Journals / Fırat Üniversitesi Sağlık Bilimleri Veteriner Dergisi / 2022 / Cilt: 36 - Sayı: 1

Effects of Arginine Silicate Inositol Complex on Bone Damage in Rats Treated with Methotrexate

Metotreksat Uygulanan Ratlarda Arjinin Silikat İnositol Kompleksinin Kemik Hasarı Üzerine Etkileri

Pages
42–48
Publication Date
2022-10-18
DOI
—
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AI Summary & Key Takeaways

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

MTX significantly increased aspartateaminotransferase (AST), alanineaminotransferase (ALT), urea (BUN) and creatine levels, while decreased tibia osteocalcin levels (P

📌 3 Key Takeaways

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Objective & Hypothesis:Methotrexate (MTX), an antineoplastic drug, causes bone deformations.
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Key Findings & Data:For this purpose, a total of 28 Sprague-Dawley male rats were divided into four groups: i) Control; ii) ASI, the rats were treated orally with 25 mg/kg/day of ASI for 15 days; iii) MTX, the rats were injected subcutaneously with 0.75 mg/kg of MTX on 8th and 12th days for 5 days, and iv) ASI+ MTX, the rats were treated orally with 25 mg/kg/day of ASI for 15 days and injected with MTX on 8th and 12th days for 5 days.
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Conclusion & Impact:MTX significantly increased aspartateaminotransferase (AST), alanineaminotransferase (ALT), urea (BUN) and creatine levels, while decreased tibia osteocalcin levels (P
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Methotrexate (MTX), an antineoplastic drug, causes bone deformations. Arginine-silicate- inositol (ASI) complex is a combination of arginine, silicon and inositol that have been shown to have beneficial effects on bone health. In this study, it was investigated the potential protective role of ASI against MTX induced bone damage in rats. For this purpose, a total of 28 Sprague-Dawley male rats were divided into four groups: i) Control; ii) ASI, the rats were treated orally with 25 mg/kg/day of ASI for 15 days; iii) MTX, the rats were injected subcutaneously with 0.75 mg/kg of MTX on 8th and 12th days for 5 days, and iv) ASI+ MTX, the rats were treated orally with 25 mg/kg/day of ASI for 15 days and injected with MTX on 8th and 12th days for 5 days. MTX significantly increased aspartateaminotransferase (AST), alanineaminotransferase (ALT), urea (BUN) and creatine levels, while decreased tibia osteocalcin levels (P

Özet

Antineoplastik bir ilaç olan metotreksat (MTX), kemik deformasyonlarına neden olmaktadır. Arjinin- silikat-inositol (ASİ) kompleksi, kemik sağlığı üzerinde faydalı etkileri olduğu gösterilen arginin, silikon ve inositolün bir bileşimidir. Bu çalışmada, ratlarda ASİ uygulamasının MTX kaynaklı kemik hasarına karşı potansiyel koruyucu rolü araştırıldı. Bu amaçla toplam 28 adet Sprague-Dawley erkek rat dört gruba ayrıldı: i) Kontrol, ii) ASİ; ratlara 15 gün boyunca 25 mg/kg/gün dozunda oral gavaj ile ASİ verildi, iii) MTX; ratlara 8-12. günler arasında 5 gün boyunca subkutan olarak 0.75 mg/kg dozunda MTX enjekte edildi, iv) ASİ+MTX; ratlara 15 gün boyunca 25 mg/kg/gün dozda oral gavaj ile ASİ verildi ve 8-12. günler arasında 5 gün boyunca subkutan olarak 0.75 mg/kg dozunda MTX enjekte edildi. MTX; serum aspartat aminotransferaz (AST), alanin aminotransferaz (ALT), üre (BUN) ve kreatin düzeylerini anlamlı derecede artırırken, tibia osteokalsin düzeyini azaltmıştır (P

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Cite This Article

TUZCU, M., BALCI, T. A., ER, B., TUZCU, Z., ERDOĞAN, M. (2022). Effects of Arginine Silicate Inositol Complex on Bone Damage in Rats Treated with Methotrexate. Fırat Üniversitesi Sağlık Bilimleri Veteriner Dergisi, Cilt: 36 - Sayı: 1, 42–48. https://ajindex.com/articles/514810

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References (13)

  1. Chen J, Chen X, Yang Z, et al. Preparation and characterization of folic acid functionalized bioactive glass for targeted delivery and sustained release of methotrexate. J Biomed Mater Res A 2018; 1: 1-11
  2. Fan C, Cool JC, Scherer MA, et al. Damaging effects of chronic low-dose methotrexate usage on primary bone formation in young rats and potential protective effects of folinic acid supplementary treatment. Bone 2009; 44: 61- 70
  3. Fan C, Foster BK, Hui SK et al. Prevention of bone growth defects, ıncreased bone resorption and marrow adiposity with folinic acid in rats receiving long-term methotrexate. PLoS One 2012; 7: e46915
  4. Fan C, Garcia M, Scherer M, et al. Potential roles of metallothioneins I and II in protecting bone growth following acute methotrexate chemotherapy. J Chemotherapy 2014; 26: 37-48
  5. Gao Q, Zhou G, Lin SJ, et al. How chemotherapy and radiotherapy damage the tissue: comparative biology lessons from feather and hair models. Exp Dermatol 2018; 1: 1-18
  6. Athanassiadou F, Tragiannidis A, Rousso I, et al. Bone mineral density in survivors of childhood acute lymphoblastic leukemia. Turk J Pediatr 2006; 48: 101- 104
  7. Brufsky AM. Cancer treatment-ınduced bone loss: Pathophysiology and clinical perspectives. The Oncologist 2008; 13: 187-195
  8. Fan J, Su YW, Hassanshahi MH, et al. β-Catenin signaling is important for osteogenesis and hematopoiesis recovery following methotrexate chemotherapy in rats. J Cell Physiol 2021; 236: 3740-3751
  9. Nadhanan RR, Fan CM, Su YW, et al. Fish oil in comparison to folinic acid for protection against adverse effects of methotrexate chemotherapy on bone. J Orthop Res 2014; 32: 587-596
  10. King TJ, Georgiou KR, Cool JC, et al. Methotrexate chemotherapy promotesosteoclast formation in the long bone of rats via increased pro-inflammatory cytokines and enhanced nf-kappab activation. Am J Pathol 2012; 181: 121-129
  11. King TJ, Shandala T, Lee AM, et al. Potential effects of phytoestrogen genistein in modulating acute methotrexate chemotherapy-ınduced osteoclastogenesis and bone damage in rats. Int J Mol Sci 2015; 16: 18293-18311
  12. Al Maruf A, O'Brien PJ, Naserzadeh P, et al. Methotrexate induced mitochondrial injury and cytochrome c release in rat liver hepatocytes. Drug and Chem Toxicol 2017; 1: 1- 11
  13. Crofton PM, Ahmed SF, Wade JC, et al. Effects of intensive chemotherapy on bone and collagen turnover and the growth hormone axis in childrenwith acute lymphoblastic leukemia. J Clin Endocr