Taylor A N, Tio D L, Yirmiya R
Department of Neurobiology and Brain Research Institute, School of Medicine, University of California Los Angeles, 90095, USA.
J Neuroimmunol. 1999 Sep 1;99(1):44-52. doi: 10.1016/s0165-5728(99)00102-2.
Central mechanisms for the attenuating effects of fetal alcohol exposure (FAE) on interleukin-1beta (IL-1beta)-induced fever were studied in adult male offspring of dams fed a liquid diet supplemented with ethanol (E), in pair-fed (P) control and in normal (N) offspring. Hypothalamic levels of IL-1 were significantly lower in E than in N rats at 2 h, but not at 4 and 6 h, after intraperitoneal administration of lipopolysaccharide. Fever induced by intracerebroventricular (i.c.v.) IL-1 was significantly lower in E than in N and P rats. In contrast, E rats showed a normal febrile response to i.c.v. prostaglandin-E2. Thus, whereas FAE does not affect central thermoregulatory mechanisms, per se, FAE alters the kinetics of hypothalamic IL-1 production/appearance and decreases the responsiveness of central mechanisms which mediate the febrile response to IL-1.
在成年雄性子代大鼠中研究了胎儿酒精暴露(FAE)对白细胞介素-1β(IL-1β)诱导发热的减弱作用的中枢机制,这些子代大鼠来自喂食添加乙醇(E)的液体饲料的母鼠、配对喂食(P)对照母鼠以及正常(N)母鼠。在腹腔注射脂多糖后2小时,E组大鼠下丘脑IL-1水平显著低于N组,但在4小时和6小时时并非如此。脑室内(i.c.v.)注射IL-1诱导的发热在E组大鼠中显著低于N组和P组大鼠。相反,E组大鼠对i.c.v.前列腺素-E2表现出正常的发热反应。因此,虽然FAE本身并不影响中枢体温调节机制,但FAE改变了下丘脑IL-1产生/出现的动力学,并降低了介导对IL-1发热反应的中枢机制的反应性。