Journals / Turkish journal of nephrology (Online) / 2021 / Cilt: 30 - Sayı: 3

The Protective Effect of Rutin Against MethotrexateInduced Nephrotoxicity in Rats

Pages
218–223
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Biochemical andhistopathological analyzes were performed on kidney tissues of rats at the end of the study.Results: It was determined that kidney tissue damage determined in the MTX group was decreased in the MTX+RUT group;there were no degenerative changes in the tubular epithelium of the MTX+RUT group, and only mild degenerative changeswere observed rather than hydropic degeneration seen in MTX group.Conclusion: This study suggests that rutin can be effective in preventing the toxic effects of methotrexate on the kidney

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Objective: This study was purposed to investigate the possible protective effects of rutin on kidney tissue in a methotrexate-induced nephrotoxicity rat model.Methods: Rats were randomly divided into 4 groups: control group, methotrexate (MTX, 20 mg/kg) group, rutin (RUT,50 mg/kg/day) group, and methotrexate + rutin (MTX+RUT, 20 mg/kg+ 50 mg/kg/day, respectively) group.
📊
Key Findings & Data:Objective: This study was purposed to investigate the possible protective effects of rutin on kidney tissue in a methotrexate-induced nephrotoxicity rat model.Methods: Rats were randomly divided into 4 groups: control group, methotrexate (MTX, 20 mg/kg) group, rutin (RUT,50 mg/kg/day) group, and methotrexate + rutin (MTX+RUT, 20 mg/kg+ 50 mg/kg/day, respectively) group.
💡
Conclusion & Impact:Biochemical andhistopathological analyzes were performed on kidney tissues of rats at the end of the study.Results: It was determined that kidney tissue damage determined in the MTX group was decreased in the MTX+RUT group;there were no degenerative changes in the tubular epithelium of the MTX+RUT group, and only mild degenerative changeswere observed rather than hydropic degeneration seen in MTX group.Conclusion: This study suggests that rutin can be effective in preventing the toxic effects of methotrexate on the kidney
🔬Design:Modeling & Simulation
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

Objective: This study was purposed to investigate the possible protective effects of rutin on kidney tissue in a methotrexate-induced nephrotoxicity rat model.Methods: Rats were randomly divided into 4 groups: control group, methotrexate (MTX, 20 mg/kg) group, rutin (RUT,50 mg/kg/day) group, and methotrexate + rutin (MTX+RUT, 20 mg/kg+ 50 mg/kg/day, respectively) group. Biochemical andhistopathological analyzes were performed on kidney tissues of rats at the end of the study.Results: It was determined that kidney tissue damage determined in the MTX group was decreased in the MTX+RUT group;there were no degenerative changes in the tubular epithelium of the MTX+RUT group, and only mild degenerative changeswere observed rather than hydropic degeneration seen in MTX group.Conclusion: This study suggests that rutin can be effective in preventing the toxic effects of methotrexate on the kidney

🔖

Cite This Article

TAMBAĞ, A. K., KAZAK, F., AKALIN, P. P., KUTLU, T. (2021). The Protective Effect of Rutin Against MethotrexateInduced Nephrotoxicity in Rats. Turkish journal of nephrology (Online), Cilt: 30 - Sayı: 3, 218–223. https://ajindex.com/articles/374801

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (14)

  1. Sherif IO, Al-Shaalan NH, Sabry D. Ginkgo biloba extract alleviates methotrexate-induced renal injury: new impact on PI3K/Akt/ mTOR signaling and MALAT1 expression. Biomolecules. 2019
  2. 9(11). [CrossRef] 2. Bleyer WA. The clinical pharmacology of methotrexate: new applications of an old drug. Cancer. 1978
  3. 41(1):36-51. [CrossRef] 3. Khoshnoud S, Mohseni Kouchesfahani H, Nabiuni M. Evaluation of the protective effect of hydro-alcoholic extract of raspberry fruit on aquaporin1 expression in rats kidney treated by methotrexate. Cell J. 2017
  4. 19(2):306-313. [CrossRef] 4. Bath RK, Brar NK, Forouhar FA, Wu GY. A review of methotrexate‐ associated hepatotoxicity. J Dig Dis. 2014
  5. 15(10):517-524. [CrossRef] 5. Widemann BC, Adamson PC. Understanding and managing methotrexate nephrotoxicity. Oncologist. 2006
  6. 11(6):694-703. [CrossRef] 6. Ulusoy HB, Öztürk İ, Sönmez MF. Protective effect of propolis on methotrexate-induced kidney injury in the rat. Ren Fail. 2016
  7. 38(5):744-750. [CrossRef] 7. Al-Rashidy AH, Salem RR, Alhosary AA, et al. Role of erythropoietin in methotrexate-induced nephrotoxicity in adult male albino rats. J Nephropharmacol. 2018
  8. 7(2):156-163. [CrossRef] 8. Jalili C, Ghanbari A, Roshankhah S, Salahshoor MR. Toxic effects of methotrexate on rat kidney recovered by crocin as a consequence of antioxidant activity and lipid peroxidation prevention. Iran Biomed J. 2020
  9. 24(1):39-46. [CrossRef] 9. Dalaklioglu S, Sahin P, Ordueri EG, Celik-Ozenci C, Tasatargil A. Potential role of poly(ADP-ribose) polymerase (PARP) activation in methotrexate-induced nephrotoxicity and tubular apoptosis. Int J Toxicol. 2012
  10. 31(5):430-440. [CrossRef] 10. Kolli VK, Abraham P, Isaac B, Selvakumar D. Neutrophil infiltration and oxidative stress may play a critical role in methotrexateinduced renal damage. Chemotherapy. 2009
  11. 55(2):83-90. [CrossRef] 11. Sakalli ÇE, Tetiker H, İlhan Çelik Ö, Yılmaz N, Ciğerci İH. Methotrexate-induced nephrotoxicity in rats: protective effect of mistletoe (Viscum album L.) extract. Complement Med. Resources. 2017
  12. 24(6):364-370. 12. Oktem F, Yilmaz HR, Ozguner F, et al. Methotrexate-induced renal oxidative stress in rats: the role of a novel antioxidant caffeic acid phenethyl ester. Toxicol Ind Health. 2006
  13. 22(6):241-247. [CrossRef] 13. Bozkurt M, Em S, Oktayoglu P, et al. Carvacrol prevents methotrexate-induced renal oxidative injury and renal damage in rats. Clin Invest Med. 2014
  14. 37(1):E19-E25. [CrossRef] 14. Asci H, Ozmen O, Ellidag HY, et al. The imp