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谷胱甘肽和过氧化氢酶在脂多糖激活的肝内皮细胞和库普弗细胞中对过氧化氢解毒的作用。

Role of glutathione and catalase in H2O2 detoxification in LPS-activated hepatic endothelial and Kupffer cells.

作者信息

Spolarics Z, Wu J X

机构信息

Department of Anatomy, Cell Biology, and Injury Sciences, University of Medicine and Dentistry of New Jersey, New Jersey Medical School, Newark 07103, USA.

出版信息

Am J Physiol. 1997 Dec;273(6):G1304-11. doi: 10.1152/ajpgi.1997.273.6.G1304.

Abstract

The present study investigated the effect of lipopolysaccharide (LPS; from Escherichia coli, 2 mg/kg body wt ip) on selected aspects of the antioxidant status in Kupffer and sinusoidal endothelial cells. Cells were isolated 18 h after the injection of saline or LPS. In fresh suspension cultures, cellular reduced glutathione (GSH) and H2O2 were determined by monochlorobimane, and 2',7'-dichlorofluorescein diacetate, respectively, using a fluorescence plate reader. LPS injection increased GSH content two- to threefold in Kupffer cells compared with cells from control rats. Cellular GSH content was higher in endothelial than Kupffer cells. However, LPS did not increase GSH content in endothelial cells. Addition of H2O2 (40-200 microM) to Kupffer or endothelial cells caused a transient decrease in GSH, which was more pronounced in cells from control rats (approximately 45% drop) than in LPS-exposed cells (approximately 25% drop). Depleted GSH levels were accompanied by a proportional increase in cellular H2O2. After inhibition of catalase by 3-amino-1,2,4-triazole, the presence of 0.2 mM H2O2 depleted GSH content by 75% and 40% in Kupffer cells from saline- or LPS-injected rats, respectively. The same treatments caused a similar 50% decrease in both activated and control endothelial cells. LPS decreased catalase activity by 45% in Kupffer cells, whereas it had no effect on catalase in endothelial cells. Glutathione reductase activity was not altered by LPS in either cell type. These data show that in activated Kupffer cells the elevated level of cellular glutathione plays an augmented role in the protection against reactive oxygen species, whereas the contribution of catalase to H2O2 detoxification is attenuated. In LPS-stimulated endothelial and Kupffer cells, the efficient maintenance of GSH is consistent with upregulated production of reducing power through the hexose phosphate shunt observed previously.

摘要

本研究调查了脂多糖(LPS;来自大肠杆菌,2mg/kg体重,腹腔注射)对库普弗细胞和肝血窦内皮细胞抗氧化状态某些方面的影响。在注射生理盐水或LPS后18小时分离细胞。在新鲜悬浮培养物中,分别使用荧光酶标仪,通过单氯双马来酰亚胺和2',7'-二氯荧光素二乙酸酯测定细胞内还原型谷胱甘肽(GSH)和过氧化氢(H2O2)。与对照大鼠的细胞相比,LPS注射使库普弗细胞内的GSH含量增加了两到三倍。内皮细胞中的细胞GSH含量高于库普弗细胞。然而,LPS并未增加内皮细胞中的GSH含量。向库普弗细胞或内皮细胞中添加H2O2(40 - 200μM)会导致GSH短暂下降,对照大鼠的细胞中这种下降更为明显(约45%),而LPS处理的细胞中下降约25%。GSH水平的降低伴随着细胞内H2O2的相应增加。在用3 - 氨基 - 1,2,4 - 三唑抑制过氧化氢酶后,0.2mM H2O2分别使注射生理盐水或LPS大鼠的库普弗细胞中的GSH含量降低75%和40%。相同处理使活化的内皮细胞和对照内皮细胞中的GSH含量均下降约50%。LPS使库普弗细胞中的过氧化氢酶活性降低45%,而对内皮细胞中的过氧化氢酶没有影响。两种细胞类型中,LPS均未改变谷胱甘肽还原酶活性。这些数据表明,在活化的库普弗细胞中,细胞内谷胱甘肽水平的升高在抵御活性氧方面发挥了增强作用,而过氧化氢酶对H2O2解毒的贡献减弱。在LPS刺激的内皮细胞和库普弗细胞中,GSH的有效维持与先前观察到的通过磷酸己糖旁路上调还原力的产生一致。

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