Regulation of the cerebral circulation: Role of endothelium and potassium channels

被引:622
作者
Faraci, FM [1 ]
Heistad, DD
机构
[1] Univ Iowa, Dept Internal Med, Iowa City, IA 52242 USA
[2] Univ Iowa, Dept Pharmacol, Iowa City, IA 52242 USA
[3] Univ Iowa, Ctr Cardiovasc, Iowa City, IA 52242 USA
[4] Univ Iowa, Ctr Aging, Iowa City, IA 52242 USA
关键词
D O I
10.1152/physrev.1998.78.1.53
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Several new concepts have emerged in relation to mechanisms that contribute to regulation of the cerebral circulation. This review focuses on some physiological mechanisms of cerebral vasodilatation and alteration of these mechanisms by disease states. One mechanism involves release of vasoactive factors by the endothelium that affect underlying vascular muscle. These factors include endothelium-derived relaxing factor (nitric oxide), prostacyclin, and endothelium-derived hyperpolarizing factor(s). The normal vasodilator influence of endothelium is impaired by some disease states. Under pathophysiological conditions, endothelium may produce potent contracting factors such as endothelin. Another major mechanism of regulation of cerebral vascular tone relates to potassium channels. Activation of potassium channels appears to mediate relaxation of cerebral vessels to diverse stimuli including receptor-mediated agonists, intracellular second messengers, and hypoxia. Endothelial-and potassium channel-based mechanisms are related because several endothelium-derived factors produce relaxation by activation of potassium channels. The influence of potassium channels may be altered by disease states including chronic hypertension, subarachnoid hemorrhage, and diabetes.
引用
收藏
页码:53 / 97
页数:45
相关论文
共 876 条
[51]   APPARENT HYDROXYL RADICAL PRODUCTION BY PEROXYNITRITE - IMPLICATIONS FOR ENDOTHELIAL INJURY FROM NITRIC-OXIDE AND SUPEROXIDE [J].
BECKMAN, JS ;
BECKMAN, TW ;
CHEN, J ;
MARSHALL, PA ;
FREEMAN, BA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (04) :1620-1624
[52]  
Beckman JS, 1996, AM J PHYSIOL-CELL PH, V271, pC1424
[53]  
BECKMAN JS, 1991, J DEV PHYSIOL, V15, P53
[54]   EXTENSIVE NITRATION OF PROTEIN TYROSINES IN HUMAN ATHEROSCLEROSIS DETECTED BY IMMUNOHISTOCHEMISTRY [J].
BECKMANN, JS ;
YE, YZ ;
ANDERSON, PG ;
CHEN, J ;
ACCAVITTI, MA ;
TARPEY, MM ;
WHITE, CR ;
BECKMAN, JS .
BIOLOGICAL CHEMISTRY HOPPE-SEYLER, 1994, 375 (02) :81-88
[55]   HYPERPOLARIZING FACTORS [J].
BENY, JL ;
VONDERWEID, PY .
CORONARY ARTERY DISEASE, 1991, 2 (03) :300-306
[56]   Stimulatory effect of ouabain on VCAM-1 and iNOS expression in murine endothelial cells: Involvement of NF-kappa B [J].
Bereta, J ;
Cohen, MC ;
Bereta, M .
FEBS LETTERS, 1995, 377 (01) :21-25
[57]   STIMULATION OF GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE MESSENGER-RNA LEVELS BY ENDOGENOUS NITRIC-OXIDE IN CYTOKINE-ACTIVATED ENDOTHELIUM [J].
BERETA, J ;
BERETA, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 217 (01) :363-369
[58]   Inhibitory effect of di-catechol rooperol on VCAM-1 and iNOS expression in cytokine-stimulate endothelium [J].
Bereta, J ;
Bereta, M ;
Allison, AC ;
Kruger, PB ;
Koj, A .
LIFE SCIENCES, 1996, 60 (4-5) :325-334
[59]   METHYLXANTHINES AND CALCIUM-MOBILIZING AGENTS INHIBIT THE EXPRESSION OF CYTOKINE-INDUCIBLE NITRIC-OXIDE SYNTHASE AND VASCULAR CELL-ADHESION MOLECULE-1 IN MURINE MICROVASCULAR ENDOTHELIAL-CELLS [J].
BERETA, M ;
BERETA, J ;
GEORGOFF, I ;
COFFMAN, FD ;
COHEN, S ;
COHEN, MC .
EXPERIMENTAL CELL RESEARCH, 1994, 212 (02) :230-242
[60]   HAEMOPHILUS-INFLUENZAE TYPE-B IMPAIRMENT OF PIAL VESSEL AUTOREGULATION IN RATS [J].
BERKOWITZ, ID ;
HAYDEN, WR ;
TRAYSTMAN, RJ ;
JONES, MD .
PEDIATRIC RESEARCH, 1993, 33 (01) :48-51