Effects of chronic mild stress on sexual behavior, locomotor activity and consumption of sucrose and saccharine solutions

被引:317
作者
Gronli, J
Murison, R
Fiske, E
Bjorvatn, B
Sorensen, E
Portas, CM
Ursin, R
机构
[1] Univ Bergen, Dept Biomed, Physiol Sect, N-5009 Bergen, Norway
[2] Haukeland Hosp, Norwegian Competence Ctr Sleep Disorders, N-5021 Bergen, Norway
[3] Univ Bergen, Dept Biol & Med Psychol, N-5009 Bergen, Norway
[4] Univ Bergen, Fac Med, Locus Neurosci, N-5009 Bergen, Norway
[5] Univ Bergen, Dept Publ Hlth & Primary Hlth Care, N-5018 Bergen, Norway
关键词
animal model of depression; chronic mild stress; sucrose intake; saccharine intake; sexual activity; open field behavior;
D O I
10.1016/j.physbeh.2005.02.007
中图分类号
B84 [心理学];
学科分类号
04 [教育学]; 0402 [心理学];
摘要
Many symptoms of human depressive disorders are also observed in animals after exposure to unpredictable stressors. The chronic mild stress (CMS) paradigm was developed in order to better model the human situation by using chronic mild stressors over a longer period. It is claimed that the model induces anhedonia in the animals, a core symptom of depression in humans. Despite the fact that the CMS model has a high degree of face validity, there are a number of laboratories in which the establishment of the model is less reliably observed. We have examined behavior (sexual activity and open field activity) together with hedonic measures (sucrose and saccharine intake) after exposure to CMS. CMS decreased male sexual activity (e.g. reduced capability to ejaculate) and increased activity in an open field test. The hedonic measures showed diverging results after CMS in our laboratory. Sucrose consumption was reduced, while saccharine consumption did not show a comparable change. It is concluded that CMS induces comparable alterations to some depression-like symptoms in humans. Saccharine consumption is not a reliable indicator of the hedonic responsiveness to CMS. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:571 / 577
页数:7
相关论文
共 43 条
[1]
TASTE AND SMELL PERCEPTION IN DEPRESSION [J].
AMSTERDAM, JD ;
SETTLE, RG ;
DOTY, RL ;
ABELMAN, E ;
WINOKUR, A .
BIOLOGICAL PSYCHIATRY, 1987, 22 (12) :1481-1485
[2]
STIMULUS CHANGE INFLUENCES ESCAPE PERFORMANCE - DEFICITS INDUCED BY UNCONTROLLABLE STRESS AND BY HALOPERIDOL [J].
ANISMAN, H ;
ZACHARKO, RM .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1982, 17 (02) :263-269
[3]
MULTIPLE NEUROCHEMICAL AND BEHAVIORAL CONSEQUENCES OF STRESSORS - IMPLICATIONS FOR DEPRESSION [J].
ANISMAN, H ;
ZACHARKO, RM .
PHARMACOLOGY & THERAPEUTICS, 1990, 46 (01) :119-136
[4]
The effects of chronic mild stress on male Sprague-Dawley and Long Evans rats I. Biochemical and physiological analyses [J].
Bielajew, C ;
Konkle, ATM ;
Merali, Z .
BEHAVIOURAL BRAIN RESEARCH, 2002, 136 (02) :583-592
[5]
LIFE EVENTS AND AFFECTIVE-DISORDER - REPLICATIONS AND LIMITATIONS [J].
BROWN, GW .
PSYCHOSOMATIC MEDICINE, 1993, 55 (03) :248-259
[6]
Exploratory behaviour and grooming after repeated restraint and chronic mild stress: effect of desipramine [J].
D'Aquila, PS ;
Peana, AT ;
Carboni, V ;
Serra, G .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2000, 399 (01) :43-47
[7]
EFFECTS OF CHRONIC MILD STRESS ON PERFORMANCE IN BEHAVIORAL-TESTS RELEVANT TO ANXIETY AND DEPRESSION [J].
DAQUILA, PS ;
BRAIN, P ;
WILLNER, P .
PHYSIOLOGY & BEHAVIOR, 1994, 56 (05) :861-867
[8]
DEPRESSION AND 5HT [J].
DEAKIN, JFW .
INTERNATIONAL CLINICAL PSYCHOPHARMACOLOGY, 1991, 6 :23-31
[9]
OPEN-FIELD BEHAVIOR IN RAT - WHAT DOES IT MEAN [J].
DENENBERG, VH .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1969, 159 (A3) :852-+
[10]
DIVERGENT RESPONSES TO SACCHARIN VS SUCROSE AVAILABILITY AFTER STRESS IN RATS [J].
DESS, NK .
PHYSIOLOGY & BEHAVIOR, 1992, 52 (01) :115-125