首页> 外文期刊>The Egyptian Journal of Hospital Medicine >Effects Of Aging On Pancreatic Islet Cell Function : An Experimental Immunohistochemical And Ultrastructural Study
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Effects Of Aging On Pancreatic Islet Cell Function : An Experimental Immunohistochemical And Ultrastructural Study

机译:衰老对胰腺胰岛细胞功能的影响:实验性免疫组织化学和超微结构研究

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A strong relationship between aging and diabetes mellitus has been clinically suggested, however, none of the previous published data had clearly focused on the age-related cytomorphological changes in the pancreas which are the goal of this study.Three groups of male apparently healthy rabbits have been used, ten animals each; classified as group-1 (3- 5months old); group-2 (9-12 months old) and group-3 (24-36 months old). After sacrification, sections from the pancreas were stained by Haematoxylin and Eosin (H&E), Gomori trichromic stain & ultrastructurally to detect aging histologic changes as well as immunohistochemically to identify insulin and glucagon secreting cells using their appropriate monoclonal antibodies . A progressive histological distortion with fibrosis and fatty changes were directly proportional to age, being mild in group-2 and severe in group-3. Morphometric studies by computerized image analysis showed that the mean number of islets was significantly higher in group2 (8.98±1.51), lowest in group-1 (5.08±1.48) and intermediate in group-3 (6.37±1.37). The mean diameter and square area of islets were significantly higher in group-2 compared to other groups (P< 0.05). The mean number of cells per islet & their secretary granules were significantly (P <0.05) higher in group-2, intermediate in group-1 and lowest in group-3.In contrast, the mean number of cells per islet and their secretory granules were insignificantly (P< 0.05) higher in group -2, intermediate in group-3 and lowest in group-1.Also, the / ratio ( cells/ cells) was greatest in group-2 (3.059:1), intermediate in group-1 (3.37:1), and lowest in group-3 (2.479:1). The increased number of cells may be due to a compensatory process to correct the hormonal feedback mechanism of insulin .The results of this work suggest that cells are generally more vulnerable to aging, an observation which might be correlated clinically with higher incidence of diabetes in older ages
机译:临床上已提出衰老与糖尿病之间有很强的关系,但是,以前的发表数据均未明确关注胰腺与年龄相关的细胞形态学变化,这是本研究的目标。三组雄性健康的雄性兔使用过,每只动物十只;归类为第1组(3-5个月大);第2组(9-12个月大)和第3组(24-36个月大)。处死后,用苏木精和曙红(H&E),Gomori三色染色和超微结构对胰腺切片进行染色,以检测衰老的组织学变化以及免疫组化,以使用其适当的单克隆抗体鉴定胰岛素和胰高血糖素分泌细胞。具有纤维化和脂肪变化的进行性组织学变形与年龄成正比,在第2组为轻度,在第3组为重度。通过计算机图像分析进行的形态计量学研究表明,胰岛的平均数量在第2组中显着更高(8.98±1.51),在第1组中最低(5.08±1.48),在第3组中处于中间水平(6.37±1.37)。第2组的胰岛平均直径和平方面积显着高于其他各组(P <0.05)。第2组的每个胰岛细胞平均数及其秘书颗粒均显着(P <0.05),第1组为中间,第3组最低(P <0.05)。相反,每个胰岛的平均细胞数及其分泌颗粒在-2组中微不足道(P <0.05),在组3中处于中间,在组1中最低。此外,在组2中的/比(细胞/细胞)最大(3.059:1),在组中处于中间-1(3.37:1),在第3组中最低(2.479:1)。细胞数量的增加可能是由于纠正胰岛素激素反馈机制的代偿过程所致。这项工作的结果表明,细胞通常更容易衰老,这一发现可能与老年人中较高的糖尿病发生率相关年龄

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