Factors influencing the hypertensive effect of eserine in the rat.
Several factors influencing the hypertensive effect of eserine in the rat were investigated. Pretreatment with reserpine regularly depressed or abolished the hypertensive response to eserine. The slow intravenous infusion of either noradrenaline, dihydroxyphenylalanine or 5-hydroxytryptamine only occasionally restored the hypertensive effect of eserine in reserpine-treated rats. Bretylium and choline 2,6-xylyl ether bromide significantly depressed or even abolished the hypertensive effect of eserine. The effect of bretylium was stronger than that of choline 2,6-xylyl ether bromide. Cocaine was found to antagonize the action of bretylium on the response to eserine. In doses which significantly depressed the action of eserine bretylium did not inhibit the hypertension due to excitation of medullary centres induced by clamping the common carotid arteries. Lowering of body temperature abolished the hypertensive effect of eserine. Pretreatment with isopropylisoniazid did not antagonize the inhibitory action of reserpine on the hypertensive response to eserine. It is concluded that the present experiments indicate that the hypertensive effect of eserine in the rat is due to central activation of adrenergic nervous elements. Liberation of noradrenaline (and adrenaline) from the adrenals and from the blood vessels by eserine is an insignificant factor in producing the hypertensive response to eserine.
D000311:Adrenal Glands; D000818:Animals; D001794:Blood Pressure / Q000494:pharmacology*; D001949:Bretylium Compounds; D002794:Choline; D004837:Epinephrine; D006973:Hypertension; D009638:Norepinephrine; D010830:Physostigmine; D051381:Rats; D012110:Reserpine; D012701:Serotonin; D013566:Sympathomimetics / Q000494:pharmacology*
D001949:Bretylium Compounds; D013566:Sympathomimetics; D012701:Serotonin; D012110:Reserpine; D010830:Physostigmine; D002794:Choline; C045166:bretylium; D009638:Norepinephrine; D004837:Epinephrine
BLOOD PRESSURE/pharmacology; SYMPATHOMIMETICS/pharmacology