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三种黄酮类化合物对乐伐替尼代谢的影响。

Effects of three flavonoids on the metabolism of lenvatinib.

作者信息

Yang Jinzhao, Chen Jie, Li Qingqing, Xu Ren-Ai, Chen Xiaohai

机构信息

Wenzhou People's Hospital, The Third Clinical Institute Affiliated to Wenzhou Medical University, Wenzhou, Zhejiang, China.

The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, Zhejiang, China.

出版信息

Front Pharmacol. 2024 Aug 20;15:1438259. doi: 10.3389/fphar.2024.1438259. eCollection 2024.

Abstract

Lenvatinib is a first-line therapy for the treatment of hepatocellular carcinoma (HCC), an active multi-target tyrosine kinase inhibitor (TKI). The interaction between Traditional Chinese Medicine (TCM) and chemicals has increasingly become a research hotspot. The objective of this study was to pinpoint the effects of three flavonoids on the metabolism of lenvatinib. Enzyme reaction system was established and optimized , and experiments were conducted in Sprague-Dawley (SD) rats, where the analytes were detected by ultra performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS). We found that among three flavonoids, luteolin and myricetin had strong inhibitory effects on lenvatinib metabolism, with half-maximal inhibitory concentration (IC) values of 11.36 ± 0.46 µM and 11.21 ± 0.81 µM in rat liver microsomes (RLM), respectively, and 6.89 ± 0.43 µM and 12.32 ± 1.21 µM in human liver microsomes (HLM), respectively. In Sprague-Dawley rats, the combined administration of lenvatinib and luteolin obviously expanded the exposure to lenvatinib; however, co-administered with myricetin did not have any changes, which may be due to the poor bioavailability of myricetin . Furthermore, the inhibitory type of luteolin on lenvatinib showed an un-competitive in RLM and a mixed in HLM. Collectively, flavonoids with liver protection, especially luteolin, may inhibit lenvatinib metabolism and .

摘要

仑伐替尼是一种用于治疗肝细胞癌(HCC)的一线疗法,是一种活性多靶点酪氨酸激酶抑制剂(TKI)。中药与化学药物之间的相互作用日益成为研究热点。本研究的目的是确定三种黄酮类化合物对仑伐替尼代谢的影响。建立并优化了酶反应体系,并在Sprague-Dawley(SD)大鼠中进行实验,通过超高效液相色谱串联质谱(UPLC-MS/MS)检测分析物。我们发现,在三种黄酮类化合物中,木犀草素和杨梅素对仑伐替尼代谢具有较强的抑制作用,在大鼠肝微粒体(RLM)中的半数最大抑制浓度(IC)值分别为11.36±0.46 μM和11.21±0.81 μM,在人肝微粒体(HLM)中的IC值分别为6.89±0.43 μM和12.32±1.21 μM。在Sprague-Dawley大鼠中,仑伐替尼与木犀草素联合给药明显增加了仑伐替尼的暴露量;然而,与杨梅素联合给药则没有任何变化,这可能是由于杨梅素的生物利用度较差。此外,木犀草素对仑伐替尼的抑制类型在RLM中表现为非竞争性,在HLM中表现为混合型。总的来说,具有肝脏保护作用的黄酮类化合物,尤其是木犀草素,可能会抑制仑伐替尼的代谢。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b334/11368737/40144f5e1e58/fphar-15-1438259-g001.jpg

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