Regulation of 11 beta-hydroxylase cytochrome p450 expression by cholesterol in spontaneously hypertensive rats

J Hypertens. 1995 Nov;13(11):1253-8. doi: 10.1097/00004872-199511000-00006.

Abstract

Objective: To investigate whether hypercholesterolaemia interferes with the expression of the enzymes involved in steroid biosynthesis in the adrenal cortex.

Methods: Twenty-four 5-week-old male spontaneously hypertensive rats (SHR) were randomly assigned to a high (1%) cholesterol diet (n = 8) or to a matched cholesterol-free diet (n = 8) for 6 weeks. A third group (n = 8) was studied after 2 weeks of washout from the high-cholesterol intake. A cohort of age- and sex-matched normotensive Wistar-Kyoto (WKY) rats (n = 24) underwent the same treatments and was used as a control.

Results: In SHR cholesterol feeding reduced urinary sodium excretion (0.8 +/- 0.1 versus 1.4 +/- 0.1 mmol/24 h in the cholesterol-free group), increased plasma aldosterone levels (299 +/- 60 versus 154 +/- 24) and reduced plasma corticosterone levels (142 +/- 21 versus 278 +/- 35 ng/ml). Those responses were associated with a reduction of 11 beta-hydroxylase cytochrome P450 messenger RNA (mRNA) in the adrenal cortex (-52.3 +/- 3.4%) whereas aldosterone synthase mRNA remained unchanged. That effect and the changes in electrolyte excretion and steroid levels were no longer detectable after withdrawal of the diet. In WKY rats high-cholesterol diet induced no significant changes in urinary electrolyte excretion, steroid levels and expression of 11 beta-hydroxylase cytochrome P450 and aldosterone synthase in the adrenals.

Conclusions: The present results indicate that in SHR hypercholesterolaemia selectively interferes with the adrenal steroid biosynthetic pathway by reducing the expression of 11 beta-hydroxylase, leading to accumulation of mineralocorticoids and sodium retention.

MeSH terms

  • Adrenal Cortex / enzymology
  • Aldosterone / blood
  • Animals
  • Cholesterol, Dietary / administration & dosage
  • Cholesterol, Dietary / pharmacology*
  • Cohort Studies
  • Corticosterone / blood
  • Cytochrome P-450 CYP11B2 / metabolism
  • Electrolytes / urine
  • Hypertension / physiopathology*
  • Male
  • Natriuresis / drug effects
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Inbred SHR / physiology*
  • Rats, Inbred WKY
  • Steroid 11-beta-Hydroxylase / genetics
  • Steroid 11-beta-Hydroxylase / metabolism*
  • Steroids / blood

Substances

  • Cholesterol, Dietary
  • Electrolytes
  • RNA, Messenger
  • Steroids
  • Aldosterone
  • Cytochrome P-450 CYP11B2
  • Steroid 11-beta-Hydroxylase
  • Corticosterone