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芍药苷、甘草酸和甘草次酸对卵巢雄激素生成的影响。

Effect of paeoniflorin, glycyrrhizin and glycyrrhetic acid on ovarian androgen production.

作者信息

Takeuchi T, Nishii O, Okamura T, Yaginuma T

机构信息

Department of Obstetrics and Gynecology, University of Tokyo, Japan.

出版信息

Am J Chin Med. 1991;19(1):73-8. doi: 10.1142/S0192415X91000119.

Abstract

We have shown that traditional herbal medicine, Shakuyaku-Kanzo-To consisted of Shakuyaku and Kanzo decreased serum testosterone levels in woman and rat. Therefore, paeoniflorin and glycyrrhizin, a main component of Shakuyaku and Kanzo, respectively, and glycyrrhetic acid, a metabolite of glycyrrhizin in vivo, were investigated for the steroid production in the rat ovary on the morning of proestrus. The homogenized tissues of one ovary were incubated in the Dulbecco's modified Eagle medium (pH 7.5) with 100 micrograms/ml of paeoniflorin, glycyrrhetic acid and glycyrrhizin and the medium only (the control) at 37 degrees C for 270 min. After the centrifugation, the concentrations of delta 4-androstenedione, testosterone and estradiol in the supernatants were determined by RIA. The production of the hormones expressed by [concentration x supernatant volume/weight of the ovary] was compared to the control. Paeoniflorin, glycyrrhetic acid and glycyrrhizin decreased significantly the testosterone production but did not change that of delta 4-androstenedione and estradiol. Testosterone/delta 4-androstenedione production ratio was lowered significantly by paeoniflorin, glycyrrhetic acid and glycyrrhizin. Estradiol/testosterone production ratio was increased significantly by glycyrrhetic acid and not changed by paeoniflorin and glycyrrhizin. These results suggest that paeoniflorin, glycyrrhetic acid and glycyrrhizin affect the conversion between delta 4-androstenedione and testosterone to inhibit testosterone synthesis and stimulate the aromatase activity to promote estradiol synthesis by the direct action on the rat proestrous ovary.

摘要

我们已经证明,由芍药和甘草组成的传统草药方剂芍药甘草汤可降低女性和大鼠的血清睾酮水平。因此,分别研究了芍药苷和甘草甜素(芍药和甘草的主要成分)以及甘草次酸(甘草甜素在体内的代谢产物)对动情前期大鼠卵巢类固醇生成的影响。将一个卵巢的匀浆组织在含有100微克/毫升芍药苷、甘草次酸和甘草甜素的杜氏改良 Eagle 培养基(pH 7.5)中,以及仅在培养基(对照)中,于37℃孵育270分钟。离心后,通过放射免疫分析法测定上清液中δ4-雄烯二酮、睾酮和雌二醇的浓度。将激素生成量(以[浓度×上清液体积/卵巢重量]表示)与对照进行比较。芍药苷、甘草次酸和甘草甜素显著降低了睾酮的生成,但对δ4-雄烯二酮和雌二醇的生成没有影响。芍药苷、甘草次酸和甘草甜素显著降低了睾酮/δ4-雄烯二酮生成比率。甘草次酸显著提高了雌二醇/睾酮生成比率,而芍药苷和甘草甜素对此没有影响。这些结果表明,芍药苷、甘草次酸和甘草甜素通过直接作用于大鼠动情前期卵巢,影响δ4-雄烯二酮和睾酮之间的转化,从而抑制睾酮合成,并刺激芳香化酶活性以促进雌二醇合成。

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