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白细胞介素-1受体拮抗剂可抑制大鼠内毒素性发热及全身性白细胞介素-6的诱导。

Interleukin-1 receptor antagonist inhibits endotoxin fever and systemic interleukin-6 induction in the rat.

作者信息

Luheshi G, Miller A J, Brouwer S, Dascombe M J, Rothwell N J, Hopkins S J

机构信息

School of Biological Sciences, University of Manchester, United Kingdom.

出版信息

Am J Physiol. 1996 Jan;270(1 Pt 1):E91-5. doi: 10.1152/ajpendo.1996.270.1.E91.

Abstract

Although a number of studies indicate that the pyrogenic activity of lipopolysaccharide (LPS) and/or interleukin (IL)-1 is mediated via induction of IL-6, this has been questioned by recent evidence demonstrating a dissociation between fever and circulating IL-6. The present study reexamines this relationship by use of human recombinant interleukin-1 receptor antagonist (IL-1ra). Injection of LPS (100 micrograms/kg ip) into rats induced fever (2.0 degrees C) that was significantly inhibited (P < 0.05) when IL-1ra (16 mg/kg ip) was given 1 and 2 h after LPS. The rise in plasma IL-6 preceded the febrile response by 1-1.5 h and, although the concentrations of bioactive IL-6 in plasma and cerebrospinal fluid (CSF) were not reduced at 4 h, at 2 h plasma and CSF IL-6 bioactivity was inhibited by 80 and 70%, respectively, after a single injection of IL-1ra (16 mg/kg ip). Intracerebroventricular injection of IL-1ra (200 micrograms/rat) inhibited LPS fever but did not affect the plasma IL-6 bioactivity measured 2 or 4 h after intraperitoneal LPS. These data show that peripheral IL-1 plays a part in the induction of both fever and the rise in plasma IL-6 that precedes it, and that IL-1 within the brain is also important in the induction of fever by LPS.

摘要

尽管多项研究表明脂多糖(LPS)和/或白细胞介素(IL)-1的致热活性是通过诱导IL-6介导的,但最近有证据表明发热与循环中的IL-6之间存在分离,这对上述观点提出了质疑。本研究通过使用人重组白细胞介素-1受体拮抗剂(IL-1ra)重新审视了这种关系。给大鼠腹腔注射LPS(100微克/千克)可诱导发热(2.0摄氏度),在LPS注射后1小时和2小时给予IL-1ra(16毫克/千克腹腔注射)时,发热明显受到抑制(P<0.05)。血浆IL-6的升高比发热反应提前1 - 1.5小时,尽管在4小时时血浆和脑脊液(CSF)中生物活性IL-6的浓度没有降低,但单次注射IL-1ra(16毫克/千克腹腔注射)后,在2小时时血浆和脑脊液中IL-6的生物活性分别被抑制了80%和70%。脑室内注射IL-1ra(200微克/只大鼠)可抑制LPS引起的发热,但不影响腹腔注射LPS后2小时或4小时测得的血浆IL-6生物活性。这些数据表明,外周IL-1在发热诱导以及之前血浆IL-6升高过程中均起作用,并且脑内的IL-1在LPS诱导发热过程中也很重要。

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