Activation of three types of voltage-independent Ca2+ channel in A7r5 cells by endothelin-1 as revealed by a novel Ca2+ channel blocker LOE 908

British Journal of Pharmacology

Volumn 126, Issue 5, 1999, Pages 1107-1114

  Iwamuro, Yasushi ^a   Miwa, Soichi ^a   Zhang, Xiao Feng ^a   Minowa, Tetsuya ^a   Enoki, Taijiro ^a   Okamoto, Yasuo ^a   Hasegawa, Hiroshi ^a   Furutani, Hidekatsu ^a   Okazawa, Makoto ^a   Ishikawa, Masatsune ^a   Hashimoto, Nobuo ^a   Masaki, Tomoh ^b  

^a KYOTO UNIVERSITY FACULTY OF MEDICINE   (Japan)

^b NATIONAL CEREBRAL AND CARDIOVASCULAR CENTER   (Japan)

Author keywords

A7r5 cell; Endothelin 1; LOE 908; SK and F 96365; Voltage independent calcium channel

Indexed keywords

1 [2 (4 METHOXYPHENYL) 2 [3 (4 METHOXYPHENYL)PROPOXY]ETHYL] 1H IMIDAZOLE; 2 (3,4 DIHYDRO 6,7 DIMETHOXY 1 ISOQUINOLINYL) 2 PHENYL N,N BIS[2 (2,3,4 TRIMETHOXYPHENYL)ETHYL]ACETAMIDE; CALCIUM CHANNEL; CALCIUM CHANNEL BLOCKING AGENT; CALCIUM ION; ENDOTHELIN 1; IONOMYCIN; NIFEDIPINE; THAPSIGARGIN; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; CALCIUM CELL LEVEL; CALCIUM CURRENT; CONTROLLED STUDY; EXTRACELLULAR CALCIUM; NONHUMAN; PRIORITY JOURNAL; RAT;

EID: 0033009716     PISSN: 00071188     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.bjp.0702416     Document Type: Article

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