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[沉默调节蛋白1(SIRT1)的表达及活性在癫痫患者和大鼠模型的脑组织中上调]

[SIRT1 expression and activity are up-regulated in the brain tissue of epileptic patients and rat models].

作者信息

Chen Yongping, Xie Yunlan, Wang Heng, Chen Yangmei

机构信息

Department of Neurology, Second Affiliated Hospital of Chongqing Medical University, China.

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2013 Apr;33(4):528-32.

Abstract

OBJECTIVE

To investigate the expression and activity of silent information regulator 1 (SIRT1) in the temporal lobe of epileptic patients and rat models and explore its role in the occurrence and progression of epilepsy.

METHODS

The temporal lobe tissue of epileptic patients and rat models (induced by lithium-pilocarpine) were examined for SIRT1 expression using immunohistochemistry and Western blotting and also for SIRT1 activity using SIRT1 Deacetylase Assay Kit.

RESULTS

Immunohistochemistry detected positive SIRT1 expression mainly in the cytoplasm of the neurons in both human and rat brains, and the epileptic groups showed stronger SIRT1 immunoreactivity than the control group. Western blotting and activity assay showed that the expression and activity of SIRT1 were significantly increased in the temporal lobe of patients with refractory epilepsy as compared with the tissues samples from non-epileptic patients (P<0.05). In the rat models of epilepsy, SIRT1 expression was up-regulated at 6, 24, and 72 h and at 7, 14, 30, and 60 days after kindling (P<0.05) and SIRT1 activity was significantly increased at 6, 24, and 72 h and at 7 and 14 days (P<0.05), with the peak level of SIRT1 expression and activity occurring at 72 h.

CONCLUSION

Up-regulation of SIRT1 expression and activity in the temporal lobe of epileptic patients and rat models may play an important role in the pathogenesis of epilepsy.

摘要

目的

研究沉默信息调节因子1(SIRT1)在癫痫患者及大鼠模型颞叶中的表达及活性,探讨其在癫痫发生发展中的作用。

方法

采用免疫组织化学和蛋白质印迹法检测癫痫患者及锂-匹罗卡品诱导的大鼠模型颞叶组织中SIRT1的表达,并用SIRT1去乙酰化酶检测试剂盒检测SIRT1活性。

结果

免疫组织化学检测显示,人和大鼠脑组织中SIRT1阳性表达主要位于神经元细胞质中,癫痫组SIRT1免疫反应性强于对照组。蛋白质印迹法和活性检测显示,与非癫痫患者组织样本相比,难治性癫痫患者颞叶中SIRT1的表达和活性显著增加(P<0.05)。在癫痫大鼠模型中,点燃后6、24和72小时以及7、14、30和60天SIRT1表达上调(P<0.05),6、24和72小时以及7和14天SIRT1活性显著增加(P<0.05),SIRT1表达和活性的峰值水平出现在72小时。

结论

癫痫患者及大鼠模型颞叶中SIRT1表达和活性上调可能在癫痫发病机制中起重要作用。

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