Augmentation of cocaine hyperactivity in rats by systemic ghrelin

The feeding-relevant pathway by which food deprivation (FD) augments cocaine action is unknown. Systemic administration of the 28 amino acid acylated peptide ghrelin (1–10 nmol) increases food intake in rats and circulating levels of rat ghrelin are up-regulated by FD. The present experiment examine...

Full description

Saved in:
Bibliographic Details
Published inRegulatory peptides Vol. 125; no. 1; pp. 151 - 154
Main Authors Wellman, Paul J., Davis, Kristina W., Nation, Jack R.
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 15.02.2005
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:The feeding-relevant pathway by which food deprivation (FD) augments cocaine action is unknown. Systemic administration of the 28 amino acid acylated peptide ghrelin (1–10 nmol) increases food intake in rats and circulating levels of rat ghrelin are up-regulated by FD. The present experiment examined the impact of ghrelin or vehicle pretreatment on the locomotion and stereotypy induced by systemic cocaine hydrochloride. Male Sprague–Dawley rats were pretreated at −60 min with 0 or 5 nmol rat ghrelin (IP) and then injected (IP) at time 0 with 0, 2.5, 5.0, or 10.0 mg/kg cocaine. Locomotor activity was monitored over a 45-min post-cocaine period. Rats received the same ghrelin dose, but a different cocaine dose (in random order) on each of the four drug trials, with each drug trial separated by at least 2 days. Administration of 5 nmol ghrelin–0 mg/kg cocaine slightly increased locomotion relative to that of 0 nmol ghrelin–0 mg/kg cocaine. Cocaine increased locomotion as a function of dose in the 0 nmol ghrelin group, but the effect of cocaine was even greater when preceded by 5 nmol ghrelin. These results indicate that acute injection of ghrelin, at a feeding-relevant dose, augments the acute effects of cocaine on locomotion in rats.
ISSN:0167-0115
1873-1686
DOI:10.1016/j.regpep.2004.08.013