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前列腺素E2受体亚型EP1拮抗剂可能抑制大鼠中枢白细胞介素-1β诱导的发热。

PGE2 receptor subtype EP1 antagonist may inhibit central interleukin-1beta-induced fever in rats.

作者信息

Oka K, Oka T, Hori T

机构信息

Department of Physiology, Faculty of Medicine, Kyushu University, Fukuoka 812-8582, Japan.

出版信息

Am J Physiol. 1998 Dec;275(6):R1762-5. doi: 10.1152/ajpregu.1998.275.6.R1762.

Abstract

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.

摘要

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。

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