Maternal deprivation of rat pups increases clinical symptoms of experimental autoimmune encephalomyelitis at adult age

被引:35
作者
Teunis, MAT
Heijnen, CJ
Sluyter, F
Bakker, JM
Van Dam, AMMW
Hof, M
Cools, AR
Kavelaars, A
机构
[1] Univ Utrecht, Med Ctr, Wilhelmina Childrens Hosp, Dept Immunol,Lab Psychoneuroimmunol, NL-3584 EA Utrecht, Netherlands
[2] Univ Nijmegen, Inst Neurosci, Dept Psychoneuropharmacol, NL-6500 HB Nijmegen, Netherlands
[3] Vrije Univ Amsterdam, Med Ctr, Neurosci Res Inst, Dept Med Pharmacol, Amsterdam, Netherlands
关键词
maternal deprivation; experimental autoimmune encephalomyelitis; autoimmunity; neuroendocrine system; disease susceptibility; Th1/Th2 cytokine balance; HPA axis;
D O I
10.1016/S0165-5728(02)00351-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
Maternal deprivation of neonatal animals has been shown to induce long-lasting changes in the reactivity of the neuroendocrine system. The aim of the present study was to investigate whether maternal deprivation also affects susceptibility to immune-mediated diseases such as experimental autoimmune encephalomyelitis (FAE) in adult life. To this end, 9-day-old rat pups were subjected to a short-lasting maternal deprivation for a period of 24 h. At the age of 8 weeks, we induced EAE in these rats by immunization with myelin basic protein (MBP) in complete Freund's adjuvant. Our data demonstrate that short-lasting maternal deprivation induces a marked increase in the severity of EAE in the animals in later life. The histopathological evaluation of spinal cord and cerebellum corresponded with the observed differences in clinical symptoms of EAE. Moreover, neonatal maternal deprivation affects macrophage functioning at adult age. In contrast, no differences were observed in in vitro mitogen- and MBP-induced cytokine production by splenocytes. LPS-induced corticosterone release did not differ either between maternally deprived and control animals. We conclude that short-lasting neonatal maternal deprivation of rat pups has long-lasting consequences for macrophage activity and for susceptibility to the inflammatory autoimmune disease EAE. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:30 / 38
页数:9
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