Beta-cell mass depletion precedes the onset of hyperglycaemia in the GK rat, a genetic model of non-insulin-dependent diabetes mellitus.

Diabete & metabolisme Pub Date : 1995-12-01
J Movassat, C Saulnier, B Portha
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Abstract

It is unclear whether reported histopathological changes in the endocrine pancreas of the GK rat (a spontaneous model of non-insulin-dependent diabetes) are related to the pathogenesis of hyperglycaemia or occur secondarily to metabolic alterations. We found that total pancreatic insulin stores in GK rats from the Paris colony were depleted by 62% (p < 0.01) in adult (4-month-old) overtly hyperglycaemic animals compared to those of normal Wistar control rats, and that beta-cell mass in GK pancreata was decreased to a similar extent (51%, p < 0.05). This indicates that decreased in vivo and in vitro insulin secretory response to glucose in GK rats could be due not only to impaired stimulus-secretion coupling for glucose in their beta cells but also to a reduced number of beta cells. Reduced total beta-cell mass in adult GK rats was associated with a noticeable alteration in the architecture of a subpopulation of islets: only large islets displayed signs of disorganization of the mantle-core relationship due to prominent fibrosis, with clusters of beta cells widely separated by strands of connective tissue. Our study also provides a first record of the pathophysiologic changes occurring in the GK rat from the neonatal period. Four-day-old GK pups demonstrated normal basal glycaemia compared to Wistar rats of the same age. GK islets displayed a well-preserved architecture, with normal staining of beta cells and no fibrosis. However, their total pancreatic insulin stores and total beta-cell mass were significantly lower [59% (p < 0.01) and 64% (p < 0.05) respectively] than those of controls. These data indicate that a reduction in islet tissue clearly predates the onset of diabetes (hyperglycaemia). Therefore, a reduction of total beta-cell mass should be considered as a primary feature in the pathological sequence leading to diabetes in GK rats, at least in those originating from the Paris colony.

在GK大鼠(非胰岛素依赖型糖尿病的遗传模型)中,β细胞质量耗竭先于高血糖的发作。
目前尚不清楚GK大鼠(非胰岛素依赖型糖尿病的自发模型)内分泌胰腺的组织病理学改变是否与高血糖的发病机制有关,还是继发于代谢改变。我们发现,与正常Wistar对照大鼠相比,来自Paris群体的GK大鼠成年(4月龄)明显高血糖动物的胰腺总胰岛素储存减少了62% (p < 0.01), GK胰腺的β细胞质量减少了相似程度(51%,p < 0.05)。这表明,GK大鼠体内和体外胰岛素分泌对葡萄糖的反应下降,不仅是由于β细胞中葡萄糖的刺激-分泌偶联受损,而且是由于β细胞数量减少。成年GK大鼠β细胞总质量的减少与胰岛亚群结构的明显改变有关:只有大的胰岛由于明显的纤维化而显示出衣核关系的紊乱迹象,β细胞簇被结缔组织链广泛分离。我们的研究也首次记录了GK大鼠从新生儿期开始发生的病理生理变化。与Wistar大鼠相比,4天大的GK幼鼠表现出正常的基础血糖。GK胰岛结构保存完好,细胞染色正常,无纤维化。胰腺总胰岛素储存量和总β细胞质量显著低于对照组[分别为59% (p < 0.01)和64% (p < 0.05)]。这些数据表明,胰岛组织的减少明显早于糖尿病(高血糖)的发病。因此,总β细胞质量的减少应该被认为是导致GK大鼠糖尿病的病理序列的主要特征,至少在那些来自巴黎群体的大鼠中是这样。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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