Short and long restraint differentially affect humoral and cellular immune functions

被引:51
作者
Millan, S
GonzalezQuijano, MI
Giordano, M
Soto, L
Martin, AI
LopezCalderon, A
机构
[1] UNIV COMPLUTENSE MADRID,DEPT FISIOL,FAC MED,MADRID 280409,SPAIN
[2] UNIV COMPLUTENSE MADRID,ESCUELA ENFERMERIA FISIOTERAPIA & PODOL,DPT ENFERMERIA,MADRID 280409,SPAIN
[3] ACAD NACL MED BUENOS AIRES,INST INVEST HEMATOL,LAB INMUNOL,BUENOS AIRES,DF,ARGENTINA
关键词
restraint stress; antibody production; lymphoproliferative response; corticosterone;
D O I
10.1016/0024-3205(96)00471-7
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
The aim of this work was to examine the effect of different periods of restraint on the humoral and cellular immune functions in adult male rats. Short restraint stress (2 h over 2 consecutive days) enhanced the primary serum antibody response to sheep red blood cells. The enhancement of this humoral response was dependent on the restraint period, since long restraint stress (6 h over 4 days) failed to modify this response. Short and long restraint decreased both the number of lymphocytes and the T-lymphocyte response to Con A stimulation in the peripheral blood. Neither 2 h over 2 days nor 6 h over 4 days modified the splenic lymphoproliferative response to Con A stimulation, but restraint stress progressively decreased the number of mononuclear splenic cells. Both periods of restraint significantly increased plasma concentration of corticosterone, however plasma prolactin levels were significantly lower after 4 days of restraint but not after short restraint (2 h over 2 days). These results indicate that although some immune functions can be increased after acute or short stress, long stress has an immunosuppressive effect, above all on the cellular immunity which is more susceptible to this effect than the humoral response.
引用
收藏
页码:1431 / 1442
页数:12
相关论文
共 45 条
[1]   CHRONIC VARIABLE STRESS FACILITATES TUMORAL GROWTH - REVERSAL BY IMIPRAMINE ADMINISTRATION [J].
BASSO, AM ;
DEPIANTEDEPAOLI, M ;
MOLINA, VA .
LIFE SCIENCES, 1992, 50 (23) :1789-1796
[2]  
BENSCHOP RJ, 1994, CIRCULATION, V89, P765
[3]   NEUROENDOCRINE AND IMMUNOLOGICAL MECHANISMS IN STRESS-INDUCED IMMUNOMODULATION [J].
BERKENBOSCH, F ;
WOLVERS, DAW ;
DERIJK, R .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1991, 40 (4-6) :639-647
[4]   MODULATION OF THE IMMUNE-RESPONSE BY EMOTIONAL-STRESS [J].
CROISET, G ;
HEIJNEN, CJ ;
VELDHUIS, HD ;
DEWIED, D ;
BALLIEUX, RE .
LIFE SCIENCES, 1987, 40 (08) :775-782
[5]   EVIDENCE THAT SHOCK-INDUCED IMMUNE SUPPRESSION IS MEDIATED BY ADRENAL HORMONES AND PERIPHERAL BETA-ADRENERGIC RECEPTORS [J].
CUNNICK, JE ;
LYSLE, DT ;
KUCINSKI, BJ ;
RABIN, BS .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1990, 36 (03) :645-651
[6]   STRESS AND IMMUNITY - AN INTEGRATED VIEW OF RELATIONSHIPS BETWEEN THE BRAIN AND THE IMMUNE-SYSTEM [J].
DANTZER, R ;
KELLEY, KW .
LIFE SCIENCES, 1989, 44 (26) :1995-2008
[7]   PROLACTIN RECEPTOR EXPRESSION IN HUMAN HEMATOPOIETIC TISSUES ANALYZED BY FLOW CYTOFLUOROMETRY [J].
DARDENNE, M ;
DEMORAES, MDL ;
KELLY, PA ;
GAGNERAULT, MC .
ENDOCRINOLOGY, 1994, 134 (05) :2108-2114
[8]  
ESTERLING B, 1987, BEHAV NEUROSCI, V101, P115
[9]   OPTIMIZING WHOLE-BLOOD LYMPHOCYTE-PROLIFERATION IN THE RAT [J].
FASANMADE, AA ;
JUSKO, WJ .
JOURNAL OF IMMUNOLOGICAL METHODS, 1995, 184 (02) :163-167
[10]   REDUCED SERUM ANTIBODIES ASSOCIATED WITH SOCIAL DEFEAT IN RATS [J].
FLESHNER, M ;
LAUDENSLAGER, ML ;
SIMONS, L ;
MAIER, SF .
PHYSIOLOGY & BEHAVIOR, 1989, 45 (06) :1183-1187