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内吗啡肽-2(Endo2)与P物质(SubP)共同应用可减弱SubP诱导的兴奋,并改变新生大鼠体外制备物中的频率可塑性。

Endomorphin-2 (Endo2) and substance P (SubP) co-application attenuates SubP-induced excitation and alters frequency plasticity in neonatal rat in vitro preparations.

作者信息

Johnson Stephen M, Johnson Sarah M, Watters Jyoti J, Baker Tracy L

机构信息

Department of Comparative Biosciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, WI, United States.

Department of Comparative Biosciences, School of Veterinary Medicine, University of Wisconsin-Madison, Madison, WI, United States.

出版信息

Respir Physiol Neurobiol. 2025 Jan;331:104351. doi: 10.1016/j.resp.2024.104351. Epub 2024 Sep 19.

DOI:10.1016/j.resp.2024.104351
PMID:39303801
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11614698/
Abstract

Substance P (SubP) and endomorphin-2 (Endo2) are co-localized presynaptically in vesicles of neurons adjacent to inspiratory rhythm-generating pre-Botzinger Complex (preBotC) neurons but the effects of co-released SubP and Endo2 on respiratory motor control are not known. To address this question, SubP alone or a combination of SubP and Endo2 (SubP/Endo2) were bath-applied in a sustained (15-min) or intermittent (5-min application, 5-min washout, x3) pattern at 10-100 nM to neonatal rat brainstem-spinal cord preparations. During neuropeptide application, SubP/Endo2 co-applications generally attenuated SubP-induced increases in burst frequency and decreases in burst amplitude. With respect to frequency plasticity (long-lasting increase in burst frequency 60 min post-neuropeptide application), SubP-induced frequency plasticity was increased with sustained SubP/Endo2 co-applications at 20 and 100 nM. Intermittent SubP/Endo2 co-applications tended to decrease the level of frequency plasticity induced by intermittent SubP alone applications. SubP/Endo2 co-applications revealed potentially new functions for neurokinin-1 (NK1R) and mu-opioid (MOR) receptors on respiratory rhythm-generating medullary neurons.

摘要

P物质(SubP)和内吗啡肽-2(Endo2)在与吸气节律产生前包钦格复合体(preBotC)神经元相邻的神经元囊泡中共同突触前定位,但共同释放的SubP和Endo2对呼吸运动控制的影响尚不清楚。为了解决这个问题,将单独的SubP或SubP与Endo2的组合(SubP/Endo2)以10-100 nM的浓度,以持续(15分钟)或间歇(5分钟应用,5分钟洗脱,共3次)模式浴用于新生大鼠脑干-脊髓标本。在应用神经肽期间,SubP/Endo2共同应用通常会减弱SubP诱导的爆发频率增加和爆发幅度降低。关于频率可塑性(神经肽应用后60分钟爆发频率的持久增加),在20和100 nM时,持续的SubP/Endo2共同应用会增加SubP诱导的频率可塑性。间歇性SubP/Endo2共同应用倾向于降低单独间歇性应用SubP诱导的频率可塑性水平。SubP/Endo2共同应用揭示了神经激肽-1(NK1R)和μ-阿片受体(MOR)在呼吸节律产生延髓神经元上潜在的新功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/521a/11614698/83aa2cfbf281/nihms-2024725-f0008.jpg
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本文引用的文献

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Respir Physiol Neurobiol. 2024 Feb;320:104186. doi: 10.1016/j.resp.2023.104186. Epub 2023 Nov 7.
2
Maternal opioids age-dependently impair neonatal respiratory control networks.母体阿片类药物会随年龄对新生儿呼吸控制网络造成损害。
Front Physiol. 2023 Mar 16;14:1109754. doi: 10.3389/fphys.2023.1109754. eCollection 2023.
3
Respiratory neuroplasticity: Mechanisms and translational implications of phrenic motor plasticity.呼吸神经可塑性:膈神经运动可塑性的机制和转化意义。
Handb Clin Neurol. 2022;188:409-432. doi: 10.1016/B978-0-323-91534-2.00016-3.
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Mu-opioid receptor-dependent transformation of respiratory motor pattern in neonates .新生儿中μ-阿片受体依赖性呼吸运动模式的转变
Front Physiol. 2022 Jul 22;13:921466. doi: 10.3389/fphys.2022.921466. eCollection 2022.
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Selective G protein signaling driven by substance P-neurokinin receptor dynamics.由 P 物质神经激肽受体动力学驱动的选择性 G 蛋白信号转导。
Nat Chem Biol. 2022 Jan;18(1):109-115. doi: 10.1038/s41589-021-00890-8. Epub 2021 Oct 28.
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Dynamic Rhythmogenic Network States Drive Differential Opioid Responses in the Respiratory Network.动态节律生成网络状态驱动呼吸网络中阿片类药物反应的差异。
J Neurosci. 2021 Dec 1;41(48):9919-9931. doi: 10.1523/JNEUROSCI.1329-21.2021. Epub 2021 Oct 25.
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Evaluation of G protein bias and β-arrestin 2 signaling in opioid-induced respiratory depression.评估阿片类药物引起的呼吸抑制中 G 蛋白偏向和β-arrestin 2 信号转导。
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