Diurnal variation and cholesterol regulation of hepatic HMG-CoA reductase activity

David J. Shapiro, Victor W. Rodwell

Research output: Contribution to journalArticle

Abstract

HMG-CoA reductase exhibits a diurnal rhythm. Cycloheximide injection completely prevents both the observed 9.5 fold rise in activity and the loss of activity during daylight. This is compatible with the existence of a specific, labile,degradative or inactivating protein for HMG-CoA reductase. Effects of cholesterol on reductase activity were also studied. KM and Vmax for reductase from normal- and cholesterol-fed rats are 8.1×10-5 M and 0.33 nmole/min/mg and 6.9x10-5 M and 0.0404 nmole/min/mg respectively. Reductase from both sources is substrate-inhibited by HMG-CoA. Mixing experiments suggest that a soluble inhibitor of IM -CoA reductase does not cause the profound drop in activity observed in cholesterol-fed rats.

Original languageEnglish (US)
Pages (from-to)867-872
Number of pages6
JournalBiochemical and Biophysical Research Communications
Volume37
Issue number5
DOIs
StatePublished - Nov 20 1969

ASJC Scopus subject areas

  • Biophysics
  • Biochemistry
  • Molecular Biology
  • Cell Biology

Fingerprint Dive into the research topics of 'Diurnal variation and cholesterol regulation of hepatic HMG-CoA reductase activity'. Together they form a unique fingerprint.

  • Cite this