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saRNA 介导的 iNOS 上调改善糖尿病大鼠的勃起功能。

saRNA guided iNOS up-regulation improves erectile function of diabetic rats.

机构信息

Department of Urology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, People's Republic of China.

出版信息

J Urol. 2013 Aug;190(2):790-8. doi: 10.1016/j.juro.2013.03.043. Epub 2013 Mar 19.

Abstract

PURPOSE

Promoter targeted saRNAs mediate sequence specific up-regulation of gene expression. We explored the therapeutic effect of RNA activation mediated iNOS gene activation on improving erectile function in a rat model of diabetes mellitus.

MATERIALS AND METHODS

An optimal saRNA sequence specific for iNOS promoter was cloned into an adenoviral vector, resulting in AdU6/shiNOS and AdU6/shControl. The corresponding viruses were used to transduce cultured rat cavernous smooth muscle cells. Streptozotocin induced diabetes models were established in rats and used to test the effects of intracavernous delivery of iNOS saRNA viruses on erectile function. iNOS expression in the cavernous smooth muscle cells or penile tissue of treated rats was assessed by reverse transcriptase-polymerase chain reaction and Western blot. Cyclic guanosine monophosphate was analyzed by enzyme-linked immunosorbent assay. Intracavernous pressure in response to cavernous nerve stimulation was measured using a data acquisition system on post-injection days 1, 3, 5, 7, 10 and 14.

RESULTS

Adenovirus mediated expression of iNOS saRNA caused sustained up-regulation of iNOS in cavernous smooth muscle cells. Intracavernous injection of AdU6/shiNOS activated iNOS expression in vivo and significantly increased peak intracavernous pressure in streptozotocin induced diabetic rats via nitric oxide/intracellular cyclic guanosine monophosphate activation.

CONCLUSIONS

Results show that saRNA mediated iNOS over expression in the penis can restore erectile function in streptozocin diabetic rats via the nitric oxide-cyclic guanosine monophosphate pathway.

摘要

目的

启动子靶向的 saRNA 介导序列特异性基因表达上调。我们探索了通过 RNA 激活介导 iNOS 基因激活改善糖尿病大鼠模型勃起功能的治疗效果。

材料与方法

将针对 iNOS 启动子的最佳 saRNA 序列克隆到腺病毒载体中,得到 AdU6/shiNOS 和 AdU6/shControl。使用相应的病毒转染培养的大鼠海绵体平滑肌细胞。建立链脲佐菌素诱导的糖尿病模型,用于测试 iNOS saRNA 病毒经海绵体内给药对勃起功能的影响。通过逆转录-聚合酶链反应和 Western blot 评估治疗大鼠海绵体平滑肌细胞或阴茎组织中的 iNOS 表达。通过酶联免疫吸附试验分析环鸟苷单磷酸。在注射后第 1、3、5、7、10 和 14 天,使用数据采集系统测量对海绵体神经刺激的海绵体内压力。

结果

腺病毒介导的 iNOS saRNA 表达导致海绵体平滑肌细胞中 iNOS 的持续上调。AdU6/shiNOS 的海绵体内注射在体内激活了 iNOS 表达,并通过一氧化氮/细胞内环鸟苷单磷酸激活显著增加了链脲佐菌素诱导的糖尿病大鼠的峰值海绵体内压力。

结论

结果表明,saRNA 介导的阴茎内 iNOS 过表达可以通过一氧化氮-环鸟苷单磷酸途径恢复链脲佐菌素糖尿病大鼠的勃起功能。

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