In order to elucidate whether diabetic microangiopathy is attributable to metabolic derangement based on insulinopenia or to genetic factor concomitant with diabetes mellitus, diabetic monkeys induced by streptozotocin were investigated. Sixteen Japanese monkeys and ten crab-eating monkeys were used for experiment and streptozotocin was intraveneously injected. After the injection, body weight, urine sugar, fasting blood sugar, IRI, IRG, serum cholesterol, triglyceride, ketone bodies, LPO, lipoprotein fractions, glycosylated Hb etc were analysed at intervals and simultaneously ocular fundus, peripheral nerve conduction velocity, electrocardiogram, thickness of gastrocnemius capillary basement membrane were surveyed. Duration of diabetes millitus ranged from 3 months to 16 months. All diabetic monkeys showed glycosuria and weight loss but insulin therapy was not necessary for the survival. Laboratory data were as follows (diabetic vs control); fasting blood sugar 241±27, 83±6 mg/dl (p<0.01), IRI 24±6, 45±107μU/ml (p<0.05), IRG 416±51, 340±33pg/ml, GH 12.5±4.2, 3.5±1.1ng/ml, ketone bodies 751±255, 174±30μM/l (p<0.05), 3-hydroxy butyric acid 533±198, 99±23μM/l (p<0.01), acetoacetate 218±58, 75±10μCM/l (p<0.05), 3-hydroxy butyric acid to acetoacetate ratio 2.1±0.3, 1.3±0.3 (p<0.05), LPO 5.4±0.3, 5.2±0.3μM/ml, electrophoretic lipid staining of plasma lipoprotein (%), α 34±5, 43±3, β 55±2, 56±3, preβ 10±6%, not detected, cholesterol contents in plasma lipoprotein fractions, HDL 59±7, 55±3, LDL 102±15, 76±6, VLDL 20±4, 14±4, total 191±15, 145±8mg/dl, TG contents in plasma lipoprotein, HDL 25±4, 11±2 (p<0.05), LDL 29±6, 14±2, VLDL 44±6, 11±1 (p<0.01), total 98±5, 36±4mg/dl (p<0.01). Thus, these diabetic monkeys bear resemblance to human insulin independent diabetes mellitus in blood analysis. Although HDL cholesterol was not lowered in the diabetic group, atherogenic index expressed as LDL-chol/HDL-chol and β+preβ/α were significantly higher in the diabetic group than in the control. On electrocardiogram in 4 of 6 diabetic monkeys, ST depression was observed but not in the control. In addition, the initial stage of atherosclerosis in the intimal layer of the abdominal aorta was observed on electron microscopy in the diabetic Japanese monkey died at the eighteen months after the injection of streptozotocin. On the other hand, ocular fundi did not show diabetic changes with color photograph and fluorescein angiogram in either groups. However, basement membrane in gastrocnemius muscle capillary tended to be thickened in the diabetic group.These results indicated that diabetic monkeys are useful for the elucidation of pathogenesis of diabetic macro-and micro-angiopathy.