基础医学与临床 ›› 2016, Vol. 36 ›› Issue (6): 728-733.

• 研究论文 • 上一篇    下一篇

4-PBA抗糖尿病大鼠内质网应激作用及机制

杨燕丽1,向若兰2,孙琦3,冯凯3,张文龙3   

  1. 1. 中国医学科学院北京协和医学院北京协和医院
    2. 北京大学医学部生理学与病理生理学系
    3. 中国医学科学院 北京协和医学院
  • 收稿日期:2015-11-24 修回日期:2016-01-25 出版日期:2016-06-05 发布日期:2016-05-27
  • 通讯作者: 孙琦 E-mail:qisun50@hotmail.com
  • 基金资助:
    国家临床重点专科建设项目

4-Phenylbutyric acid attenuates the endoplasmic reticulum stress in type 2 diabetes rats

  • Received:2015-11-24 Revised:2016-01-25 Online:2016-06-05 Published:2016-05-27

摘要: 目的 探讨4-苯基丁酸(4-PBA)对2型糖尿病(T2DM)大鼠的治疗作用及其抗胰腺β细胞凋亡的作用机制。方法 高脂饮食喂养加小剂量链佐霉素(STZ)腹腔注射建立大鼠T2DM模型,造模成功后第10天灌胃给予4-PBA 20d。用real-time PCR和Western blot法检测内质网(ER)应激相关分子CHOP、GRP78、caspase-3、Bax、Bcl-2和细胞色素C的mRNA及蛋白表达水平,同时检测MAPK通路相关蛋白的磷酸化水平。 结果 高脂喂养和T2DM组大鼠胰岛β细胞出现明显的凋亡,4-PBA治疗显著降低caspase-3的活性,减轻了凋亡。高脂喂养和T2DM组大鼠CHOP、Bax和细胞色素C的mRNA及蛋白表达水平显著升高,Bcl-2的表达降低(P<0.05)。4-PBA治疗显著降低了CHOP的表达,但对GRP78的表达没有影响;4-PBA治疗降低Bax和细胞色素C的mRNA及蛋白表达水平,并增加了Bcl-2的表达(P<0.05)。T2DM组可见ERK1/2磷酸化的增加,4-PBA治疗后降低了ERK1/2的磷酸化水平(P<0.05)。结论 4-PBA通过CHOP途径减轻高脂喂养和STZ导致ER应激增加诱导的胰岛β细胞凋亡,进而抑制了下游的线粒体途径,最终减轻ER应激诱导的胰岛β细胞凋亡,这一过程可能还与ERK1/2途径有关。

关键词: 2型糖尿病, 内质网应激, 凋亡, 4-PBA, CHOP

Abstract: Objective To evaluate the effect of 4-PBA in high-fat diets-fed with/without streptozotocin (STZ)-induced diabetic rats and to clarify the underlying mechanisms. Methods Type 2 diabetic animal model was developed by high-fat diets-fed with/without low-dose STZ injection. Diabetic rats were orally gavages each day with 4-PBA for 20 days. The expressions of mRNA and protein were detected by real-time PCR and Western blot analysis. Results 4-PBA treatment significantly reduced the pancreas apoptosis induced by high-fat diets-fed with/without STZ. High-fat diets with/without STZ-induced increase in expression of CHOP mRNA and protein, p53 mRNA, Bax mRNA and protein, and cytochrome c protein, decrease in mRNA and protein levels of Bcl-2 were attenuated by 4-PBA treatment. 4-PBA also attenuated the increase of ERK1/2 phosphorylation induced by high-fat diets with/without STZ. Conclusion Treatment with 4-PBA significantly inhibits the process of type 2 diabetes in rats through the ER stress and mitochondria-dependent apoptotic pathway.

Key words: type 2 diabetic rat, endoplasmic reticulum stress, apoptosis, 4-phenylbutyric acid, CHOP

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