单磷酸腺苷和三磷酸腺苷联合l -精氨酸对雄性兔海绵体组织的影响

V. Hupertan, Y. Neuzillet, O. Stücker, C. Pons, E. Leammel, T. Lebret
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引用次数: 17

摘要

嘌呤,特别是单磷酸腺苷(AMP)和三磷酸腺苷(ATP)对狗、兔和人海绵体的平滑肌细胞有很强的松弛作用,其程度与一氧化氮(NO)大致相同。然而,嘌呤被认为是勃起功能的调节剂而不是关键介质。这表明嘌呤与NO供体联合使用可有效治疗某些特定的勃起障碍。在兔海肌体模型上,研究了NO合成酶天然底物l-精氨酸(Arg)联合嘌呤核苷酸(AMP、ATP)诱导的松弛作用,以确定这些物质是否能相互增强作用。当苯肾上腺素诱导预收缩时,AMP单独诱导的CC松弛率为43%,ATP单独诱导的CC松弛率为26%。Arg诱导的弛豫率较低(5.10−4 m为8%,AMP 5.10−4 m为25%,ATP 5.10−4 m为15%)。NO合成酶抑制剂n-硝基-l-精氨酸没有改变AMP引起的松弛作用,提示该核苷酸的作用机制不涉及NO途径。5.10−4 m的Arg与5.10−4 ~ 10−3 m范围内不同剂量的AMP或ATP联合使用可显著增强松弛反应,分别达到62%和80%,产生协同效应。目前的数据表明,“NO供体”与“腺苷供体”联合可能是一种有效的治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Effects of nucleotides adenosine monophosphate and adenosine triphosphate in combination with L-arginine on male rabbit corpus cavernosum tissue

Effects of nucleotides adenosine monophosphate and adenosine triphosphate in combination with L-arginine on male rabbit corpus cavernosum tissue

Purines and more specifically adenosine monophosphate (AMP) and adenosine triphosphate (ATP) have a strong relaxant effect on smooth muscle cells of the dog, rabbit and human corpus cavernosum, to approximately the same degree as nitric oxide (NO). However, purines are considered as modulators of erectile function rather than key mediators. This suggests that the use of purines combined with NO donors could be effective to treat some specific erectile disorders. The relaxation induced by the combination of l-arginine (Arg), a natural substrate for NO synthase, was assessed with a purine-nucleotide (AMP, ATP) on a rabbit corpus cavernosum model, to determine if these substances could potentiate each other’s effect. When a pre-contraction was induced by phenylephrine, AMP alone induced a 43% CC relaxation rate and ATP alone a 26% rate. The relaxation rate induced by Arg was lower in comparison (8% at 5.10−4m vs. 25% at AMP 5.10−4 m and 15% at ATP 5.10−4 m). NO synthase inhibitor n-nitro-l-arginine did not modify the relaxing effect provoked by AMP suggesting that the mechanism of action of this nucleotide does not involve the NO pathway. The combination of Arg at 5.10−4 m with either AMP or ATP at different doses ranging from 5.10−4 to 10−3m significantly enhanced the relaxing response reaching rates of 62 and 80% respectively, leading to a synergistic effect. The present data indicate that a ‘NO donor’ combined with an ‘adenosine donor’ could be an effective therapeutic approach.

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