丝胶对2型糖尿病大鼠胰岛细胞凋亡的保护作用  被引量:8

Protective effects of sericin on islet cells apoptosis of type 2 diabetes rats

在线阅读下载全文

作  者:刘晓燕[1] 付秀美[2] 高宇[1] 陈志宏[2] 

机构地区:[1]承德医学院附属医院内分泌科,河北承德067000 [2]承德医学院人体解剖学教研室

出  处:《中国老年学杂志》2012年第12期2525-2527,共3页Chinese Journal of Gerontology

基  金:河北省科技厅项目(No.08276101D-19);河北省教育厅项目(No.2006301)

摘  要:目的观察丝胶对2型糖尿病大鼠胰岛细胞凋亡的保护作用。方法雄性SD大鼠36随机分为3组:正常对照组、糖尿病模型组和丝胶治疗组。链脲佐菌素(STZ,25 mg/kg,连续3 d)腹腔注射建立2型糖尿病大鼠模型;待模型成功建立后,丝胶治疗组大鼠给予丝胶灌胃(2.4 g.kg-1.d-1)35 d。免疫组织化学染色观察胰岛β细胞Bcl-2和Bax蛋白的表达。结果与正常对照组大鼠相比,模型组大鼠胰岛β细胞Bax蛋白的表达明显升高(P<0.01),Bcl-2蛋白的表达明显降低(P<0.01);与模型大鼠相比,丝胶治疗组大鼠胰岛β细胞Bax蛋白的表达明显降低(P<0.01),Bcl-2蛋白的表达明显升高(P<0.01)。结论丝胶可通过上调胰岛β细胞Bcl-2蛋白的表达、下调胰岛β细胞Bax蛋白的表达,抑制2型糖尿病大鼠胰岛细胞凋亡,对糖尿病时胰岛细胞损伤具有一定的保护作用。Objective To observe the protective effects of sericin on islet cells apoptosis of type 2 diabetes rats.Methods 36 male SD rats were randomly divided into 3 groups and each group had 12 rats: normal control,diabetes model and sericin treatment groups.Diabetes model were made by injecting 2% STZ(25 mg/kg,3 d) into the abdominal cavity continuously.After the diabetes model was successfully established,the rats in model group had no more treatment;the rats in sericin treatment group were lavaged with sericin(2.4 g·kg-1·d-1) for 35 days.SP immunohistochemical staining was used to observe the expression of Bcl-2 and Bax protein in β cells of islet.Results Compared with normal control rats,the Bcl-2 expression in β cells of islet of rats in model group was decreased obviously,Bax expression increased obviously(P0.01).Compared with model rats,the Bcl-2 expression in β cells of islet of rats in sericin treatment was increased obviously,Bax expression decreased obviously(P0.01).Conclusions Sericin can inhibit β cell apoptosis by up-regulating Bcl-2 expression and downregulating Bax expression and have protective effects on β cells injury during diabetes.

关 键 词:丝胶 2型糖尿病 胰岛Β细胞 BCL-2 BAX 

分 类 号:R587[医药卫生—内分泌]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象