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重新审视通过乙酰辅酶 A 羧化酶抑制作用对肝脏代谢的影响。

Revisiting liver metabolism through acetyl-CoA carboxylase inhibition.

机构信息

Department of Science, University "ROMA TRE", 00146, Rome, Italy.

Obesity, Diabetes and Metabolism Laboratory, Biomedical Research Institute of Murcia (IMIB), 30120 Murcia, Spain.

出版信息

Trends Endocrinol Metab. 2024 Jul;35(7):563-565. doi: 10.1016/j.tem.2024.04.010. Epub 2024 Apr 24.

DOI:10.1016/j.tem.2024.04.010
PMID:38664153
Abstract

Liver-targeted acetyl-coenzyme A (CoA) carboxylase (ACC) inhibitors in metabolic dysfunction-associated steatotic liver disease (MASLD) trials reveal notable secondary effects: hypertriglyceridemia and altered glucose metabolism, paradoxically with reduced hepatic steatosis. In their study, Deja et al. explored how hepatic ACC influences metabolism using different pharmacological and genetic methods, coupled with targeted metabolomics and stable isotope-based tracing techniques.

摘要

在代谢功能障碍相关脂肪性肝病 (MASLD) 试验中,靶向肝脏的乙酰辅酶 A (CoA) 羧化酶 (ACC) 抑制剂揭示了显著的次要作用:高甘油三酯血症和葡萄糖代谢改变,与肝脂肪变性减少相反。在他们的研究中,Deja 等人使用不同的药理学和遗传学方法,结合靶向代谢组学和基于稳定同位素的示踪技术,探索了肝脏 ACC 如何影响代谢。

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引用本文的文献

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Targeting Metabolism: Innovative Therapies for MASLD Unveiled.靶向代谢:非酒精性脂肪性肝炎的创新疗法揭秘。
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Metabolomics-driven approaches for identifying therapeutic targets in drug discovery.代谢组学驱动的药物发现中治疗靶点识别方法。
MedComm (2020). 2024 Nov 11;5(11):e792. doi: 10.1002/mco2.792. eCollection 2024 Nov.