Zawada W M, Ruwe W D, Clarke J, Wall P T, Myers R D
Department of Clinical Pharmacology, University of Colorado Health Sciences Center, Denver 80262.
Neuroreport. 1994 Jun 27;5(11):1365-8. doi: 10.1097/00001756-199406270-00018.
The central pyrogenic actions in the rat of doublet macrophage inflammatory protein-1 (MIP-1) and MIP-1 alpha were determined by their intracerebroventricular infusion. Doses of 560 pg and 11.2 ng of MIP-1 or 10.0 ng MIP-1 alpha infused into the third cerebral ventricle induced a long lasting fever. However, MIP-1 alpha was much less potent than MIP-1 in terms of intensity and longer latency. Overall, these cytokines are pyrogenic when acting on the walls of the third ventricle; however, a dose 10 times greater than that injected directly into the anterior hypothalamus is required to evoke fever, as based on earlier experiments. Finally, circulating MIP-1 could act centrally by its entry through the choroid plexus into the ventricular system of the brain.
通过脑室内注射双重巨噬细胞炎性蛋白-1(MIP-1)和MIP-1α,确定了它们在大鼠体内的中枢致热作用。向第三脑室注射560 pg和11.2 ng的MIP-1或10.0 ng的MIP-1α可引起持久发热。然而,就强度和较长潜伏期而言,MIP-1α的效力远低于MIP-1。总体而言,这些细胞因子作用于第三脑室壁时具有致热作用;然而,根据早期实验,引发发热所需的剂量是直接注入下丘脑前部剂量的10倍。最后,循环中的MIP-1可通过脉络丛进入脑室系统而在中枢发挥作用。