{"title":"Bone Marrow Mesenchymal Stem Cells Alleviate Methotrexate-Induced Renal Toxicity in leukemia Rats","authors":"Hanan abdellatief","doi":"10.21608/besps.2023.226616.1150","DOIUrl":null,"url":null,"abstract":"Background: The chemotherapeutic drug methotrexate (MTX) is administered for managing multiple kinds of cancer. Aim: To determine if bone marrow mesenchymal stem cells (BM-MSCs) might protect rats against renal damage brought on by MTX. Materials and Methods : Rats were divided into five groups : (i) Control group received 2.5 ml saline. (ii) group received MTX as a single IP of 20 mg/Kg body weight. (iii) LEUK group: Benzene-induced leukemia group was injected intravenously every 2 days for 3 consecutive weeks by 0.2 ml benzene. (iv) LEUK/MTX group was injected intravenously every 2 days for 3 consecutive weeks by 0.2 ml benzene and treated by intraperitoneal injection of 2.5 mg/kg.bw/week MTX for 4 consecutive weeks. (v) (LEUK/ MTX/MSCs) group was injected intravenously every 2 days for 3 consecutive weeks by 0.2 ml benzene and treated by intraperitoneal injection of 2.5 mg/kg.bw/week MTX for 4 consecutive weeks. This group was also left for 8 days for kidney injury induction then injected intravenously with a single dose of 3x10 6 MSCs. After 4 weeks of MSCs transplantation. Kidney histopathology, Catalase and Superoxide dismutase activities as well as Capase-3 expression levels were examined. Results: Methotrexate induced marked pathological lesion which characterized by focal necrosis, cell infiltration and high immuno-expression ofTGF-β1 . Besides, treatment with MSCs successfully improved the severe effects of MTX on the kidney and restored histological architecture which confirmed by oxidative enzymes and apoptosis marker","PeriodicalId":9347,"journal":{"name":"Bulletin of Egyptian Society for Physiological Sciences","volume":"45 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bulletin of Egyptian Society for Physiological Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21608/besps.2023.226616.1150","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Background: The chemotherapeutic drug methotrexate (MTX) is administered for managing multiple kinds of cancer. Aim: To determine if bone marrow mesenchymal stem cells (BM-MSCs) might protect rats against renal damage brought on by MTX. Materials and Methods : Rats were divided into five groups : (i) Control group received 2.5 ml saline. (ii) group received MTX as a single IP of 20 mg/Kg body weight. (iii) LEUK group: Benzene-induced leukemia group was injected intravenously every 2 days for 3 consecutive weeks by 0.2 ml benzene. (iv) LEUK/MTX group was injected intravenously every 2 days for 3 consecutive weeks by 0.2 ml benzene and treated by intraperitoneal injection of 2.5 mg/kg.bw/week MTX for 4 consecutive weeks. (v) (LEUK/ MTX/MSCs) group was injected intravenously every 2 days for 3 consecutive weeks by 0.2 ml benzene and treated by intraperitoneal injection of 2.5 mg/kg.bw/week MTX for 4 consecutive weeks. This group was also left for 8 days for kidney injury induction then injected intravenously with a single dose of 3x10 6 MSCs. After 4 weeks of MSCs transplantation. Kidney histopathology, Catalase and Superoxide dismutase activities as well as Capase-3 expression levels were examined. Results: Methotrexate induced marked pathological lesion which characterized by focal necrosis, cell infiltration and high immuno-expression ofTGF-β1 . Besides, treatment with MSCs successfully improved the severe effects of MTX on the kidney and restored histological architecture which confirmed by oxidative enzymes and apoptosis marker