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五味子酯甲在小鼠皮肤两阶段致癌过程中抑制12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯的促癌作用。

Gomisin A inhibits tumor promotion by 12-O-tetradecanoylphorbol-13-acetate in two-stage carcinogenesis in mouse skin.

作者信息

Yasukawa K, Ikeya Y, Mitsuhashi H, Iwasaki M, Aburada M, Nakagawa S, Takeuchi M, Takido M

机构信息

College of Pharmacy, Nihon University, Chiba, Japan.

出版信息

Oncology. 1992;49(1):68-71. doi: 10.1159/000227014.

Abstract

Gomisin A, isolated from the fruits of Schisandra chinensis, is one of the dibenzocyclooctadiene lignans. Application of 12-O-tetradecanoylphorbol-13-acetate (TPA, 1 microgram/ear), a tumor-promoting agent, to the ears of mice induces inflammation. Among seven dibenzocyclooctadiene lignans assayed, gomisin A, gomisin J, and wuweizisu C inhibited the inflammatory activity induced by TPA in mice. The ED50 of these compounds for TPA-induced inflammation was 1.4-4.4 mumol. Gomisin A, with an ED50 of 1.4 mumol, showed the strongest inhibitory effect. Furthermore, at 5 mumol/mouse, it markedly suppressed the promotion effect of TPA (2.5 micrograms/mouse) on skin tumor formation in mice following initiation with 7,12-dimethylbenz[a]anthracene (50 micrograms/mouse). It is assumed that the inhibition of tumor promotion by gomisin A is due to its anti-inflammatory activity.

摘要

从五味子果实中分离得到的戈米辛A是二苯并环辛二烯木脂素之一。将肿瘤促进剂12 - O - 十四烷酰佛波醇-13 - 乙酸酯(TPA,1微克/耳)涂抹于小鼠耳部会诱发炎症。在所检测的七种二苯并环辛二烯木脂素中,戈米辛A、戈米辛J和五味子素C抑制了TPA在小鼠中诱导的炎症活性。这些化合物对TPA诱导炎症的半数有效量(ED50)为1.4 - 4.4微摩尔。戈米辛A的ED50为1.4微摩尔,显示出最强的抑制作用。此外,在5微摩尔/小鼠的剂量下,它显著抑制了TPA(2.5微克/小鼠)对经7,12 - 二甲基苯并[a]蒽(50微克/小鼠)启动后的小鼠皮肤肿瘤形成的促进作用。据推测,戈米辛A对肿瘤促进的抑制作用归因于其抗炎活性。

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