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围产期高脂肪饮食可导致肌间神经丛氮能神经元丢失,并增加肠神经胶质密度,而肥胖尚未发生。

High-Fat Diet During the Perinatal Period Induces Loss of Myenteric Nitrergic Neurons and Increases Enteric Glial Density, Prior to the Development of Obesity.

机构信息

Department of Neural and Behavioral Sciences, Penn State College of Medicine, Hershey, PA 17033, United States.

Department of Neural and Behavioral Sciences, Penn State College of Medicine, Hershey, PA 17033, United States.

出版信息

Neuroscience. 2018 Nov 21;393:369-380. doi: 10.1016/j.neuroscience.2018.09.033.

DOI:10.1016/j.neuroscience.2018.09.033
PMID:30454864
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6251501/
Abstract

Diet-induced obesity induces peripheral inflammation accompanied by a loss of myenteric neurons. Few studies, however, have investigated the effects of a high-fat diet (HFD) on either the development of myenteric neurons or prior to the occurrence of obesity. The present study assessed the effects of maternal HFD on the density and neurochemical phenotype of myenteric ganglia in the upper gastrointestinal tract. Sprague-Dawley rats were fed either a control or HFD (14% or 60% kcal from fat, respectively) from embryonic day 13; the fundus, corpus and duodenum were fixed thereafter at postnatal 2, 4, 6 and 12 weeks of age for subsequent immunohistochemical studies. While myenteric ganglion size did not differ throughout the study, HFD exposure decreased the number of nitrergic neurons by 6 weeks of age in all regions. This decrease was accompanied by a loss of PGP-immunoreactive neurons, suggesting a decline in myenteric neuronal number. HFD also increased myenteric plexus glial cell density in all regions by 4 weeks of age. These changes occurred in the absence of an increase in serum or gastric inflammatory markers. The present study suggests that exposure to a HFD during the perinatal time period results in glial proliferation and loss of inhibitory nitrergic neurons prior to the onset of obesity, suggesting that dietary alterations may affect gastrointestinal functions independently of increased adiposity or glycemic dysregulation.

摘要

饮食诱导的肥胖会引起外周炎症,同时伴随着肠神经元的丧失。然而,很少有研究调查高脂肪饮食(HFD)对肠神经元的发育或肥胖发生前的影响。本研究评估了母体 HFD 对胃上部消化道肠神经节密度和神经化学表型的影响。Sprague-Dawley 大鼠从胚胎第 13 天开始分别喂食对照饮食或 HFD(分别来自脂肪的 14%或 60%卡路里);此后,在出生后 2、4、6 和 12 周时固定胃底、胃体和十二指肠,以便随后进行免疫组织化学研究。虽然整个研究期间肠神经节大小没有差异,但 HFD 暴露在所有区域都使 6 周龄时的氮能神经元数量减少。这种减少伴随着 PGP 免疫反应性神经元的丧失,表明肠神经元数量下降。HFD 还使所有区域的肠神经丛胶质细胞密度在 4 周龄时增加。这些变化发生在血清或胃炎症标志物没有增加的情况下。本研究表明,在围产期期间暴露于 HFD 会导致肥胖发生前胶质细胞增殖和抑制性氮能神经元丧失,这表明饮食改变可能会独立于肥胖或血糖失调影响胃肠道功能。

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