首页> 中文期刊> 《亚太热带生物医学杂志(英文版)》 >A novel polyherbal formulation containing thymoquinone attenuates carbon tetrachloride-induced hepatorenal injury in a rat model

A novel polyherbal formulation containing thymoquinone attenuates carbon tetrachloride-induced hepatorenal injury in a rat model

         

摘要

Objective:To evaluate a novel polyherbal formulation(BSVT)containing the standardized extracts from the leaves of Boerhavia diffusa,Solidago virgaurea,Vitex negundo,and thymoquinone in CCl4 induced hepatorenal toxicity in rats.Methods:A total of 36 rats were divided into six groups including normal control,CCl4(2 mL/kg,i.p.),CCl4(2 mL/kg,i.p.)+Cystone?(750 mg/kg p.o.),CCl4(2 mL/kg,i.p.)+BSVT(25 mg/kg,p.o.),CCl4(2 mL/kg,i.p.)+BSVT(50 mg/kg,p.o.),and CCl4(2 mL/kg,i.p.)+BSVT(100 mg/kg,p.o.).All treatments were given for four weeks.Serum levels of aspartate transaminase,alanine transaminase,alkaline phosphatase,cholesterol,total protein,serum urea,blood urea nitrogen and creatinine were assessed.Superoxide dismutase,malondialdehyde,and glutathione peroxidase were evaluated in tissue homogenate.The histopathological study of liver and kidney tissues was also done.Results:Aspartate transaminase,alanine transaminase,alkaline phosphatase,cholesterol,serum urea,blood urea nitrogen and creatinine were significantly elevated(P<0.001)while total protein was considerably reduced in the CCl4 group as compared to the normal control(P<0.001),which indicated hepatorenal toxicity.In addition,superoxide dismutase and glutathione peroxidase activities were significantly decreased(P<0.001)while malondialdehyde levels were increased markedly(P<0.001).Treatment with BSVT formulation recovered these parameters towards a normal level in a dose-dependent manner.Conclusions:BSVT formulation ameliorates the hepatorenal toxicity in a dose-dependent manner.Furthermore,clinical studies are required to confirm its efficacy.

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  • 来源
    《亚太热带生物医学杂志(英文版)》 |2020年第4期|147-155|共9页
  • 作者单位

    Health Information Technology Department Faculty of Applied Studies King Abdulaziz University Jeddah-21589 Kingdom of Saudi Arabia;

    Department of Medical Laboratory Technology Faculty of Applied Medical Sciences King Abdulaziz University P. O. Box 80402 Jeddah-21589 Jeddah Kingdom of Saudi Arabia;

    Department of Pharmacology Faculty of Medicine King Abdulaziz University Jeddah Saudi Arabia;

    Department of Pharmacy Practice Faculty of Pharmacy King Abdulaziz University Jeddah Saudi Arabia;

    Department of Genetic Medicine Faculty of Medicine King Abdulaziz University Jeddah Saudi Arabia;

    Department of Public Health College of Health Sciences Saudi Electronic University Riyadh Kingdom of Saudi Arabia;

    Department of Pharmaceutical Chemistry School of Pharmaceutical Education and Research Jamia Hamdard (Hamdard University) New Delhi 110062 India;

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