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体外内皮细胞和肾小管上皮细胞的抗氧化防御机制:谷胱甘肽氧化还原循环和过氧化氢酶的作用

Antioxidant defense mechanisms of endothelial cells and renal tubular epithelial cells in vitro: role of the glutathione redox cycle and catalase.

作者信息

Andreoli S P, Mallett C, McAteer J A, Williams L V

机构信息

Department of Pediatrics, Indiana University Medical Center, Indianapolis 46202-5225.

出版信息

Pediatr Res. 1992 Sep;32(3):360-5. doi: 10.1203/00006450-199209000-00023.

Abstract

We recently demonstrated that endothelial cells are more susceptible than renal tubular epithelial cells to oxidant injury and that renal tubular epithelial cells with proximal tubular characteristics including porcine proximal tubular epithelial cells, opossum kidney proximal tubular epithelial cells, and normal human kidney cortical epithelial cells are more susceptible to oxidant injury than the distal nephron-derived Madin Darby canine kidney cell line. To determine the basis of this differential response, we evaluated several antioxidant defenses in the five cell lines. Glutathione levels were not significantly different among the five cell lines, but catalase and glutathione reductase levels were significantly (p less than 0.01) lower in endothelial cells compared to all renal tubular epithelial cells. Among renal tubular epithelial cells, Madin Darby canine kidney cells had significantly (p less than 0.05) higher glutathione peroxidase activity. To further evaluate the role of antioxidant defenses in limiting oxidant injury, we determined two responses to oxidant injury (ATP depletion and 51Cr release) when glutathione was depleted with buthionine sulfoxamine and when catalase was inhibited with aminotriazole. Oxidant-induced ATP depletion was accentuated when catalase was inhibited as well as when glutathione was depleted with buthionine sulfoxamine. In contrast, inhibition of catalase had little or no effect on 51Cr release, whereas glutathione depletion resulted in accentuated 51Cr release. We conclude that the increased susceptibility of endothelial cells to oxidant injury as compared with epithelial cells is associated with lower antioxidant defenses. Disruption of the glutathione redox cycle results in accentuated ATP depletion and lytic injury, whereas inhibition of catalase results in accentuated ATP depletion with little effect on lytic injury.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

我们最近证明,内皮细胞比肾小管上皮细胞更容易受到氧化损伤,并且具有近端肾小管特征的肾小管上皮细胞,包括猪近端肾小管上皮细胞、负鼠肾近端肾小管上皮细胞和正常人肾皮质上皮细胞,比远端肾单位来源的Madin Darby犬肾细胞系更容易受到氧化损伤。为了确定这种差异反应的基础,我们评估了这五种细胞系中的几种抗氧化防御机制。五种细胞系中的谷胱甘肽水平没有显著差异,但与所有肾小管上皮细胞相比,内皮细胞中的过氧化氢酶和谷胱甘肽还原酶水平显著降低(p小于0.01)。在肾小管上皮细胞中,Madin Darby犬肾细胞的谷胱甘肽过氧化物酶活性显著更高(p小于0.05)。为了进一步评估抗氧化防御机制在限制氧化损伤中的作用,我们在使用丁硫氨酸亚砜胺耗尽谷胱甘肽以及使用氨基三唑抑制过氧化氢酶时,测定了对氧化损伤的两种反应(ATP消耗和51Cr释放)。当过氧化氢酶被抑制以及谷胱甘肽被丁硫氨酸亚砜胺耗尽时,氧化诱导的ATP消耗会加剧。相比之下,抑制过氧化氢酶对51Cr释放几乎没有影响,而谷胱甘肽耗竭会导致51Cr释放加剧。我们得出结论,与上皮细胞相比,内皮细胞对氧化损伤的易感性增加与较低的抗氧化防御有关。谷胱甘肽氧化还原循环的破坏导致ATP消耗加剧和溶解性损伤,而过氧化氢酶的抑制导致ATP消耗加剧,但对溶解性损伤影响很小。(摘要截短至250字)

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