral health and decreases the chances of cardiovascular diseases, cancer and acts as an anti-hypertensive, anti-bacterial, anti-viral agent. It also exhibits protection against ultraviolet radiations, helps in weight loss, causes increase in bone mineral density and provides neuro-protective power. Other than the mentioned advantages of green tea, it is popularly utilized for the treatment of stomach discomfort, indigestion, vomiting, diarrhea and flatulence. It also enhances brain functioning and helps in maintaining blood glucose balance and body weight [15]. Due to numerous health benefits, there has been a significant increase in the popularity and consumption of green tea among various cultures and populations.

GREEN TEA EFFECT ON ORAL TISSUES

Green tea which is essential source for providing polyphenol antioxidants has the ability to protect against various oral diseases such as dental caries, gingivitis, periodontitis, halitosis and oral malignancy (protection and regression). In addition it can prevent from oral oxidative stress, inflammation resulting due to cigarette smoke and reduces dentin erosion and abrasion. The therapeutic roles of green tea related to oral health are given.

a) Role as Antioxidants

Polyphenols have shown anti-oxidative activity by neutralization of free radicals in the body. They are also known to reduce or prevent their detrimental effects and restrain ROS generation to inhibit the lysosomal secretions. The hydrogen releasing property of catechin and epicatechin results in scavenging effects [16]. Polyphenols have following processes that reduce oxidation level (Fig. 5).

Fig. (5).

Fig. (5)

Representing steps of oxidative reduction mechanism by polyphenols.

b) Therapeutic Effects on Periodontal and Gingival Health

The gingival crevice is a physiological zone surrounded by gingiva and tooth margins. A colony of microorganisms resides in this space and most common of that are anaerobes. In pathological conditions, these spaces extend and periodontal pockets filled with serum exudates and large colonies of polymorphs. Additionally, oxidative stress supports the development of diseased conditions. The microbes commonly present in such conditions are Prevotella spp and Porphyromonas gingivalis (black pigmented anaerobes) [18].

Periodontal health is inversely related to consumption of green tea, an epidemiological study proves that people have better periodontal health if they drink green tea very often for example during meals or at breaks from work [19]. Green tea plays supportive role in the maintenance of periodontal health, as suggested by an in vitro study catechins (e.g. EGCG) restrict the development and colonization of harmful bacteria such as Porphyromonas gingivalis, Prevotella intermedia, and Prevotella nigrescens [20]. These bacteria cause severe harm to periodontal tissues for example Porphyromonas gingivalis develop adhesion to buccal mucosa and cause destruction [21]. Recently, Nadeem et al. [22] studied the influence of green tea consumption versus black tea on periodontal health of 240 dental students and noticed that students who were consuming green tea had good periodontal health status with minimal plaque accumulation in comparison with consumers of black tea. Literature exhibited that better periodontal health status of regular green tea using individuals is mainly due to catechins, as these are steric structures of 3-galloyl radial, ECG, EGCG and gallocatechin gallate (GCG) (major polyphenols) and responsible for restrain release of toxic end metabolites from Porphyromonas gingivalis [23].

c) Dental Caries

Dental carries is a pathological condition resulting due to demineralization of tooth structure because of bacterial infections and/or deficiency of nutrients. Oral microbes are responsible for carries development, out of which mainly streptococcus mutants are most active [24]. The oral antimicrobial peptides are known to reduce the bacterial activity [25]. Green tea leaves are known to be rich in fluoride and other components such as polyphenols (catechins) that play a supportive role in resisting dental carried as reported in many studies [23, 26-28]. The beneficial role of fluoride is well known as it inhibits the bacterial growth and helps re-mineralization of dental tissues [29, 30]. Cariogenic bacteria release glucans with the help of glucosyltransferase (GTase) which are branched and facilitate adherence of microbes to tooth surface [24]. GC and EGC are the catechins that restrict the growth of 10 types of carries causing bacteria. Otake et al. [31] showed that total amount of catechins, mainly EGCG and its epimer gallocatechin, EC and ECG present in one cup of green tea prevent streptococcus mutants from adhering to tooth surfaces. The catechins were extracted from green tea with concentration of 100mg/L and their effects on bacterial adhesion to salivary coated hydroxyapatites were observed. Other studies also exhibit that consumption of tea constrains the release of salivary enzyme, amylase as observed by Kashket and Paolino [32]. Later it was supported by Zhang and Kashket [33] proving that tea, either black or green restrains the enzymatic activity of Streptococcus mutans’ amylase on tooth structure preventing deminerlization.

d) Bad Breath (halitosis)

The main reagents responsible for halitosis (bad breath) are volatile sulfide compounds such as hydrogen sulfide (H2S), dimethylsulfide [(CH3)2S] and methyl mercaptan (CH3SH). These reagents degrade in the oral cavity by proteolytic reactions primarily by anaerobic gram negative bacteria consuming numerous sulfur-containing substrates including saliva, food debris, epithelial cells and blood [34]. Green tea is well known for antibacterial properties against anaerobic microorganisms. Green tea can abolish bad breath by suppressing anaerobic bacteria and eliminating the production of volatile sulfur compounds [35]. Deodorant action of ingredients decreases in the following order: EGCG > EGC > ECG > EC. The deodorizing action of EGCG is based on a chemical reaction of EGCG and MSH and introducing methylsulfinyl/methylthio group into the B ring of EGCG. During this reaction, a methylthio group is supplemented in orthoquinone form of the catechin produced by oxidation, hence eliminating the halitosis [36].

e) Cigarette Smoke Induced Inflammation

Smoking affects the homeostasis and injurious to oral health [37, 38]. The effects of smoking range from simple mucosal erythema to premalignant conditions and oral cancer. Smoking intensifies oral malignancies in response to oral inflammatory diseases due to compromised status of salivary antioxidants [39]. Diminished activity of numerous salivary enzymes is observed during smoking hence compromising the protection against oxidative damage [17]. In addition, smoke coming from tobacco comprised of reactive oxygen species (ROS) including superoxides, hydroxyl radical/hydrogen peroxide. The toxicity is further added due to the formation of nitric oxide (NO). Superoxide reacts chemically with NO to form peroxynitrite (ONOO). The inflammatory transcription factor pathway (NFkB) is triggered by ONOO due to activation of IkB kinase (IKK). The cascade of changes results in the intensification of expressions, iNOS activity and chronic inflammation in tissues even by exposing to a very minute dose of smoke [40].

Green tea can be beneficial for cigarette smokers. Catechins present in green tea are capable of scavenging superoxide oxide, NO, and ONOO [41, 42]. In addition, EGCG has the ability to suppress activation of NF-kB that leads to inhibition of phosphorylation. It can further trigger the collapse of the inhibitory sections IkB-a in human pulp cells. The IkBa is also accountable for overturning nuclear transfer of NF-kB operating subunits (p65 and p50) and stimulation of pro-inflammatory genes [43, 44]. EGCG resulted in decreased NF-kB expression and reduction of proteins facilitated including matrix metalloproteinase9 (MMP-9). The MMP-9 is implicated in the breakdown of extracellular matrix, nterleukin-8 (IL-8) and iNOS present in bronchial epithelium [14]. There are more than 4700 oxygen/nitrogen species and reactive chemical compounds in the cigarette smoke. Nicotine is the main chemical compound released from cigarettes that affects gingival and periodontal health [45]. Nicotine stimulates apoptosis across ROS generations of human gingival fibroblasts (HuGF) [45]. The metabolites of nicotine such as tobacco-specific nitrosamines (TSNAs) are considered major carcinogens.

Weitberg et al. [46] treated cultured human pulmonary cells through EGCG prior to introducing to TSNA 4-(Nmethyl- N-n-trosamino)-1-(3-pyridyl)-1-butanone (NNK). EGCG exhibited the ability to protect against the initiation of genetic injury to DNA of cultivated human pulmonary cells [46]. Another smoke compound (acrolein) is a risk factor for developing periodontal diseases and toxic to HuGF. It inhibits normal functioning of gingival fibroblasts due to interruption with cells attachment and proliferation [47]. In advance stages, acrolein can prompt inflammatory conditions and cancer onset. Green tea extract and EGCG can extinguish acrolein and other unsaturated aldehydes, hence reducing acrolein toxicity [48]. Green tea consumption can diminish oxidative and inflammatory tissue injuries in the oral cavity caused by cigarette smoking.

CONCLUSION

There are numerous beneficial effects of green tea on oral health. Green tea has valuable effects on oral conditions such as dental caries, periodontal disease and halitosis. Research suggests that green tea helps to reduce the bacterial activity in the oral cavity that in turn, can reduce the aforementioned oral afflictions. Furthermore, the antioxidant effect of the tea may reduce the chances of oral cancer in tobacco users. However, more clinical data is require to ascertain benefits of using green tea for oral tissues and prevention of oral diseases

ACKNOWLEDGEMENTS

Declared none.

CONFLICT OF INTEREST

The authors confirm that this article content has no conflict of interest.

REFERENCES

  • 1.Almas K. Miswak (chewing stick) and its role in oral health. Postgrad. Dent. 1993;3:214–218. [Google Scholar]
  • 2.Al-Bayaty F.H. AI-Koubaisi AH, Ali Naw, Abdulla MA. Effect of mouth wash extracted from Salvadora persica (Miswak) on dental plaque formation: A clinical trial. J Medicinal Plants Res. 2010;4(14):1446–1454. [Google Scholar]
  • 3.Sofrata A., Lingström P., Baljoon M., Gustafsson A. The effect of miswak extract on plaque pH. An in vivo study. Caries Res. 2007;41(6):451–454. doi: 10.1159/000107931. [DOI] [PubMed] [Google Scholar]
  • 4.Batwa M., Bergstrom J., Batwa S., Al-Otaibi M.F. The effectiveness of chewing stick miswak on plaque removal. Saudi Dent. J. 2006;18(3):125–133. [Google Scholar]
  • 5.Duke J.A., Atchley A.A. CRC handbook of proximate analysis tables of higher plants. USA: CRC Press; 1986. [Google Scholar]
  • 6.Ferrara L., Montesano D., Senatore A. The distribution of minerals and flavonoids in the tea plant (Camellia sinensis). Farmaco. 2001;56(5-7):397–401. doi: 10.1016/S0014-827X(01)01104-1. [DOI] [PubMed] [Google Scholar]
  • 7.Chen L., Zhou Z.X. Variations of main quality components of tea genetic resources [Camellia sinensis (L.) O. Kuntze] preserved in the China National Germplasm Tea Repository. Plant Foods Hum. Nutr. 2005;60(1):31–35. doi: 10.1007/s11130-005-2540-1. [DOI] [PubMed] [Google Scholar]
  • 8.Banerjee S., Chatterjee J. Efficient extraction strategies of tea (Camellia sinensis) biomolecules. J Food Sci Technol; 2014. pp. 1–11. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Hamilton-Miller J.M. Anti-cariogenic properties of tea (Camellia sinensis). J. Med. Microbiol. 2001;50(4):299–302. doi: 10.1099/0022-1317-50-4-299. [DOI] [PubMed] [Google Scholar]
  • 10.Cabrera C., Artacho R., Giménez R. Beneficial effects of green tea-a review. J. Am. Coll. Nutr. 2006;25(2):79–99. doi: 10.1080/07315724.2006.10719518. [DOI] [PubMed] [Google Scholar]
  • 11.Astill C., Birch M.R., Dacombe C., Humphrey P.G., Martin P.T. Factors affecting the caffeine and polyphenol contents of black and green tea infusions. J. Agric. Food Chem. 2001;49(11):5340–5347. doi: 10.1021/jf010759+. [DOI] [PubMed] [Google Scholar]
  • 12.Mahmood T., Akhtar N., Khan B.A. The morphology, characteristics, and medicinal properties of Camellia sinensis’ tea. J Med Plants Res. 2010;4(19):2028–2033. [Google Scholar]
  • 13.McKay D.L., Blumberg J.B. The role of tea in human health: an update. J. Am. Coll. Nutr. 2002;21(1):1–13. doi: 10.1080/07315724.2002.10719187. [DOI] [PubMed] [Google Scholar]
  • 14.Syed D.N., Afaq F., Kweon M.H., Hadi N., Bhatia N., Spiegelman V.S., Mukhtar H. Green tea polyphenol EGCG suppresses cigarette smoke condensate-induced NF-kappaB activation in normal human bronchial epithelial cells. Oncogene. 2007;26(5):673–682. doi: 10.1038/sj.onc.1209829. [DOI] [PubMed] [Google Scholar]
  • 15.Namita P., Mukesh R., Vijay K.J. Camellia Sinensis (green tea): a review. Global J Pharmacol. 2012;6:52–59. [Google Scholar]
  • 16.Nugala B., Namasi A., Emmadi P., Krishna P.M. Role of green tea as an antioxidant in periodontal disease: The Asian paradox. J. Indian Soc. Periodontol. 2012;16(3):313–316. doi: 10.4103/0972-124X.100902. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Narotzki B., Reznick A.Z., Aizenbud D., Levy Y. Green tea: a promising natural product in oral health. Arch. Oral Biol. 2012;57(5):429–435. doi: 10.1016/j.archoralbio.2011.11.017. [DOI] [PubMed] [Google Scholar]
  • 18.Chapple I.L. Reactive oxygen species and antioxidants in inflammatory diseases. J. Clin. Periodontol. 1997;24(5):287–296. doi: 10.1111/j.1600-051X.1997.tb00760.x. [DOI] [PubMed] [Google Scholar]
  • 19.Kushiyama M., Shimazaki Y., Murakami M., Yamashita Y. Relationship between intake of green tea and periodontal disease. J. Periodontol. 2009;80(3):372–377. doi: 10.1902/jop.2009.080510. [DOI] [PubMed] [Google Scholar]
  • 20.Makimura M., Hirasawa M., Kobayashi K., Indo J., Sakanaka S., Taguchi T., Otake S. Inhibitory effect of tea catechins on collagenase activity. J. Periodontol. 1993;64(7):630–636. doi: 10.1902/jop.1993.64.7.630. [DOI] [PubMed] [Google Scholar]
  • 21.Magnusson I., Lindhe J., Yoneyama T., Liljenberg B. Recolonization of a subgingival microbiota following scaling in deep pockets. J. Clin. Periodontol. 1984;11(3):193–207. doi: 10.1111/j.1600-051X.1984.tb01323.x. [DOI] [PubMed] [Google Scholar]
  • 22.Nadeem M, Datoo F, Bugti AA, Ayaz A, Mahfooz M. Effects of black tea and green tea on periodontal health status among dental students at pakistan. 2014.
  • 23.Sakanaka S., Okada Y. Inhibitory effects of green tea polyphenols on the production of a virulence factor of the periodontal-disease-causing anaerobic bacterium Porphyromonas gingivalis. J. Agric. Food Chem. 2004;52(6):1688–1692. doi: 10.1021/jf0302815. [DOI] [PubMed] [Google Scholar]
  • 24.Hamada S., Slade H.D. Biology, immunology, and cariogenicity of Streptococcus mutans. Microbiol. Rev. 1980;44(2):331–384. doi: 10.1128/mr.44.2.331-384.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Khurshid Z, Naseem M, Sheikh Z, Najeeb S, Shahab S, Zafar MS. Oral Antimicrobial Peptides: Types and Role in the Oral Cavity. . Saudi Pharmaceut J . 2015. [In press] [DOI] [PMC free article] [PubMed]
  • 26.Wu C., Wei G., Wilson M. Tea as a functional food for oral health. Food constituents and oral health. In: Wilson M., editor. Food constituents and oral health: Epigallocatechin gallate Suppresses Cariogenic Viru- Current status and future prospects. Florida, U.S.A.: CRC Press LLC; 2009. pp. 396–417. [DOI] [Google Scholar]
  • 27.Sakanaka S., Kim M., Taniguchi M., Yamamoto T. Antibacterial substances in Japanese green tea extract against Streptococcus mutans, a cariogenic bacterium. Agric. Biol. Chem. 1989;53(9):2307–2311. [Google Scholar]
  • 28.Sakanaka S., Sato T., Kim M., Yamamoto T. Inhibitory effects of green tea polyphenols on glucan synthesis and cellular adherence of cariogenic streptococci. Agric. Biol. Chem. 1990;54(11):2925–2929. [Google Scholar]
  • 29.Zafar MS, Ahmed N. Therapeutic roles of fluoride released from restorative dental materials Res Rev Fluoride. 2015;48(3):184–194. [Google Scholar]
  • 30.Zafar M.S. Effects of surface pre-reacted glass particles on fluoride release of dental restorative materials. World Appl Sci J. 2013;28(4):457–462. [Google Scholar]
  • 31.Otake S., Makimura M., Kuroki T., Nishihara Y., Hirasawa M. Anticaries effects of polyphenolic compounds from Japanese green tea. Caries Res. 1991;25(6):438–443. doi: 10.1159/000261407. [DOI] [PubMed] [Google Scholar]
  • 32.Kashket S., Paolino V.J. Inhibition of salivary amylase by water-soluble extracts of tea. Arch. Oral Biol. 1988;33(11):845–846. doi: 10.1016/0003-9969(88)90110-0. [DOI] [PubMed] [Google Scholar]
  • 33.Zhang J., Kashket S. Inhibition of salivary amylase by black and green teas and their effects on the intraoral hydrolysis of starch. Caries Res. 1998;32(3):233–238. doi: 10.1159/000016458. [DOI] [PubMed] [Google Scholar]
  • 34.Tonzetich J. Production and origin of oral malodor: a review of mechanisms and methods of analysis. J. Periodontol. 1977;48(1):13–20. doi: 10.1902/jop.1977.48.1.13. [DOI] [PubMed] [Google Scholar]
  • 35.Liao S., Kao Y.H., Hiipakka R.A. Green tea: biochemical and biological basis for health benefits. Vitam. Horm. 2001;62:1–94. doi: 10.1016/S0083-6729(01)62001-6. [DOI] [PubMed] [Google Scholar]
  • 36.Yasuda H., Arakawa T. Deodorizing mechanism of (–)-epigallocatechin gallate against methyl mercaptan. Biosci. Biotechnol. Biochem. 1995;59(7):1232–1236. doi: 10.1271/bbb.59.1232. [DOI] [Google Scholar]
  • 37.Javed F., Al-Rasheed A., Almas K., Romanos G.E., Al-Hezaimi K. Effect of cigarette smoking on the clinical outcomes of periodontal surgical procedures. Am. J. Med. Sci. 2012;343(1):78–84. doi: 10.1097/MAJ.0b013e318228283b. [DOI] [PubMed] [Google Scholar]
  • 38.Fahad K., Aziz A., Shahab S., Zafar M. Laboratorial and clinical impacts of tobacco on periodontal health: A systematic review. Int Dental J Student’s Res. 2015;3(2):72–78. [Google Scholar]
  • 39.Greabu M., Totan A., Battino M., Mohora M., Didilescu A., Totan C., Spinu T. Cigarette smoke effect on total salivary antioxidant capacity, salivary glutathione peroxidase and gamma-glutamyltransferase activity. Biofactors. 2008;33(2):129–136. doi: 10.1002/biof.5520330205. [DOI] [PubMed] [Google Scholar]
  • 40.Hasnis E., Bar-Shai M., Burbea Z., Reznick A.Z. Mechanisms underlying cigarette smoke-induced NF-kappaB activation in human lymphocytes: the role of reactive nitrogen species. J. Physiol. Pharmacol. 2007;58(1) Suppl. 5:275–287. [PubMed] [Google Scholar]
  • 41.Nakagawa T., Yokozawa T. Direct scavenging of nitric oxide and superoxide by green tea. Food Chem. Toxicol. 2002;40(12):1745–1750. doi: 10.1016/S0278-6915(02)00169-2. [DOI] [PubMed] [Google Scholar]
  • 42.Chung H.Y., Yokozawa T., Soung D.Y., Kye I.S., No J.K., Baek B.S. Peroxynitrite-scavenging activity of green tea tannin. J. Agric. Food Chem. 1998;46(11):4484–4486. doi: 10.1021/jf980556u. [DOI] [Google Scholar]
  • 43.Hirao K., Yumoto H., Nakanishi T., Mukai K., Takahashi K., Takegawa D., Matsuo T. Tea catechins reduce inflammatory reactions via mitogen-activated protein kinase pathways in toll-like receptor 2 ligand-stimulated dental pulp cells. Life Sci. 2010;86(17-18):654–660. doi: 10.1016/j.lfs.2010.02.017. [DOI] [PubMed] [Google Scholar]
  • 44.Kundu J.K., Surh Y.J. Inflammation: gearing the journey to cancer. Mutat. Res. 2008;659(1-2):15–30. doi: 10.1016/j.mrrev.2008.03.002. [DOI] [PubMed] [Google Scholar]
  • 45.Kang S.W., Park H.J., Ban J.Y., Chung J.H., Chun G.S., Cho J.O. Effects of nicotine on apoptosis in human gingival fibroblasts. Arch. Oral Biol. 2011;56(10):1091–1097. doi: 10.1016/j.archoralbio.2011.03.016. [DOI] [PubMed] [Google Scholar]
  • 46.Weitberg A.B., Corvese D. The effect of epigallocatechin galleate and sarcophytol A on DNA strand breakage induced by tobacco-specific nitrosamines and stimulated human phagocytes. J. Exp. Clin. Cancer Res. 1999;18(3):433–437. [PubMed] [Google Scholar]
  • 47.Cattaneo V., Cetta G., Rota C., Vezzoni F., Rota M.T., Gallanti A., Boratto R., Poggi P. Volatile components of cigarette smoke: effect of acrolein and acetaldehyde on human gingival fibroblasts in vitro. J. Periodontol. 2000;71(3):425–432. doi: 10.1902/jop.2000.71.3.425. [DOI] [PubMed] [Google Scholar]
  • 48.Beretta G., Furlanetto S., Regazzoni L., Zarrella M., Facino R.M. Quenching of α,β-unsaturated aldehydes by green tea polyphenols: HPLC-ESI-MS/MS studies. J. Pharm. Biomed. Anal. 2008;48(3):606–611. doi: 10.1016/j.jpba.2008.05.036. [DOI] [PubMed] [Google Scholar]

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