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首页> 外文期刊>Xenobiotica: the fate of foreign compounds in biological systems >Activation of CYP3A-mediated testosterone 6beta-hydroxylation by tanshinone IIA and midazolam 1-hydroxylation by cryptotanshinone in human liver microsomes.
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Activation of CYP3A-mediated testosterone 6beta-hydroxylation by tanshinone IIA and midazolam 1-hydroxylation by cryptotanshinone in human liver microsomes.

机译:CYP3A介导的睾酮6β-丹参酮和咪达唑仑1-羟基化对人肝微粒体的Chedpotalshinonation的激活。

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摘要

This study evaluated the in vitro activation of CYP3A-mediated midazolam 1-hydroxylation and testosterone 6beta-hydroxylation by tanshinone I, tanshinone IIA, and cryptotanshinone. The abilities of tanshinones to activate CYP3A-mediated midazolam 1-hydroxylation and testosterone 6beta-hydroxylation in human liver microsomes (HLMs) were tested. Substrate- and effector-dependent activation of CYP3A by tanshinones were both observed. Cryptotanshinone was shown to activate CYP3A-mediated midazolam 1-hydroxylation in a concentration-dependent manner. In contrast, tanshinone IIA and tanshinone I did not activate this hydroxylation reaction. In addition, tanshinone IIA activated CYP3A-mediated testosterone 6beta-hydroxylation, whereas cryptotanshinone and tanshinone I did not. The results from our study enhance the understanding of CYP3A activation by tanshinone IIA and cryptotanshinone in HLMs. Additionally, these data allow for an accurate prediction of the magnitude and likelihood of Danshen-drug interactions.
机译:该研究评估了CYP3A介导的Midazolam 1-羟基化和睾酮6β-羟基化的体外活化,由丹参酮I,丹参酮IIA和Cryptot anshinone。测试了丹参酮激活CYP3A介导的咪达唑仑1-羟基化和睾酮6β-羟基化的能力,在人肝微粒体(HLMS)中。观察到甲藻酮的CYP3A的基质和效应依赖性活化。显示Cryptotanshinone以浓度依赖性方式激活CYP3A介导的Midazolam 1-羟基化。相比之下,丹参酮IIa和丹参酮我没有激活这种羟基化反应。此外,丹参酮IIA活化CYP3A介导的睾酮6beta-羟基化,而Cryptotalshinone和丹参酮我没有。我们的研究结果增强了丹参酮IIA和Cryptotanshinone对HLMS的CYP3A活化的理解。另外,这些数据允许准确地预测丹参 - 药物相互作用的幅度和可能性。

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