Keochanthala-Bounthanh C, Haag-Berrurier M, Beck J P, Anton R
Laboratoire de Pharmacognosie, Faculté de Pharmacie, Université Louis Pasteur, 1 Illkirch, France.
Planta Med. 1990 Apr;56(2):190-2. doi: 10.1055/s-2006-960923.
The antagonistic activity of various thiol compounds versus the cytotoxic effects of valtrate and didrovaltrate has been evaluated on cultured hepatoma cells. Compounds with free SH groups like cysteine, mercaptoethanol, dithioerythritol, and glutathione were able to suppress the cytotoxicity of the valepotriates in a dose-dependent way, whereas compounds with blocked SH groups did not antagonize these toxic effects. The possible interactions between the valepotriates and thiol compounds are discussed.
已在培养的肝癌细胞上评估了各种硫醇化合物对缬草酸盐和二氢缬草酸盐细胞毒性作用的拮抗活性。具有游离巯基的化合物,如半胱氨酸、巯基乙醇、二硫苏糖醇和谷胱甘肽,能够以剂量依赖的方式抑制缬草三酯的细胞毒性,而巯基被封闭的化合物则不能拮抗这些毒性作用。本文讨论了缬草三酯与硫醇化合物之间可能的相互作用。