脂肪变性
乙酰辅酶A羧化酶
新陈代谢
丙酮酸羧化酶
脂肪生成
辅酶A
脂肪肝
高甘油三酯血症
内分泌学
内科学
医学
生物
生物化学
化学
疾病
酶
甘油三酯
还原酶
胆固醇
作者
Armando Jesús Pérez-Díaz,María A. Núñez‐Sánchez,Bruno Ramos‐Molina
标识
DOI:10.1016/j.tem.2024.04.010
摘要
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.
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