2012
DOI: 10.1016/j.archoralbio.2011.11.017
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Green tea: A promising natural product in oral health

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Cited by 129 publications
(114 citation statements)
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“…Bioactive natural metabolites derived from various plant extracts have shown potential oral benefits (Shinada et al, 2007;Macedo et al, 2009;Bedran-Russo et al, 2011;Pavan et al, 2011;Narotzki et al, 2012). To the best of our knowledge, this is the first study to systematically evaluate the dentin bioactivity of different and well-defined sources of PACs and correlate these findings with their phytoconstituent profiles.…”
Section: Discussionmentioning
confidence: 99%
“…Bioactive natural metabolites derived from various plant extracts have shown potential oral benefits (Shinada et al, 2007;Macedo et al, 2009;Bedran-Russo et al, 2011;Pavan et al, 2011;Narotzki et al, 2012). To the best of our knowledge, this is the first study to systematically evaluate the dentin bioactivity of different and well-defined sources of PACs and correlate these findings with their phytoconstituent profiles.…”
Section: Discussionmentioning
confidence: 99%
“…Yet, another publication demonstrates on a large number of volunteers that green tea does not alter liver functions in any way [158]. The most recent publications have examined the biochemical and pharmaceutical properties of tea catechins and their impact on human health [159][160][161][162][163][164]. We would like to conclude this review with an appeal, 'Drink tea for the benefits to your health!'…”
Section: Resultsmentioning
confidence: 99%
“…Besides polyphenols, GTE contains additional antioxidants such as carotenoids, tocopherols (vitamin E derivatives) and vitamin C. Tea contains also minerals that function as co-factors in antioxidant enzymes: zinc, selenium and manganese. Polyphenols have additional mechanisms in which they reduce oxidation level besides direct role as antioxidants [32,33]. The antifibrotic effect of GTE explained by some authors who reported that it might be through the inhibition exerted by GTE on gelatinases involved in the damage to lung extracellular matrix, matrix metalloproteinases [18] and others have demonstrated that GTE both inhibits the signal transduction of TGF-β by binding to transforming growth factor receptor II (TGFR) and attenuates the expression of α-smooth muscle actin (α-SMA) in MRC-5 cells (human lung fibroblasts), which is a myofibroblast cell line, when it is stimulated by TGF-β.…”
Section: Discussionmentioning
confidence: 99%