INTERACTION OF AMILORIDE WITH RAT PAROTID MUSCARINIC AND ALPHA-ADRENERGIC RECEPTORS

被引:6
作者
DEHAYE, JP
VERHASSELT, V
机构
[1] Department of Biochemistry, Institute of Pharmacy, Université libre de Bruxelles, Bruxelles
来源
GENERAL PHARMACOLOGY-THE VASCULAR SYSTEM | 1995年 / 26卷 / 01期
关键词
AMYLASE; CARBAMYLCHOLINE; EPINEPHRINE; SUBSTANCE P; NA+/H+ ANTIPORTER;
D O I
10.1016/0306-3623(94)00153-E
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1. In rat parotid acini, amiloride inhibited the secretion of amylase and the efflux of calcium and rubidium in response to carbamylcholine and to norepinephrine. 2. Amiloride competitively inhibited the binding of [H-3]N-methylscopolamine and [H-3] is thus a competitive antagonist of muscarinic and norepinephrine alpha-adrenergic receptors. 3. Amiloride did not affect the response to substance P with respect to secretion or ion movements. 4. Thus the Na+/H+ antiporter is not involved in the short-term regulation of amylase secretion and calcium and potassium movements in rat parotid gland function.
引用
收藏
页码:155 / 159
页数:5
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