Rho-kinase Inhibition Improves Erectile Function in Aging Male Brown-Norway Rats

Mahadevan Rajasekaran, Steven White, Angelo Baquir, Nathan Wilkes
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引用次数: 75

Abstract

ABSTRACT: Physiological aging is a significant risk factor in the on-set of male erectile dysfunction (ED) and an imbalance in factors that modulate cavernosal smooth-muscle tone may play a role in these altered penile hemodynamic mechanisms. To evaluate the association between aging and male erectile function, we monitored neurogenic erectile response and its correlation to systemic arterial pressure changes in old (21–23 months of age) vs young (6–9 months of age) Brown-Norway (BN) rats. We tested the hypothesis that age-associated ED is due to unregulated vasoconstrictive tone, contributed in part by an increased Rho-kinase activity, and that antagonism of Rho-kinase activity attenuates the age-related decline in male erectile function. We also examined the hypothesis that a combination of Rho-kinase antagonism and phosphodiesterase-5 (PDE-5) inhibition has a synergistic effect in improving the erectile response in these aging animals. Erectile function in old BN rats was evaluated before and after intracavernosal injection of a specific inhibitor of Rho-kinase (Y-27632) alone or in combination with zaprinast, a PDE-5 inhibitor. Erectile capabilities of the young and old BN rat groups were significantly different in corpus cavernosum pressure response after electrical-field stimulation of the major pelvic ganglion. Y-27632 administration attenuated the aging-related changes in male erectile function seen in BN rats. Rho-kinase antagonism and PDE-5 inhibition had a synergistic effect in improving erectile function in old rats. Our data indicate that aging leads to impairment in the neurogenic erectile response in BN rats involving a possible derangement in penile hemodynamic mechanisms of the erectile tissue. Rho-kinase inhibition may be of value in treating age-related ED.

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rho激酶抑制可改善雄性褐挪威大鼠的勃起功能
摘要:生理性衰老是男性勃起功能障碍(ED)发生的重要危险因素,海绵体平滑肌张力调节因子的失衡可能在这些改变的阴茎血流动力学机制中发挥作用。为了评估衰老与雄性勃起功能之间的关系,我们监测了老年(21-23月龄)和年轻(6-9月龄)布朗-挪威(BN)大鼠的神经源性勃起反应及其与全身动脉压变化的关系。我们测试了年龄相关ED是由于血管收缩张力不调节,部分原因是rho激酶活性增加,而rho激酶活性的拮抗作用减弱了年龄相关的男性勃起功能下降的假设。我们还检验了rho激酶拮抗剂和磷酸二酯酶-5 (PDE-5)抑制的组合在改善这些衰老动物的勃起反应方面具有协同作用的假设。老年BN大鼠在海绵内单独注射rho激酶特异性抑制剂(Y-27632)或与PDE-5抑制剂zaprinast联合注射前后评估勃起功能。电场刺激盆腔神经节后,年轻和年老BN大鼠海绵体压力反应的勃起能力有显著差异。Y-27632可减轻BN大鼠雄性勃起功能的衰老相关变化。rho激酶拮抗剂和PDE-5抑制剂在改善老年大鼠勃起功能方面具有协同作用。我们的数据表明,衰老导致BN大鼠的神经源性勃起反应受损,可能涉及勃起组织的阴茎血流动力学机制紊乱。rho激酶抑制可能对治疗年龄相关性ED有价值。
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来源期刊
Journal of andrology
Journal of andrology 医学-男科学
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5.6 months
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