Rotondo D, Abul H T, Milton A S, Davidson J
Department of Pharmacology, Marischal College, University of Aberdeen, Scotland, U.K.
Eur J Pharmacol. 1988 Sep 13;154(2):145-52. doi: 10.1016/0014-2999(88)90091-x.
Blood prostaglandin E2 (PGE2) levels, estimated by radioimmunoassay, and body temperatures of conscious rabbits were measured simultaneously during fever in response to polyinosinic: polycytidylic acid, lipopolysaccharide and interleukin 1/endogenous pyrogen. The effects of the antipyretic agent ketoprofen on both parameters was also studied. Significant rises (in the order of 6- to 8-fold) in the PGE2 level were observed after injection of either of the three pyrogens and occurred simultaneously with the rise in temperature. Ketoprofen given after the onset of fever in response to the pyrogens produced an immediate defervescence and a simultaneous decrease in plasma PGE2. Ketoprofen given before the pyrogens prevented any rise in either body temperature or plasma PGE2 level. When animals were subjected to an environmental temperature of 34 degrees C a hyperthermia was observed without any change in the blood PGE2 level. These results suggest that an increase in the blood PGE2 level may contribute to the pathogenesis of fever.
聚胞苷酸、脂多糖和白细胞介素1/内源性致热原引起发热期间的血液前列腺素E2(PGE2)水平,并同时测量其体温。还研究了解热剂酮洛芬对这两个参数的影响。注射三种致热原中的任何一种后,均观察到PGE2水平显著升高(约6至8倍),且与体温升高同时出现。在因致热原引起发热后给予酮洛芬,可立即退热,并同时使血浆PGE2水平降低。在给予致热原之前给予酮洛芬可防止体温或血浆PGE2水平升高。当动物处于34摄氏度的环境温度时,观察到体温过高,但血液PGE2水平无任何变化。这些结果表明,血液PGE2水平升高可能与发热的发病机制有关。