CARDIOVASCULAR EFFECTS OF N-ETHYL PERHEXILINE MALEATE IN ANIMALS
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Abstract
N-ethyl perhexiline maleate (1,1-dicyclohexyl-2(N-ethyl) pyridinyl ethane maleate, NEP) is a derivative of perhexiline maleate (Per). NEP was demonstrated to produce more potent inhibiting effects than Per in a series of experimental arrhythmia models induced by BaCl2, CaCl2, aconitine and ouabain. Its negative chronotropic action, negative automaticity action and negative conduction action may be the pharmacological basis for antiarrhythmia. In anesthetized open-chest dogs, NEP (4 mg/kg ⅳ)significantly decreased blood pressure (—20.1%), heart rate (—26.5%), myocardium oxygen consumption (—53.6%) and coronary resistance (—19.1%). It appears that NEP may have an anti-ischemia effect on the heart.
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