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中枢注射血管紧张素转换酶抑制剂和血管紧张素1型受体拮抗剂对脂多糖诱导大鼠发热及脑白细胞介素-1β反应的影响。

The effect of central injection of angiotensin-converting enzyme inhibitor and the angiotensin type 1 receptor antagonist on the induction by lipopolysaccharide of fever and brain interleukin-1beta response in rats.

作者信息

Shimizu Hideki, Miyoshi Michio, Matsumoto Kenji, Goto Osamu, Imoto Toshiaki, Watanabe Tatsuo

机构信息

Department of Functional, Morphological, and Regulatory Science, Tottori University Faculty of Medicine, Yonago, Tottori, Japan.

出版信息

J Pharmacol Exp Ther. 2004 Mar;308(3):865-73. doi: 10.1124/jpet.103.060392. Epub 2003 Nov 14.

Abstract

We recently reported an involvement of peripheral angiotensin II (ANG II) in the development of both the fever and the peripheral interleukin (IL)-1beta production induced in rats by a systemic injection of lipopolysaccharide (LPS). The present study was performed to investigate whether brain ANG II contributes to the fever and IL-1beta production in the rat brain induced by i.c.v. injection of LPS. LPS (0.2 and 2 microg i.c.v.) induced dose-related fevers and increases in the brain (hypothalamus, hippocampus, and cerebellum) concentrations of IL-1beta. These effects were significantly inhibited by i.c.v. administration of either an angiotensin-converting-enzyme (ACE) inhibitor or an angiotensin type 1 (AT(1)) receptor antagonist. By contrast, the ACE inhibitor had no effect on the IL-1beta (i.c.v.)-induced fever, whereas the AT(1) receptor antagonist enhanced (rather than reduced) it. The AT(1) receptor antagonist had no effect on the brain levels of prostaglandin E(2) in rats given an i.c.v. injection of IL-1beta. These results suggest that in rats, brain ANG II and AT(1) receptors are involved in the LPS-induced production of brain IL-1beta, thus contributing to the fever induced by the presence of LPS within the brain.

摘要

我们最近报道,外周血管紧张素II(ANG II)参与了全身注射脂多糖(LPS)诱导的大鼠发热及外周白细胞介素(IL)-1β产生的过程。本研究旨在探讨脑内ANG II是否参与了脑室内注射LPS诱导的大鼠脑内发热及IL-1β产生。脑室内注射LPS(0.2和2微克)可诱导剂量相关的发热,并使脑内(下丘脑、海马和小脑)IL-1β浓度升高。血管紧张素转换酶(ACE)抑制剂或血管紧张素1型(AT(1))受体拮抗剂脑室内给药可显著抑制这些作用。相比之下,ACE抑制剂对IL-1β(脑室内注射)诱导的发热无影响,而AT(1)受体拮抗剂则增强(而非降低)了该发热。AT(1)受体拮抗剂对脑室内注射IL-1β的大鼠脑内前列腺素E2水平无影响。这些结果表明,在大鼠中,脑内ANG II和AT(1)受体参与了LPS诱导的脑内IL-1β产生,从而导致脑内LPS存在时引发的发热。

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