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糖尿病大鼠海绵体组织中 SK3 和 IK1 通道蛋白表达减少。

Reduced expression of SK3 and IK1 channel proteins in the cavernous tissue of diabetic rats.

机构信息

Department of Urology, Nanjing First Hospital Affiliated to Nanjing Medical University, Nanjing, China.

出版信息

Asian J Androl. 2010 Jul;12(4):599-604. doi: 10.1038/aja.2009.97. Epub 2010 Apr 5.

Abstract

The small (SK3) and intermediate (IK1) conductance calcium-activated potassium channels could have key roles in the endothelium-dependent hyperpolarization factor pathway, which is believed to contribute to normal penile erection function. We aimed to investigate the expression of SK3 and IK1 in diabetic rodents. The experimental diabetes model was induced in 8-week-old male Sprague-Dawley rats (250-300 g) by a single administration of streptozotocin. Both the diabetes mellitus group (DM group, n = 20) and the control group (NDM group, n = 10) were injected with a low dose of apomorphine to allow for the measurement and comparison of the corresponding penile erections. The mRNA and protein expression levels of SK3 and IK1 were measured by reverse transcription polymerase chain reaction and western blot, respectively. Erectile function was significantly decreased in the DM group compared with control group (P < 0.05). The mRNA and protein expression levels of SK3 and IK1 were reduced in the cavernous tissue of diabetic rats compared with the control group (P < 0.05). Diabetes inhibits mRNA and protein expression of both SK3 and IK1 in the cavernous tissue of diabetic rats. This could play a key role in the development of erectile dysfunction in diabetic rats.

摘要

小(SK3)和中电导钙激活钾通道(IK1)可能在血管内皮依赖性超极化因子通路中起关键作用,该通路被认为有助于正常的阴茎勃起功能。我们旨在研究 SK3 和 IK1 在糖尿病啮齿动物中的表达。通过单次给予链脲佐菌素诱导 8 周龄雄性 Sprague-Dawley 大鼠(250-300g)建立实验性糖尿病模型。糖尿病组(DM 组,n=20)和对照组(NDM 组,n=10)均给予低剂量阿扑吗啡注射,以允许测量和比较相应的阴茎勃起。通过逆转录聚合酶链反应和 Western blot 分别测量 SK3 和 IK1 的 mRNA 和蛋白表达水平。与对照组相比,DM 组的勃起功能显著降低(P<0.05)。与对照组相比,糖尿病大鼠海绵体组织中 SK3 和 IK1 的 mRNA 和蛋白表达水平降低(P<0.05)。糖尿病抑制糖尿病大鼠海绵体组织中 SK3 和 IK1 的 mRNA 和蛋白表达。这可能在糖尿病大鼠勃起功能障碍的发展中起关键作用。

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