Long term modulation of the HPA axis by the hippocampus - Behavioral, biochemical and immunological endpoints in rats exposed to chronic mild stress

被引:38
作者
Bratt, AM
Kelley, SP
Knowles, JP
Barrett, J
Davis, K
Davis, M
Mittleman, G
机构
[1] Univ Memphis, Dept Psychol, Memphis, TN 38152 USA
[2] Cat & Cow Vet Clin, Olive Branch, MS 38654 USA
[3] Univ Memphis, Dept Biol, Memphis, TN 38152 USA
关键词
hippocampus; fimbria-fornix; subiculum; amphetamine; metryapone; corticosterone; locomotion;
D O I
10.1016/S0306-4530(00)00033-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mature rats were given lesions of the hippocampus (HIPPO), subiculum (SUBIC) or fimbria-fornix (FIFO) and then received the mild chronic stressors of food deprivation and isolation housing for ten months prior to testing. Group differences in circadian activity were investigated along with locomotion elicited by amphetamine (AMP 1.0-2.0 mg/kg i.p.) alone, and following the corticosterone (CORT) synthesis inhibitor, metyrapone (MET 10.0-25.0 mg/kg i.p.), Basal levels of plasma CORT, (ng/ml), plasma glucose (GLUC, mmol/l), thymic and splenic wet weights were subsequently determined along with complete blood counts (CBC). In comparison to age matched, unoperated controls, selective SUBIC lesions altered the circadian periodicity of locomotion, while rats with FIFO lesions were spontaneously hyperactive. Both HIPPO and FIFO animals showed significantly higher levels of amphetamine-induced locomotion. In all groups metyrapone significantly enhanced locomotion elicited by amphetamine, probably due to a pharmacokinetic interaction between these drugs. In comparison to controls, animals in the HIPPO group showed significant reductions in plasma glucose levels, decreased thymic wet weights and reductions in lymphocyte numbers, indicating lesion-related immune-suppression. These findings highlight a functional difference among the effects of these specific hippocampal lesions on neural regulation of the HPA axis, under conditions of chronic mild stress, suggesting that the modulatory influence of the hippocampus on the stress axis is dependent on the neuroanatomical location and total extent of cell loss within this structure. They further suggest that the heightened response to amphetamine occurs independently of any lesion-induced changes in modulation of the HPA axis. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:121 / 145
页数:25
相关论文
共 77 条
[1]   Effects of corticosteroid synthesis inhibitors on the sensitization of reward by food restriction [J].
Abrahamsen, GC ;
Carr, KD .
BRAIN RESEARCH, 1996, 726 (1-2) :39-48
[2]   INVOLUTION OF THE THYMUS REVISITED - IMMUNOLOGICAL TRADE-OFFS AS AN ADAPTATION TO AGING [J].
ARONSON, M .
MECHANISMS OF AGEING AND DEVELOPMENT, 1993, 72 (01) :49-55
[3]   THE IMMUNE-HYPOTHALAMIC-PITUITARY-ADRENAL AXIS [J].
BATEMAN, A ;
SINGH, A ;
KRAL, T ;
SOLOMON, S .
ENDOCRINE REVIEWS, 1989, 10 (01) :92-112
[4]   EFFECTS OF REPEATED STRESS ON T-CELL NUMBERS AND FUNCTION IN RATS [J].
BATUMAN, OA ;
SAJEWSKI, D ;
OTTENWELLER, JE ;
PITMAN, DL ;
NATELSON, BH .
BRAIN BEHAVIOR AND IMMUNITY, 1990, 4 (02) :105-117
[5]   CYTOKINE REGULATION OF CORTICOSTEROID RECEPTORS IN THE RAT HIPPOCAMPUS - EFFECTS OF INTERLEUKIN-1, INTERLEUKIN-6, TUMOR-NECROSIS-FACTOR AND LIPOPOLYSACCHARIDE [J].
BETANCUR, C ;
BORRELL, J ;
GUAZA, C .
NEUROENDOCRINOLOGY, 1995, 62 (01) :47-54
[6]   Stimulation of the ventral subiculum of the hippocampus evokes glutamate receptor-mediated changes in dopamine efflux in the rat nucleus accumbens [J].
Blaha, CD ;
Yang, CR ;
Floresco, SB ;
Barr, AM ;
Phillips, AG .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1997, 9 (05) :902-911
[7]  
BOHUS B, 1994, STRESS NEUROENDOCRIN, P607
[8]   LESIONS OF THE HIPPOCAMPAL EFFERENT PATHWAY (FIMBRIA-FORNIX) DO NOT ALTER SENSITIVITY OF ADRENOCORTICOTROPIN TO FEEDBACK INHIBITION BY CORTICOSTERONE IN RATS [J].
BRADBURY, MJ ;
STRACK, AM ;
DALLMAN, MF .
NEUROENDOCRINOLOGY, 1993, 58 (04) :396-407
[9]  
BRATT AM, 1995, EXP BRAIN RES, V102, P429
[10]   Fimbria-fornix lesions do not block sensitization to the psychomotor activating effects of amphetamine [J].
Browman, KE ;
Badiani, A ;
Robinson, TE .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1996, 53 (04) :899-902