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七鳃鳗呼吸网络中阿片类药物诱导的抑郁

Opioid-induced depression in the lamprey respiratory network.

作者信息

Mutolo D, Bongianni F, Einum J, Dubuc R, Pantaleo T

机构信息

Dipartimento di Scienze Fisiologiche, Università degli Studi di Firenze, Viale G.B. Morgagni 63, 50134 Firenze, Italy.

出版信息

Neuroscience. 2007 Dec 12;150(3):720-9. doi: 10.1016/j.neuroscience.2007.09.028. Epub 2007 Sep 20.

Abstract

The role of opioid receptors in modulating respiratory activity was investigated in in vitro brainstem preparations of adult lampreys by bath application of agonists and antagonists. The vagal motor output was used to monitor respiratory activity. Neuronal recordings were also performed to characterize the rostrolateral trigeminal region that has been suggested to be critical for respiratory rhythmogenesis. Microinjections of the micro-opioid receptor agonist [d-Ala(2), N-Me-Phe(4), Gly(5)-ol]-enkephalin (DAMGO) were also made into this region and at different locations within the brainstem. Bath application of DAMGO (0.5-2 microM) caused marked decreases in respiratory frequency up to complete apnea. Bath application of the delta-opioid receptor agonist [d-Pen(2,5)]-enkephalin (DPDPE) at 10-40 microM induced less pronounced depressant respiratory effects, while no changes in respiratory activity were induced by the kappa-opioid receptor agonist trans-(1S,2S)-3,4-dichloro-N-methyl-N-[2-(1-pyrrolidinyl)cyclohexyl] benzeneacetamide (U50488) at 10-40 microM. Bath application of the opioid receptor antagonists naloxone and naltrindole did not affect baseline respiratory activity, but prevented agonist-induced effects. DAMGO microinjections (1 mM; 0.5-1 nl) at sites rostrolateral to the trigeminal motor nucleus, where respiration-related neuronal activity was recorded, abolished the respiratory rhythm. The results show that opioids may have an important role in the lamprey respiratory network and that micro-opioid receptor activation is the most effective in causing respiratory depression. They also indicate that endogenous opioids are not required for the generation of baseline respiratory activity. Apneic responses induced by DAMGO microinjections support the hypothesis that a specific opioid-sensitive region rostrolateral to the trigeminal motor nucleus, that we have termed the paratrigeminal respiratory group (pTRG), likely has a pivotal role in respiratory rhythmogenesis. Since the lamprey diverged from the main vertebrate line around 450 million years ago, our results also imply that the inhibitory role of opioids on respiration is present at an early stage of vertebrate evolution.

摘要

通过在成体七鳃鳗的离体脑干制剂中浴加激动剂和拮抗剂,研究了阿片受体在调节呼吸活动中的作用。迷走神经运动输出用于监测呼吸活动。还进行了神经元记录,以表征已被认为对呼吸节律发生至关重要的嘴侧外侧三叉神经区域。微阿片受体激动剂[d-Ala(2),N-Me-Phe(4),Gly(5)-ol]-脑啡肽(DAMGO)也被微量注射到该区域以及脑干内的不同位置。浴加DAMGO(0.5 - 2 microM)导致呼吸频率显著降低直至完全呼吸暂停。浴加10 - 40 microM的δ阿片受体激动剂[d-Pen(2,5)]-脑啡肽(DPDPE)诱导的呼吸抑制作用较不明显,而10 - 40 microM的κ阿片受体激动剂反式-(1S,2S)-3,4-二氯-N-甲基-N-[2-(1-吡咯烷基)环己基]苯乙酰胺(U50488)未引起呼吸活动变化。浴加阿片受体拮抗剂纳洛酮和纳曲吲哚不影响基线呼吸活动,但可防止激动剂诱导的效应。在记录到与呼吸相关神经元活动的三叉神经运动核嘴侧外侧部位微量注射DAMGO(1 mM;0.5 - 1 nl)可消除呼吸节律。结果表明,阿片类物质可能在七鳃鳗呼吸网络中起重要作用,且微阿片受体激活在引起呼吸抑制方面最为有效。它们还表明,基线呼吸活动的产生不需要内源性阿片类物质。DAMGO微量注射诱导的呼吸暂停反应支持了这样一种假说,即我们称为三叉旁呼吸组(pTRG)的位于三叉神经运动核嘴侧外侧的特定阿片敏感区域可能在呼吸节律发生中起关键作用。由于七鳃鳗在约4.5亿年前从主要脊椎动物谱系中分化出来,我们的结果还意味着阿片类物质对呼吸的抑制作用在脊椎动物进化的早期阶段就已存在。

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