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首页> 外文期刊>Biochimica et biophysica acta: international journal of biochemistry and biophysics >Comparative cytotoxic and cytoprotective effects of taurohyodeoxycholic acid (THDCA) and tauroursodeoxycholic acid (TUDCA) in HepG2 cell line.
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Comparative cytotoxic and cytoprotective effects of taurohyodeoxycholic acid (THDCA) and tauroursodeoxycholic acid (TUDCA) in HepG2 cell line.

机译:牛磺去氧胆酸(THDCA)和牛磺去氧胆酸(TUDCA)在HepG2细胞系中的比较细胞毒性和细胞保护作用。

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摘要

This study was performed to compare the effects of two hydrophilic bile acids, taurohyodeoxycholic acid (THDCA) and tauroursodeoxycholic acid (TUDCA), on HepG2 cells. Cytotoxicity was evaluated at different times of exposure by incubating cells with increasing concentrations (50-800 micromol/l) of either bile acid, while their cytoprotective effect was tested in comparison with deoxycholic acid (DCA) (350 micromol/l and 750 micromol/l)-induced cytotoxicity. Culture media, harvested at the end of each incubation period, were analyzed to evaluate aspartate transaminase (AST), alanine transaminase and gamma-glutamyltranspeptidase release. In addition, the hemolytic effect of THDCA and TUDCA on human red blood cells was also determined. At 24 h of incubation neither THDCA nor TUDCA was cytotoxic at concentrations up to 200 and 400 micromol/l. At 800 micromol/l both THDCA and TUDCA induced a slight increase in AST release. At this concentration and with time of exposure prolonged up to 72 h, THDCA and TUDCA induced a progressive increase of AST release significantly (P<0.05) higher than that of controls being AST values for THDCA (2.97+/-0.88 time control value (tcv) at 48 h and 4.50+/-1.13 tcv at 72 h) significantly greater than those of TUDCA (1.50+/-0.20 tcv at 48 h and 1.80+/-0.43 tcv at 72 h) (P<0.01). In cytoprotection experiments, the addition of 50 micromol/l THDCA decreased only slightly (-5%) AST release induced by 350 micromol/l DCA, while the addition of 50 micromol/l TUDCA was significantly effective (-23%; P<0.05). Higher doses of THDCA or TUDCA did not reduce toxicity induced by 350 micromol/l DCA, but were much less toxic than an equimolar dose of DCA alone. At the concentration used in this experimental model neither THDCA nor TUDCA was hemolytic; however at a very high concentration (6 mmol/l) both bile acids induced 5-8% hemolysis. We conclude that bile acid molecules with a similar degree of hydrophilicity may show different cytotoxic and cytoprotective properties.
机译:进行这项研究以比较两种亲水性胆汁酸,牛磺去氧胆酸(THDCA)和牛磺去氧胆酸(TUDCA)对HepG2细胞的影响。通过将细胞与浓度较高的胆汁酸(50-800 micromol / l)一起孵育来评估在不同暴露时间的细胞毒性,同时与脱氧胆酸(DCA)(350 micromol / l和750 micromol / l)相比,测试了它们的细胞保护作用l)诱导的细胞毒性。分析在每个温育期结束时收获的培养基,以评估天冬氨酸转氨酶(AST),丙氨酸转氨酶和γ-谷氨酰转肽酶的释放。另外,还测定了THDCA和TUDCA对人红细胞的溶血作用。孵育24小时后,THDCA和TUDCA在浓度高达200和400 micromol / l时都不具有细胞毒性。 THDCA和TUDCA浓度均为800 micromol / l时,AST释放均略有增加。在此浓度下,随着暴露时间延长至72小时,THDCA和TUDCA诱导的AST释放进行性增加明显高于对照组(P <0.05),高于THDCA的AST值(2.97 +/- 0.88时间控制值( 48小时的tcv)和72小时的4.50 +/- 1.13 tcv)显着大于TUDCA的tcv(48小时为1.50 +/- 0.20 tcv,72小时为1.80 +/- 0.43 tcv)(P <0.01)。在细胞保护实验中,添加50 micromol / l的THDCA仅会轻微降低(-5%)350 micromol / l的DCA诱导的AST释放,而添加50 micromol / l的TUDCA则显着有效(-23%; P <0.05 )。较高剂量的THDCA或TUDCA不会降低350微摩尔/升DCA诱导的毒性,但其毒性要比等摩尔量的DCA单独得多。在该实验模型中使用的浓度下,THDCA和TUDCA均不溶血。但是,在很高的浓度(6 mmol / l)下,两种胆汁酸均会引起5-8%的溶血。我们得出结论,具有相似程度的亲水性的胆汁酸分子可能显示出不同的细胞毒性和细胞保护特性。

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