基础医学与临床 ›› 2014, Vol. 34 ›› Issue (1): 68-71.

• 研究论文 • 上一篇    下一篇

苯丙酸诺龙促进胰岛NIT-1细胞Nampt表达和胰岛素分泌

陈洁润,吴雅婷,冯乔,沈旺,冯乐平   

  1. 桂林医学院
  • 收稿日期:2013-10-08 修回日期:2013-11-15 出版日期:2014-01-05 发布日期:2013-12-26
  • 通讯作者: 冯乐平 E-mail:lpfeng1226@sina.com
  • 基金资助:
    国家自然科学基金课题资助;广西科技厅科研基金资助;广西教育厅2013年自治区大学生创新创业训练计划立项项目((桂教高教[2013]14号);广西教育厅科研资助课题

Benzyl propionate nandrolone enhences Nampt expression and insulin secretion in NIT-1 islet cells

  • Received:2013-10-08 Revised:2013-11-15 Online:2014-01-05 Published:2013-12-26
  • Contact: le-ping FENG E-mail:lpfeng1226@sina.com

摘要: 目的 探讨雄性激素苯丙酸诺龙在氧化应激条件下对胰岛细胞的作用,为2型糖尿病治疗提供理论依据。方法 将培养的NIT-1细胞按不同葡萄糖浓度(5.6、11.1、16.7和27.6 mmol/L)分为4组,分别用10 μg/mL苯丙酸诺龙处理48h,之后用流式细胞仪检测细胞周期;用Western blot 检测Nampt和FOXO1蛋白表达和用放射免疫法测定细胞胰岛素分泌。结果 用苯丙酸诺龙处理48 h后,1)低糖条件下细胞G0/G1期阻滞明显改善(p<0.01);2)高糖条件下细胞G2/M期阻滞得到缓解(p<0.01);3)高糖氧化应激状态下,苯丙酸诺龙促进胰岛细胞Nampt表达(p<0.05)和抑制非磷酸化的FOXO1蛋白表达(p<0.01),细胞分泌胰岛素增加。结论 苯丙酸诺龙能够在高浓度葡萄糖条件下改善胰岛细胞生存状况和促进胰岛素分泌,这些效应可能与促进细胞内Nampt表达和抑制FOXO1密切相关。

Abstract: Objective To discuss the effects of nandrolone styrene acrylic acid on islet cells under the condition of oxidative stress for the theoretical basis of the treatment of type 2 diabetes. Methods NIT-1 cell were divided into four groups which in different concentrations of glucose (5.6,11.1,16.7 and 27.6 mmol/L),then treat with 10μg/mL Benzyl propionate nandrolone for 48h. Nampt and FOXO1 protein expression were detected by Western blot assay. Cell cycle was determined by FCM and cell insulin secreted level was measured with radioimmuno-assay. Results Treated with benzyl propionate nandrolone for 48 h,1) G0/G1 phase retardation effect of the cell cycle was relieved(p﹤0.01)when the cell cultured in lower energy, but 2) G2/M block effect of the cell significantly remitted(p﹤0.01)under the condition of high glucose concentration. 3) Benzyl propionate nandrolone can promote Nampt protein expression(p﹤0.05) and promote insulin secretion, but inhibiting the dephosphorylated FOXO1 expression(p﹤0.01). Conclusion Benzyl propionate nandrolone would promote islet NIT-1 cell proliferation and insulin secretion, those effects are closely related to increase Nampt expression inhibit of FOXO1.