Ji Guang-Chen, Ma Fei, Zhang Yu-Qiu, Wu Gen-Cheng
Department of Neurobiology, State Key Laboratory of Medical Neurobiology, Medical Center of Fudan University (The Former Shanghai Medical University), Shanghai 200032.
Sheng Li Xue Bao. 2002 Aug 25;54(4):325-8.
The present study was to investigate the effects of intracerebroventricular (i.c.v.) injection of interleukin-1beta (IL-1beta) on thermal nociception in SD rats. The rats were divided into control and drug-administration groups. The animals of control group were given vehicle solution via i.c.v. injection. The animals of drug-administered groups were given IL-1beta at different doses (5, 50 and 500 pg/kg b.w.) via i.c.v. injection. IL-1 receptor antagonist (IL-1ra, 50 ng/kg) was injected 20 min before injection of IL-1beta or vehicle solution. The nociceptive threshold, which was represented as paw withdrawal latency (PWL), to a noxious thermal stimulation was measured using an analgesiameter. I.c.v. injection of IL-1beta dose-dependently shortened the PWL. At the dose of 500 pg/kg, the shortening of the PWL occurred at 20 min, reaching a peak within 40 min, lasted 100 min after injection, then gradually returned to the baseline level. Pretreatment with IL-1ra completely blocked the effects of IL-1beta-induced shortening in PWL. The results obtained suggest that IL-1beta may induce hyperalgesia in rats through binding to IL-1 receptors in the brain.
本研究旨在探讨脑室内注射白细胞介素-1β(IL-1β)对SD大鼠热痛觉的影响。将大鼠分为对照组和给药组。对照组动物通过脑室内注射给予赋形剂溶液。给药组动物通过脑室内注射给予不同剂量(5、50和500 pg/kg体重)的IL-1β。在注射IL-1β或赋形剂溶液前20分钟注射白细胞介素-1受体拮抗剂(IL-1ra,50 ng/kg)。使用痛觉测定仪测量对有害热刺激的痛觉阈值,以爪退缩潜伏期(PWL)表示。脑室内注射IL-1β剂量依赖性地缩短了PWL。在500 pg/kg的剂量下,PWL在注射后20分钟开始缩短,40分钟内达到峰值,注射后持续100分钟,然后逐渐恢复到基线水平。用IL-1ra预处理完全阻断了IL-1β诱导的PWL缩短效应。所得结果表明,IL-1β可能通过与脑中的IL-1受体结合在大鼠中诱导痛觉过敏。