Oka K, Oka T, Hori T
Department of Physiology, Faculty of Medicine, Kyushu University, Fukuoka 812-8582, Japan.
Am J Physiol. 1998 Dec;275(6):R1762-5. doi: 10.1152/ajpregu.1998.275.6.R1762.
We have previously reported that central injection of PGE2 induces hyperthermia through its actions on EP1 receptors in rats. Because the increase in local synthesis of PGE2 is assumed to be a necessary process in a fever caused by central injection of interleukin-1beta (IL-1beta), an EP1 receptor antagonist (SC-19220) should inhibit the IL-1beta-induced fever. To test this hypothesis, we observed the effect of SC-19220 on the fever produced by injection of recombinant human IL-1beta (rhIL-1beta) into the lateral cerebroventricle (LCV) in conscious rats. Administration of SC-19220 (100 microgram) into the LCV 15 min before LCV injection of rhIL-1beta (4 ng) suppressed an initial rise in colonic temperature for 30 min, producing a fever with a longer latency to onset and a longer time to peak elevation. SC-19220, given 60 min after the central administration of rhIL-1beta, also suppressed the rhIL-1beta-induced fever 15-60 min after its injection. These findings suggest that the central IL-1beta-induced fever in rats is mediated, at least partly, by activation of EP1 receptors by PGE2.
我们之前报道过,在大鼠中,向中枢注射前列腺素E2(PGE2)可通过其对EP1受体的作用诱导体温升高。由于局部PGE2合成增加被认为是中枢注射白细胞介素-1β(IL-1β)引起发热的必要过程,因此EP1受体拮抗剂(SC-19220)应能抑制IL-1β诱导的发热。为了验证这一假设,我们观察了SC-19220对清醒大鼠侧脑室(LCV)注射重组人IL-1β(rhIL-1β)所产生发热的影响。在向LCV注射rhIL-1β(4 ng)前15分钟,向LCV注射SC-19220(100微克)可抑制结肠温度的初始升高30分钟,使发热的起始潜伏期延长,达到峰值升高的时间延长。在中枢注射rhIL-1β 60分钟后给予SC-19220,也可在注射后15 - 60分钟抑制rhIL-1β诱导的发热。这些发现表明,大鼠中枢IL-1β诱导的发热至少部分是由PGE2激活EP1受体介导的。