Schneider K, Laube H, Linn T
Department of Internal Medicine, Justus Liebig University, Giessen, Germany.
Acta Diabetol. 1996 Sep;33(3):236-40. doi: 10.1007/BF02048550.
Diet modifies the development of insulin-dependent diabetes mellitus in animals and in humans. We examined female non-obese-diabetic (NOD) mice, a diabetes-prone mouse strain with 70% spontaneous diabetes incidence and metabolic abnormalities in non-overtly diabetic litters. They were fed a diet containing 55% (n = 27) or 15% (n = 26) protein, respectively, after weaning. At an age of 30 weeks, non-diabetic NOD mice were submitted to an intravenous glucose tolerance test (0.5 g/kg body weight; blood samples were taken after 2, 4, 8, 10, 15, 20 and 30 min) and to perfusion of the pancreas (stimulation media were Krebs-Ringer-Hepes buffer with 5 mmol/l glucose, 30 mmol/l glucose and 5 mmol/l glucose plus 19 mmol/l arginine). Diabetic mice were removed from the experiment. Serum glucose concentration and body weight were monitored weekly. Food ingestion was checked at an age of 11 weeks. On average, the onset of diabetes was diagnosed in mice on a high-protein diet (19.7 +/- 1.3 weeks) 4 weeks earlier than in mice on a low-protein diet (23.5 +/- 1.1 weeks; P < 0.05). Non-diabetic NOD mice on a high-protein diet showed significantly better glucose tolerance (as determined by the glucose disappearance rate) and mean insulin secretion (at 30 mmol/l glucose). No difference in the serum glucose concentration between non-diabetic mice on the low-protein diet or high-protein diet could be proved. In non-diabetic mice on the high-protein diet the body weight and food ingestion exceeded those of mice on the low-protein diet (P < 0.05). High insulin secretion and glucose tolerance in non-diabetic mice may reflect the capacity of beta-cells to adapt; however, beta-cells tend to be destroyed under such circumstances. Thus, a high-protein diet promoted the onset of diabetes, but it did not increase significantly the incidence of the disease.
饮食会改变动物和人类中胰岛素依赖型糖尿病的发展。我们研究了雌性非肥胖糖尿病(NOD)小鼠,这是一种易患糖尿病的小鼠品系,在非显性糖尿病窝中自发糖尿病发病率为70%且存在代谢异常。断奶后,它们分别被喂食含55%(n = 27)或15%(n = 26)蛋白质的饮食。在30周龄时,对非糖尿病的NOD小鼠进行静脉葡萄糖耐量试验(0.5 g/kg体重;在2、4、8、10、15、20和30分钟后采集血样)以及胰腺灌注(刺激介质为含5 mmol/l葡萄糖、30 mmol/l葡萄糖和5 mmol/l葡萄糖加19 mmol/l精氨酸的 Krebs-Ringer-Hepes缓冲液)。将糖尿病小鼠排除在实验之外。每周监测血清葡萄糖浓度和体重。在11周龄时检查食物摄入量。平均而言,高蛋白饮食组小鼠(19.7 +/- 1.3周)糖尿病发病时间比低蛋白饮食组小鼠(23.5 +/- 1.1周;P < 0.05)早4周。高蛋白饮食的非糖尿病NOD小鼠表现出明显更好的葡萄糖耐量(由葡萄糖消失率确定)和平均胰岛素分泌(在30 mmol/l葡萄糖时)。无法证明低蛋白饮食或高蛋白饮食的非糖尿病小鼠之间血清葡萄糖浓度存在差异。高蛋白饮食的非糖尿病小鼠的体重和食物摄入量超过低蛋白饮食的小鼠(P < 0.05)。非糖尿病小鼠的高胰岛素分泌和葡萄糖耐量可能反映了β细胞的适应能力;然而,在这种情况下β细胞往往会被破坏。因此,高蛋白饮食促进了糖尿病的发病,但并未显著增加疾病的发病率。