
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.
Male, Venoms, Anxiety, Motor Activity, Glucagon-Like Peptide-1 Receptor, Rats, Rats, Sprague-Dawley, Amphetamine, Antimanic Agents, Glucagon-Like Peptide 1, Receptors, Glucagon, Animals, Conditioning, Operant, Exenatide, Central Nervous System Stimulants, Lithium Chloride, Peptides
Male, Venoms, Anxiety, Motor Activity, Glucagon-Like Peptide-1 Receptor, Rats, Rats, Sprague-Dawley, Amphetamine, Antimanic Agents, Glucagon-Like Peptide 1, Receptors, Glucagon, Animals, Conditioning, Operant, Exenatide, Central Nervous System Stimulants, Lithium Chloride, Peptides
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| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
