Cytochrome P450 in livers of diabetic rats: regulation by growth hormone and insulin

Arch Biochem Biophys. 1989 Feb 1;268(2):567-75. doi: 10.1016/0003-9861(89)90324-x.


The effects of pituitary and pancreatic hormones on the change in hepatic cytochrome P450s were studied in alloxan- or streptozotocin-induced male rats. In two major sex-specific forms, P450-male and P450(6 beta-1), the former was decreased in chronic (5 week) diabetes to only less than one-third of controls and the latter was also reduced in early (1 week) diabetes. In contrast, a main phenobarbital-inducible form, P450b, was enhanced 25- to 30-fold in these diabetic rats. 3-Methylcholanthrene-inducible P448H was also elevated 3-fold in alloxan-induced diabetes. These changes in hepatic contents of P450-male, P450-6 beta-1, and P450b, which are under the regulation of pituitary growth hormone, associated well with the reported results of time-dependent changes in growth hormone levels in diabetes (G.S. Tannenbaum (1981) Endocrinology 108, 76-82), suggesting that the change in growth hormone level is a factor responsible for alterations in hepatic cytochrome P450s. Normalizing effects of insulin on these forms were also studied. Treatment of diabetic rats with insulin reversed the decreased amounts of both P450-male protein and mRNA. Insulin also normalized hepatic contents of P450b, P4506 beta-1, and P448H. However, the treatment of hypophysectomized rats with insulin had no effect, and treatment of diabetic rats with growth hormone or a suppressing agent of somatostatin, cysteamine, showed trivial effects on P450-male and P450b. These results suggest that insulin does not act directly as a substitute of growth hormone, but exerts its effect indirectly through the normalization of a growth hormone-mediated process(es) in diabetic rats.

MeSH terms

  • Alloxan / pharmacology
  • Animals
  • Blotting, Western
  • Cytochrome P-450 Enzyme System / genetics
  • Cytochrome P-450 Enzyme System / immunology
  • Cytochrome P-450 Enzyme System / metabolism*
  • Diabetes Mellitus, Experimental / enzymology*
  • Growth Hormone / pharmacology*
  • Insulin / pharmacology*
  • Liver / enzymology*
  • Male
  • Microsomes, Liver / enzymology
  • RNA, Messenger / genetics
  • Streptozocin / pharmacology
  • Testosterone / metabolism
  • Time Factors


  • Insulin
  • RNA, Messenger
  • Testosterone
  • Streptozocin
  • Alloxan
  • Growth Hormone
  • Cytochrome P-450 Enzyme System