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Effect of buthionine sulfoximine on acute N-(3,5-dichlorophenyl)succinimide-induced nephrotoxicity in Fischer 344 rats.

作者信息

Rankin G O, Teets V J, Nicoll D W, Brown P I

机构信息

Department of Pharmacology, Marshall University School of Medicine, Huntington, WV 25755-9310.

出版信息

Toxicol Lett. 1990 Jun;52(1):91-100. doi: 10.1016/0378-4274(90)90169-m.

DOI:10.1016/0378-4274(90)90169-m
PMID:2356574
Abstract

The experimental agricultural fungicide N-(3,5-dichlorophenyl)succinimide (NDPS) has been shown to be a nephrotoxicant in Fischer 344 rats. Results of a previous study conducted in our laboratory suggested that glutathione might be an important modulator of NDPS-induced nephrotoxicity. The purpose of this study was to examine the effect of DL-buthionine-(S,R)-sulfoximine (BSO), an inhibitor of glutathione synthesis, on NDPS-induced renal effects. Male Fischer 344 rats received an intraperitoneal (i.p.) injection of BSO (890 mg/kg) in 0.9% saline (10 ml/kg) followed 2 h later by an i.p. injection of NDPS (0.4 or 1.0 mmol/kg) or sesame oil (2.5 ml/kg), and renal function monitored at 24 and 48 h. BSO pretreatment attenuated the diuresis, proteinuria, elevation in blood urea nitrogen (BUN) concentration and kidney weight, and decreases in organic ion accumulation by renal cortical slices induced by NDPS (0.4 or 1.0 mmol/kg) administration. Proximal tubular necrosis induced by NDPS administration also was attenuated by BSO pretreatment. These results indicate that BSO pretreatment attenuates NDPS-induced renal effects and that glutathione is important for modulating acute NDPS-induced nephropathy.

摘要

相似文献

1
Effect of buthionine sulfoximine on acute N-(3,5-dichlorophenyl)succinimide-induced nephrotoxicity in Fischer 344 rats.
Toxicol Lett. 1990 Jun;52(1):91-100. doi: 10.1016/0378-4274(90)90169-m.
2
Buthionine sulfoximine (BSO) and N-(3,5-dichlorophenyl)succinimide nephrotoxicity: temporal aspects of BSO administration and BSO effects on renal transport systems.丁硫氨酸亚砜胺(BSO)和N-(3,5-二氯苯基)琥珀酰亚胺的肾毒性:BSO给药的时间因素以及BSO对肾脏转运系统的影响。
Toxicology. 1997 Feb 28;117(2-3):207-17. doi: 10.1016/s0300-483x(96)03581-0.
3
Effect of buthionine sulfoximine on N-(3,5-dichlorophenyl)-2-hydroxysuccinimide and N-(3,5-dichlorophenyl)-2-hydroxysuccinamic acid nephrotoxicity.丁硫氨酸亚砜胺对N-(3,5-二氯苯基)-2-羟基琥珀酰亚胺和N-(3,5-二氯苯基)-2-羟基琥珀酰胺酸肾毒性的影响。
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4
Role of glutathione in acute N-(3,5-dichlorophenyl) succinimide-induced nephrotoxicity in Sprague-Dawley and Fischer 344 rats.谷胱甘肽在急性N-(3,5-二氯苯基)琥珀酰亚胺诱导的Sprague-Dawley大鼠和Fischer 344大鼠肾毒性中的作用
Toxicology. 1987 Jul;45(1):25-44. doi: 10.1016/0300-483x(87)90112-0.
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The effect of probenecid on acute N-(3,5-dichlorophenyl)succinimide-induced nephrotoxicity in the Fischer 344 rat.丙磺舒对费希尔344大鼠急性N-(3,5-二氯苯基)琥珀酰亚胺诱导的肾毒性的影响。
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Sodium sulfate potentiates N-(3,5-dichlorophenyl)-2-hydroxysuccinimide (NDHS) and N-(3,5-dichlorophenyl)-2-hydroxysuccinamic acid (2-NDHSA) nephrotoxicity in the Fischer 344 rat.在费希尔344大鼠中,硫酸钠可增强N-(3,5-二氯苯基)-2-羟基琥珀酰亚胺(NDHS)和N-(3,5-二氯苯基)-2-羟基琥珀酰胺酸(2-NDHSA)的肾毒性。
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7
Acute N-(3,5-dichlorophenyl)succinimide nephrotoxicity in female Fischer 344 rats.雌性Fischer 344大鼠急性N-(3,5-二氯苯基)琥珀酰亚胺肾毒性
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N-(3,5-dichlorophenyl)succinimide nephrotoxicity: evidence against the formation of nephrotoxic glutathione or cysteine conjugates.N-(3,5-二氯苯基)琥珀酰亚胺肾毒性:反对形成肾毒性谷胱甘肽或半胱氨酸共轭物的证据。
Toxicology. 1991;68(3):307-25. doi: 10.1016/0300-483x(91)90077-e.
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Acute nephrotoxicity of N-phenyl and N-(monochlorophenyl) succinimides in Fischer 344 and Sprague-Dawley rats.N-苯基和N-(一氯苯基)琥珀酰亚胺对Fischer 344和Sprague-Dawley大鼠的急性肾毒性
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N-(3,5-Dichlorophenyl)succinimide nephrotoxicity in the Fischer-344 rat.N-(3,5-二氯苯基)琥珀酰亚胺对费希尔344大鼠的肾毒性
Toxicol Lett. 1985 Jan;24(1):99-105. doi: 10.1016/0378-4274(85)90146-8.

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