首页> 外文期刊>Free radical research >Modulation of tea and tea polyphenols on benzo(a)pyrene-induced DNA damage in Chang liver cells.
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Modulation of tea and tea polyphenols on benzo(a)pyrene-induced DNA damage in Chang liver cells.

机译:茶和茶多酚对苯并(a)re诱导的昌肝细胞DNA损伤的调节作用。

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摘要

The protective effects of three tea extracts (green tea, GTE; oolong tea, OTE; and black tea, BTE) and five tea polyphenols (epicatechin, EC; epicatechin gallate, ECG; epigallocatechin, EGC; epigallocatechin gallate, EGCG; and theaflavins, THFs) on benzo[a]pyrene (B[a]P)-induced DNA damage in Chang liver cells were evaluated using the comet assay. B[a]P-induced DNA damage in Chang liver cells was significantly (p < 0.05) inhibited by GTE and OTE at a concentration of 10 microg/ml and by BTE at 25 microg/ml. At a concentration of 100 microg/ml, the % tail DNA was reduced from 33% (B[a]P treated only) to 10, 9, 13%, by GTE, OTE and BTE, respectively. EC and ECG did not cause DNA damage in cells according to the results of the comet assay; however, EGC, EGCG and theaflavins caused DNA damage in cells at a concentration of 100 microM. The results indicated that EC and ECG had protective effects against B[a]P-induced DNA damage in cells at a concentration of 10-100 microM. Although EGC, EGCG and the theaflavins caused DNA damage at a high concentration, but they had protective effects against B[a]P-induced DNA damage in cells at a low concentration of 10-50 microM. The results also showed that the DNA damage in cells induced by EGC, EGCG, and the theaflavins was due to the generation of superoxide during incubation with cells at a higher concentration. Therefore, tea catechins and THFs play an important role in enabling tea extracts to inhibit DNA damage in Chang liver cells.
机译:三种茶提取物(绿茶,GTE;乌龙茶,OTE;和红茶,BTE)和五种茶多酚(表皮茶碱,EC;表儿茶素没食子酸酯,ECG;表没食子儿茶素,EGC;表没食子儿茶素没食子酸酯,EGCG和茶黄素的保护作用,使用彗星试验评估了苯​​并[a] py(B [a] P)诱导的Chang肝细胞DNA损伤后的THFs)。在浓度为10 microg / ml的GTE和OTE和在浓度为25 microg / ml的BTE中,B [a] P诱导的Chang肝细胞DNA损伤被显着抑制(p <0.05)。在浓度为100微克/毫升时,GTE,OTE和BTE的尾巴DNA百分比分别从33%(仅B [a] P处理)降低到10%,9%,13%。根据彗星试验的结果,EC和ECG不会引起细胞DNA损伤。然而,EGC,EGCG和茶黄素以100 microM的浓度引起细胞DNA损伤。结果表明,EC和ECG在10-100 microM的浓度下对B [a] P诱导的细胞DNA损伤具有保护作用。尽管EGC,EGCG和茶黄素在高浓度下会引起DNA损伤,但是在10-50 microM的低浓度下它们对B [a] P诱导的DNA损伤具有保护作用。结果还表明,由EGC,EGCG和茶黄素诱导的细胞DNA损伤是由于与较高浓度细胞孵育过程中产生了超氧化物。因此,茶儿茶素和四氢呋喃在使茶提取物抑制长肝细胞中的DNA损伤中起重要作用。

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