Editor-in-Chief Hatice Kübra Elçioğlu Vice Editors Levent Kabasakal Esra Tatar Online ISSN 2630-6344 Publisher Marmara University Frequency Bimonthly (Six issues / year) Abbreviation J.Res.Pharm. Former Name Marmara Pharmaceutical Journal
Journal of Research in Pharmacy 2023 , Vol 27 , Issue 5
Panax ginseng extract ameliorates methotrexate-induced multi-organ damage via the regulation of oxidative stress
Caglar MACİT1,Seren EDE-PAZARBASI2,Sümeyye YILMAZ-KARAOGLU2,Tugba TUNALIAKBAY3,Fatma Bedia KARAKAYA-ÇİMEN4,Feriha ERCAN5,Goksel SENER7
1Department of Pharmacology, School of Pharmacy, İstanbul Medipol University, İstanbul, Turkey
2Vocational School of Health Services, Fenerbahçe University, Ataşehir/İstanbul, Turkey
3Department of Basic Medical Sciences, Faculty of Dentistry, Marmara University, İstanbul, Turkey
4Department of Histology and Embryology, Institute of Health Science, Marmara University, İstanbul, Turkey
5Department of Histology and Embryology, School of Medicine, Marmara University, İstanbul, Turkey
6Department of Histology and Embryology, School of Medicine, Bezmialem Vakıf University, İstanbul, Turkey
7Department of Pharmacology, School of Pharmacy, Fenerbahçe University, Ataşehir/İstanbul, Turkey
DOI : 10.29228/jrp.477 Oxidative damage plays an important role in organ toxicities caused by methotrexate (MTX). This study aimed to determine the antioxidant effects of Panax ginseng (PxG) extract against MTX-induced liver, lung, ileum and kidney damage. Twenty-four Sprague Dawley male rats (weight 250-300 g) were used in the study. The animals were randomly separated into three groups: a) Control, b) MTX-treated (MTX) and c) MTX+PxG-treated (MTX+PxG) groups. MTX was administered intraperitoneally at 20 mg/kg, as a single dose to MTX and MTX+PxG groups. PxG was administered orally at 100 mg/kg to the MTX+PxG group for five days. Saline was given to the control and MTX groups for 5 days. At the end of the experiment, liver, lung, ileum, and kidney samples were obtained. Malondialdehyde (MDA) and glutathione (GSH) levels, superoxide dismutase (SOD), glutathione-S-transferase (GST) and tissue factor (TF) activities were determined in all tissues. In addition, histological examinations were done through light microscopy. GraphPad Prism 5v. was used for statistics, and p<0.05 were considered significant. Administration of MTX caused severe injury in tissues. Findings showed that MDA level, SOD, and GST activities were significantly normalized in the MTX+PxG group compared to the control group. A significant reduction in GSH level observed in the MTX group was reversed with PxG administration In addition, TF activity and total protein levels were found to be impaired in the MTX group, but TF activity was significantly improved in liver and lung tissues and total protein level was significantly reversed in lung and ileum in MTX+PxG group. The results of histological examinations showed that MTX-induced damage was ameliorated with the PxG administration. In conclusion, this study shows that Panax ginseng, thanks to its antioxidant properties, reversed MTX-induced tissue damage and therefore may be beneficial against side effects in patients undergoing chemotherapy. Keywords : Panax ginseng extract; methotrexate; liver; lung; ileum; kidney; antioxidant activity
Marmara University