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首页> 外文期刊>Urology >Combination of phentolamine and L-arginine or sildenafil synergistically improves neurogenic relaxation of rabbit corpus cavernosum smooth muscle.
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Combination of phentolamine and L-arginine or sildenafil synergistically improves neurogenic relaxation of rabbit corpus cavernosum smooth muscle.

机译:酚妥拉明与L-精氨酸或西地那非的组合可协同改善兔海绵体平滑肌的神经源性松弛。

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OBJECTIVES: To analyze the effects of combining an alpha-adrenergic receptor antagonist, phentolamine, with an enhancer of the nitric oxide/cyclic guanosine monophosphate pathway (L-arginine or sildenafil) on neurogenic relaxations of rabbit corpus cavernosum (RCC). METHODS: Studies were performed on isolated RCC tissue in organ chambers. Transmural electrical stimulation (TES) was applied at increasing frequencies (0.5 to 6 Hz) on endothelin-contracted RCC strips, and the responses were evaluated. RESULTS: The activation of alpha(2)-adrenergic receptors with UK 14304 (0.3 microM) significantly inhibited the relaxation induced by TES in RCC strips in which adrenergic neurotransmission was blocked with guanethidine (10 microM). The relaxant responses produced by TES application on RCC strips without guanethidine were not significantly affected by the treatment with L-arginine or sildenafil but were significantly augmented by phentolamine (2.7-fold increase in maximum relaxation). Furthermore, the combinations of phentolamine with L-arginine or sildenafil markedly increased the relaxations evoked by the application of TES in RCC tissue, significantly more than those obtained in the presence of phentolamine alone (4.5 or 4.7-fold increase of maximum relaxation, respectively). CONCLUSIONS: Our results demonstrated a synergistic interaction between the alpha-adrenergic blockade and the potentiation of the nitric oxide/cyclic guanosine monophosphate pathway to increase neurogenic relaxation of trabecular smooth muscle relaxation. This fact suggests that the combination of alpha-adrenergic receptor blockade with L-arginine or sildenafil could represent a therapeutic advantage in the treatment of erectile dysfunction.
机译:目的:分析将α-肾上腺素能受体拮抗剂酚妥拉明与一氧化氮/环鸟苷单磷酸途径(L-精氨酸或西地那非)的增强剂联合使用对兔海绵体(RCC)神经源性松弛的影响。方法:对器官腔中孤立的RCC组织进行了研究。在内皮素收缩的RCC试纸上以增加的频率(0.5至6 Hz)施加经壁电刺激(TES),并评估反应。结果:UK 14304(0.3 microM)激活α(2)-肾上腺素受体可显着抑制TES在RCC条中的诱导的松弛,RCC条中肾上腺素能神经递质被胍乙啶(10 microM)阻断。在没有胍乙啶的RCC试纸上,TES施加的松弛反应不受L-精氨酸或西地那非处理的影响显着,但酚妥拉明显着增强(最大松弛度增加2.7倍)。此外,酚妥拉明与L-精氨酸或西地那非的组合显着增加了TES在RCC组织中引起的舒张作用,明显高于单独存在酚妥拉明存在时的舒张作用(最大舒张作用分别增加4.5或4.7倍) 。结论:我们的结果证明了α-肾上腺素能阻滞与一氧化氮/环鸟苷一磷酸途径的增强作用之间的协同相互作用,以增加小梁平滑肌松弛的神经源性松弛。这个事实表明,α-肾上腺素能受体阻滞剂与L-精氨酸或西地那非的组合可能代表治疗勃起功能障碍的治疗优势。

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