Department of Urology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, PRC, China.
Int J Impot Res. 2010 Mar-Apr;22(2):120-6. doi: 10.1038/ijir.2009.53. Epub 2009 Nov 26.
It has been shown that there are many Chinese traditional herbals that can enhance sexual activity. Chuanxiongzine is a vasoactive ingredient that has been isolated and purified from Ligusticum chuanxiong Hort. In previous studies, it has been found that chuanxiongzine was effective in relaxing rabbit corpus cavernosum smooth muscle. We determined the effects of chuanxiongzine on relaxation of isolated corpus cavernosum strips in vitro and on increase of intracavernous pressure (ICP) in vivo in rabbits. Chuanxiongzine caused a concentration-dependent relaxation of phenylephrine precontracted isolated corpus cavernosum strips (EC(50) 1.58 x 10(-4) mol l(-1)), which were endothelium independent and NO independent. However, the guanylyl cyclase inhibitor 1-H-[1,2,4] oxadiazolo [4,3-a] quinoxalin-1-one significantly shifted the chuanxiongzine concentration-response relationship to the right. Although there was no significant difference in the level of cyclic guanosine monophosphate (cGMP) and cyclic adenosine monophosphate (cAMP) in isolated corpus cavernosum strips treated with chuanxiongzine or vehicle, chuanxiongzine caused a significant rise in the level of cGMP and cAMP in isolated corpus cavernosum strips pretreated with the activator of adenylyl cyclase forskolin and the source of NO sodium nitroprusside. In an in vivo study, chuanxiongzine dose-dependently raised ICP after the intracavernous injection of its cumulative doses (0.5, 1, 2 and 5 mg kg(-1)). The ICP increased from baseline to 19.1+/-3.7, 24.8+/-2.1, 30.2+/-4.8 and 39.7+/-6.1 mm Hg, respectively, and the duration of tumescence ranged from 8.5+/-2.8 to 22.9+/-7.3 min. Our results show that chuanxiongzine can relax isolated corpus cavernosum strips of rabbits in vitro and increase ICP of rabbits in vivo, which is neither endothelium dependent nor NO dependent, but may be partly mediated by the inhibition of cAMP phosphodiesterase or cGMP phosphodiesterase.
已有研究表明,许多中药具有增强性活动的功效。川芎嗪是从川芎中分离提纯得到的一种血管活性成分,先前的研究发现,川芎嗪能有效舒张兔阴茎海绵体平滑肌。本研究旨在观察川芎嗪对离体兔阴茎海绵体条的舒张作用及其对兔阴茎海绵体内压(ICP)的影响。结果表明,川芎嗪能浓度依赖性舒张去甲肾上腺素预收缩的离体兔阴茎海绵体条(EC50 为 1.58×10(-4)mol/L),这种舒张作用具有非内皮依赖性和非一氧化氮(NO)依赖性,而鸟苷酸环化酶抑制剂 1-H-[1,2,4]恶二唑[4,3-a]喹喔啉-1-酮能显著右移川芎嗪的量效曲线。尽管川芎嗪处理或对照处理的离体阴茎海绵体条中环磷酸鸟苷(cGMP)和环磷酸腺苷(cAMP)水平无显著差异,但预先用激活型腺昔酸环化酶佛司可林和 NO 供体硝普钠处理的离体阴茎海绵体条中,cGMP 和 cAMP 水平显著升高。在体内研究中,静脉注射累积剂量的川芎嗪(0.5、1、2 和 5mg/kg)后,ICP 呈剂量依赖性升高。ICP 从基础值分别升高至 19.1+/-3.7、24.8+/-2.1、30.2+/-4.8 和 39.7+/-6.1mmHg,勃起持续时间分别为 8.5+/-2.8、22.9+/-7.3min。结果表明,川芎嗪既能体外舒张兔离体阴茎海绵体条,又能增加兔体内 ICP,这种作用既不依赖于内皮,也不依赖于 NO,而是可能部分通过抑制 cAMP 磷酸二酯酶或 cGMP 磷酸二酯酶而介导。