油酸
化学
月桂酸
脂肪酸
生物化学
脂肪组织
分解代谢
新陈代谢
成分
多不饱和脂肪酸
胆固醇
脂肪生成
脂质代谢
代谢途径
脂解
脂类学
脂肪酸代谢
结构-活动关系
药理学
酶
对接(动物)
作者
Yen‐Chun Koh,Sudthida Kamchonemenukool,Pin-Yu Ho,Monthana Weerawatanakorn,Min‐Hsiung Pan
标识
DOI:10.1021/acs.jafc.5c10351
摘要
Octacosanol, a major constituent of policosanol, exhibits lipid-lowering activity, particularly when esterified with fatty acids. Although its cholesterol-lowering actions have been linked to the modulation of fatty acid and cholesterol biosynthesis, its functions within adipose tissue remain poorly defined. Here, we examined nonesterified octacosanol (NO), lauric acid-esterified octacosanol (LEO), and oleic acid-esterified octacosanol (OEO) in high-fat diet-fed mice for 11 weeks. Target prediction and molecular docking identified PPARα and PPARδ as putative targets of octacosanol, guiding downstream mechanistic analyses in adipose tissue. Both NO and OEO enhanced lipolysis; NO preferentially increased fatty acid β-oxidation, whereas OEO specifically promoted thermogenic remodeling, indicating distinct metabolic consequences driven by ester chemistry. Together, these findings demonstrate that structural modification, particularly oleic acid esterification, substantially augments the metabolic activity of octacosanol in lipid catabolism and thermogenesis, underscoring its potential relevance in obesity-associated metabolic regulation.
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