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Abstract

Antagonism by naltrexone of the hypotension and bradycardia induced by alpha-methyldopa in conscious normotensive rats.

P L van Giersbergen and W de Jong
Journal of Pharmacology and Experimental Therapeutics January 1988, 244 (1) 341-347;
P L van Giersbergen
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W de Jong
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Abstract

The possible role of the endogenous opioid system in the central hypotensive mechanism of action of alpha-methyldopa was investigated. Conscious normotensive Wistar rats were used in this study and all treatments were given intracisternally. Pretreatment with the opiate receptor antagonist naltrexone resulted in a parallel shift to the right of the dose-response curve for alpha-methyldopa, both for blood pressure and heart rate. In addition, when increasing doses of naltrexone and a constant dose of alpha-methyldopa were used the opiate receptor antagonist inhibited dose-dependently alpha-methyldopa-induced hypotension but not the bradycardia. Administration of naltrexone after the injection of alpha-methyldopa failed to reverse or inhibit alpha-methyldopa-induced hypotension, indicating that the interaction between alpha-methyldopa and the endogenous opioid system occurs at the start of the action of alpha-methyldopa. An antiserum against endorphins also inhibited the fall in blood pressure after alpha-methyldopa. These findings indicate that stimulation of opiate receptors, probably by an endorphin, is involved in the mechanism of action of alpha-methyldopa and that this stimulation seems to occur at the start of the action of alpha-methyldopa.

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Journal of Pharmacology and Experimental Therapeutics
Vol. 244, Issue 1
1 Jan 1988
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Abstract

Antagonism by naltrexone of the hypotension and bradycardia induced by alpha-methyldopa in conscious normotensive rats.

P L van Giersbergen and W de Jong
Journal of Pharmacology and Experimental Therapeutics January 1, 1988, 244 (1) 341-347;

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Abstract

Antagonism by naltrexone of the hypotension and bradycardia induced by alpha-methyldopa in conscious normotensive rats.

P L van Giersbergen and W de Jong
Journal of Pharmacology and Experimental Therapeutics January 1, 1988, 244 (1) 341-347;
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