酮发生
NEFA公司
内科学
内分泌学
β氧化
酮体
脂肪酸
激素
过氧化物酶体增殖物激活受体
脂肪肝
化学
生物
新陈代谢
受体
医学
生物化学
疾病
胰岛素
作者
Philip M.M. Ruppert,Sander Kersten
标识
DOI:10.1016/j.tem.2023.10.002
摘要
Abstract
Fasting is part of many weight management and health-boosting regimens. Fasting causes substantial metabolic adaptations in the liver that include the stimulation of fatty acid oxidation and ketogenesis. The induction of fatty acid oxidation and ketogenesis during fasting is mainly driven by interrelated changes in plasma levels of various hormones and an increase in plasma nonesterified fatty acid (NEFA) levels and is mediated transcriptionally by the peroxisome proliferator-activated receptor (PPAR)α, supported by CREB3L3 (cyclic AMP-responsive element-binding protein 3 like 3). Compared with men, women exhibit higher ketone levels during fasting, likely due to higher NEFA availability, suggesting that the metabolic response to fasting shows sexual dimorphism. Here, we synthesize the current molecular knowledge on the impact of fasting on hepatic fatty acid oxidation and ketogenesis.
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