Exendin-4 decreases amphetamine-induced locomotor activity |
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Authors: | Erreger Kevin Davis Adeola R Poe Amanda M Greig Nigel H Stanwood Gregg D Galli Aurelio |
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Affiliation: | Department of Molecular Physiology & Biophysics, Vanderbilt University, Nashville, TN 37232, USA. kevin.erreger@vanderbilt.edu |
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Abstract: | Glucagon-like peptide-1 (GLP-1) is released in response to nutrient ingestion and is a regulator of energy metabolism and consummatory behaviors through both peripheral and central mechanisms. The GLP-1 receptor (GLP-1R) is widely distributed in the central nervous system, however little is known about how GLP-1Rs regulate ambulatory behavior. The abused psychostimulant amphetamine (AMPH) promotes behavioral locomotor activity primarily by inducing the release of the neurotransmitter dopamine. Here, we identify the GLP-1R agonist exendin-4 (Ex-4) as a modulator of behavioral activation by AMPH. We report that in rats a single acute administration of Ex-4 decreases both basal locomotor activity as well as AMPH-induced locomotor activity. Ex-4 did not induce behavioral responses reflecting anxiety or aversion. Our findings implicate GLP-1R signaling as a novel modulator of psychostimulant-induced behavior and therefore a potential therapeutic target for psychostimulant abuse. |
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