Journals / Kafkas Üniversitesi Veteriner Fakültesi Dergisi / 2020 / Cilt: 26 - Sayı: 1

Protective Effect of Resveratrol on Kidney and Liver Histopathology Induced by NMDA Receptor Antagonist Mk-801 in Mice

Farelerde NMDA Reseptör Antagonisti Mk-801 İle Böbrek ve Karaciğerde Oluşan Histopatolojik Değişikliklere Karşı Resveratrolün Koruyucu Etkisi

Pages
83–87
Publication Date
2022-10-18
DOI
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AI Summary & Key Takeaways

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

In conclusion, MK-801 caused histopathological changes in both kidney and livertissues, and resveratrol had a significantly protective role on this injury.

📌 3 Key Takeaways

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Objective & Hypothesis:TMK-801 is an antagonist of N-methyl-D-aspartate (NMDA) receptors.
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Key Findings & Data:Sub-chronic administration of 1 mg / kg dose of MK-801 resultedin schizophrenia-like symptoms and degeneration in the brain of mice.
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Conclusion & Impact:In conclusion, MK-801 caused histopathological changes in both kidney and livertissues, and resveratrol had a significantly protective role on this injury.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

TMK-801 is an antagonist of N-methyl-D-aspartate (NMDA) receptors. Sub-chronic administration of 1 mg / kg dose of MK-801 resultedin schizophrenia-like symptoms and degeneration in the brain of mice. In this study, it was investigated whether this dose could causehistopathological changes in kidney and liver tissues and resveratrol had a protective role against these changes. For this aim, 24 malemice were obtained and divided equally into 4 groups. The animals in the control group were intraperitoneally (i.p.) given 10 mL/kg salinesolution, the animals in the experiment groups were i.p. given 1 mg/kg MK-801 alone, 40 mg/kg resveratrol alone and MK-801 by 1 mg/kg for14 days. The kidney and the liver of the sacrificed mice were collected and routine histology procedure was applied. Glomerular shrinkagewas observed in the kidneys after the measurements. Besides this finding, histopathological changes were observed in both kidney and livertissue and resveratrol inhibited most of the harmful effcts. In conclusion, MK-801 caused histopathological changes in both kidney and livertissues, and resveratrol had a significantly protective role on this injury.

Özet

MK-801 N-methyl-D-aspartate (NMDA) reseptör antagonisti bir kimyasal ajandır. Bu kimyasalın sub-kronik 1 mg/kg dozunda uygulanması farelerde şizofreni benzeri semptomlar görülmesine ve beyinde dejenerasyona yol açmaktadır. Resveratrolünse hem böbrek hem de karaciğer üzerinde koruyucu etkisi vardır. Sunulan bu çalışmada hem bu dozun karaciğer ve böbrek gibi organlara histopatalojik bir zararının olup olmadığı hem de resveratrolün koruyucu etkisinin olup olmadığı araştırılmıştır. Bu amaçla 24 erkek fare alınmış ve 4 eşit gruba bölünmüştür. Kontrol grubuna intraperitoneal (i.p.) olarak %0.9’luk (10 mL/kg) fizyolojik tuzlu su verilmiştir. Deney gruplarındaki hayvanlara 14 gün boyunca MK-801 tek başına 1 mg / kg, resveratrol tek başına 40 mg/kg ve MK-801 ile birlikte i.p. verildi. Farelerin sakrifikasyonundan sonra karaciğer ve böbrek dokuları çıkartılmış, histolojik işlemlerden sonra hematoksilen-eozinle boyanmıştır. Ölçümler sonucunda glomeruluslarda istatistiksel olarak küçülme ile birlikte karaciğer ve böbrek dokusunda histopatolojik değişikliklere rastlanmıştır. Resveratrolün bu zararlı değişikliklere karşı oldukça fazla koruyucu etkisinin olduğu gözlenmiştir. Sonuç olarak MK-801’in kronik dozunun karaciğer ve böbrek üzerine zararlı etkileri olduğu ve resveratrolün bu zararlı etkilere karşı önemli miktarda bir koruyucu özelliğinin olduğu gözlemlenmiştir.

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Cite This Article

TÜRKMEN, R., AKOSMAN, M. S., DEMİREL, H. H. (2022). Protective Effect of Resveratrol on Kidney and Liver Histopathology Induced by NMDA Receptor Antagonist Mk-801 in Mice. Kafkas Üniversitesi Veteriner Fakültesi Dergisi, Cilt: 26 - Sayı: 1, 83–87. https://ajindex.com/articles/569630

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References (7)

  1. Vandongen MA: Biology of the NMDA Receptor. 1-8, CRC Press Taylor and Francis Group, USA, 2009
  2. IOM (Institute of Medicine): Glutamate-related biomarkers in drug development for disorders of the nervous system: A workshop summary. 5-8, Washington, DC: The National Academies Press, 2011
  3. Verbeek R, van Tol EAF, van Noort JM: Oral flvonoids delay recovery from experimental autoimmune encephalomyelitis in SJL mice. Biochem Pharmacol, 70, 220-228, 2005. DOI: 10.1016/j.bcp.2005.04.041 4. Sato F, Martinez NE, Shahid M, Rose JW, Carlson NG, Tsunoda I: Resveratrol exacerbates both autoimmune and viral models of multiple sclerosis. Am J Pathol, 183, 1390-1396, 2013. DOI: 10.1016/j. ajpath.2013.07.006 5. Kruk-Slomka M, Budzynska B, Slomka T, Banaszkiewicz I, Biala G: The inflence of the CB1 receptor ligands on the schizophrenia-like effcts in mice induced by MK-801. Neurotox Res, 30, 658-676, 2016
  4. Ozyurt H, Ozyurt B, Sarsilmaz M, Kus I, Songur A, Akyol O: Potential role of some oxidant/antioxidant status parameters in prefrontal cortex of rat brain in an experimental psychosis model and the protective effcts of melatonin. Eur Rev Med Pharmacol Sci, 18 (15): 2137-2144, 2014
  5. Xiu Y, Kong XR, Zhang L, Qiu X, Chao FL, Peng C, Gao Y, Huang CX, Wang SR, Tang Y: White matter injuries induced by MK-801 in a mouse model of schizophrenia based on NMDA antagonism. Anat Rec (Hoboken), 297 (8): 1498-1507, 2014. DOI: 10.1002/ar.22942 8. Xiu Y, Kong XR, Zhang L, Qiu X, Gao Y, Huang CX, Chao FL, Wang SR, Tang Y: The Myelinated fiber loss in the corpus callosum of mouse model of schizophrenia induced by MK-801. J Psychiatr Res, 63, 132-140, 2015. DOI: 10.1016/j.jpsychires.2015.02.013 9. Hu JH, Yang N, Ma YH, Jiang J, Zhang JF, Fei J, Guo LH: Identification of glutamate transporters and receptors in mouse testis. Acta Pharmacol Sin, 25, 366-371, 2004
  6. Dryer SE: Glutamate receptors in the kidney. Nephrol Dial Transplant, 30 (10): 1630-1638, 2015. DOI: 10.1093/ndt/gfv028 11. Leung JC, Ragland N, Marphis T, Silverstein DM: NMDA agonists and antagonists induce renal culture cell toxicity. Med Chem, 4 (6): 565- 571, 2008
  7. Roshanravan H, Kim EY, Dryer SE: NMDA receptors as potential therapeutic targets in diabetic nephropathy: Increased renal nmda receptor subunit expression in akita mice and reduced nephropathy following sustained treatment with memantine or MK-801. Diabetes, 65 (10): 3139-1350, 2016. DOI: 10.2337/db16-0209 13. Lin CS, Hung SF, Huang HS, Ma MC: Blo