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姜黄素对大鼠敌稗所致肝毒性的保护作用

Protective Effect of Curcumin against the Liver Toxicity Caused by Propanil in Rats.

作者信息

Otuechere Chiagoziem A, Abarikwu Sunny O, Olateju Victoria I, Animashaun Azeezat L, Kale Oluwafemi E

机构信息

Department of Chemical Sciences, Redeemer's University, PMB 2011, Mowe, Ogun, Nigeria.

Department of Pharmacology, College of Medicine, University of Lagos, PMB 12003, Lagos, Nigeria.

出版信息

Int Sch Res Notices. 2014 Oct 29;2014:853697. doi: 10.1155/2014/853697. eCollection 2014.

Abstract

We investigated the protective effects of curcumin on propanil-induced alterations in biochemical indices in blood and liver of male Wistar rats. The study consisted of four treatment groups, with six animals each, designated as control, propanil (20mg/kg), curcumin(50 mg/kg), and curcumin (50 mg/kg) + propanil (20 mg/kg). Rats were administered their respective doses orally, every other day, for 28 days. Propanil administration elicited significant (P < 0.001) increases in plasma aspartate aminotransferase and alkaline phosphatase activities, by 24% and 56%, respectively, compared to the control. Treatment with propanil elevated bilirubin, creatinine, and total cholesterol levels in rats, but these were not significant relative to controls. Administration of propanil to rats significantly (P < 0.001) increased lipid peroxidation levels. However, catalase activity, vitamin C, and reduced glutathione levels were significantly reduced. Exposure to propanil did not produce any significant changes in packed cell volume, neutrophils, and leukocyte counts. The supplementation of curcumin attenuated the adverse effects of propanil intoxication by reducing lipid peroxidation levels and restored the levels of serum enzymes and reduced glutathione. The present study showed that propanil increased oxidative stress and altered some biochemical parameters in the rats but curcumin could afford some protection to attenuate propanil-induced toxicity in the liver.

摘要

我们研究了姜黄素对稗草畏诱导的雄性Wistar大鼠血液和肝脏生化指标变化的保护作用。该研究包括四个治疗组,每组六只动物,分别指定为对照组、稗草畏(20mg/kg)、姜黄素(50mg/kg)和姜黄素(50mg/kg)+稗草畏(20mg/kg)。大鼠每隔一天口服各自的剂量,持续28天。与对照组相比,施用稗草畏使血浆天冬氨酸转氨酶和碱性磷酸酶活性分别显著(P<0.001)增加24%和56%。施用稗草畏使大鼠体内胆红素、肌酐和总胆固醇水平升高,但与对照组相比无显著差异。给大鼠施用稗草畏显著(P<0.001)增加脂质过氧化水平。然而,过氧化氢酶活性、维生素C和还原型谷胱甘肽水平显著降低。接触稗草畏对红细胞压积、中性粒细胞和白细胞计数未产生任何显著变化。补充姜黄素可通过降低脂质过氧化水平减轻稗草畏中毒的不良反应,并恢复血清酶和还原型谷胱甘肽水平。本研究表明,稗草畏增加了大鼠的氧化应激并改变了一些生化参数,但姜黄素可以提供一定的保护,减轻稗草畏对肝脏的毒性作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/21a8/4897076/e3fdb0f28726/ISRN2014-853697.001.jpg

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