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首页> 外文期刊>International Journal of Preventive Medicine >Commentary on Prevention a Possible Drug–Drug Interaction: Is Concurrent Administration of Orlistat and Pioglitazone Increase the Risk of Durg-Induced Hepatotoxicity?
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Commentary on Prevention a Possible Drug–Drug Interaction: Is Concurrent Administration of Orlistat and Pioglitazone Increase the Risk of Durg-Induced Hepatotoxicity?

机译:关于预防可能发生的药物相互作用的评论:奥利司他和吡格列酮的同时给药是否会增加杜格诱导的肝毒性的风险?

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Background: Drug–drug interactions (DDIs) are an emerging threat to public health and are difficult to detect. To prevent DDIs and their burden, the possible DDIs should be kept in mind. We know that the obesity predisposes to the development of insulin resistance and type 2 diabetes. Therefore, combinational uses of antiobesity drugs and glucose-lowering drugs are very common. As the hepatotoxicity of both pioglitazone (an antidiabetic drug) and orlistat (an antiobesity drug) has been shown in some cases, the aim of this study was to evaluate the interaction of pioglitazone and orlistat in human hepatocellular cell line human hepatocellular carcinoma (HepG2) cells to determine their effect on liver toxicity. Methods: Human hepatocellular carcinoma cells were treated with 25 μM Pioglitazon (Pio), 20 μM Orlistat (Orl) pioglitazone, orlistat or combination of them. The MTT assay was used to assess cell viability. Results: Pioglitazone and orlistat combination caused a loss of HepG2 cell viability. While pioglitazone (25 μM) and orliatat (20 μM) alone decreased the cell viability around 91% and 85% respectively (notsignificant, P 0.05), the combination of these two drugs reduced the amount of viable cells to 55% which was significant when compared with each drug alone ( P 0.001). Conclusions: Revealing the significant loss of viability of HepG2 cells in the combination use of pioglitazone and orlistat indicates these two drugs should not be administered at the same time to prevent their hepatotoxic effects especially in patients with liver dysfunction.
机译:背景:药物相互作用(DDI)是对公共卫生的新兴威胁,难以发现。为了防止DDI及其负担,应牢记可能的DDI。我们知道,肥胖易患胰岛素抵抗和2型糖尿病。因此,抗肥胖药和降糖药的联合使用非常普遍。由于在某些情况下已经显示了吡格列酮(抗糖尿病药)和奥利司他(抗肥胖药)的肝毒性,因此本研究的目的是评估吡格列酮和奥利司他在人肝细胞系人肝细胞癌(HepG2)中的相互作用。以确定它们对肝毒性的作用。方法:用25μM吡格列酮(Pio),20μM奥利司他(Orl)吡格列酮,奥利司他或它们的组合处理人肝癌细胞。使用MTT测定法评估细胞活力。结果:吡格列酮和奥利司他的组合导致HepG2细胞活力丧失。吡格列酮(25μM)和奥里亚特(20μM)单独将细胞活力分别降低了约91%和85%(无显着性,P> 0.05),但这两种药物的组合将活细胞数量降低至55%,这是显着的与每种药物单独比较时(P <0.001)。结论:吡格列酮和奥利司他联用显示HepG2细胞活力显着降低,表明这两种药物不应同时给药以预防其肝毒性作用,尤其是在肝功能不全的患者中。

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