Blunted sensitivity to sucrose in autoimmune MRL-Ipr mice: A curve-shift study

被引:66
作者
Sakic, B
Denburg, JA
Denburg, SD
Szechtman, H
机构
[1] MCMASTER UNIV, DEPT MED, HAMILTON, ON L8N 3Z5, CANADA
[2] MCMASTER UNIV, DEPT PSYCHIAT, HAMILTON, ON L8N 3Z5, CANADA
基金
加拿大自然科学与工程研究理事会;
关键词
autoimmunity; stress; depression; concentration/intake function; curve shift; one-bottle sucrose test; MRL-Ipr mice; cyclophosphamide; behavioral immunology;
D O I
10.1016/S0361-9230(96)00190-6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Lupus-prone MRL-lpr mice show an autoimmunity-associated behavioral syndrome that has many features similar to the effects of chronic stress. The present study evaluated whether autoimmune MRL-lpr mice show reduced responsiveness to sucrose, as observed in normal animals exposed to chronic mild stress. Sixteen-week old MRL-lpr mice and their age-matched congenic MRL +/+ controls were given 0%, 0.5% 1%, 2%, 4%, 8%, or 16% sucrose solution to drink every 48 h in a one-bottle test. The MRL-lpr mice drank less than controls at all concentrations, except at 16%, The amount of sucrose consumed vs. solution concentration followed a saturation curve. Estimates were obtained for the concentration yielding the half-maximum response (X(50)) and the response at saturating concentration of sucrose (R(max)). The X(50) was significantly higher in MRL-lpr than in MRL +/+ mice, indicating a shift to the right of the concentration-intake curve. The R(max) did not differ significantly between substrains, suggesting that the autoimmune process did not affect performance capacity. Pretreatment with the immunosuppressant cyclophosphamide diminished the substrain difference in X(50), suggesting that reduced sensitivity to sucrose is related to autoimmune/inflammatory factors. These results support the similarity between autoimmunity-associated behavioral syndrome and behavioral changes produced by chronic stress, and suggest common neuroendocrine mechanisms. Because reduced sensitivity to palatable stimulus may reflect blunted hedonic responsiveness (''anhedonia''), it is hypothesized that an autoimmune/inflammatory factor(s) produces the depression found in human lupus, and some cases of affective disorder. Copyright (C) 1996 Elsevier Science Inc.
引用
收藏
页码:305 / 311
页数:7
相关论文
共 52 条
[1]   SPONTANEOUS MURINE LUPUS-LIKE SYNDROMES - CLINICAL AND IMMUNOPATHOLOGICAL MANIFESTATIONS IN SEVERAL STRAINS [J].
ANDREWS, BS ;
EISENBERG, RA ;
THEOFILOPOULOS, AN ;
IZUI, S ;
WILSON, CB ;
MCCONAHEY, PJ ;
MURPHY, ED ;
ROTHS, JB ;
DIXON, FJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1978, 148 (05) :1198-1215
[2]   DEPRESSION AS A CONSEQUENCE OF INADEQUATE NEUROCHEMICAL ADAPTATION IN RESPONSE TO STRESSORS [J].
ANISMAN, H ;
ZACHARKO, RM .
BRITISH JOURNAL OF PSYCHIATRY, 1992, 160 :36-43
[3]   BEHAVIORAL AND NEUROCHEMICAL CONSEQUENCES ASSOCIATED WITH STRESSORS [J].
ANISMAN, H ;
ZACHARKO, RM .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1986, 467 :205-225
[4]   MULTIPLE NEUROCHEMICAL AND BEHAVIORAL CONSEQUENCES OF STRESSORS - IMPLICATIONS FOR DEPRESSION [J].
ANISMAN, H ;
ZACHARKO, RM .
PHARMACOLOGY & THERAPEUTICS, 1990, 46 (01) :119-136
[5]  
[Anonymous], REINFORCEMENT BEHAV
[6]   HEDONIC REACTIVITY TO SUCROSE IN RATS - MODIFICATION BY PIMOZIDE [J].
BAILEY, CS ;
HSIAO, S ;
KING, JE .
PHYSIOLOGY & BEHAVIOR, 1986, 38 (04) :447-452
[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]  
DUNN AJ, 1993, CIBA F SYMP, V172, P226
[9]   PARAMETRIC ANALYSIS OF BRAIN-STIMULATION REWARD IN RAT .3. EFFECT OF PARAMETRIC ANALYSIS OF BRAIN-STIMULATION REWARD IN RAT .3. EFFECT OF PERFORMANCE VARIABLES ON REWARD SUMMATION FUNCTION [J].
EDMONDS, DE ;
GALLISTEL, CR .
JOURNAL OF COMPARATIVE AND PHYSIOLOGICAL PSYCHOLOGY, 1974, 87 (05) :876-883
[10]   PARAMETRIC ANALYSIS OF BRAIN-STIMULATION REWARD IN RAT .2. TEMPORAL SUMMATION IN REWARD SYSTEM [J].
EDMONDS, DE ;
STELLAR, JR ;
GALLISTEL, CR .
JOURNAL OF COMPARATIVE AND PHYSIOLOGICAL PSYCHOLOGY, 1974, 87 (05) :860-869