Relaxation Effects of Epimedium Koreanum Nakai in Isolated Rabbit Corpus Cavernosum Smooth Muscle

Tae Yeon Kim
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引用次数: 0

Abstract

This study aimed to investigate the relaxation effects and its underlying mechanisms of Epimedium koreanum Nakai(EK) in phenylephrine(PE) treated isolated rabbit corpus cavernosum smooth muscle. The dose-dependent relaxation responses of phenylephrine(PE, 1×10 M)-precontracted strips to EK at 0.01-3.0 mg/ml were measured and also observed after endothelial denudation using organ bath. To analyze the underlying mechanisms of EK-induced relaxation, Nω-nitro-L-arginine(L-NNA), methylene blue(MB), tetraethylammonium chloride(TEA), indomethacin(IM) were pretreated before EK extract infused into precontracted strips induced by PE. To investigate cytotoxic activity and nitric oxide(NO) concentration of EK extract on EA.hy926 cells, mitochondrial dehydrogenase activity(MTT) assay and nitric oxide detection kit were used. The cavernous strips were significantly relaxed by EK extract at 0.3 mg/ml, 1.0 mg/ml, 3.0 mg/ml and the relaxation responses of PE-precontracted strips denuded endothelium also inhibited in comparison with intact endothelium. The pretreatment of L-NNA, MB, TEA reduced EK extract-induced endothelium-dependent relaxation, but the pretreatment of IM didn't affect EK extract-induced endothelium-dependent relaxation. When EK extract was applicated on EA.hy926 cells, the NO concentration was increased. Our findings have shown that EK extract exerts a relaxing effect on corpus cavernosum in part by suppressing influx of extracellular Ca through activating the NO-cGMP system. 
韩国淫羊藿对兔离体海绵体平滑肌的松弛作用
本研究旨在探讨韩国淫羊藿(Epimedium koreanum Nakai, EK)对苯肾上腺素(PE)处理兔离体海绵体平滑肌的松弛作用及其机制。测定了苯肾上腺素(PE, 1×10 M)预收缩条在0.01 ~ 3.0 mg/ml浓度下对EK的剂量依赖性松弛反应,并在内皮剥脱后用器官浴法观察。为了分析EK诱导松弛的机制,将ω-硝基- l -精氨酸(L-NNA)、亚甲基蓝(MB)、四乙基氯化铵(TEA)、吲哚美辛(IM)预处理后注入PE诱导的预收缩条中。采用线粒体脱氢酶活性(MTT)法和一氧化氮(NO)检测试剂盒研究EK提取物对EA.hy926细胞的细胞毒活性和一氧化氮(NO)浓度。0.3 mg/ml、1.0 mg/ml、3.0 mg/ml的EK提取物均能使海绵状条带松弛,剥去内皮后pe预收缩条带的松弛反应也受到抑制。L-NNA、MB、TEA预处理可降低EK提取物诱导的内皮依赖性舒张,而IM预处理对EK提取物诱导的内皮依赖性舒张无影响。当EK提取物作用于EA.hy926细胞时,一氧化氮浓度升高。我们的研究结果表明,EK提取物对海绵体的松弛作用部分是通过激活NO-cGMP系统来抑制细胞外Ca的流入。
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