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α2 -肾上腺素能受体激动剂赛拉嗪对绵羊的脊髓抗伤害感受活性

The spinal antinociceptive activity of the alpha 2-adrenoceptor agonist, xylazine in sheep.

作者信息

Kyles A E, Waterman A E, Livingston A

机构信息

Department of Veterinary Surgery, University of Bristol, Langford.

出版信息

Br J Pharmacol. 1993 Apr;108(4):907-13. doi: 10.1111/j.1476-5381.1993.tb13485.x.

Abstract
  1. The intrathecal administration of xylazine (100 micrograms), via a chronic indwelling, cervical intrathecal catheter, produced a marked elevation of the mechanical nociceptive thresholds in the sheep. This antinociceptive effect was abolished by the prior intrathecal administration of the alpha 2-adrenoceptor antagonist, idazoxan. 2. The intrathecal administration of the selective alpha 2-antagonists, idazoxan (100 micrograms) and RX811059 (33 micrograms), significantly attenuated the antinociceptive activity of intravenous xylazine, with a 60-65% reduction in the area under the antinociceptive curve. The intrathecal administration of the antagonists alone had no significant effect on nociceptive thresholds. 3. Examination of the distribution of tritiated idazoxan (25 microCi in 100 microliters) indicated that the site of action of the drug was limited to the cervical spinal cord after intrathecal administration. 4. These studies demonstrate that a significant proportion of the antinociceptive effect of systemically administered xylazine is mediated by spinal alpha 2-adrenoceptors.
摘要
  1. 通过慢性留置的颈段鞘内导管鞘内注射赛拉嗪(100微克),可使绵羊的机械性伤害感受阈值显著升高。鞘内预先注射α2肾上腺素能受体拮抗剂咪唑克生可消除这种抗伤害感受作用。2. 鞘内注射选择性α2拮抗剂咪唑克生(100微克)和RX811059(33微克)可显著减弱静脉注射赛拉嗪的抗伤害感受活性,抗伤害感受曲线下面积减少60 - 65%。单独鞘内注射拮抗剂对伤害感受阈值无显著影响。3. 对氚标记的咪唑克生(100微升中含25微居里)分布的研究表明,鞘内给药后药物的作用部位局限于颈段脊髓。4. 这些研究表明,全身给药的赛拉嗪的抗伤害感受作用很大一部分是由脊髓α2肾上腺素能受体介导的。

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