The concurrent therapeutic potential of adipose-derived mesenchymal stem cells on Gentamycin-induced hepatorenal toxicity in rats

dc.AffiliationOctober University for modern sciences and Arts (MSA)
dc.contributor.authorRawash, Mohamed A
dc.contributor.authorMohamed, Ayman Saber
dc.contributor.authorEl-Zayat, Emad M
dc.date.accessioned2021-10-17T14:10:27Z
dc.date.available2021-10-17T14:10:27Z
dc.date.issued2021-10
dc.description.abstractBackground: Adipose mesenchymal stem cells (AMSCs) are a type of stem cell employed to repair damaged organs. This study aimed to see how effective AMSCs are at treating gentamycin-induced hepatorenal damage in rats. Methods: 18 male Wister rats were assigned into three groups; control, Gentamycin (GM), and GM+AMSCs. GM induced hepatorenal toxicity through daily injection (100 mg/kg, i.p.) for eight days. On day 9, AMSC (106 cells/ml/rat) was injected intravenously. Results: Creatinine, urea, uric acid, AST, ALP, ALT, TNF-, and MDA levels decreased, whereas IL-10, GSH, and CAT levels increased, indicating the therapeutic potency of intravenous injection AMSCs. Conclusion: The current study demonstrated the simultaneous therapeutic efficacy of adipose mesenchymal stem cells on the liver and kidney in the treatment of Gentamycin-induced hepatotoxicity. These data show that AMSCs could be a feasible therapy option for liver and kidney diseaseen_US
dc.identifier.doihttps://doi.org/10.2174/1574888X16666211011124154
dc.identifier.otherhttps://doi.org/10.2174/1574888X16666211011124154
dc.identifier.urihttps://cutt.ly/zRsYT43
dc.language.isoen_USen_US
dc.publisherBentham Science Publisheren_US
dc.relation.ispartofseriesCurrent Stem Cell Research & Therapy;
dc.subjectAdipose-derived mesenchymal stem cellsen_US
dc.subjectGentamycinen_US
dc.subjectAminoglycosidesen_US
dc.subjectHepatorenal toxicityen_US
dc.subjectOxidative stressen_US
dc.subjectHistologyen_US
dc.subjectInflammationen_US
dc.titleThe concurrent therapeutic potential of adipose-derived mesenchymal stem cells on Gentamycin-induced hepatorenal toxicity in ratsen_US
dc.typeArticleen_US

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