Abstract:Tea polyphenols have been demonstrated as chemopreventive agents in a number of experimental models. However, less is known about the mechanism of chemoprevention by black tea compared with that of green tea. Some beneficial properties of theaflavins, the black tea polyphenols, were investigated in the present study. Theaflavins showed inhibitory effects on H(2)O(2)- and tert-butyl hydroperoxide (tBuOOH)-induced cytotoxicity (evaluated by tetrazolium bromide reduction), cellular oxidative stress (detected by o… Show more
“…Notable among the literature on antioxidants are studies on various teas, especially green tea (51,52). For example, polyphenols in green tea include catechins (‰avan-3-ols) (53,54), while in black tea, thea‰avin formation may be important (54,55). Polyphenols from green and black tea are eŠective antioxidants in model test systems, while tea polyphenols may also chelate pro-oxidant metals (56).…”
Section: Examples Of Anti-mutagen Protection Against Dišerent Classesmentioning
confidence: 99%
“…Various types of anti-mutagen appear to act through inhibiting induction of these enzymes, or otherwise interfering with the activation process. For example, black tea polyphenol (thea‰avin) has been shown to be able to reduce the induction of CYP1A1, at least in a human cultured cell line, and this has been suggested as one mechanism by which this class of chemicals can reduce DNA damage, and possibly also reduce cancer risk (55). The activation of speciˆc groups of mutagens resides with other speciˆc classes of enzymes.…”
Section: Examples Of Mechanisms Of Anti-mutagen Protection Against DImentioning
An anti-mutagen is any substance that reduces the rate of spontaneous mutations or counteracts or reverses the action of a mutagen, or any technique that protects cells against the eŠects of mutagens. Studies as early as the 1940s reported on substances that delayed detection of radiation-induced mutations, or reduced the appearance of mutations induced by chemicals such as acridine orange. However, a far more sophisticated range of anti-mutagens is now being identiˆed. Mutagen scavengers act through absorption onto a larger molecule that is readily excreted. Good examples are provided by dietaryˆbre sources, such as wheat bran, or the planar molecule, chlorophyll and its stabilised derivative, chlorophyllin. Mutagens may be actively extruded from human cells through the action of one or more of a series of ATP-binding cassette (ABC) drug transporter proteins, including the multidrug resistance proteins (P-glycoproteins), multidrug resistance-associated proteins (MRP1-7) and the breast cancer resistance protein (BCRP). These proteins can aŠect the absorption, distribution and excretion of mutagens and carcinogens, as well as of their metabolites and conjugates. Even if the undesirable compound enters the cells, there are several mechanisms by which it may be prevented from interaction with DNA. Detoxiˆcation mechanisms are of increasing interest, especially those where transcription is regulated through the antioxidant response element (ARE), whose own transcription factor, Nrf2, is repressed under basal conditions. While much of the early literature on mutagenesis and carcinogenesis implicated exogenous chemicals, it is increasingly realised that unrepaired oxidative DNA lesions are important mutational precursors, and anti-oxidants represent an important class of anti-mutagens. It is also recognised that deˆciency of certain micronutrients may lead to cell mutation, and that restoring nutrient balance is an important mechanism of antimutagenesis. An increasing number of studies focus on DNA repair and stress responses as novel mechanisms of anti-mutagenesis.
“…Notable among the literature on antioxidants are studies on various teas, especially green tea (51,52). For example, polyphenols in green tea include catechins (‰avan-3-ols) (53,54), while in black tea, thea‰avin formation may be important (54,55). Polyphenols from green and black tea are eŠective antioxidants in model test systems, while tea polyphenols may also chelate pro-oxidant metals (56).…”
Section: Examples Of Anti-mutagen Protection Against Dišerent Classesmentioning
confidence: 99%
“…Various types of anti-mutagen appear to act through inhibiting induction of these enzymes, or otherwise interfering with the activation process. For example, black tea polyphenol (thea‰avin) has been shown to be able to reduce the induction of CYP1A1, at least in a human cultured cell line, and this has been suggested as one mechanism by which this class of chemicals can reduce DNA damage, and possibly also reduce cancer risk (55). The activation of speciˆc groups of mutagens resides with other speciˆc classes of enzymes.…”
Section: Examples Of Mechanisms Of Anti-mutagen Protection Against DImentioning
An anti-mutagen is any substance that reduces the rate of spontaneous mutations or counteracts or reverses the action of a mutagen, or any technique that protects cells against the eŠects of mutagens. Studies as early as the 1940s reported on substances that delayed detection of radiation-induced mutations, or reduced the appearance of mutations induced by chemicals such as acridine orange. However, a far more sophisticated range of anti-mutagens is now being identiˆed. Mutagen scavengers act through absorption onto a larger molecule that is readily excreted. Good examples are provided by dietaryˆbre sources, such as wheat bran, or the planar molecule, chlorophyll and its stabilised derivative, chlorophyllin. Mutagens may be actively extruded from human cells through the action of one or more of a series of ATP-binding cassette (ABC) drug transporter proteins, including the multidrug resistance proteins (P-glycoproteins), multidrug resistance-associated proteins (MRP1-7) and the breast cancer resistance protein (BCRP). These proteins can aŠect the absorption, distribution and excretion of mutagens and carcinogens, as well as of their metabolites and conjugates. Even if the undesirable compound enters the cells, there are several mechanisms by which it may be prevented from interaction with DNA. Detoxiˆcation mechanisms are of increasing interest, especially those where transcription is regulated through the antioxidant response element (ARE), whose own transcription factor, Nrf2, is repressed under basal conditions. While much of the early literature on mutagenesis and carcinogenesis implicated exogenous chemicals, it is increasingly realised that unrepaired oxidative DNA lesions are important mutational precursors, and anti-oxidants represent an important class of anti-mutagens. It is also recognised that deˆciency of certain micronutrients may lead to cell mutation, and that restoring nutrient balance is an important mechanism of antimutagenesis. An increasing number of studies focus on DNA repair and stress responses as novel mechanisms of anti-mutagenesis.
“…15 Studies also demonstrated the anti-cancerous activity and suppression of oral squamous cell carcinoma by Curcuma longa 16 Mentha spicata, 17 Withania somnifera, 18 Nigella sativa 19 and Azadirachta indica. 20 Feng, et al 21 reported that Camellia sinensis protects buccal cells from DNA damage caused by reactive oxygen species. Flower sap of Echinacea sp.…”
“…Natural products are important ingredients for medicines, in recent years a variety of natural products have been found to inhibit ONOO¯ damage, a large number of studies have shown that flavonoids compounds have strong antioxidant activity [9][10][11][12], and also these compounds have obvious pharmacological effects on cardiovascular disease treatment and anti-tumor [13]. Studies have shown that the antioxidant effect of flavonoids is closely related to the phenol hydroxyl group in the adjacent position.…”
Peroxynitrite (ONOO¯), a powerful oxidant, is produced by nitric oxide (NO . ) and superoxide anion (O 2 .¯) . Under the physiological condition, the ONOO¯ could oxidize the lipids, nitrifyproteins, damage DNA and others biomolecules, thereby harm human health. The study used natural products Capsanthin, Myricetin and Capsaicin as the research object and controlled with Vc, and developed the method of HPLC-DAD to separate the components of nitrification damage system, which could determine the inhibition rate of natural products on the formation of 3-nitrotyrosine (3-NT). The fluorescence spectrometry was employed to determine the ability of these substances to inhibit tyrosine dimer and inhibit the self-oxidation of phthalate. The results showed that Capsanthin, Myricetin and Capsaicin had strong inhibitory effect on the generation capacity of 3-NT and tyrosine dimer, and strong inhibitory effect on the self-oxidation of phthalate.
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