Naloxone and vitamin E block stress-induced reduction of locomotor activity and elevation of plasma corticosterone

被引:14
作者
Ainsah, O
Nabishah, BM
Osman, CB
Khalid, BAK
机构
[1] Hosp Univ Kebangsaan Malaysia, Dept Psychiat, Kuala Lumpur, Malaysia
[2] Hosp Univ Kebangsaan Malaysia, Dept Physiol, Kuala Lumpur, Malaysia
[3] Hosp Univ Kebangsaan Malaysia, Dept Med, Kuala Lumpur, Malaysia
关键词
vitamin E; restraint stress; locomotor activity; plasma corticosterone;
D O I
10.1055/s-0029-1212139
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Normal rats, on being repetitively stressed by being restrained in a tight container for two hours, had higher levels of plasma corticosterone compared to pre stress values These rats also reacted to the stress by a behavioral response in which there was marked decrease in locomotor activity assessed by the open field test (pre stress: 71.3 +/- 2.6 squares crossed versus post stress: 14.3 +/- 2.5 squares crossed) by counting the number of squares entered by the rat over 5 minutes. By the 6th to 7th exposures to the repetitive stress, the rats adapted to the stress and had normal plasma corticosterone levels and locomotor activity scores comparable to the pre stress values These responses to stress were completely blocked by the administration of 0.32 mu g/100 g BW of naloxone i.p at 10 minutes prior to the stress. In rats fed with rat chow supplemented with 90 mg/kg rat chow or 150 mg/kg rat chow of vitamin E, there was significant reduction of the plasma corticosterone levels and improvement in the locomotor activity. Stress thus caused opioid mediated increase in plasma corticosterone and reduction in locomotor activity which could be blocked by naloxone. These stress responses probably also involved generation of oxygen free radicals which were scavenged by the vitamin E, thus reducing the effects of repetitive stress on locomotor activity and serum corticosterone levels.
引用
收藏
页码:462 / 467
页数:6
相关论文
共 51 条
[1]  
AlShabanah OA, 1996, RES COMMUN MOL PATH, V92, P95
[2]   VITAMIN-E-SUPPLEMENTED DIETS REDUCE LIPID-PEROXIDATION BUT DO NOT ALTER EITHER PITUITARY-ADRENAL, GLUCOSE, AND LACTATE RESPONSES TO IMMOBILIZATION STRESS OR GASTRIC-ULCERATION [J].
ARMARIO, A ;
CAMPMANY, L ;
BORRAS, M ;
HIDALGO, J .
FREE RADICAL RESEARCH COMMUNICATIONS, 1990, 9 (02) :113-118
[3]   Oxidative stress following traumatic brain injury in rats [J].
Awasthi, D ;
Church, DF ;
Torbati, D ;
Carey, ME ;
Pryor, WA .
SURGICAL NEUROLOGY, 1997, 47 (06) :575-581
[4]  
BLOOM F, 1976, SCIENCE, V197, P1367
[5]   INTERRELATIONSHIPS OF OPIOIDERGIC AND ADRENERGIC-MECHANISMS CONTROLLING THE SECRETION OF CORTICOTROPIN RELEASING-FACTOR IN THE RAT [J].
BUCKINGHAM, JC ;
COOPER, TA .
NEUROENDOCRINOLOGY, 1987, 46 (03) :199-206
[6]   EFFECTS OF NALOXONE ON HYPOTHALAMO-PITUITARY-ADRENOCORTICAL ACTIVITY IN THE RAT [J].
BUCKINGHAM, JC ;
COOPER, TA .
NEUROENDOCRINOLOGY, 1986, 42 (05) :421-426
[7]   REDUCTION OF HEART LESIONS AFTER EXPERIMENTAL RESTRAINT STRESS - A STUDY IN STRESS-SUSCEPTIBLE PIGS [J].
CARLSTEN, J ;
BJURSTROM, S ;
HAGGENDAL, J ;
JONSSON, L .
JOURNAL OF VETERINARY MEDICINE SERIES A-PHYSIOLOGY PATHOLOGY CLINICAL MEDICINE, 1994, 41 (10) :722-730
[8]   PHYSICAL CONDITIONING FACILITATES THE EXERCISE-INDUCED SECRETION OF BETA-ENDORPHIN AND BETA-LIPOTROPIN IN WOMEN [J].
CARR, DB ;
BULLEN, BA ;
SKRINAR, GS ;
ARNOLD, MA ;
ROSENBLATT, M ;
BEITINS, IZ ;
MARTIN, JB ;
MCARTHUR, JW .
NEW ENGLAND JOURNAL OF MEDICINE, 1981, 305 (10) :560-563
[9]   ANTIOXIDANTS AND PHYSICAL PERFORMANCE [J].
CLARKSON, PM .
CRITICAL REVIEWS IN FOOD SCIENCE AND NUTRITION, 1995, 35 (1-2) :131-141
[10]   OXYGEN RADICALS AND HUMAN-DISEASE [J].
CROSS, CE ;
HALLIWELL, B ;
BORISH, ET ;
PRYOR, WA ;
AMES, BN ;
SAUL, RL ;
MCCORD, JM ;
HARMAN, D .
ANNALS OF INTERNAL MEDICINE, 1987, 107 (04) :526-545