Stroke, Vol 23, 1643-1650, Copyright © 1992 by American Heart Association
AL Siren, E Heldman, D Doron, PG Lysko, TL Yue, Y Liu, G Feuerstein and JM Hallenbeck
BACKGROUND AND PURPOSE: We reported previously that stroke risk factors
prepared the brain stem for the development of ischemia and hemorrhage and
induced the production of tumor necrosis factor following an intrathecal
injection of lipopolysaccharide, a prototypic monocyte- activating
stimulus. This study evaluates whether blood or brain cells of hypertensive
rats produce more proinflammatory and prothrombotic mediators than do blood
or brain cells of normotensive rats. METHODS: Levels of tumor necrosis
factor, platelet-activating factor, 6- ketoprostaglandin F1 alpha, and
thromboxane B2 in the cerebrospinal fluid and blood of spontaneously
hypertensive and normotensive Wistar- Kyoto rats were monitored before and
after a challenge with lipopolysaccharide. RESULTS: Little or no activity
from these mediators was found in the cerebrospinal fluid or blood of
saline-injected control animals. Intravenous administration of
lipopolysaccharide (0.001, 0.1, and 1.8 mg/kg) produced dose-dependent
increases in blood levels of all mediators in hypertensive rats. In
normotensive rats the levels were less than in hypertensive rats and were
not clearly dose- related. When lipopolysaccharide was injected
intracerebroventricularly, more tumor necrosis factor was measured in the
cerebrospinal fluid than in the blood, suggesting local synthesis of this
cytokine. Levels of tumor necrosis factor and platelet- activating factor
in the cerebrospinal fluid were higher in hypertensive than in normotensive
rats. The thromboxane A2/prostacyclin ratio was not altered significantly
between the two rat strains. CONCLUSIONS: It is suggested that the higher
incidence of brain stem ischemia and hemorrhage after the intrathecal
injection of lipopolysaccharide in hypertensive rats than in normotensive
rats might be related to the higher levels of the two cytotoxic factors
tumor necrosis factor and platelet-activating factor produced in response
to such challenge.
ARTICLES
Release of proinflammatory and prothrombotic mediators in the brain and peripheral circulation in spontaneously hypertensive and normotensive Wistar-Kyoto rats
Department of Neurology, Uniformed Services University of the Health Sciences, Bethesda, MD 20814.
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