Tyrosine hydroxylase gene expression in the locus coeruleus of depression-model rats and rats exposed to short- and long-term forced walking stress

被引:30
作者
Wang, P [1 ]
Kitayama, I [1 ]
Nomura, J [1 ]
机构
[1] Mie Univ, Sch Med, Dept Psychiat, Tsu, Mie 514, Japan
关键词
walking stress; locus coeruleus; tyrosine hydroxylase mRNA; in situ hybridization; animal model; depression;
D O I
10.1016/S0024-3205(98)00183-0
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Abnormal brain noradrenergic function is thought to cause depressive illnesses which are sometimes manifested or aggravated under stressful conditions. To investigate the effect of chronic stress on noradrenaline (NA) synthesis in the brain we used in situ hybridization to examine the expression of tyrosine hydroxylase (TH) mRNA in the locus coeruleus (LC) of "depression-model rats" that exhibit reduced activity following exposure to long-term (14 days) forced walking stress (FWS). We also examined TH mRNA expression in rats stressed for 30 minutes, 3 hours and 1, 2 (short-term), 6 or 12 (long-term) days. The expression of TH mRNA increased markedly following 1 to 12 days of FWS, but not in rats exposed to FWS for 30 minutes or 3 hours. The expression also increased significantly in the depression-model rats, but not in the "spontaneous recovery rats" whose activity was restored after long-term stress. Our results suggest that NA synthesis remains high in the FWS-induced depression-model rats because of the high levels of TH mRNA expression in the LC. Our results also suggest that FWS is initially a mild stress but gradually becomes a severe form of unadaptable stress as reflected by delayed but persistent increases in TH mRNA expression.
引用
收藏
页码:2083 / 2092
页数:10
相关论文
共 32 条
[1]   IMMUNOCYTOCHEMICAL EVIDENCE FOR STIMULATORY CONTROL BY THE VENTRAL NORADRENERGIC BUNDLE OF PARVOCELLULAR NEURONS OF THE PARAVENTRICULAR NUCLEUS SECRETING CORTICOTROPIN RELEASING HORMONE AND VASOPRESSIN IN RATS [J].
ALONSO, G ;
SZAFARCZYK, A ;
BALMEFREZOL, M ;
ASSENMACHER, I .
BRAIN RESEARCH, 1986, 397 (02) :297-307
[2]  
ANISMAN H, 1984, J NEUROBIOLOGY MOOD, P407
[3]  
BARNETT JE, 1979, STRESS MENTAL DISORD, P71
[4]   LIFE STRESS AND PSYCHOLOGICAL WELL-BEING - REPLICATION OF LANGNERS ANALYSIS IN MIDTOWN MANHATTAN STUDY [J].
BERKMAN, PL .
JOURNAL OF HEALTH AND SOCIAL BEHAVIOR, 1971, 12 (01) :35-45
[5]   Influence of corticotropin-releasing hormone on electrophysiological activity of locus coeruleus neurons [J].
Borsody, MK ;
Weiss, JM .
BRAIN RESEARCH, 1996, 724 (02) :149-168
[6]   URINARY MHPG, STRESS RESPONSE, PERSONALITY-FACTORS AND SOMATOSENSORY EVOKED-POTENTIALS IN NORMAL SUBJECTS AND PATIENTS WITH MAJOR AFFECTIVE-DISORDERS [J].
BUCHSBAUM, MS ;
MUSCETTOLA, G ;
GOODWIN, FK .
NEUROPSYCHOBIOLOGY, 1981, 7 (04) :212-224
[7]   CATECHOLAMINE EFFECTS UPON RAT HYPOTHALAMIC CORTICOTROPIN-RELEASING HORMONE-SECRETION INVITRO [J].
CALOGERO, AE ;
GALLUCCI, WT ;
CHROUSOS, GP ;
GOLD, PW .
JOURNAL OF CLINICAL INVESTIGATION, 1988, 82 (03) :839-846
[8]  
Curtis AL, 1997, J PHARMACOL EXP THER, V281, P163
[9]   SHOULD PLASMA OR URINARY MHPG BE MEASURED IN PSYCHIATRIC RESEARCH - A CRITICAL COMMENT [J].
FILSER, JG ;
MULLER, WE ;
BECKMANN, H .
BRITISH JOURNAL OF PSYCHIATRY, 1986, 148 :95-97
[10]  
HAMANAKA H, IN PRESS J NEUROENDO