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黄酮类化合物对活性氧诱导的细胞毒性的抑制作用。

Suppression of active oxygen-induced cytotoxicity by flavonoids.

作者信息

Nakayama T, Yamada M, Osawa T, Kawakishi S

机构信息

Department of Food Science and Technology, Nagoya University, Japan.

出版信息

Biochem Pharmacol. 1993 Jan 7;45(1):265-7. doi: 10.1016/0006-2952(93)90402-i.

Abstract

The flavonoids quercetin, kaempferol, catechin and taxifolin suppressed cytotoxicity of active oxygen species (O2- and H2O2) on Chinese hamster V79 cells. Cytotoxicity of active oxygen species was assessed with a colony formation assay. The flavonoids prevented the decrease in the number of colonies caused by H2O2 or O2- at concentrations which were not themselves cytotoxic. There was a very substantial difference in the dose-dependency of the protective effects brought about by quercetin and kaempferol in contrast to catechin and taxifolin. The structure-activity relationship revealed that either the o-dihydroxy structure in the B ring or certain structures in the A and C rings of the flavonoids are necessary for the protective activities.

摘要

黄酮类化合物槲皮素、山奈酚、儿茶素和紫杉叶素可抑制活性氧(超氧阴离子和过氧化氢)对中国仓鼠V79细胞的细胞毒性。采用集落形成试验评估活性氧的细胞毒性。这些黄酮类化合物在自身无细胞毒性的浓度下,可防止由过氧化氢或超氧阴离子导致的集落数量减少。与儿茶素和紫杉叶素相比,槲皮素和山奈酚所产生的保护作用在剂量依赖性上存在非常显著的差异。构效关系表明,黄酮类化合物B环中的邻二羟基结构或A环和C环中的某些结构对于保护活性是必需的。

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