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坦索罗辛与酚妥拉明对阴茎勃起协同作用的比较:体内外研究

Comparison of the synergistic effects of tamsulosin versus phentolamine on penile erection: in vitro and in vivo studies.

作者信息

Kim S C, Seo K K, Lee S K, Song E S, Lee M Y

机构信息

Department of Urology, Chung-Ang University Yongsan Hospital, Seoul, Korea.

出版信息

Urol Res. 1999 Dec;27(6):437-44. doi: 10.1007/s002400050133.

Abstract

In vitro and in vivo studies were performed to determine the potential use of tamsulosin (TAM) versus phentolamine (PHE) for intracavernosal injection (ICI) therapy when mixed with papaverine (PAP) and/or prostagladin E1 (PGE1) or with vasoactive intestinal polypeptide (VIP) for the treatment of erectile dysfunction. We performed isometric tension studies on rabbit (n = 15), dog (n = 5), and human (n = 10) cavernous smooth muscle strips with TAM, PAP, PHE, VIP, PGE1, and the combinations of PAP and PHE; PAP and TAM; VIP and PHE; VIP and TAM; PAP, PGE1 and PHE; and PAP, PGE1 and TAM. TAM-containing trimix (PAP 18.75 mg, PGE1 6.25 micromg, and TAM 0.875 mg per ml) or PHE-containing trimix (PAP, PGE1, and PHE 0.625 mg per ml) were also injected into the cavernous bodies of ten mongrel dogs. Among the single agents, TAM and PGE1 (only in human) had the strongest effect on the relaxation of cavernous muscles in rabbit, dog, and human strips (P<0.05). Relaxation responses to 2- or 3-drug mixtures containing tamsulosin were also significantly better (P<0.05) than PHE-containing ones in rabbit, dog, and human strips. The increase in intracavernosal pressure with a TAM-containing trimix was higher than with a PHE-containing one (0.03 ml; 81.2 vs. 75.8 mm Hg, 0.04 ml; 103.2 vs. 94.3 mm Hg), although not statistically different. The drop in systemic blood pressure was lower after injection of a TAM-containing trimix than a PHE-containing one, although not statistically different. In conclusion, tamsulosin might be a more efficacious and safer agent to use for ICI therapy than phentolamine.

摘要

进行了体外和体内研究,以确定坦索罗辛(TAM)与酚妥拉明(PHE)在与罂粟碱(PAP)和/或前列腺素E1(PGE1)混合用于海绵体内注射(ICI)治疗,或与血管活性肠肽(VIP)混合用于治疗勃起功能障碍时的潜在用途。我们对兔(n = 15)、犬(n = 5)和人(n = 10)的海绵体平滑肌条进行了等长张力研究,使用了TAM、PAP、PHE、VIP、PGE1,以及PAP和PHE的组合;PAP和TAM;VIP和PHE;VIP和TAM;PAP、PGE1和PHE;以及PAP、PGE1和TAM。含坦索罗辛的三联混合液(每毫升含PAP 18.75毫克、PGE1 6.25微克和坦索罗辛0.875毫克)或含酚妥拉明的三联混合液(每毫升含PAP、PGE1和酚妥拉明0.625毫克)也被注射到10只杂种犬的海绵体内。在单一药物中,TAM和PGE1(仅在人体中)对兔、犬和人平滑肌条的海绵体舒张作用最强(P<0.05)。在兔、犬和人平滑肌条中,含坦索罗辛的两药或三药混合物的舒张反应也明显优于含酚妥拉明的混合物(P<0.05)。含坦索罗辛的三联混合液引起的海绵体内压升高高于含酚妥拉明的三联混合液(0.03毫升时分别为81.2与75.8毫米汞柱,0.04毫升时分别为103.2与94.3毫米汞柱),尽管无统计学差异。注射含坦索罗辛的三联混合液后,全身血压下降幅度低于含酚妥拉明的三联混合液,尽管无统计学差异。总之,对于ICI治疗,坦索罗辛可能比酚妥拉明更有效、更安全。

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