Literature DB >> 8242396

Peptide-induced grooming behavior and caudate nucleus dopamine release.

W J Florijn1, A J Holtmaat, H de Lang, H Spierenburg, W H Gispen, D H Versteeg.   

Abstract

We simultaneously measured the display of grooming behavior and, by monitoring the extracellular dopamine concentration via transversal microdialysis, the release of dopamine in the caudate nucleus in freely moving rats after i.c.v. administration of 1 micrograms adrenocorticotropic hormone-(1-24) (ACTH-(1-24)). During a period of 1 h after administration of the peptide, the incidence of excessive grooming behavior was increased. Concomitantly, the concentration of dopamine in the caudate nucleus dialysates was significantly increased (maximal effect 151% of basal release) whereas that of its metabolite DOPAC was unchanged. The potent alpha-melanocyte stimulating hormone (alpha-MSH) receptor agonist, [Nle4,D-Phe7]alpha-MSH, induced grooming behavior and stimulated caudate nucleus dopamine release (maximal effect 148% of basal release) whereas ACTH-(7-16)-NH2 did neither induce grooming behavior nor cause an increase in caudate nucleus dopamine release. Single-dose tolerance was observed for ACTH-induced grooming but not for ACTH-induced dopamine release. These data are in support of the proposed involvement of brain dopamine systems in grooming behavior of the rat but at the same time suggest that the effect of ACTH/MSH-like peptides on dopaminergic transmission in the caudate nucleus is proximal to the final neural pathway involved in ACTH-induced grooming behavior.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8242396     DOI: 10.1016/0006-8993(93)90151-c

Source DB:  PubMed          Journal:  Brain Res        ISSN: 0006-8993            Impact factor:   3.252


  3 in total

1.  Effects of Semax on dopaminergic and serotoninergic systems of the brain.

Authors:  K O Eremin; V S Kudrin; I A Grivennikov; N F Miasoedov; K S Rayevsky
Journal:  Dokl Biol Sci       Date:  2004 Jan-Feb

2.  Semax, an ACTH(4-10) analogue with nootropic properties, activates dopaminergic and serotoninergic brain systems in rodents.

Authors:  Kirill O Eremin; Vladimir S Kudrin; Pirjo Saransaari; Simo S Oja; Igor A Grivennikov; Nikolay F Myasoedov; Kirill S Rayevsky
Journal:  Neurochem Res       Date:  2005-12       Impact factor: 3.996

3.  Blockade of melanocortin transmission inhibits cocaine reward.

Authors:  Richard Hsu; Jane R Taylor; Samuel S Newton; John D Alvaro; Colin Haile; G Han; Victor J Hruby; Eric J Nestler; Ronald S Duman
Journal:  Eur J Neurosci       Date:  2005-04       Impact factor: 3.386

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.