Pharmacological differences between muscarinic receptors coupled to phosphoinositide turnover and those coupled to adenylate cyclase inhibition-Reference-Cited by-同舟云学术

Pharmacological differences between muscarinic receptors coupled to phosphoinositide turnover and those coupled to adenylate cyclase inhibition

Published:1989-05 Issue:10 Volume:38 Page:1605-1616
ISSN:0006-2952
Container-title:Biochemical Pharmacology
language:en
Short-container-title:Biochemical Pharmacology

Author:

Baumgold Jesse,White Thomas

Publisher

Elsevier BV

Subject

Pharmacology,Biochemistry

Reference34 articles.

1. Burgen ASV and Hulme EC, Pirenzepine distinguishes between different subclasses of muscarinic receptors;Hammer;Nature,1980

2. Biochemical and functional basis of putative muscarinic receptor subtypes and its implications;Watson;Trends Pharmacol Sci,1986

3. Inositol lipids and signal transduction at CNS muscarinic receptors;Fisher;Trends Pharmacol Sci,1986

4. The putative M1 muscarinic receptor does not regulate phospho-inositide hydrolysis. Studies with pirenzepine and McN-A343 in chick heart and astrocytoma cells;Brown;Mol Pharmacol,1985

5. AF-DX 116, a cardioselective muscarinic antagonist;Micheletti;J Pharmacol Exp Ther,1987

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4. Polygodial induces inositol phosphate turnover in human neuroblastoma SH-SY5Y cells;Neuroscience Letters;1996-10

5. Pharmacological evidence for the existance of different subtypes of muscarinic acetylcholine receptors for phosphoinositide hydrolysis in neonatal versus adult rat atria;Journal of Lipid Mediators and Cell Signalling;1995-07