CENTRAL BUT NOT PERIPHERAL OPIATE RECEPTOR BLOCKADE PROLONGED PITUITARY-ADRENAL RESPONSES TO STRESS

被引:22
作者
ODIO, M
BRODISH, A
机构
[1] Department of Physiology and Pharmacology, Bowman Gray School, Medicine Wake Forest University, Winston-Salem
关键词
Stress-induced ACTH corticosterone and prolactin responses; Tertiary and quaternary naltrexone;
D O I
10.1016/0091-3057(90)90386-V
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Evidence from pharmacological studies suggests that opiate systems may serve either inhibitory or stimulatory functions on stress-induced reponses of the hypothalamic-pituitary-adrenocortical (HPA) axis. The objective of these experiments was to determine whether these discrepant findings may result, in part, from differential effects of central or peripheral opiate receptor blockade on HPA axis responses. To this effect, groups of rats received injections of either saline, naltrexone (NHCl) or the quaternary analogue naltrexone methobromide (NMBr). The animals were then exposed to 30 min of a motion stressor and blood samples were obtained from each rat for analysis of ACTH, corticosterone, and prolactin. The data showed that resting and stress-induced levels of prolactin were decreased by NHCl only. Although neither drug affected the magnitude of the stress-induced ACTH and corticosterone responses, treatment with NHCl, but not NMBr, delayed the poststress decline of these responses. Hence, we concluded that central opiate mechanisms may be important for cessation of HPA axis activity, after exposure to stressful situations. © 1990.
引用
收藏
页码:963 / 969
页数:7
相关论文
共 35 条
[1]   SYSTEMIC NALOXONE ADMINISTRATION POTENTIATES LOCUS COERULEUS NORADRENERGIC NEURONAL-ACTIVITY UNDER STRESSFUL BUT NOT NON-STRESSFUL CONDITIONS [J].
ABERCROMBIE, ED ;
JACOBS, BL .
BRAIN RESEARCH, 1988, 441 (1-2) :362-366
[2]   EVIDENCE THAT LONG-TERM ADMINISTRATION OF A METHIONINE-ENKEPHALIN ANALOG STIMULATES THE GROWTH AND STEROIDOGENIC CAPACITY OF RAT INNER ADRENOCORTICAL-CELLS [J].
ANDREIS, PG ;
BELLONI, AS ;
CAVALLINI, L ;
MAZZOCCHI, G ;
NUSSDORFER, GG .
NEUROPEPTIDES, 1988, 12 (03) :165-170
[3]   AGE-DEPENDENT EFFECTS OF CHRONIC STRESS ON ACTH AND CORTICOSTERONE RESPONSES TO AN ACUTE NOVEL STRESS [J].
BRODISH, A ;
ODIO, M .
NEUROENDOCRINOLOGY, 1989, 49 (05) :496-501
[5]   ANTAGONISM OF STRESS-INDUCED ANALGESIA BY QUATERNARY NALOXONE [J].
CHANCE, WT ;
NELSON, JL .
BRAIN RESEARCH, 1986, 380 (02) :394-396
[6]   AN ADRENAL-MEDIATED, NALOXONE-REVERSIBLE INCREASE IN REACTION-TIME IN THE TAIL-FLICK TEST FOLLOWING INTRATHECAL ADMINISTRATION OF SUBSTANCE-P AT THE LOWER THORACIC SPINAL LEVEL IN THE RAT [J].
CRIDLAND, RA ;
HENRY, JL .
NEUROSCIENCE, 1988, 26 (01) :243-251
[7]   D-ALA2-MET-ENKEPHALINAMIDE, A POTENT OPIOID PEPTIDE, ALTERS PITUITARY-ADRENOCORTICAL SECRETION IN RATS [J].
DESOUZA, EB ;
VANLOON, GR .
ENDOCRINOLOGY, 1982, 111 (05) :1483-1490
[8]   EFFECTS OF NALOXONE ON PLASMA-CORTICOSTERONE IN THE OPIATE-NAIVE RAT [J].
EISENBERG, RM .
LIFE SCIENCES, 1980, 26 (12) :935-943
[9]  
Ferri S, 1980, Adv Biochem Psychopharmacol, V22, P347
[10]   HYPERALGESIA INDUCED BY NALOXONE FOLLOWS DIURNAL RHYTHM IN RESPONSIVITY TO PAINFUL STIMULI [J].
FREDERICKSON, RCA ;
BURGIS, V ;
EDWARDS, JD .
SCIENCE, 1977, 198 (4318) :756-758