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锌在细胞内氧化还原平衡中的作用。

Involvement of zinc in intracellular oxidant/antioxidant balance.

作者信息

Parat M O, Richard M J, Béani J C, Favier A

机构信息

Laboratoire de Biochimie C, Groupe de Recherche sur les Pathologies Oxydatives, CHU Albert Michallon, Grenoble, France.

出版信息

Biol Trace Elem Res. 1997 Dec;60(3):187-204. doi: 10.1007/BF02784439.

Abstract

The effect of zinc (Zn) on cellular oxidative metabolism is complex and could be explained by multiple complementary interactions. In this study, we evaluated the impact of Zn on the pro-oxidant/antioxidant balance of HaCaT keratinocytes. Cells were submitted to a diffusible metal chelator able to induce intracellular Zn deprivation, TPEN, in combination or not with Zn chloride (ZnCl2), in the culture medium. The intracellular amount of Zn, copper (Cu), and iron (Fe) was determined, as well as CuZnSOD and MnSOD activities and glutathione reserves. The consequence of the modulation of Zn concentration on lipid peroxidation was also evaluated. TPEN induced a significant dose-dependent decrease in intracellular Zn and Cu (from 394-181 and 43-21 microg/g protein, respectively, after 6 h of TPEN 50 microM). No significant change in intracellular Fe concentration was found following TPEN exposure. The SOD activities were unchanged after 6 h of TPEN 50 microM application, either CuZnSOD or MnSOD. Cells exposure to TPEN induced a deep time- and dose-dependent decrease in their glutathione content (from 65-8 microM/g protein after 6 h of TPEN 50 microM), and a concomitant increase in glutathione in the cell-culture supernatants. No significant change in lipid peroxidation products was detected.

摘要

锌(Zn)对细胞氧化代谢的影响较为复杂,可通过多种互补性相互作用来解释。在本研究中,我们评估了锌对HaCaT角质形成细胞促氧化剂/抗氧化剂平衡的影响。将细胞置于一种能够诱导细胞内锌缺乏的可扩散金属螯合剂三-(2-吡啶甲基)胺(TPEN)中,在培养基中单独使用或与氯化锌(ZnCl2)联合使用。测定细胞内锌、铜(Cu)和铁(Fe)的含量,以及铜锌超氧化物歧化酶(CuZnSOD)和锰超氧化物歧化酶(MnSOD)的活性和谷胱甘肽储备。还评估了锌浓度调节对脂质过氧化的影响。TPEN诱导细胞内锌和铜显著的剂量依赖性降低(在50μM TPEN处理6小时后,分别从394 - 181和43 - 21μg/g蛋白质下降)。TPEN处理后细胞内铁浓度未发现显著变化。在应用50μM TPEN 6小时后,CuZnSOD或MnSOD的超氧化物歧化酶活性均未改变。细胞暴露于TPEN会导致其谷胱甘肽含量出现深度的时间和剂量依赖性降低(在50μM TPEN处理6小时后,从65 - 8μg/g蛋白质下降),同时细胞培养上清液中的谷胱甘肽增加。未检测到脂质过氧化产物有显著变化。

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