de Koning E J, Bodkin N L, Hansen B C, Clark A
Diabetes Research Laboratories, Radcliffe Infirmary, Oxford, UK.
Diabetologia. 1993 May;36(5):378-84. doi: 10.1007/BF00402271.
Diabetes mellitus in Macaca mulatta rhesus monkeys is preceded by phases of obesity and hyperinsulinaemia and is similar to Type 2 (non-insulin-dependent) diabetes mellitus in man. To relate the progression of the disease to quantitative changes in islet morphology, post-mortem pancreatic tissue from 26 monkeys was examined. Four groups of animals were studied: group I--young, lean and normal (n = 3); group II--older (> 10 years), lean and obese, normoglycaemic (n = 9); group III--normoglycaemic and hyperinsulinaemic (n = 6); group IV--diabetic (n = 8). Areas of islet amyloid, beta cells and islets were measured on stained histological sections. Islet size was larger in animals from groups III (p < 0.01) and IV (p < 0.0001) compared to groups I and II. The mean beta-cell area per islet in micron 2 was increased in group III (p < 0.05) and reduced in group IV (p < 0.001) compared to groups I and II. Mean beta-cell area per islet correlated with fasting plasma insulin (r = 0.76, p < 0.001) suggesting that hyper- and hypoinsulinaemia are related to the beta-cell population. Amyloid was absent in group I but small deposits were present in three of nine (group II) and in four of six (group III) animals, occupying between 0.03-45% of the islet space. Amyloid was present in eight of eight diabetic animals (group IV) occupying between 37-81% of the islet area. Every islet was affected in seven of eight diabetic monkeys. There was no correlation of degree of amyloidosis with age, body weight, body fat proportion or fasting insulin. Islet amyloid appears to precede the development of overt diabetes in Macaca mulatta and is likely to be a factor in the destruction of islet cells and onset of hyperglycaemia.
恒河猴的糖尿病在肥胖和高胰岛素血症阶段之后出现,与人类的2型(非胰岛素依赖型)糖尿病相似。为了将疾病进展与胰岛形态的定量变化相关联,对26只猴子的死后胰腺组织进行了检查。研究了四组动物:第一组——年轻、瘦且正常(n = 3);第二组——年龄较大(> 10岁)、瘦且肥胖、血糖正常(n = 9);第三组——血糖正常且高胰岛素血症(n = 6);第四组——糖尿病组(n = 8)。在染色的组织学切片上测量胰岛淀粉样变区域、β细胞和胰岛的面积。与第一组和第二组相比,第三组(p < 0.01)和第四组(p < 0.0001)动物的胰岛尺寸更大。与第一组和第二组相比,第三组每个胰岛的平均β细胞面积(单位:平方微米)增加(p < 0.05),第四组减少(p < 0.001)。每个胰岛的平均β细胞面积与空腹血浆胰岛素相关(r = 0.76,p < 0.001),表明高胰岛素血症和低胰岛素血症与β细胞数量有关。第一组没有淀粉样变,但九只动物中的三只(第二组)和六只动物中的四只(第三组)有少量沉积物,占胰岛空间的0.03 - 45%。八只糖尿病动物(第四组)中的八只都有淀粉样变,占胰岛面积的37 - 81%。八只糖尿病猴子中有七只的每个胰岛都受到影响。淀粉样变程度与年龄、体重、体脂比例或空腹胰岛素均无相关性。胰岛淀粉样变似乎先于恒河猴明显糖尿病的发生,并且可能是胰岛细胞破坏和高血糖症发作的一个因素。