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The role of cytochrome p-450 in salt-sensitive stroke in stroke-prone spontaneously hypertensive rats.

Abstract
Stroke-prone spontaneously hypertensive rats (SHRSP/Izm) are salt sensitive: they develop severe hypertension and die of stroke within a short time after salt loading. We studied the role of cytochrome P-450 (CYP) isoforms in the brain and the effect of clofibrate to investigate the mechanism of salt sensitive stroke-proneness in SHRSP/Izm. Male SHRSP/Izm at 9 weeks of age were fed a regular diet with or without 0.25% clofibrate and given a 1% NaCl solution for drinking water for 10 d. The expression levels of CYP4A1, 2C11, and 2C23 were measured by Western blotting. Cerebral blood flow was measured with a laser Doppler method and blood vessel diameters were measured under microscopic observation. SHRSP/Izm died within 60 d after salt loading; however, clofibrate prolonged the survival (mean life span, 33+/-7 vs. 215+/-23 d, p<0.0001) without significant attenuation of the severe hypertension. CYP4A1 and CYP2C11 expression levels were lower in SHRSP/Izm than those in age-matched male spontaneously hypertensive rats (SHR/Izm) in the cerebral cortex (p<0.05). Salt loading down-regulated CYP2C11 expression in the cerebral cortex of SHRSP/Izm (p<0.05). No obvious change in cerebral CYP4A1 was observed in either salt-loaded SHRSP/Izm or SHR/Izm. Clofibrate significantly up-regulated the expression of cerebral CYP2C11 and significantly attenuated its salt-induced suppression (p<0.05). Additionally, clofibrate significantly increased blood vessel diameters (p<0.01) and cerebral blood flow (p<0.0001). CYP2C11 plays an important role in regulating cerebral blood flow and, as a result, in preventing stroke in the salt-sensitive stroke-prone SHRSP/Izm.
AuthorsChen-Jiang Ying, Takanori Noguchi, Hiroaki Aso, Katsumi Ikeda, Yukio Yamori, Yasuo Nara
JournalHypertension research : official journal of the Japanese Society of Hypertension (Hypertens Res) Vol. 31 Issue 9 Pg. 1821-7 (Sep 2008) ISSN: 0916-9636 [Print] England
PMID18971561 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Anticholesteremic Agents
  • PPAR alpha
  • Sodium Chloride, Dietary
  • Cytochrome P-450 Enzyme System
  • Aryl Hydrocarbon Hydroxylases
  • CYP2C11 protein, rat
  • Cytochrome P-450 CYP2J2
  • Cytochrome P450 Family 2
  • Steroid 16-alpha-Hydroxylase
  • Cytochrome P-450 CYP4A
  • Clofibrate
Topics
  • Animals
  • Anticholesteremic Agents (pharmacology)
  • Arterioles (drug effects, physiology)
  • Aryl Hydrocarbon Hydroxylases (metabolism)
  • Blood Pressure (drug effects, physiology)
  • Cerebral Cortex (blood supply, metabolism)
  • Cerebrovascular Circulation (drug effects, physiology)
  • Clofibrate (pharmacology)
  • Cytochrome P-450 CYP2J2
  • Cytochrome P-450 CYP4A (metabolism)
  • Cytochrome P-450 Enzyme System (metabolism)
  • Cytochrome P450 Family 2
  • Hypertension (drug therapy, metabolism)
  • Male
  • Microsomes (metabolism)
  • PPAR alpha (metabolism)
  • Rats
  • Rats, Inbred SHR
  • Sodium Chloride, Dietary (pharmacology)
  • Steroid 16-alpha-Hydroxylase (metabolism)
  • Stroke (metabolism, prevention & control)

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