Progressive atrophy of pyramidal neuron dendrites in autoimmune MRL-lpr mice

被引:68
作者
Sakic, B
Szechtman, H
Denburg, JA
Gorny, G
Kolb, B
Whishaw, IQ
机构
[1] McMaster Univ, Dept Psychiat, Hamilton, ON L8N 3Z5, Canada
[2] McMaster Univ, Dept Biomed Sci, Hamilton, ON, Canada
[3] McMaster Univ, Dept Med, Hamilton, ON, Canada
[4] Univ Lethbridge, Dept Psychol & Neurosci, Lethbridge, AB T1K 3M4, Canada
[5] Univ Lethbridge, NeuroDetect Inc, Lethbridge, AB T1K 3M4, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
autoimmunity; dendrites; spines; inflammation; hippocampus; parietal cortex; lupus; interleukin-6; stress; MRL-lpr mice; behavioral immunology;
D O I
10.1016/S0165-5728(98)00085-X
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The autoimmune-prone MRL-lpr substrain of mice develop an autoimmunity-associated behavioral syndrome (AABS) which resembles in many respects the behavior of animals exposed to chronic stress. The present study examined whether these mice show changes in the morphology of neuronal dendrites, as found in animals exposed to chronic stress. A modified Golgi-Cox procedure was used to visualize the dendrites of pyramidal neurons in the parietal cortex and in the CA1 hippocampal field of 5-week and 14-week old MRL-lpr mice and MRL +/+ controls. Reduced dendritic branching and length, and an up to 20% loss of dendritic spines were observed in parietal and hippocampal pyramidal neurons of MRL-lpr mice at both ages. In the parietal cortex, there was an age-dependent potentiation in the reduction of basilar, but not apical, dendrite branching and length, as well as in the loss of spines on basilar segments. Loss of spines in the hippocampus followed an age-related course for apical but not basilar dendrites, Moreover, compared to age-matched controls, brain weight was smaller in MRL-lpr mice at 14 but not 5 weeks of age. Considering that dendritic atrophy becomes more extensive when autoimmune disease is florid in MRL-lpr mice, it is proposed that immune/inflammatory factor(s) produce dendritic loss. Reduced dendritic complexity may represent, at least in part, a structural basis for the altered behavioral profile of MRL-lpr mice. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:162 / 170
页数:9
相关论文
共 62 条
[31]   RECOMBINANT INTERLEUKIN-6 ACTIVATES THE HYPOTHALAMIC-PITUITARY-ADRENAL AXIS IN HUMANS [J].
MASTORAKOS, G ;
CHROUSOS, GP ;
WEBER, JS .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1993, 77 (06) :1690-1694
[32]   THE VULNERABILITY OF THE HIPPOCAMPUS TO PROTECTIVE AND DESTRUCTIVE EFFECTS OF GLUCOCORTICOIDS IN RELATION TO STRESS [J].
MCEWEN, BS ;
GOULD, EA ;
SAKAI, RR .
BRITISH JOURNAL OF PSYCHIATRY, 1992, 160 :18-24
[33]   INTERLEUKIN-6 STIMULATES THE SECRETION OF ADRENOCORTICOTROPIC HORMONE IN CONSCIOUS, FREELY-MOVING RATS [J].
NAITOH, Y ;
FUKATA, J ;
TOMINAGA, T ;
NAKAI, Y ;
TAMAI, S ;
MORI, K ;
IMURA, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 155 (03) :1459-1463
[34]  
PERRELLA O, 1992, J NEUROL, V239, P387
[35]  
Perrella O, 1992, Arq Neuropsiquiatr, V50, P180
[36]   IMMUNOREGULATORS IN THE NERVOUS-SYSTEM [J].
PLATASALAMAN, CR .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 1991, 15 (02) :185-215
[37]   DEVELOPMENTAL EXPRESSION OF CYTOKINE GENES IN THE CORTEX AND HIPPOCAMPUS OF THE RAT CENTRAL-NERVOUS-SYSTEM [J].
POUSSET, F .
DEVELOPMENTAL BRAIN RESEARCH, 1994, 81 (01) :143-146
[38]  
Sakic B, 1997, NEUROSCI BIOBEHAV R, V21, P327
[39]  
SAKIC B, 1992, BRAIN BEHAV IMMUN, V6, P265
[40]   Blunted sensitivity to sucrose in autoimmune MRL-Ipr mice: A curve-shift study [J].
Sakic, B ;
Denburg, JA ;
Denburg, SD ;
Szechtman, H .
BRAIN RESEARCH BULLETIN, 1996, 41 (05) :305-311