Stroke, Vol 24, 1561-1566, Copyright © 1993 by American Heart Association
S Sadoshima, K Fujii, H Ooboshi, S Ibayashi and M Fujishima
BACKGROUND AND PURPOSE: Angiotensin converting enzyme (ACE) inhibitors are
expected to modulate neuronal activities. The present study was designed to
examine the beneficial effects of ACE inhibitors on microcirculation and
metabolism in the ischemic brain. METHODS: Cerebral ischemia was developed
for 60 minutes in spontaneously hypertensive rats (SHR, n = 35) by
bilateral carotid artery occlusion. ACE inhibitor (0.1 or 10 mg/kg SQ
29,852 or captopril) were intravenously injected 15 minutes before cerebral
ischemia. Cerebral blood flow to the parietal cortex was measured with the
H2 clearance technique. Lactate, pyruvate, and ATP in the brain were
estimated by the enzymatic method. RESULTS: Before cerebral ischemia, high
doses of both SQ 29,852 and captopril significantly decreased mean arterial
pressure by 15 to 25 mm Hg and reduced cerebral vascular resistance by 13%
to 17% of the resting values. Cerebral blood flow and arterial pressure
during ischemia were not altered by these ACE inhibitors. After 60 minutes
of cerebral ischemia, tissue lactate in vehicle- treated SHR increased
6.6-fold and ATP decreased to 65% of the control values. Administration of
SQ 29,852 or captopril significantly reduced the lactate levels to 1.6- to
3.1-fold and well preserved the ATP levels to 82% to 93% of the control.
CONCLUSIONS: These results suggest that inhibition of ACE activities may be
protective for cerebral metabolism against ischemic insult.
ARTICLES
Angiotensin converting enzyme inhibitors attenuate ischemic brain metabolism in hypertensive rats
Second Department of Internal Medicine, Faculty of Medicine, Kyushu University, Fukuoka, Japan.
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