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多奈哌齐可逆转麻醉兔中丁丙诺啡引起的中枢性呼吸抑制。

Donepezil reverses buprenorphine-induced central respiratory depression in anesthetized rabbits.

机构信息

Department of Anesthesiology, Clinical Care Medicine, Kanagawa Dental College, Kanagawa, Japan.

出版信息

Biol Res. 2009;42(4):469-75. Epub 2010 Jan 29.

Abstract

Buprenorphine is a mixed opioid receptor agonist-antagonist used in acute and chronic pain management. Although this agent's analgesic effect increases in a dose-dependent manner, buprenorphine-induced respiratory depression shows a marked ceiling effect at higher doses, which is considered to be an indicator of safety. Nevertheless, cases of overdose mortality or severe respiratory depression associated with buprenorphine use have been reported. Naloxone can reverse buprenorphine-induced respiratory depression, but is slow-acting and unstable, meaning that new drug candidates able to specifically antagonize buprenorphine-induced respiratory depression are needed in order to enable maximal analgesic effect without respiratory depression. Acetylcholine is an excitatory neurotransmitter in central respiratory control. We previously showed that a long-acting acetylcholinesterase inhibitor, donepezil, antagonizes morphine-induced respiratory depression. We have now investigated how donepezil affects buprenorphine-induced respiratory depression in anesthetized, paralyzed, and artificially ventilated rabbits. We measured phrenic nerve discharge as an Index of respiratory rate and amplitude, and compared discharges following the injection of buprenorphine with discharges following the injection of donepezil. Buprenorphine-induced suppression of the respiratory rate and respiratory amplitude was antagonized by donepezil (78.4 +/- 4.8 %, 92.3% +/- 22.8 % of control, respectively). These findings indicate that systemically administered donepezil restores buprenorphine-induced respiratory depression in anesthetized rabbits.

摘要

丁酰苯类是一种混合阿片受体激动-拮抗剂,用于急性和慢性疼痛管理。尽管该药物的镇痛效果呈剂量依赖性增加,但丁丙诺啡引起的呼吸抑制在较高剂量时表现出明显的天花板效应,这被认为是安全性的指标。然而,已经报道了与丁丙诺啡使用相关的过量死亡率或严重呼吸抑制的病例。纳洛酮可以逆转丁丙诺啡引起的呼吸抑制,但作用缓慢且不稳定,这意味着需要新的药物候选物,能够特异性拮抗丁丙诺啡引起的呼吸抑制,以便在不引起呼吸抑制的情况下实现最大的镇痛效果。乙酰胆碱是中枢呼吸控制中的一种兴奋性神经递质。我们之前表明,长效乙酰胆碱酯酶抑制剂多奈哌齐拮抗吗啡引起的呼吸抑制。我们现在研究了多奈哌齐如何影响麻醉、麻痹和人工通气的兔中丁丙诺啡引起的呼吸抑制。我们测量膈神经放电作为呼吸频率和幅度的指标,并比较了丁丙诺啡注射后的放电和多奈哌齐注射后的放电。多奈哌齐拮抗丁丙诺啡引起的呼吸频率和呼吸幅度抑制(分别为 78.4 +/- 4.8%,92.3% +/- 22.8%的对照)。这些发现表明,系统给予多奈哌齐可恢复麻醉兔中丁丙诺啡引起的呼吸抑制。

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