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本文引用的文献

1
Immunolocalization of muscarinic M1 receptor in the rat medial prefrontal cortex.毒蕈碱M1受体在大鼠内侧前额叶皮质中的免疫定位
J Comp Neurol. 2018 Jun 1;526(8):1329-1350. doi: 10.1002/cne.24409. Epub 2018 Feb 28.
2
Post-inflammatory Ileitis Induces Non-neuronal Purinergic Signaling Adjustments of Cholinergic Neurotransmission in the Myenteric Plexus.炎症后回肠炎诱导肌间神经丛中胆碱能神经传递的非神经元嘌呤能信号调节。
Front Pharmacol. 2017 Nov 8;8:811. doi: 10.3389/fphar.2017.00811. eCollection 2017.
3
Gliotransmission and adenosinergic modulation: insights from mammalian spinal motor networks.胶质细胞传递与腺苷能调节:来自哺乳动物脊髓运动网络的见解
J Neurophysiol. 2017 Dec 1;118(6):3311-3327. doi: 10.1152/jn.00230.2017. Epub 2017 Sep 27.
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P2Y Receptors - Properties and Functional Activities.P2Y 受体——特性与功能活动。
Adv Exp Med Biol. 2017;1051:71-89. doi: 10.1007/5584_2017_57.
5
Ganglionic GFAP glial Gq-GPCR signaling enhances heart functions in vivo.神经节细胞胶质纤维酸性蛋白(GFAP) 神经胶质 Gq-GPCR 信号增强体内心脏功能。
JCI Insight. 2017 Jan 26;2(2):e90565. doi: 10.1172/jci.insight.90565.
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Astrocytic control of synaptic function.星形胶质细胞对突触功能的调控。
Philos Trans R Soc Lond B Biol Sci. 2017 Mar 5;372(1715). doi: 10.1098/rstb.2016.0154.
7
Enteric glial activity regulates secretomotor function in the mouse colon but does not acutely affect gut permeability.肠道神经胶质细胞的活动调节小鼠结肠的分泌运动功能,但不会急性影响肠道通透性。
J Physiol. 2017 Jun 1;595(11):3409-3424. doi: 10.1113/JP273492. Epub 2017 Feb 22.
8
The acute inhibition of enteric glial metabolism with fluoroacetate alters calcium signaling, hemichannel function, and the expression of key proteins.用氟乙酸对肠神经胶质细胞代谢进行急性抑制会改变钙信号传导、半通道功能以及关键蛋白的表达。
J Neurophysiol. 2017 Jan 1;117(1):365-375. doi: 10.1152/jn.00507.2016. Epub 2016 Oct 26.
9
Enteric neuropathies: Yesterday, Today and Tomorrow.肠道神经病:昨天、今天与明天。
Adv Exp Med Biol. 2016;891:123-33. doi: 10.1007/978-3-319-27592-5_12.
10
Enteric glia: the most alimentary of all glia.肠神经胶质细胞:所有神经胶质细胞中与营养关系最为密切的细胞。
J Physiol. 2017 Jan 15;595(2):557-570. doi: 10.1113/JP271021. Epub 2016 May 29.

肠神经胶质细胞的胆碱能激活是一种生理机制,有助于调节胃肠道蠕动。

Cholinergic activation of enteric glia is a physiological mechanism that contributes to the regulation of gastrointestinal motility.

机构信息

Neuroscience Program, Michigan State University , East Lansing, Michigan.

Department of Physiology, Michigan State University , East Lansing, Michigan.

出版信息

Am J Physiol Gastrointest Liver Physiol. 2018 Oct 1;315(4):G473-G483. doi: 10.1152/ajpgi.00155.2018. Epub 2018 Jun 21.

DOI:10.1152/ajpgi.00155.2018
PMID:29927320
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6230698/
Abstract

The reflexive activities of the gastrointestinal tract are regulated, in part, by precise interactions between neurons and glia in the enteric nervous system (ENS). Intraganglionic enteric glia are a unique type of peripheral glia that surround enteric neurons and regulate neuronal function, activity, and survival. Enteric glia express numerous neurotransmitter receptors that allow them to sense neuronal activity, but it is not clear if enteric glia monitor acetylcholine (ACh), the primary excitatory neurotransmitter in the ENS. Here, we tested the hypothesis that enteric glia detect ACh and that glial activation by ACh contributes to the physiological regulation of gut functions. Our results show that myenteric enteric glia express both the M3 and M5 subtypes of muscarinic receptors (MRs) and that muscarine drives intracellular calcium (Ca) signaling predominantly through M3R activation. To elucidate the functional effects of activation of glial M3Rs, we used GFAP::hM3Dq mice that express a modified human M3R (hM3Dq) exclusively on glial fibrillary acidic protein (GFAP) positive glia to directly activate glial hM3Dqs using clozapine- N-oxide. Using spatiotemporal mapping analysis, we found that the activation of glial hM3Dq receptors enhances motility reflexes ex vivo. Continuous stimulation of hM3Dq receptors in vivo, drove changes in gastrointestinal motility without affecting neuronal survival in the ENS and glial muscarinic receptor activation did not alter neuron survival in vitro. Our results provide the first evidence that GFAP intraganglionic enteric glia express functional muscarinic receptors and suggest that the activation of glial muscarinic receptors contributes to the physiological regulation of functions. NEW & NOTEWORTHY Enteric glia are emerging as novel regulators of enteric reflex circuits, but little is still known regarding the effects of specific transmitter pathways on glia and the resulting consequences on enteric reflexes. Here, we provide the first evidence that enteric glia monitor acetylcholine in the enteric nervous system and that glial activation by acetylcholine is a physiological mechanism that contributes to the functional regulation of intestinal reflexes.

摘要

胃肠道的反射活动部分受到肠神经系统 (ENS) 中神经元和神经胶质之间精确相互作用的调节。肠神经节内的肠神经胶质是一种独特的外周神经胶质,环绕肠神经元并调节神经元的功能、活动和存活。肠神经胶质表达许多神经递质受体,使它们能够感知神经元活动,但目前尚不清楚肠神经胶质是否监测乙酰胆碱 (ACh),ACh 是 ENS 中的主要兴奋性神经递质。在这里,我们检验了这样一个假设,即肠神经胶质检测 ACh,并且 ACh 对神经胶质的激活有助于肠道功能的生理调节。我们的研究结果表明,肌间神经节内的肠神经胶质表达 M3 和 M5 两种毒蕈碱受体 (MR) 亚型,而毒蕈碱主要通过 M3R 激活来驱动细胞内钙 (Ca) 信号。为了阐明激活神经胶质 M3R 的功能影响,我们使用了 GFAP::hM3Dq 小鼠,该小鼠在 GFAP 阳性神经胶质上仅表达一种修饰的人 M3R (hM3Dq),使用氯氮平-N-氧化物直接激活神经胶质 hM3Dqs。通过时空映射分析,我们发现激活神经胶质 hM3Dq 受体增强了离体运动反射。体内连续刺激 hM3Dq 受体驱动胃肠道运动发生变化,而不影响 ENS 中的神经元存活,并且神经胶质毒蕈碱受体的激活并未改变体外神经元的存活。我们的研究结果首次提供了证据表明 GFAP 肌间神经节内的肠神经胶质表达功能性毒蕈碱受体,并表明神经胶质毒蕈碱受体的激活有助于功能的生理调节。