[The effect of Shakuyaku-kanzo-to on prostaglandin production in human uterine myometrium].

Nihon Sanka Fujinka Gakkai zasshi Pub Date : 1996-05-01
T Shibata, T Morimoto, A Suzuki, H Saito, T Yanaihara
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引用次数: 0

Abstract

Shakuyaku-kanzo-to (SK), a Chinese herb medicine consisting of Shakuyaku (Paeoniae Radix) and Kanzo (Glycyrrhizae Radix) has been used for the treatment of dysmenorrhea. It is reported that prostaglandin (PG) production increased during menstruation in uterine myometrium. To know the effect of SK on PG production in the uterine myometrium, the following in vitro study was undertaken. Human uterine myometrium was obtained from patients who underwent hysterectomy. 1. Myometrial cells were cultured and, SK, Shakuyaku (S), Kanzo (K), or glycyrrhetinic acid (GA), which is the major component of K, were added to the culture medium. Concentrations of PGE2, PGF2 alpha, and 6-ketoPGF1 alpha in the medium measured by RIA were significantly decreased by the addition of SK, K or GA but no effect was observed when S. 2. [3H]-arachidonic acid (AA) was added to culture medium and incorporated into the Sn-2 of phospholipids. [3H]-AA release and PG production in the medium were determined. PG were extracted and the radioactivity of PG was measured. The production of PGE2, PGE2 alpha and 6-ketoPGF1 alpha from labeled cells was significantly reduced by the addition of SK, K and GA. 3. Phosphatidylcholine containing [14C]-AA in Sn-2 (150,000 dpm) was incubated with cytosol of uterine myometrium and the amounts of [14C]-AA released were calculated as Phospholipase A2 activity. The amount of [14C]-AA release was inhibited dose-dependently by SK, K and GA. It is the first time that SK has been shown to suppress PG production in the myometrium by inhibiting cPLA2 activity.

[尺骨丸对人子宫肌层前列腺素生成的影响]。
由芍药(芍药根)和甘草根(甘草根)组成的中药“芍药Kanzo -to”(SK)被用于治疗痛经。据报道,月经期间子宫肌层中前列腺素(PG)的产生增加。为了了解SK对子宫肌层PG生成的影响,我们进行了以下的体外研究。人子宫肌层取自子宫切除术患者。1. 培养子宫肌瘤细胞,在培养基中加入SK、Shakuyaku (S)、Kanzo (K)或K的主要成分甘草酸(GA)。在RIA测定的培养基中,添加SK、K或GA显著降低了PGE2、PGF2 α和6-ketoPGF1 α的浓度,但在s。在培养基中加入[3H]-花生四烯酸(AA),加入磷脂的Sn-2中。测定培养基中[3H]-AA的释放量和PG的产量。提取PG,测定PG的放射性。添加SK、K和GA显著降低了标记细胞的PGE2、PGE2 α和6-ketoPGF1 α的生成。3.将Sn-2中含有[14C]-AA的磷脂酰胆碱(150000 dpm)与子宫肌层胞浆孵育,以磷脂酶A2活性计算[14C]-AA的释放量。SK、K和GA对[14C]-AA的释放量有剂量依赖性。这是SK首次通过抑制cPLA2活性来抑制肌层中PG的产生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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