Augmentation of cocaine hyperactivity in rats by systemic ghrelin

被引:86
作者
Wellman, PJ [1 ]
Davis, KW [1 ]
Nation, JR [1 ]
机构
[1] Texas A&M Univ, Dept Psychol, Behav Neurosci Program, College Stn, TX 77843 USA
关键词
food deprivation; locomotion; stereotypy; growth hormone;
D O I
10.1016/j.regpep.2004.08.013
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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. Mate 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. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:151 / 154
页数:4
相关论文
共 30 条
[1]   Stomach is a major source of circulating ghrelin, and feeding state determines plasma ghrelin-like immunoreactivity levels in humans [J].
Ariyasu, H ;
Takaya, K ;
Tagami, T ;
Ogawa, Y ;
Hosoda, K ;
Akamizu, T ;
Suda, M ;
Koh, T ;
Natsui, K ;
Toyooka, S ;
Shirakami, G ;
Usui, T ;
Shimatsu, A ;
Doi, K ;
Hosoda, H ;
Kojima, M ;
Kangawa, K ;
Nakao, K .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (10) :4753-4758
[2]   Antagonism of ghrelin receptor reduces food intake and body weight gain in mice [J].
Asakawa, A ;
Inui, A ;
Kaga, T ;
Katsuura, G ;
Fujimiya, M ;
Fujino, MA ;
Kasuga, M .
GUT, 2003, 52 (07) :947-952
[3]   A role of ghrelin in neuroendocrine and behavioral responses to stress in mice [J].
Asakawa, A ;
Inui, A ;
Kaga, T ;
Yuzuriha, H ;
Nagata, T ;
Fujimiya, M ;
Katsuura, G ;
Makino, S ;
Fujino, MA ;
Kasuga, M .
NEUROENDOCRINOLOGY, 2001, 74 (03) :143-147
[4]   Endogenous ghrelin is an orexigenic peptide acting in the arcuate nucleus in response to fasting [J].
Bagnasco, M ;
Tulipano, G ;
Melis, MR ;
Argiolas, A ;
Cocchi, D ;
Muller, EE .
REGULATORY PEPTIDES, 2003, 111 (1-3) :161-167
[5]   Decisions, decisions [J].
Bell, J .
NATURE REVIEWS IMMUNOLOGY, 2001, 1 (01) :8-8
[6]   Effects of ghrelin and amylin on dopamine, norepinephrine and serotonin release in the hypothalamus [J].
Brunetti, L ;
Recinella, L ;
Orlando, G ;
Michelotto, B ;
Di Nisio, C ;
Vacca, M .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2002, 454 (2-3) :189-192
[7]   POTENTIATION OF AMPHETAMINE-INDUCED AROUSAL BY STARVATION [J].
CAMPBELL, BA ;
FIBIGER, HC .
NATURE, 1971, 233 (5319) :424-&
[8]   Effects of ketoconazole on the acquisition of intravenous cocaine self-administration under different feeding conditions in rats [J].
Campbell, UC ;
Carroll, ME .
PSYCHOPHARMACOLOGY, 2001, 154 (03) :311-318
[9]   Ghrelin increases anxiety-like behavior and memory retention in rats [J].
Carlini, VP ;
Monzón, ME ;
Varas, MM ;
Cragnolini, AB ;
Schiöth, HB ;
Scimonelli, TN ;
de Barioglio, SR .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 299 (05) :739-743
[10]   Feeding, drug abuse, and the sensitization of reward by metabolic need [J].
Carr, KD .
NEUROCHEMICAL RESEARCH, 1996, 21 (11) :1455-1467