Ruwe W D, Myers R D
Brain Res Bull. 1979 Nov-Dec;4(6):741-5. doi: 10.1016/0361-9230(79)90007-8.
In the unrestrained cat, the inhibition of protein synthesis by anisomycin, given either subcutaneously (5.0--25.0 mg/kg) or directly into the anterior hypothalamic, preoptic area (1.0--25.0 micrograms) impaired the development of a bacterial fever. S. typhosa infused intravenously (1:10 dilution in 1 ml) or into AH/POA (1.0 microliter) evoked an intense fever which was either significantly delayed or prevented by anisomycin. Conversely, anisomycin failed to affect the typical hyperthermia evoked by 100 ng PGE2 or 1.0--7.0 micrograms 5-HT similarly infused into AH/POA. These data demonstrate that an intermediary humoral factor of unknown nature is required in the hyperthermic effector pathway underlying the febrile response.
在未加约束的猫中,皮下注射(5.0 - 25.0毫克/千克)或直接注入下丘脑前部视前区(1.0 - 25.0微克)茴香霉素对蛋白质合成的抑制作用,会损害细菌性发热的发展。静脉注射(1毫升中1:10稀释)或注入AH/POA(1.0微升)的伤寒沙门氏菌会引起强烈发热,而茴香霉素会显著延迟或阻止这种发热。相反,茴香霉素未能影响由同样注入AH/POA的100纳克前列腺素E2或1.0 - 7.0微克5 - 羟色胺引起的典型体温过高。这些数据表明,在发热反应的热效应途径中,需要一种性质未知的中间体液因子。