Hepatoprotective efficacy of quinoa seed extract against CCl4‐ induced acute liver toxicity in rat model

Author:

Arshad Maria1ORCID,Kousar Shabana1,Din Ahmad1,Afzaal Muhammad2ORCID,Faisal Muhammad Naeem1ORCID,Sharif Mian Kamran1,Rasheed Hina1,Saeed Farhan2ORCID,Akram Noor3ORCID,Ahmed Faiyaz4,Khan Mahbubur Rahman5ORCID

Affiliation:

1. National Institute of Food Science and Technology (NIFSAT), University of Agriculture Faisalabad Pakistan

2. Department of Food Science Government College University Faisalabad Faisalabad Pakistan

3. Food Safety & Biotechnology Lab, Department of Food Science Government College University Faisalabad Faisalabad Pakistan

4. Department of Clinical Nutrition, College of Applied Sciences in Ar Rass Qassim University Buraydah Saudi Arabia

5. Department of Food Processing and Preservation Hajee Mohammad Danesh Science & Technology University Dinajpur Bangladesh

Abstract

AbstractThe current research explored the possible protective effect of chenopodium quinoa extract against CCl4 acute liver toxicity in Sprague Dawley rats. Thirty rats were divided into five groups with six rats in each group. CCl4 (Carbon tetrachloride) was administered at a dose rate of 2 mL/kg b.w. intra‐peritoneally once a week for 3 weeks. The plant extract was given through oral gavage for a period of 21 days. Group I served as a normal group which was given with basal diet. Group II was referred to as a positive control group and received CCl4 2 mL/kg body weight (i.p.). Group III was the standard treatment group and received 2 mL/kg CCl4 (i.p.) and 16 mg/kg body weight (p.o.) silymarin. Group IV was the plant treatment group, which received 2 mL/kg CCl4 (i.p.) and 600 mg/kg body weight of quinoa seed extract (p.o.). Group V was the combined treatment group, which received 2 mL/kg CCl4 (i.p.) accompanied with a combination of silymarin (p.o.) 16 mg/kg body weight and quinoa seed extract (p.o.) 600 mg/kg body weight. The liver biomarkers were assessed along with histopathological analysis to observe the changes in the liver. The outcome suggested that the treatment, which was given with the combination of silymarin and quinoa seed extract, significantly enhanced the antioxidant levels, reduced the oxidative stress, and restored the liver function as evidenced by biochemical parameters histopathological studies. The hepatoprotective potential may be due to the antioxidant and anti‐inflammatory properties of quinoa seed extract.

Publisher

Wiley

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