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Attenuation of uremia by orally feeding alpha-lipoic acid on acetaminophen induced uremic rats

机译:在对乙酰氨基酚引起的尿毒症大鼠中口服α-硫辛酸可减轻尿毒症

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Uremia means excess nitrogenous waste products in the blood & their toxic effects. An acute acetaminophen (paracetamol, N-acetyl p-aminophenol; APAP) overdose may result into potentially fatal hepatic and renal necrosis in humans and experimental animals. The aims of this present study were to investigate the protective effect of alpha-lipoic acid (ALA) on oxidative stress & uremia on male albino rats induced by acetaminophen. The study was performed by 24 albino male Wister strain rats which were randomly divided into four groups: Group I, control – receives normal food and water, Groups II, III & IV receive acetaminophen interperitoneally at the dose of 500 mg/kg/day for 10 days, from 11th day Groups III & IV were treated with ALA at the dose of 5 mg & 10 mg/100 g/day for 15 days, respectively. After 25 days of treatment, it was observed that there was a significant increase in plasma urea, creatinine, sodium and malondialdehyde (MDA) levels (p 0.05) but a significant decrease in super oxide dismutase (SOD) & catalase activity & potassium level in uremic group is compared with control group & there was a significant increase in SOD & catalase (p 0.05) & a significant decrease in serum urea, creatinine & Na and MDA (p 0.05) in Group III & Group IV is compared with Group II & significant changes were observed in high ALA dose group. In conclusion it was observed that the ALA has nephroprotective activities by biochemical observations against acetaminophen induced uremic rats.
机译:尿毒症是指血液中过量的含氮废物及其毒性作用。急性对乙酰氨基酚(扑热息痛,N-乙酰基对氨基苯酚; APAP)过量服用可能导致人和实验动物潜在的致命性肝和肾坏死。本研究的目的是研究α-硫辛酸(ALA)对对乙酰氨基酚诱导的雄性白化病大鼠氧化应激和尿毒症的保护作用。该研究是由24只白化病雄性Wister品系大鼠进行的,将其随机分为四组:第一组,对照组-接受正常食物和水,第二,第三和第四组以500 mg / kg /天的剂量腹膜内接受对乙酰氨基酚。从第11天起第10天,分别以5 mg和10 mg / 100 g /天的剂量用ALA治疗III和IV组15天。治疗25天后,发现血浆尿素,肌酐,钠和丙二醛(MDA)水平显着增加(p <0.05),但超氧化物歧化酶(SOD),过氧化氢酶活性和钾水平显着下降与第三组和第四组相比,尿毒症组与对照组相比,SOD和过氧化氢酶显着增加(p <0.05),血清尿素,肌酐和Na和MDA显着降低(p <0.05)。在高ALA剂量组中观察到第二组和显着变化。总之,通过生化观察观察到,ALA对对乙酰氨基酚引起的尿毒症大鼠具有肾保护活性。

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