Chiu J-H, Chen K-K, Chien T-M, Chiou W-F, Chen C-C, Wang J-Y, Lui W-Y, Wu C-W
Institute of Traditional Medicine, School of Medicine, National Yang-Ming University, Peitou, Taipei, Taiwan, ROC.
Int J Impot Res. 2006 Jul-Aug;18(4):335-42. doi: 10.1038/sj.ijir.3901437. Epub 2006 Jan 5.
Epimedium brevicornum Maxim (EbM) has been reputed to have sexual stimulation effects on males. The study is aimed to test the hypothesis that EbM extracts relaxed the corpus cavernosum (CC) smooth muscle through activation of multitargets on nitric oxide (NO)/cyclic guanosine monophosphate (cGMP) signaling pathway. Water extract of EbM and its subfraction (EP-20) were prepared and standardized by high-performance liquid chromatography. Isolated rabbit CC strips were mounted in organ baths and isometric tension was recorded in the presence or absence of specific inhibitors related to NO/cGMP signaling such as L-N(G)-nitro-arginine methyl ester (L-NAME), 1H-[1,2,4]oxadiazolo-[4,3-a] quinoxalin-1-one (ODQ, a guanylyl cyclase inhibitor) or phosphodiesterase 5 (PDE 5) inhibitors. cGMP level was determined in EP-20-treated CC strips. The results showed that EP-20 enriched the content of L-arginine in the process of purification and relaxed the CC smooth muscle precontracted with phenylephrine (PE, 1 microM) in a concentration-dependent manner. Besides, EP-20 increased the amount of cGMP production in rabbit CC tissues. Coincubation with EP-20 and L-NAME or ODQ significantly decreased EP-20-induced relaxation whereas EP-20 increased sodium nitroprusside-induced relaxation in PE-precontracted CC strips. Besides, EP-20 increased the potency and the duration of the relaxation effects caused by electrical field stimulation. Finally, EP-20 could potentiate PDE 5 inhibitors in relaxation of PE-precontracted CC strips. We concluded that extract of EbM relax the CC smooth muscle through multitargets in NO/cGMP/PDE 5 pathway and might bring into perspective the treatment strategy for those patients with erectile dysfunction.
淫羊藿一直被认为对男性有性刺激作用。本研究旨在验证以下假设:淫羊藿提取物通过激活一氧化氮(NO)/环磷酸鸟苷(cGMP)信号通路的多靶点来舒张海绵体(CC)平滑肌。制备了淫羊藿水提取物及其亚组分(EP - 20),并通过高效液相色谱进行标准化。将分离的兔CC条带安装在器官浴槽中,在存在或不存在与NO/cGMP信号相关的特异性抑制剂(如L - N(G)-硝基精氨酸甲酯(L - NAME)、1H - [1,2,4]恶二唑并[4,3 - a]喹喔啉 - 1 - 酮(ODQ,一种鸟苷酸环化酶抑制剂)或磷酸二酯酶5(PDE 5)抑制剂)的情况下记录等长张力。测定了EP - 20处理的CC条带中的cGMP水平。结果表明,EP - 20在纯化过程中富集了L - 精氨酸的含量,并以浓度依赖的方式舒张了用去氧肾上腺素(PE,1 microM)预收缩的CC平滑肌。此外,EP - 20增加了兔CC组织中cGMP的生成量。与EP - 20和L - NAME或ODQ共同孵育显著降低了EP - 20诱导的舒张作用,而在PE预收缩的CC条带中,EP - 20增加了硝普钠诱导的舒张作用。此外,EP - 20增加了电场刺激引起的舒张作用的效力和持续时间。最后,EP - 20可增强PDE 5抑制剂对PE预收缩的CC条带的舒张作用。我们得出结论,淫羊藿提取物通过NO/cGMP/PDE 5途径的多靶点舒张CC平滑肌,这可能为勃起功能障碍患者带来治疗策略的新视角。