9-METHYL-7-BROMOEUDISTOMIN-D INDUCES CA2-RETICULUM( RELEASE FROM CARDIAC SARCOPLASMIC)

Citation
A. Seinoumeda et al., 9-METHYL-7-BROMOEUDISTOMIN-D INDUCES CA2-RETICULUM( RELEASE FROM CARDIAC SARCOPLASMIC), European journal of pharmacology, 357(2-3), 1998, pp. 261-265
Citations number
15
Categorie Soggetti
Pharmacology & Pharmacy
ISSN journal
00142999
Volume
357
Issue
2-3
Year of publication
1998
Pages
261 - 265
Database
ISI
SICI code
0014-2999(1998)357:2-3<261:9ICRFC>2.0.ZU;2-Q
Abstract
9-Methyl-7-bromoeudistomin D (MBED), the most powerful caffeine-like r eleaser of Ca2+ from skeletal muscle sarcoplasmic reticulum, induced C a2+ release from the cardiac sarcoplasmic reticulum, MEED (5 mu M) and caffeine (I mM) caused rapid Ca2+ release from the fragmented cardiac sarcoplasmic reticulum in a Ca2+ electrode experiment. [H-3]MBED boun d to a single class of high-affinity binding sites in cardiac sarcopla smic reticulum membranes (K-d = 150 nM). These results suggest that ME ED binds to a specific binding site on cardiac sarcoplasmic reticulum membranes to induce Ca2+ release from the cardiac sarcoplasmic reticul um. Thus, MEED is a useful probe for characterizing Ca2+ release the c hannels nor only in skeletal sarcoplasmic reticulum but also in cardia c sarcoplasmic reticulum. (C) 1998 Elsevier Science B.V. AU rights res erved.