Regulation of cholesterol metabolism in adrenal cortex: effects of apoproteins on cholesterol esterase in rat adrenal glands

Endocr J. 1993 Apr;40(2):221-5. doi: 10.1507/endocrj.40.221.

Abstract

We have investigated the effects of apoproteins on cholesterol esterase (CEase) in rat adrenal glands in order to clarify the mechanism of synthesis of free cholesterol which is the most important substrate for steroidogenesis. We prepared lipid mixtures containing cholesteryl oleate plus apoproteins with and without phosphatidylcholine as a substrate for CEase in order to investigate the effect of the substrate state on CEase. The substrate containing only cholesteryl oleate and apo-HDL increased both acid and alkaline CEase activities. Both acid and alkaline CEase activities were also increased by a substrate containing apo-HDL plus cholesteryl oleate and phosphatidylcholine more than by a substrate containing cholesteryl oleate plus apo-LDL with phosphatidylcholine or cholesteryl oleate with phosphatidylcholine. We have already reported that phosphatidylcholine is an important factor for the regulation of adrenal CEase. Therefore, the present studies show that apoproteins as well as phosphatidylcholine may be important factors for the regulation of adrenal CEase.

MeSH terms

  • Adrenal Cortex / enzymology
  • Adrenal Cortex / metabolism*
  • Adrenal Glands / drug effects
  • Adrenal Glands / enzymology*
  • Animals
  • Apoproteins / pharmacology*
  • Cholesterol / metabolism*
  • Lipoproteins / blood
  • Lipoproteins, LDL / blood
  • Male
  • Phosphatidylcholines / blood
  • Rats
  • Rats, Wistar
  • Sterol Esterase / metabolism*

Substances

  • Apoproteins
  • Lipoproteins
  • Lipoproteins, LDL
  • Phosphatidylcholines
  • Cholesterol
  • Sterol Esterase