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Protection against cisplatin-induced lipid peroxidation and kidney damage by procaine in rats.

作者信息

Zhong L F, Zhang J G, Zhang M, Ma S L, Xia Y X

出版信息

Arch Toxicol. 1990;64(7):599-600. doi: 10.1007/BF01971843.

DOI:10.1007/BF01971843
PMID:2073136
Abstract
摘要

相似文献

1
Protection against cisplatin-induced lipid peroxidation and kidney damage by procaine in rats.
Arch Toxicol. 1990;64(7):599-600. doi: 10.1007/BF01971843.
2
Protection effects of procaine on oxidative stress and toxicities of renal cortical slices from rats caused by cisplatin in vitro.
Arch Toxicol. 1992;66(5):354-8. doi: 10.1007/BF01973631.
3
The iron chelator deferoxamine prevents cisplatin-induced lipid peroxidation in rat kidney cortical slices.铁螯合剂去铁胺可防止顺铂诱导的大鼠肾皮质切片中的脂质过氧化。
Jpn J Pharmacol. 1991 Oct;57(2):259-62. doi: 10.1254/jjp.57.259.
4
Carnosic acid attenuates renal injury in an experimental model of rat cisplatin-induced nephrotoxicity.迷迭香酸可减轻顺铂诱导的大鼠肾毒性实验模型的肾损伤。
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Iron- and ascorbic acid-induced lipid peroxidation in renal microsomes isolated from rats treated with platinum compounds.
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6
Vitamin C attenuates cisplatin-induced alterations in renal brush border membrane enzymes and phosphate transport.维生素C可减轻顺铂诱导的肾刷状缘膜酶和磷酸盐转运的改变。
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Ren Fail. 2012;34(3):343-9. doi: 10.3109/0886022X.2011.647305. Epub 2012 Jan 20.
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Protective effect of recombinant human erythropoietin against cisplatin-induced oxidative stress and nephrotoxicity in rat kidney.重组人促红细胞生成素对顺铂诱导的大鼠肾氧化应激和肾毒性的保护作用。
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Hydroxyl radical scavenger ameliorates cisplatin-induced nephrotoxicity by preventing oxidative stress, redox state unbalance, impairment of energetic metabolism and apoptosis in rat kidney mitochondria.羟基自由基清除剂通过防止大鼠肾线粒体中的氧化应激、氧化还原状态失衡、能量代谢受损和细胞凋亡，改善顺铂诱导的肾毒性。
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1
Oxytocin ameliorates cisplatin-induced nephrotoxicity in Wistar rats.催产素可改善顺铂诱导的Wistar大鼠肾毒性。
Ann Saudi Med. 2013 Jan-Feb;33(1):57-62. doi: 10.5144/0256-4947.2013.57.
2
WR2721 as a modulator of cisplatin- and carboplatin-induced side effects in comparison with other chemoprotective agents: a molecular approach.与其他化学保护剂相比，WR2721作为顺铂和卡铂诱导副作用的调节剂：一种分子方法。
Cancer Chemother Pharmacol. 1993;33(2):93-106. doi: 10.1007/BF00685326.
3
Iron- and ascorbic acid-induced lipid peroxidation in renal microsomes isolated from rats treated with platinum compounds.

本文引用的文献

1
Inhibition of lipid peroxidation in muscle homogenates by phospholipase A2 inhibitors.磷脂酶A2抑制剂对肌肉匀浆中脂质过氧化的抑制作用。
Biosci Rep. 1984 Jul;4(7):581-7. doi: 10.1007/BF01121915.
2
Modification of cisplatin toxicity by antioxidants.
Jpn J Pharmacol. 1986 Feb;40(2):353-5. doi: 10.1254/jjp.40.353.
3
Cisplatin-induced lipid peroxidation and decrease of gluconeogenesis in rat kidney cortex: different effects of antioxidants and radical scavengers.顺铂诱导大鼠肾皮质脂质过氧化及糖异生减少：抗氧化剂和自由基清除剂的不同作用
Cancer Chemother Pharmacol. 1991;28(6):427-33. doi: 10.1007/BF00685818.
4
Protection effects of procaine on oxidative stress and toxicities of renal cortical slices from rats caused by cisplatin in vitro.
Arch Toxicol. 1992;66(5):354-8. doi: 10.1007/BF01973631.
Toxicology. 1988 Oct;51(2-3):119-32. doi: 10.1016/0300-483x(88)90143-6.
4
Effect of cisplatin on in vitro production of lipid peroxides in rat kidney cortex.顺铂对大鼠肾皮质脂质过氧化物体外生成的影响。
Jpn J Pharmacol. 1987 May;44(1):71-6. doi: 10.1254/jjp.44.71.
5
Potentiation of cisplatin-induced lipid peroxidation in kidney cortical slices by glutathione depletion.谷胱甘肽耗竭增强顺铂诱导的肾皮质切片脂质过氧化作用。
Jpn J Pharmacol. 1989 Jun;50(2):87-92. doi: 10.1254/jjp.50.87.
6
Use of cultured renal epithelial cells for the study of cisplatin toxicity.利用培养的肾上皮细胞研究顺铂毒性。
Jpn J Pharmacol. 1989 Jun;50(2):247-9. doi: 10.1254/jjp.50.247.
7
Amelioration of cis-platinum nephrotoxicity by orgotein (superoxide dismutase).有机金属蛋白（超氧化物歧化酶）对顺铂肾毒性的改善作用。
Physiol Chem Phys. 1978;10(3):267-77.
8
Microsomal lipid peroxidation.微粒体脂质过氧化
Methods Enzymol. 1978;52:302-10. doi: 10.1016/s0076-6879(78)52032-6.
9
Toxic effects of cis-dichlorodiammineplatinum(II) in man.顺二氯二氨合铂（II）对人体的毒性作用。
Cancer Treat Rep. 1979 Sep-Oct;63(9-10):1527-31.
10
Platinum nephrotoxicity.
Am J Med. 1978 Aug;65(2):307-14. doi: 10.1016/0002-9343(78)90825-2.