Gandarias J M, Lacort M, Ochoa B
Lipids. 1984 Dec;19(12):916-22. doi: 10.1007/BF02534726.
The regulation of cholesterol ester hydrolase activity by female sex hormones was studied in cytosolic preparations from female rat liver. The investigation was undertaken in order to determine whether a reduction in the enzyme activity might be responsible for the increased content of esterified cholesterol found in rat liver after estradiol or progesterone treatments. The single injection of estradiol (0.75 mg/100 g) or progesterone (1.50 mg/100 g) produced respectively significant decreases and increases in sterol hydrolase activity. Both opposite effects were noted after a similar lag period of 3-4 hr and were of short duration. No alterations were observed in rats receiving short-term treatments. When hormones were added to the incubation medium, the activity of cholesterol ester hydrolase decreased progressively with increasing concentrations of hormones. Kinetic studies demonstrate that both estradiol and progesterone compete with the substrate (cholesteryl oleate) for the active center. The findings of the present paper exclude a direct relationship between hepatic hydrolytic activity and lipid deposition. However, they provide evidences that female sex hormones act as modulatory agents of the hydrolysis of cholesteryl esters in rat liver cytosol and suggest that other factors besides competitive inhibition are involved in such regulatory effects.
在雌性大鼠肝脏的胞质制剂中研究了雌性性激素对胆固醇酯水解酶活性的调节作用。进行该研究是为了确定酶活性的降低是否可能是雌二醇或孕酮处理后大鼠肝脏中酯化胆固醇含量增加的原因。单次注射雌二醇(0.75毫克/100克)或孕酮(1.50毫克/100克)分别使固醇水解酶活性显著降低和增加。在相似的3-4小时延迟期后均观察到这两种相反的作用,且持续时间较短。接受短期处理的大鼠未观察到变化。当将激素添加到孵育培养基中时,胆固醇酯水解酶的活性随着激素浓度的增加而逐渐降低。动力学研究表明,雌二醇和孕酮均与底物(油酸胆固醇酯)竞争活性中心。本文的研究结果排除了肝脏水解活性与脂质沉积之间的直接关系。然而,它们提供了证据表明雌性性激素作为大鼠肝脏胞质溶胶中胆固醇酯水解的调节剂,并表明除了竞争性抑制之外,其他因素也参与了这种调节作用。