Loomis C W, Arunachalam K D
School of Pharmacy, Memorial University of Newfoundland, St. John's, Canada.
J Pharmacol Exp Ther. 1992 Nov;263(2):428-35.
The purpose of this study was to determine the effect of i.t. St 587 (lumbar injection) on tail-flick (TF) latency and paw pressure (PP) withdrawal threshold in conscious rats, and the effect of i.t. (midthoracic injection) and i.v. St 587 on blood pressure in urethane-anesthetized rats. Unlike i.t. methoxamine (alpha 1 agonist), which produced antinociception, i.t. St 587 (0.5-30 micrograms) decreased TF latency and PP threshold below base line. Hyperalgesia was also produced by i.t. Wy 27127 (alpha 2-selective antagonist). At i.t. doses of St 587 > 3 micrograms, there was an apparent but incomplete return of TF latency and PP threshold toward base line. Pretreatment with i.t. prazosin (2.5 micrograms) enhanced the hyperalgesic effect of 30 micrograms, but not 1 microgram of St 587. Intrathecal St 587 and Wy 27127 each antagonized the antinociceptive effect of i.t. guanfacine (alpha 2 agonist) in the TF and PP tests. Intravenous St 587 produced a dose-dependent pressor effect that was antagonized by pretreatment with i.v. prazosin (0.14 mg/kg; 52-fold increase in the ED50), but weakly antagonized by Wy 27127 (0.5 mg/kg; 1.5-fold increase in the ED50). ST-587 also produced a dose-dependent pressor response after i.t. injection which was antagonized by i.t. prazosin (10 micrograms) or i.v. hexamethonium (10 mg/kg).(ABSTRACT TRUNCATED AT 250 WORDS)
本研究的目的是确定鞘内注射St 587(腰椎注射)对清醒大鼠甩尾(TF)潜伏期和爪部压力(PP)撤针阈值的影响,以及鞘内注射(胸段中部注射)和静脉注射St 587对乌拉坦麻醉大鼠血压的影响。与产生抗伤害感受的鞘内注射甲氧明(α1激动剂)不同,鞘内注射St 587(0.5 - 30微克)使TF潜伏期和PP阈值降至基线以下。鞘内注射Wy 27127(α2选择性拮抗剂)也产生痛觉过敏。当鞘内注射St 587的剂量>3微克时,TF潜伏期和PP阈值有明显但不完全恢复至基线的情况。鞘内注射哌唑嗪(2.5微克)预处理增强了30微克而非1微克St 587的痛觉过敏作用。在TF和PP试验中,鞘内注射St 587和Wy 27127均拮抗了鞘内注射胍法辛(α2激动剂)的抗伤害感受作用。静脉注射St 587产生剂量依赖性升压作用,静脉注射哌唑嗪(0.14毫克/千克;ED50增加52倍)预处理可拮抗该作用,但Wy 27127(0.5毫克/千克;ED50增加1.5倍)的拮抗作用较弱。鞘内注射ST - 587后也产生剂量依赖性升压反应,该反应可被鞘内注射哌唑嗪(10微克)或静脉注射六甲铵(10毫克/千克)拮抗。(摘要截选至250字)