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CEPO调控新生大鼠缺氧缺血性脑损伤Bcl-2、Bax基因表达的研究
引用本文:付中秋,姚笠,田执梁,张玉晶,邵庆亮,张海涛,赵霞霞. CEPO调控新生大鼠缺氧缺血性脑损伤Bcl-2、Bax基因表达的研究[J]. 国际遗传学杂志, 2014, 37(5): 220-223
作者姓名:付中秋  姚笠  田执梁  张玉晶  邵庆亮  张海涛  赵霞霞
作者单位:哈尔滨医科大学附属第二医院儿内科,150081
基金项目:黑龙江省教育厅科技研究项目
摘    要:目的 观察新生大鼠缺氧缺血性脑损伤(HIBD)脑组织Bcl-2、Bax基因表达变化及氨基甲酰化促红细胞生成素(CEPO)干预对其表达的影响,探讨CEPO发挥脑保护作用的可能机制.方法 将新生7日龄SD大鼠建立HIBD模型,利用RT-PCR检测缺氧缺血和CEPO干预后2h、12h、24 h、48 h、72 h凋亡基因Bcl-2、Bax的mRNA表达的改变.结果 与假手术组相比,缺氧缺组在2h、12h、24 h、48 h、72 h脑组织中Bcl-2、Bax的表达均增加(P<0.05),与缺氧缺血组相比,CEPO干预组在不同时间点Bcl-2表达增加(P<0.05),Bax表达下降(P<0.05).结论 在新生大鼠HIBD中Bcl-2、Bax mRNA的表达发生改变,调控二者的表达水平可能是CEPO发挥脑保护的作用机制之一.

关 键 词:缺氧缺血性脑损伤  CEPO  凋亡基因  新生大鼠

Effect of CEPO on the expression of Bcl-2 and Bax genes in hypoxic ischemic brains of neonatal
Fu Zhongqiu,Yao Li,Tian Zhiliang,Zhang Yujing,Shao Qingliang,Zhang Haitao,Zhao Xiaxia. Effect of CEPO on the expression of Bcl-2 and Bax genes in hypoxic ischemic brains of neonatal[J]. International JOurnal of Genetics, 2014, 37(5): 220-223
Authors:Fu Zhongqiu  Yao Li  Tian Zhiliang  Zhang Yujing  Shao Qingliang  Zhang Haitao  Zhao Xiaxia
Affiliation:( Department of Pediatrics, the Second Affiliated Hospital, Harbin Medical University, Harbin 150081 , China )
Abstract:ObjectiVe To investigated the association between the expressions of Bcl-2 and Bax genes in neonatal rats upon cerebral hypoxic-isehemia and the effects of Carbamylated Erythropoietin (CEPO) administration on both genes. Methods An animal model of neonatal hypoxic-ischemia brain damage was established. The changes of Bcl-2 and Bax mRNAs in brain tissues were detected in rats after HI or CEPO administration by RT-PCR. Results The levels of Bcl-2 and Bax mRNAs were increased upon HIBD compared with sham-operated group at 2 h, 12 h, 24 h,48 h, 72 h time points post treatment (P〈0.05). On the contrary, only the level of Bcl-2 mRNA was increased (P 〈0.05) while the level of Bax mRNA was decreased ( P 〈 0.05 ) in CEPO intervention group. Conclusion The levels of Bcl-2 and Bax mRNAs in HIBD of neonatal rats were altered. CEPO may exert some neuroprotective effects on the brain tissues via interventing the expression of Bcl-2 and Bax.
Keywords:Hypoxia-ischemia damage  CEPO  Apoptotic genes  Neonatal rat
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