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      Role of epinephrine stimulation of CNS alpha1-adrenoceptors in motor activity in mice.

      Synapse (New York, N.y.)
      Adrenergic alpha-Agonists, pharmacology, Adrenergic alpha-Antagonists, Adrenergic beta-Antagonists, Animals, Benzylamines, Betaxolol, Brain, drug effects, Cell Line, Epinephrine, administration & dosage, antagonists & inhibitors, Humans, Hydrolysis, Imidazoles, Injections, Intraventricular, Kidney, metabolism, Male, Mice, Motor Activity, Norepinephrine, analogs & derivatives, Phenylephrine, Phosphatidylinositols, Prazosin, Receptors, Adrenergic, alpha, Serotonin

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          Abstract

          The role of brain epinephrine (EPI) in the regulation of motor activity and movement in mice was examined. Blockade of EPI synthesis with i.p. 2,3-dichloro-alpha-methylbenzylamine (DCMB) or LY134046 was found to produce marked behavioral inactivity which could be significantly reversed by intraventricular injection of EPI and by three other alpha(1)-adrenoceptor agonists, norepinephrine (NE), 6-fluoronorepinephrine (6FNE), and phenylephrine (PE), as well as by serotonin (5HT). EPI had the largest effect of these agonists and also was the only one that reversed nondrug-induced inactivity of mice in their home cages during the light phase. The effects of EPI were blocked by coinfusion of an alpha(1)-adrenoceptor antagonist (terazosin) but not of an alpha(2)-(atipamezole) or beta(1) (betaxolol)-blocker. The rank order of maximal behavioral responses to EPI, 6FNE, and PE in DCMB-treated mice was the same as the rank order of their maximal stimulation of hydrolysis of phosphatidylinositol at cloned alpha(1B)-adrenoceptors in cell culture. On the basis of the above findings and of the central distributions of adrenergic neurons and alpha(1)-adrenoceptors, the existence of a central EPI-innervated alpha(1)-adrenergic receptor system is postulated which serves to coexcite or enhance signaling in several monoaminergic brain regions involved in movement and motor activity. Copyright 2003 Wiley-Liss, Inc.

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