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肠道中迷走神经传入信号的可塑性。

Plasticity of vagal afferent signaling in the gut.

作者信息

Grabauskas Gintautas, Owyang Chung

机构信息

Division of Gastroenterology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI 48019, USA.

Division of Gastroenterology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI 48019, USA.

出版信息

Medicina (Kaunas). 2017;53(2):73-84. doi: 10.1016/j.medici.2017.03.002. Epub 2017 Apr 10.


DOI:10.1016/j.medici.2017.03.002
PMID:28454890
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6318799/
Abstract

Vagal sensory neurons mediate the vago-vagal reflex which, in turn, regulates a wide array of gastrointestinal functions including esophageal motility, gastric accommodation and pancreatic enzyme secretion. These neurons also transmit sensory information from the gut to the central nervous system, which then mediates the sensations of nausea, fullness and satiety. Recent research indicates that vagal afferent neurons process non-uniform properties and a significant degree of plasticity. These properties are important to ensure that vagally regulated gastrointestinal functions respond rapidly and appropriately to various intrinsic and extrinsic factors. Similar plastic changes in the vagus also occur in pathophysiological conditions, such as obesity and diabetes, resulting in abnormal gastrointestinal functions. A clear understanding of the mechanisms which mediate these events may provide novel therapeutic targets for the treatment of gastrointestinal disorders due to vago-vagal pathway malfunctions.

摘要

迷走感觉神经元介导迷走-迷走反射,进而调节一系列广泛的胃肠功能,包括食管动力、胃容纳和胰腺酶分泌。这些神经元还将来自肠道的感觉信息传递至中枢神经系统,进而介导恶心、饱腹感和饱足感。最近的研究表明,迷走传入神经元具有非均匀特性和显著程度的可塑性。这些特性对于确保受迷走神经调节的胃肠功能对各种内在和外在因素迅速且适当地做出反应很重要。在肥胖和糖尿病等病理生理状况下,迷走神经也会发生类似的可塑性变化,从而导致胃肠功能异常。清楚了解介导这些事件的机制可能为因迷走-迷走通路功能障碍所致的胃肠疾病提供新的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01c1/6318799/2aed32294181/nihms-988077-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01c1/6318799/2aed32294181/nihms-988077-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01c1/6318799/2aed32294181/nihms-988077-f0001.jpg

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Plasticity of vagal afferent signaling in the gut.

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本文引用的文献

[1]
Increased Activation of the TRESK K Mediates Vago-Vagal Reflex Malfunction in Diabetic Rats.

Gastroenterology. 2016-11

[2]
High-Fat Diet-Induced Obesity Ablates Gastric Vagal Afferent Circadian Rhythms.

J Neurosci. 2016-3-16

[3]
One-day high-fat diet induces inflammation in the nodose ganglion and hypothalamus of mice.

Biochem Biophys Res Commun. 2015-9-4

[4]
KATP channels in the nodose ganglia mediate the orexigenic actions of ghrelin.

J Physiol. 2015-9-1

[5]
Diet-induced obesity causes peripheral and central ghrelin resistance by promoting inflammation.

J Endocrinol. 2015-7

[6]
Glucagon-like peptide 1 interacts with ghrelin and leptin to regulate glucose metabolism and food intake through vagal afferent neuron signaling.

J Nutr. 2015-4

[7]
TRPM8 function and expression in vagal sensory neurons and afferent nerves innervating guinea pig esophagus.

Am J Physiol Gastrointest Liver Physiol. 2015-3-15

[8]
The melanocortin-4 receptor is expressed in enteroendocrine L cells and regulates the release of peptide YY and glucagon-like peptide 1 in vivo.

Cell Metab. 2014-12-2

[9]
Deletion of leptin signaling in vagal afferent neurons results in hyperphagia and obesity.

Mol Metab. 2014-6-27

[10]
Ghrelin induces leptin resistance by activation of suppressor of cytokine signaling 3 expression in male rats: implications in satiety regulation.

Endocrinology. 2014-10

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