首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >High-Fat Diet During the Perinatal Period Induces Loss of Myenteric Nitrergic Neurons and Increases Enteric Glial Density, Prior to the Development of Obesity
【24h】

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

机译:在围产期期间,高脂饮食诱导肥胖症的损失,增加肠道胶质密度,在肥胖症之前增加

获取原文
获取原文并翻译 | 示例
           

摘要

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. (C) 2018 IBRO. Published by Elsevier Ltd. All rights reserved.
机译:饮食诱导的肥胖诱导外周炎症伴随着神经元的丧失。然而,少数研究已经研究了高脂饮食(HFD)对神经元的发育或在肥胖症发生之前的影响。本研究评估了母体HFD对上胃肠道中宫腔神经节的密度和神经化学表型的影响。 Sprague-Dawley大鼠从胚胎13分别喂食对照或HFD(分别从脂肪14%或60%KCAL);此后在后续免疫组化研究的产后2,4,6和12周内修复了眼底,语料库和十二指肠。虽然在整个研究中,神心神经节大小没有差异,但HFD暴露在所有地区的6周龄下降到6周龄的硝态神经元数量下降。这种减少伴随着PGP免疫反应性神经元的丧失,表明宫腔神经元数下降。 HFD在4周龄的所有地区也增加了神经聚集丛胶质细胞密度。这些变化发生在没有增加血清或胃炎标志物的情况下。本研究表明,在围产期期间暴露于HFD导致肥胖症前的胶质增殖和抑制硝基菌神经元的损失,表明饮食改变可能影响胃肠功能,这些功能可以独立于增加肥胖或血糖性失调。 (c)2018年IBRO。 elsevier有限公司出版。保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号