Glycyrrhizin inhibits prostaglandin E2 production by activated peritoneal macrophages from rats

Kazuo Ohuchi , Yuko Kamada , Lawrence Levine , Susumu Tsurufuji
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引用次数: 105

Abstract

Glycyrrhizin was found to inhibit prostaglandin E2 production by activated rat peritoneal macrophages. Preincubation of the cells with glycyrrhizin increases its inhibitory effectiveness. Glycyrrhetinic acid, the aglycone of glycyrrhizin, at a dose of 100 μg per ml also inhibited prostaglandin E2 production, but the inhibition was considered to be attributable to a toxic effect on the cells since more than 30% of the cells were detached from the dish during the 8 hr incubation period. In contrast, glycyrrhizin did not detach the cells from the dish at doses up to 3 mg per ml. Release of [3H]arachidonic acid from prelabeled cells was also inhibited by glycyrrhizin. It is likely that anti-inflammatory activity of glycyrrhizin depends at least in part on its inhibitory effect of the production of prostaglandin E2.

甘草酸通过激活大鼠腹腔巨噬细胞抑制前列腺素E2的产生
甘草素可抑制活化大鼠腹腔巨噬细胞产生前列腺素E2。用甘草酸预孵育细胞可提高其抑制效果。甘草酸的苷元甘草酸在100 μg / ml的剂量下也能抑制前列腺素E2的产生,但这种抑制作用被认为是由于对细胞的毒性作用,因为在8小时的孵育期间,超过30%的细胞从培养皿中分离出来。相比之下,甘草酸在高达3mg / ml的剂量下不会使细胞脱离培养皿。预标记细胞中[3H]花生四烯酸的释放也被甘草酸抑制。甘草酸的抗炎活性可能至少部分取决于其抑制前列腺素E2生成的作用。
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