Co-operative Effect Between γ-Aminobutyric Acid A Receptors and Central-Type Benzodiazepine Receptors on Amylase Release in Rat Parotid Acinar Cells

被引:6
|
作者
Okubo, Migiwa [1 ]
Kawaguchi, Mitsuru [1 ]
机构
[1] Tokyo Dent Coll, Dept Pharmacol, Mihama Ku, Chiba 2618502, Japan
关键词
gamma-aminobutyric acid A receptor; parotid gland; amylase release; SALIVARY-GLANDS; SYSTEM;
D O I
10.1254/jphs.09269SC
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We investigated the inhibitory role of gamma-aminobutyric acid A (GABA(A)) receptors on amylase release and the evidence for functional coupling with central-type benzodiazepine receptors In rat parotid acinar cells. Muscimol and GABA decreased isoprenaline-induced amylase release This effect was blocked by bicuculline, a GABA(A)-receptor antagonist, and enhanced by clonazepam, a central-type benzodiazepine-receptor agonist, and diazepam, a central- and peripheral-type benzodiazepine-receptor agonist. Although bicuculline completely blocked the combination effect of GABA(A)-receptor agonist and clonazepam, it did not completely block the combination effect with diazepam These results suggest that protein secretion is suppressively regulated by GABA(A) receptors coupled with central-type benzodiazepine receptors.
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页码:247 / 250
页数:4
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