首页> 美国卫生研究院文献>Translational Andrology and Urology >AB085. Improvement of erectile function through combination of anti-fibrotic effect by LIM-kinase 2 inhibitor with suppression of apoptosis and potentiation of endothelial function by type 5 phosphodiesterase inhibitor in a rat model of cavernous nerve injury
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AB085. Improvement of erectile function through combination of anti-fibrotic effect by LIM-kinase 2 inhibitor with suppression of apoptosis and potentiation of endothelial function by type 5 phosphodiesterase inhibitor in a rat model of cavernous nerve injury

机译:AB085。 LIM激酶2抑制剂的抗纤维化作用与5型磷酸二酯酶抑制剂抑制细胞凋亡和增强内皮功能相结合改善大鼠勃起功能

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摘要

BackgroundThe cavernosal apoptosis and fibrosis are considered to be important pathophysiologies of post-radical prostatectomy (RP) erectile dysfunction (ED). Recently, we demonstrated that inhibition of LIMK2 alleviate ED through suppression of cavernosal fibrosis in a rat model of cavernous nerve (CN) injury. Also, some previous studies showed that administration of PDE5 inhibitors improved both cavernosal apoptosis and endothelial dysfunction in a rat model of CN injury, leading to improvement of ED. Thus, the aim of this study was to determine whether combined administration of LIMK2 inhibitors and PDE5 inhibitors could restore erectile function by combination of anti-fibrotic effect with suppression of apoptosis or potentiation of endothelial function in a rat model of CN injury.
机译:背景海绵体细胞凋亡和纤维化被认为是根治性前列腺切除术(RP)勃起功能障碍(ED)后的重要病理生理。最近,我们证明抑制LIMK2通过抑制海绵体神经(CN)大鼠模型中的海绵体纤维化来减轻ED。同样,一些先前的研究表明,在CN损伤的大鼠模型中,施用PDE5抑制剂可改善海绵体凋亡和内皮功能障碍,从而改善ED。因此,本研究的目的是确定在CN损伤的大鼠模型中,LIMK2抑制剂和PDE5抑制剂的联合给药能否通过抗纤维化作用与抑制细胞凋亡或增强内皮功能相结合来恢复勃起功能。

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