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淫羊藿苷对体外磷酸二酯酶-5活性及海绵体平滑肌细胞中环磷酸鸟苷水平的影响。

Effects of icariin on phosphodiesterase-5 activity in vitro and cyclic guanosine monophosphate level in cavernous smooth muscle cells.

作者信息

Ning Hongxiu, Xin Zhong-Cheng, Lin Guiting, Banie Lia, Lue Tom F, Lin Ching-Shwun

机构信息

Knuppe Molecular Urology Laboratory, Department of Urology, University of California, San Francisco, School of Medicine, San Francisco, California 94115, USA.

出版信息

Urology. 2006 Dec;68(6):1350-4. doi: 10.1016/j.urology.2006.09.031.

Abstract

OBJECTIVES

To investigate the effect of icariin on the cyclic guanosine monophosphate (cGMP)-hydrolytic activity of phosphodiesterase-5 (PDE5) isoforms and the cGMP levels in cavernous smooth muscle cells treated with sodium nitroprusside (SNP).

METHODS

PDE5 isoforms (PDE5A1, A2, and A3) were isolated from sf9 insect cells infected with baculoviruses carrying PDE5 isoform cDNA. Icariin was isolated from Epimedii herba. Varying amounts (10(-6) to 10(-11) M) of icariin or zaprinast were added to reaction mixtures containing PDE5 isoforms and cGMP. The inhibitory effects of icariin and zaprinast were analyzed by GraphPad Software and are expressed as concentration that inhibits 50% (IC50) values. Cavernous smooth muscle cells were isolated from 3-month-old rats, treated with icariin (100 and 200 microM) or zaprinast (200 microM) for 15 minutes, and then with 10 microM SNP for 30, 60, 120, 240, and 360 minutes. The cells were then analyzed for the cGMP concentration using an enzyme immunoassay system.

RESULTS

Icariin inhibited PDE5A1, A2, and A3 with an IC50 value of 1.0, 0.75, and 1.1 microM, respectively. The corresponding IC50 values for zaprinast were 0.33, 0.23, and 0.32 microM. Icariin consistently outperformed the control (SNP-only treatment) in maintaining greater cGMP levels, particularly at the greater concentration of 200 microM. In contrast, zaprinast at 200 microM did better than the control only at 60 and 360 minutes.

CONCLUSIONS

Icariin was inhibitory to all three PDE5 isoforms with similar IC50 values, which were approximately three times greater than those for zaprinast. Icariin was able to enhance cGMP levels in SNP-treated cavernous smooth muscle cells.

摘要

目的

研究淫羊藿苷对磷酸二酯酶5(PDE5)亚型的环磷酸鸟苷(cGMP)水解活性以及对硝普钠(SNP)处理的海绵体平滑肌细胞中cGMP水平的影响。

方法

从感染携带PDE5亚型cDNA的杆状病毒的sf9昆虫细胞中分离出PDE5亚型(PDE5A1、A2和A3)。淫羊藿苷从淫羊藿中分离得到。将不同量(10⁻⁶至10⁻¹¹M)的淫羊藿苷或扎普司特添加到含有PDE5亚型和cGMP的反应混合物中。淫羊藿苷和扎普司特的抑制作用通过GraphPad软件进行分析,并表示为抑制50%(IC50)值的浓度。从3月龄大鼠中分离出海绵体平滑肌细胞,用淫羊藿苷(100和200μM)或扎普司特(200μM)处理15分钟,然后用10μM SNP处理30、60、120、240和360分钟。然后使用酶免疫分析系统分析细胞中的cGMP浓度。

结果

淫羊藿苷对PDE5A1、A2和A3的IC50值分别为1.0、0.75和1.1μM。扎普司特的相应IC50值分别为0.33、0.23和0.32μM。在维持更高的cGMP水平方面,淫羊藿苷始终优于对照组(仅SNP处理),尤其是在200μM的更高浓度下。相比之下,200μM的扎普司特仅在60和360分钟时比对照组表现更好。

结论

淫羊藿苷对所有三种PDE5亚型均有抑制作用,IC50值相似,约为扎普司特的三倍。淫羊藿苷能够提高SNP处理的海绵体平滑肌细胞中的cGMP水平。

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