链脲佐菌素剂量与糖尿病发病的关系。

Shika gakuho. Dental science reports Pub Date : 1989-03-01
A Nishigaki, H Noma, T Kakizawa
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引用次数: 0

摘要

采用尾静脉注射不同剂量链脲佐菌素(STZ) (20 ~ 60 mg/kg体重)诱导Sprague-Dawley株雄性大鼠糖尿病。根据各种参数(体重、血糖、血浆胰岛素、葡萄糖耐量试验、尿镜检查、血液诊断、皮肤强度)观察最终的发病情况。STZ剂量为40 mg/kg体重组(S-40组)均诱发糖尿病。该组的血糖水平约为340毫克(是对照组的3倍)。血浆胰岛素水平约8.9微u /ml(约为对照组的1/3)。葡萄糖耐量试验和尿葡萄糖观察显示葡萄糖耐量和血浆胰岛素反应降低。2. S-40组在注射STZ后30天,诱导性糖尿病的发病稳定,持续90天。3.注射STZ后20天皮肤强度下降。注射后30至90天,该水平稳定在对照皮肤强度的一半。4. STZ剂量为20 mg/kg或30 mg/kg组,部分大鼠出现糖尿病。这些动物往往会从诱导的疾病中恢复过来。5. stz50 mg/kg或60 mg/kg体重组均诱发糖尿病。注射后不久,诱导性糖尿病病变加重;并出现严重并发症(低白蛋白血症、糖尿病酮症酸中毒、糖尿病蛋白尿)。这些组中有大量的大鼠死亡。6. 本研究结果证实了STZ 40 mg/kg体重是实验研究中STZ诱导大鼠糖尿病的最佳剂量。此类研究的适宜期为注射STZ后30 - 90天。
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[The relations between doses of streptozotocin and pathosis in induced diabetes mellitus].

Tail-vein injections of streptozotocin (STZ) in various doses (20-60 mg/kg body weight) were used to induce diabetes mellitus in male rats of the Sprague-Dawley strain. Resulting pathosis was observed on the basis of various parameters (body weight, blood glucose, plasma insulin, glucose-tolerance tests, uroscopy, hemodiagnosis, and skin strength) Results 1. Diabetes mellitus was induced in all rats of the group in which the dosage was STZ 40 mg/kg body weight (S-40 group). Blood-glucose level in this group was about 340 mg (3 times the quantity in controls). Plasma-insulin level was about 8.9 microU/ml (about 1/3 the quantity in controls). Glucose-tolerance tests and observation of urino-glucose showed reductions in glucose tolerance and plasma-insulin response. 2. In the S-40 group, pathosis of induced diabetes mellitus had stabilized 30 days after and persisted for 90 days after STZ injection. 3. Skin strength decreased for 20 days after STZ injection. The level remained stable at half the strength of control skin from 30 to 90 days after the injection. 4. In groups in which doses were STZ 20 mg/kg body weight or STZ 30 mg/kg body weight, diabetes mellitus was induced in some of the rats. The animals tended to recover from the induced pathosis. 5. Diabetes mellitus was induced in all rats to which doses of STZ 50 mg/kg or STZ60 mg/kg body weight were induced. shortly after injection, the induced-diabetes pathosis changed for the worse; and grave complications (hypo-albuminosis, diabetic ketocacidosis, and diabetic proteinuria) were observed. A large number of the rats in these groups died. 6. The results of this study confirm the opinion that STZ 40 mg/kg body weight is the optimum dose for STZ induction of diabetes mellitus in rats for experimental studies. The suitable term for such studies is from 30 to 90 days after STZ injection.

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