INTRACELLULAR CALCIUM RELEASE IN N1E-115 NEUROBLASTOMA-CELLS IS MEDIATED BY THE M1 MUSCARINIC RECEPTOR SUBTYPE AND IS ANTAGONIZED BY MCN-A-343

被引:13
作者
MATHES, C
WANG, SSH
VARGAS, HM
THOMPSON, SH
机构
[1] UNIV CALIF LOS ANGELES,BRAIN RES INST,DEPT PHARMACOL,LOS ANGELES,CA 90024
[2] UNIV CALIF LOS ANGELES,BRAIN RES INST,INTERDEPT PROGRAM NEUROSCI,LOS ANGELES,CA 90024
关键词
MUSCARINIC RECEPTOR SUBTYPE; 4-DAMP; AFDX116; PIRENZEPINE; MCN-A-343; (+/-)BN228(4-[N]-(CHLOROPHENYL)CARBOXYLOXY-PENT-2-YNYLTRIMETHYLAMMONIUM BR); CALCIUM RELEASE; N1E-115; NEUROBLASTOMA;
D O I
10.1016/0006-8993(92)91225-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Experiments using muscarinic receptor antagonists were done to determine which muscarinic receptor subtype(s) mediate carbachol-evoked calcium release in N1E-115 cells. McN-A-343 and a new analog, (+/-)BN228, were weak antagonists and neither compound caused release on its own. The rank order of potency was 4-DAMP > pirenzepine > AFDX116 > (+/-)BN228 and McN-A-343. This profile, pirenzepine's high potency (19-fold greater than AFDX116) and its IC50 of 31 nM suggest that calcium release in this neuronal cell line is mediated by the M1 muscarinic receptor subtype.
引用
收藏
页码:307 / 310
页数:4
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