Acta Physiologica Scandinavica · 1987 · 10 citations · 20 references
MedicineNeurosciencePharmacologyNeurochemistryNeuropharmacologyPharmacodynamicsCholinergic PharmacologyMechanisms Of Drug ActionNeurochemical PharmacologySerotonergic Pharmacology5-Hydroxytryptamine Receptor PharmacologyMonoamine Oxidase InhibitorsMonoamine Oxidase InvolvementPharmacological Treatment Of TremorReceptor Tissue SelectivityReceptor-ligand SelectivitySotalol TherapyTremor Pathophysiology
The effect of beta-adrenoceptor antagonists, varying in lipophilicity and receptor selectivity, were studied on tremor elicited by L-5-hydroxytryptophan (L-5-HTP) in rats pretreated with a peripherally acting decarboxylase inhibitor and a monoamine oxidase inhibitor, or by the directly acting 5-HT agonist 5-methoxy-N,N-dimethyltryptamine (5-MeODMT). Plasma levels of the beta-adrenoceptor antagonists were determined simultaneously. The non-selective lipophilic adrenoceptor antagonist propranolol was found to dose-dependently reduce tremor intensity, whereas the non-selective hydrophilic adrenoceptor antagonist sotalol had no effect, indicating a central site of action. Furthermore, beta 1-selective blockade with the adrenoceptor antagonist metoprolol had no effect on tremor intensity, whereas the beta 2-selective antagonist ICI 118,551 dose-dependently suppressed tremor intensity, suggesting that the beta-adrenoceptor subtype involved is of the beta 2-type. These results suggest that blockade of centrally located beta 2-adrenoceptors are able to attenuate the tremor response following 5-hydroxytryptamine receptor activation.
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Neuropharmacology of Serotonin
P Jenner · Journal of Neurology Neurosurgery & Psychiatry · 1986 · 238 citations · Full text