A HIGHLY POTENT AND SELECTIVE H-3 AGONIST RELAXES RABBIT MIDDLE CEREBRAL-ARTERY, INVITRO

被引:50
作者
EAKIM, L
OUDART, N
机构
关键词
D O I
10.1016/0014-2999(88)90026-X
中图分类号
R9 [药学];
学科分类号
1007 ;
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页码:393 / 396
页数:4
相关论文
共 7 条
[1]   AUTO-INHIBITION OF BRAIN HISTAMINE-RELEASE MEDIATED BY A NOVEL CLASS (H-3) OF HISTAMINE-RECEPTOR [J].
ARRANG, JM ;
GARBARG, M ;
SCHWARTZ, JC .
NATURE, 1983, 302 (5911) :832-837
[2]   HIGHLY POTENT AND SELECTIVE LIGANDS FOR HISTAMINE RECEPTORS-H-3 [J].
ARRANG, JM ;
GARBARG, M ;
LANCELOT, JC ;
LECOMTE, JM ;
POLLARD, H ;
ROBBA, M ;
SCHUNACK, W ;
SCHWARTZ, JC .
NATURE, 1987, 327 (6118) :117-123
[3]   A NOVEL CLASS (H-3) OF HISTAMINE-RECEPTORS ON PERIVASCULAR NERVE-TERMINALS [J].
ISHIKAWA, S ;
SPERELAKIS, N .
NATURE, 1987, 327 (6118) :158-160
[4]  
LEVI R, 1982, PHARM HISTAMINE RECE, P236
[5]  
OUDART N, 1981, ARCH INT PHARMACOD T, V252, P196
[6]  
SERCOMBE R, 1986, BLOOD VESSELS, V23, P137
[7]  
TODA N, 1974, J PHARMACOL EXP THER, V191, P139