Department of Urology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul 135-710, Korea.
Asian J Androl. 2011 Sep;13(5):742-6. doi: 10.1038/aja.2010.184. Epub 2011 Apr 11.
In this study, we investigated the effects of a combination of Ginkgo biloba extracts (GBE) and phosphodiesterase type 5 (PDE-5) inhibitors on the muscular tone of the corpus cavernosum and potassium channel activity of corporal smooth muscle cells. Strips of corpus cavernosum from male New Zealand white rabbits were mounted in organ baths for isometric tension studies. After contraction with 1×10⁻⁵ mol l⁻¹ norepinephrine, GBE (0.01-1 mg ml⁻¹) and mirodenafil (0.01-100 nmol l⁻¹) were added together into the organ bath. In electrophysiological studies, whole-cell currents were recorded by the conventional patch-clamp technique in cultured smooth muscle cells of the human corpus cavernosum. The corpus cavernosum was relaxed in response to GBE in a dose-dependent manner (from 0.64%±8.35% at 0.01 mg ml⁻¹ to 52.28% ± 11.42% at 1 mg ml⁻¹). After pre-treatment with 0.03 mg ml⁻¹ of GBE, the relaxant effects of mirodenafil were increased at all concentrations. After tetraethylammonium (TEA) (1 mmol l⁻¹) administration, the increased effects were inhibited (P<0.01). Extracellular administration of GBE increased the whole-cell K(+) outward currents in a dose-dependent fashion. The increase of the outward current was inhibited by 1 mmol l⁻¹ TEA. These results suggest that GBE could increase the relaxant potency of mirodenafil even at a minimally effective dose. The K(+) flow through potassium channels might be one of the mechanisms involved in this synergistic relaxation.
在这项研究中,我们研究了银杏叶提取物(GBE)和磷酸二酯酶 5(PDE-5)抑制剂联合对海绵体平滑肌张力和细胞内钾通道活性的影响。新西兰白兔阴茎海绵体组织条置于离体肌槽中进行等长张力研究。在 1×10⁻⁵ mol l⁻¹去甲肾上腺素诱导收缩后,将 GBE(0.01-1 mg ml⁻¹)和米罗昔酚(0.01-100 nmol l⁻¹)联合加入到器官浴中。在电生理研究中,通过常规膜片钳技术记录培养的人海绵体平滑肌细胞的全细胞电流。GBE 呈浓度依赖性地舒张阴茎海绵体(从 0.01 mg ml⁻¹时的 0.64%±8.35%增加至 1 mg ml⁻¹时的 52.28%±11.42%)。用 0.03 mg ml⁻¹的 GBE 预处理后,米罗昔酚在所有浓度下的舒张作用均增强。加入 1 mmol l⁻¹四乙铵(TEA)后,这种增强作用被抑制(P<0.01)。GBE 细胞外给药可剂量依赖性地增加全细胞外向 K⁺电流。1 mmol l⁻¹ TEA 抑制外向电流的增加。这些结果表明,GBE 甚至在最小有效剂量下也能增强米罗昔酚的舒张作用。钾通道的钾流可能是这种协同舒张作用的机制之一。