Influence of streptozocin's dose on inductive effect of diabetes in C57BL/6J mice
10.3760/cma.j.issn.1674-1935.2009.01.008
- VernacularTitle:链脲菌素剂量对C57BL/6J小鼠糖尿病诱导效应的影响
- Author:
Chenliang SUN
;
Mingyan ZHU
;
Zhiwei WANG
;
Xiangjun FAN
;
Yuhua LU
;
Haoliang SHEN
- Publication Type:Journal Article
- Keywords:
Diabetes meilitus,experimental;
Streptozocin;
Dose-response relationship,drug;
C57 BL/6J mice
- From:
Chinese Journal of Pancreatology
2009;9(1):24-26
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the influence of streptozocin (STZ)'s dose on the inductive effect of diabetes in C57BL/6J mice, and investigate the dose-effect relationship and the optimal dose range. Methods 145 C57BL/6J mice were randomly divided into 9 diabetic groups (group A to group 1, n = 15 in each group) and I control group (n = I0) to receive intraperitoneal injection of STZ with the dosages of 30, 60, 80, 100, 120, 150, 180, 210, 240 mg/kg and same amount of buffer solution,respectively. Changes of blood glucose, body weight, survival rate at 45 day and serum insulin level were monitored, and the relationship with STZ doses was analyzed. Pancreas and kidneys of the mice were removed for morphological examination, and immunohistochemistry was used for determination of insulin in pancreas and CD<,68> in kidneys. Results Compared with control group, blood glucose in group C ~G increased significantly; body weigh, insulin level decreased significantly (P < 0.05), and the STZ dose was positively correlated with mean blood glucose (r = -0.984, P < 0.05) and was negatively correlated with mean serum insulin levels (r = 0.994, P <0.05). The diabetes modeling rates in group C ~ G (86.7% ~ 100%) were higher than those of group A and B (0 and 40%, P<0.05). At the 45th day, the survival rates of group C ~G (46.7% ~ 73.3%) were higher than those of group H and 1 (13.3% and 0, P <0.05). There was no obvious injury of pancreas and kidneys in group B, whereas, in group C and G, pancreatic island atrophy and decreased insulin secretion were observed; deposits of extracellular matrix and macrophage increased in the mesangium were also present. Conclusions 80 ~ 180 mg/kg of STZ dose was ideal for establishing diabetes model in C57BL/6J mice. Within this range, the modeling rate and survival rate was higher, and target organs injury was typical. The STZ dose was positively correlated with blood glucose and negatively correlated with serum insulin levels.