Stroke, Vol 17, 202-207, Copyright © 1986 by American Heart Association
T Tsukahara, T Taniguchi, S Shimohama, M Fujiwara and H Handa
The nature of beta adrenergic receptors in human cerebral arteries was
characterized and alteration of these receptors after subarachnoid
hemorrhage was examined using a radioligand binding assay. The specific
3H-dihydroalprenolol, a beta adrenergic antagonist, binding to human
cerebral arteries was saturable and of high affinity (KD = 12.3 nM) with a
Bmax of 790 fmol/mg protein. Ki values and Hill coefficients of adrenergic
agents for 3H-dihydroalprenolol were as follows; propranolol, 4.1 X
10(-8)M, 1.01; isoproterenol, 1.7 X 10(-6)M, 0.80; epinephrine, 8.3 X
10(-6)M, 0.48; norepinephrine, 2.3 X 10(-5)M, 0.45; metoprolol, 6.8 X
10(-8)M and 7.9 X 10(-6)M, 0.62; butoxamine, 2.2 X 10(-8)M and 2.1 X
10(-6)M, 0.43. The analysis of inhibition of specific 3H-dihydroalprenolol
binding by these adrenergic agents suggests that human cerebral arteries
contain a high density of beta adrenergic receptors and that the receptors
are classified into two types, namely beta 1 and beta 2 adrenergic
receptors. The calculated beta 1/beta 2 ratio from Hofstee plots was
approximately 4/6. KD and Bmax of 3H- dihydroalprenolol binding to the
cerebral arteries after subarachnoid hemorrhage were compared with those of
control group. KD and Bmax of 3H- dihydroalprenolol binding of subarachnoid
hemorrhage group were 13.9 nM and 1140 fmol/mg protein, respectively. The
calculated beta 1/beta 2 ratio was approximately 6/4. These data suggest
that the density of total beta adrenergic receptors increased without any
significant change in the affinity after subarachnoid hemorrhage and that
the increase of beta 1 adrenergic receptors was dominant.
ARTICLES
Characterization of beta adrenergic receptors in human cerebral arteries and alteration of the receptors after subarachnoid hemorrhage
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