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老年大鼠结肠肌层脂肪沉积及 Cajal 间质细胞和 nNOS 阳性神经元细胞减少。

Fat deposition in the tunica muscularis and decrease of interstitial cells of Cajal and nNOS-positive neuronal cells in the aged rat colon.

机构信息

Departments of Internal Medicine and.

出版信息

Am J Physiol Gastrointest Liver Physiol. 2014 Apr 15;306(8):G659-69. doi: 10.1152/ajpgi.00304.2012. Epub 2014 Feb 13.

Abstract

Little is known about the time course of aging on interstitial cells of Cajal (ICC) of colon. The aim of this study was to investigate the change of morphology, ICC, and neuronal nitric oxide synthase (nNOS)-immunoreactive cells in the aged rat. The proximal colon of 344 Fischer rats at four different ages (6, 31, 74 wk, and 2 yr) were studied. The immunoreactivity of c-Kit, nNOS, anti-protein gene product 9.5, and synaptophysin were counted after immunohistochemistry. The c-kit, stem cell factor (ligand of Kit), and nNOS mRNA were measured by real-time PCR. c-Kit and nNOS protein were assessed by Western blot. Isovolumetric contractile force measurement and electrical field stimulation (EFS) were conducted. The area of intramuscular fat deposition significantly increased with age after 31 wk. c-Kit-immunoreactive ICC and nNOS-immunoreactive neurons and nerve fibers significantly declined with age. mRNA and protein expression of c-kit and nNOS decreased with aging. The functional study showed that the spontaneous contractility was decreased in aged rat, whereas EFS responses in the presence of atropine and L-NG-Nitroarginine methyl ester were increased in aged rat. In conclusion, the decrease of proportion of proper smooth muscle, the density of ICC and nNOS-immunoreactive neuronal fibers, and the number of nNOS-immunoreactive neurons during the aging process may explain the aging-associated colonic dysmotility.

摘要

关于结肠平滑肌细胞(ICC)随年龄变化的过程知之甚少。本研究旨在探讨老年大鼠结肠形态、ICC 和神经元型一氧化氮合酶(nNOS)-免疫反应细胞的变化。研究了 344 只 Fischer 大鼠的近端结肠,分为四个不同年龄组(6、31、74 周和 2 年)。免疫组织化学后,对 c-Kit、nNOS、抗蛋白基因产物 9.5 和突触素的免疫反应性进行计数。通过实时 PCR 测量 c-kit、干细胞因子(Kit 的配体)和 nNOS mRNA。通过 Western blot 评估 c-Kit 和 nNOS 蛋白。进行等容收缩力测量和电刺激(EFS)。31 周后,随着年龄的增长,肌间脂肪沉积面积显著增加。c-Kit 免疫反应性 ICC 和 nNOS 免疫反应性神经元和神经纤维随年龄显著减少。c-kit 和 nNOS 的 mRNA 和蛋白表达随年龄增长而降低。功能研究表明,老年大鼠的自发性收缩性降低,而在阿托品和 L-NG-硝基精氨酸甲酯存在下,EFS 反应增加。总之,在老化过程中适当平滑肌比例的降低、ICC 和 nNOS-免疫反应性神经元纤维的密度以及 nNOS-免疫反应性神经元的数量的减少可能解释了与年龄相关的结肠运动障碍。

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