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Volumn 4, Issue 3, 1990, Pages 731-736
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The structurally novel Ca2+ channel blocker Ro 40-5967, which binds to the [3H] desmethoxyverapamil receptor, is devoid of the negative inotropic effects of verapamil in normal and failing rat hearts
a
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Author keywords
calcium antagonists; heart failure; myocardial contractility; Ro 40 5967; verapamil
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Indexed keywords
MIBEFRADIL;
VERAPAMIL;
BENZIMIDAZOLE DERIVATIVE;
CALCIUM CHANNEL BLOCKING AGENT;
DIAGNOSTIC AGENT;
NICOTINIC RECEPTOR;
TETRALIN DERIVATIVE;
TRITIUM;
ANIMAL CELL;
ANIMAL EXPERIMENT;
ARTICLE;
FEMALE;
HEART MUSCLE CONTRACTILITY;
INTRAVENOUS DRUG ADMINISTRATION;
MALE;
NONHUMAN;
PRIORITY JOURNAL;
RAT;
ANIMAL;
CALCIUM CHANNEL;
CHEMICAL PHENOMENA;
COMPARATIVE STUDY;
CONGESTIVE HEART FAILURE;
CORONARY ARTERY BLOOD FLOW;
DOSE RESPONSE;
DRUG EFFECT;
HEART;
HEART CONTRACTION;
HEART INFARCTION;
HEMODYNAMICS;
METABOLISM;
PATHOPHYSIOLOGY;
RAT STRAIN;
ANIMAL;
BENZIMIDAZOLES;
CALCIUM CHANNEL BLOCKERS;
CALCIUM CHANNELS;
COMPARATIVE STUDY;
CORONARY CIRCULATION;
DEPRESSION, CHEMICAL;
DOSE-RESPONSE RELATIONSHIP, DRUG;
FEMALE;
HEART;
HEART FAILURE, CONGESTIVE;
HEMODYNAMICS;
MALE;
MIBEFRADIL;
MYOCARDIAL CONTRACTION;
MYOCARDIAL INFARCTION;
RATS;
RATS, INBRED WKY;
RECEPTORS, NICOTINIC;
TETRAHYDRONAPHTHALENES;
TRITIUM;
VERAPAMIL;
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EID: 0025196303
PISSN: 09203206
EISSN: 15737241
Source Type: Journal
DOI: 10.1007/BF01856562 Document Type: Article |
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Times cited : (86)
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References (17)
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