Moltz H
University of Chicago, IL 60637.
Neurosci Biobehav Rev. 1993 Fall;17(3):237-69. doi: 10.1016/s0149-7634(05)80009-0.
The present review distinguishes pathogenic, neurogenic, and psychogenic fever, but focuses largely on pathogenic fever, the hallmark of infectious disease. The data presented show that a complex cascade of events underlies pathogenic fever, which in broad outline - and with frank disregard of contradictory data - can be described as follows. An invading microorganism releases endotoxin that stimulates macrophages to synthesize a variety of pyrogenic compounds called cytokines. Carried in blood, these cytokines reach the perivascular spaces of the organum vasculosum laminae terminalis (OVLT) and other regions near the brain where they promote the synthesis and release of prostaglandin (PGE2). This prostaglandin then penetrates the blood-brain barrier to evoke the autonomic and behavioral responses characteristic of fever. But then once expressed, fever does not continue unchecked; endogenous antipyretics likely act on the septum to limit the rise in body temperature. The present review also examines fever-resistance in neonates, the blunting of fever in the aged, and the behaviorally induced rise in body temperature following infection in ectotherms. And finally it takes up the question of whether fever enhances immune responsiveness, and through such enhancement contributes to host survival.
本综述区分了致病性发热、神经源性发热和心因性发热,但主要关注致病性发热,即传染病的标志。所呈现的数据表明,致病性发热背后存在一系列复杂的事件,大致情况如下(坦率地忽略了矛盾的数据)。入侵的微生物释放内毒素,刺激巨噬细胞合成多种称为细胞因子的致热化合物。这些细胞因子随血液到达终板血管器(OVLT)的血管周围间隙和大脑附近的其他区域,在那里它们促进前列腺素(PGE2)的合成和释放。然后这种前列腺素穿透血脑屏障,引发发热特有的自主神经和行为反应。但一旦发热表现出来,它不会不受控制地持续下去;内源性解热物质可能作用于隔膜以限制体温升高。本综述还研究了新生儿的抗热能力、老年人发热的减弱以及外温动物感染后行为诱导的体温升高。最后,它探讨了发热是否增强免疫反应性,并通过这种增强作用促进宿主存活的问题。