Wolff S M, Dinarello C A
Trans Am Clin Climatol Assoc. 1980;91:159-66.
The pathogenesis of fever in man begins with the production of endogenous pyrogen by phagocytic leukocytes in response to exogenous pyrogens (toxic, immunologic or infectious agents). Endogenous pyrogen, a protein, is released from a variety of phagocytic leukocytes and enters the circulation after new messenger RNA and protein are synthesized. Fever is caused by an interaction of endogenous pyrogen with specialized receptors on or near thermosensitive neurons in the thermoregulatory center of the anterior hypothalamus. This interaction may cause local hypothalamic production of prostaglandins, monoamines and, possibly, cyclic AMP. From the anterior hypothalamus, information is transmitted through the posterior hypothalamus to the vasomotor center, which directs sympathetic-nerve fibers to constrict peripheral vessels and decrease heat dissipation.
人类发热的发病机制始于吞噬性白细胞对外源性致热原(毒性、免疫或感染因子)作出反应而产生内源性致热原。内源性致热原是一种蛋白质,它从多种吞噬性白细胞中释放出来,在新的信使核糖核酸和蛋白质合成后进入循环系统。发热是由内源性致热原与下丘脑前部体温调节中枢中或其附近的热敏神经元上的特殊受体相互作用引起的。这种相互作用可能导致下丘脑局部产生前列腺素、单胺,可能还有环磷酸腺苷。从前部下丘脑,信息通过后部下丘脑传递到血管运动中枢,该中枢指挥交感神经纤维收缩外周血管并减少散热。