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老年Fischer 344大鼠肌间神经丛中神经胶质细胞和神经元的丧失。

Loss of glia and neurons in the myenteric plexus of the aged Fischer 344 rat.

作者信息

Phillips Robert J, Kieffer Elizabeth J, Powley Terry L

机构信息

Purdue University, Department of Psychological Sciences, 703 Third Street, West Lafayette, IN 47907-2081, USA.

出版信息

Anat Embryol (Berl). 2004 Nov;209(1):19-30. doi: 10.1007/s00429-004-0426-x.

Abstract

Over the normal lifespan, a subpopulation of myenteric neurons in the small and large intestines dies. This loss is one possible mechanism for the disruptions of gastrointestinal function seen in the elderly. Little, however, is known about how the glia constituting the supportive cells of the myenteric plexus may change with aging and the losses of the enteric neurons. The goal of the present study, therefore, was to determine what, if any, changes occur in the glia associated with myenteric neurons in the aged gut. Two experimental groups, consisting of adult (5-6 months of age, n = 8) or aged (26 months of age, n = 8) virgin male Fischer 344 rats, fed ad libitum, were examined. The duodenum, jejunum, ileum, colon, and rectum from each rat were prepared as whole mounts, and indirect immunofluorescence was used to visualize the myenteric glia and neurons (antibodies to S-100 and the HuC/D protein, respectively). Separate counts of glia and neurons from the same specimens were determined, and these counts were expressed both as per ganglionic area and as per ganglion to correct for "dilution" effects resulting from age-associated changes in tissue area. Significant reductions in both the numbers of glia as well as neurons occurred in every region of the small and large intestine sampled from aged rats, except for the rectum, where a nonsignificant decrease was observed. Glial loss was proportional to neuronal death, suggesting an interdependency between the two cell types. Thus, an understanding of the nature of the neuron-glia interaction in the enteric nervous system may provide insight into the deterioration of function seen in the aged gut.

摘要

在正常寿命期间,小肠和大肠中一部分肠肌层神经元会死亡。这种损失是老年人胃肠道功能紊乱的一种可能机制。然而,对于构成肠肌丛支持细胞的神经胶质细胞如何随衰老和肠神经元的损失而变化,人们知之甚少。因此,本研究的目的是确定老年肠道中与肠肌层神经元相关的神经胶质细胞是否发生了变化。研究人员检查了两个实验组,分别由成年(5 - 6个月大,n = 8)或老年(26个月大,n = 8)的未交配雄性Fischer 344大鼠组成,大鼠自由进食。将每只大鼠的十二指肠、空肠、回肠、结肠和直肠制成整装片,采用间接免疫荧光法观察肠肌层神经胶质细胞和神经元(分别使用针对S - 100和HuC/D蛋白的抗体)。对同一标本中的神经胶质细胞和神经元进行单独计数,并将这些计数表示为每神经节面积和每神经节数量,以校正因年龄相关的组织面积变化导致的“稀释”效应。除直肠观察到不显著的减少外,从老年大鼠取样的小肠和大肠的每个区域中,神经胶质细胞和神经元的数量均显著减少。神经胶质细胞的损失与神经元死亡成正比,表明这两种细胞类型之间存在相互依存关系。因此,了解肠神经系统中神经元 - 神经胶质细胞相互作用的本质可能有助于深入了解老年肠道中功能的恶化。

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