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中缝背核对阿片类药物引起的呼吸抑制的贡献。

Contribution of the caudal medullary raphe to opioid induced respiratory depression.

机构信息

Department of Anesthesiology, Medical College of Wisconsin, Milwaukee, WI, United States; Faculty of Medicine, University of Osijek, Osijek, Croatia.

Department of Anesthesiology, Medical College of Wisconsin, Milwaukee, WI, United States; Department of Neuroscience, Carthage College, Kenosha, WI, United States; Department of Physiology, Medical College of Wisconsin, Milwaukee, WI, United States.

出版信息

Respir Physiol Neurobiol. 2022 May;299:103855. doi: 10.1016/j.resp.2022.103855. Epub 2022 Feb 3.

Abstract

BACKGROUND

Opioid-induced respiratory depression can be partially antagonized in the preBötzinger Complex and Parabrachial Nucleus/Kölliker-Fuse Complex. We hypothesized that additional opioid antagonism in the caudal medullary raphe completely reverses the opioid effect.

METHODS

In adult ventilated, vagotomized, decerebrate rabbits, we administrated remifentanil intravenously at "analgesic", "apneic", and "very high" doses and determined the reversal with sequential naloxone microinjections into the bilateral Parabrachial Nucleus/Kölliker-Fuse Complex, preBötzinger Complex, and caudal medullary raphe. In separate animals, we injected opioid antagonists into the raphe without intravenous remifentanil.

RESULTS

Sequential naloxone microinjections completely reversed respiratory rate depression from "analgesic" and "apneic" remifentanil, but not "very high" remifentanil concentrations. Antagonist injection into the caudal medullary raphe without remifentanil independently increased respiratory rate.

CONCLUSIONS

Opioid-induced respiratory depression results from a combined effect on the respiratory rhythm generator and respiratory drive. The effect in the caudal medullary raphe is complex as we also observed local antagonism of endogenous opioid receptor activation, which has not been described before.

摘要

背景

阿片类药物引起的呼吸抑制可以在 PreBötzinger 复合体和 Parabrachial Nucleus/Kölliker-Fuse 复合体中部分拮抗。我们假设在延髓尾侧中缝核中增加阿片类拮抗剂可以完全逆转阿片类药物的作用。

方法

在成年通气、迷走神经切断、去大脑的兔子中,我们静脉给予瑞芬太尼,剂量分别为“镇痛”、“呼吸暂停”和“非常高”,并通过序贯纳洛酮微注射到双侧 Parabrachial Nucleus/Kölliker-Fuse 复合体、PreBötzinger 复合体和延髓尾侧中缝核来确定逆转情况。在单独的动物中,我们在没有静脉瑞芬太尼的情况下将阿片类拮抗剂注射到中缝核。

结果

序贯纳洛酮微注射完全逆转了“镇痛”和“呼吸暂停”瑞芬太尼引起的呼吸频率抑制,但不能逆转“非常高”瑞芬太尼浓度引起的抑制。在没有瑞芬太尼的情况下,将拮抗剂注射到延髓尾侧中缝核可独立增加呼吸频率。

结论

阿片类药物引起的呼吸抑制是由呼吸节律发生器和呼吸驱动的综合作用引起的。延髓尾侧中缝核的作用很复杂,因为我们还观察到内源性阿片受体激活的局部拮抗作用,这以前尚未描述过。

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