Long-term gender-specific effects of manipulation during pregnancy on immune and endocrine responsiveness in rat offspring

被引:22
|
作者
Bakker, JM
van den Dobbelsteen, GPJM
Kroes, H
Kavelaars, A
Heijnen, CJ
Tilders, FJH
van Rees, EP
机构
[1] Univ Hosp Children & Youth, Wilhelmina Kinderziekenhuis, Dept Immunol, NL-3501 CA Utrecht, Netherlands
[2] Free Univ Amsterdam, Fac Med, Dept Cell Biol & Immunol, NL-1081 BT Amsterdam, Netherlands
[3] Free Univ Amsterdam, Fac Med, Dept Pharmacol, NL-1081 BT Amsterdam, Netherlands
[4] Natl Inst Publ Hlth & Environm, Lab Vaccine Dev & Immune Mechanisms, NL-3721 MA Bilthoven, Netherlands
关键词
prenatal; stress; glucocorticoids; HPA-axis; immune response; in vivo;
D O I
10.1016/S0165-5728(97)00188-4
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Exposure to synthetic glucocorticoids (GCs) or other stimuli around birth may affect neuroendocrine and immune responsiveness in the offspring. Experiments were conducted to investigate whether maternal manipulation with saline or with GCs alters the corticosterone (CORT) response to a mild stressor in the offspring, and whether maternal manipulation results in long-term altered in vivo humoral and cellular immune responsiveness in the offspring. Pregnant rats were given dexamethasone(DEX, 1.2 mg/kg body weight, i.p.) or saline (SAL) at day 17 and 19 of gestation. A third group of pregnant rats was left undisturbed (UNTR-group). After maternal DEX treatment no altered CORT response was seen to a novel environment at 20 days of age. as compared to both the SAL-treated group and the UNTR-group. However, saline administration to pregnant rah caused an increased CORT response in female offspring, but not malt: offspring, as compared to the UNTR-group (P less than or equal to 0.01). Furthermore, no effects of maternal DEX exposure were seen on IgG2a production after immunization with a conjugated pneumococcal polysaccharide (PPS-14-CRM197) at 6 weeks of age. However, maternal SAL treatment enhanced anti-PPS-14 IgG2a antibody levels in female offspring, but not ill male offspring, as compared to the UNTR-group (P less than or equal to 0.05). Cellular immune responses were measured by an oxazolone-induced contact hypersensitivity response (CHS-response), at 8 weeks of age. Maternal SAL treatment increased the CHS response in adult male rats, but not in female rats;, as compared to both the UNTR-group and the DEX-group (P less than or equal to 0.005). These data suggest that manipulations during late pregnancy not only affect endocrine responsiveness, but also influence immune responsiveness in the rat offspring. Furthermore, these effects may belong-term and gender-specific. (C) 1998 Elsevier Science B.V.
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页码:56 / 63
页数:8
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