Journals / Bitlis Eren Üniversitesi Fen Bilimleri Dergisi / 2021 / Cilt: 10 - Sayı: 3

The Protective Effects of Borax on Doxorubicin Induced Cardiotoxicity In Rats

The Protective Effects of Borax on Doxorubicin Induced Cardiotoxicity in Rats

Pages
692–702
Publication Date
2021-09-17
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)

According to the results, MDA levels increased significantly in doxorubucin induced group (p

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Boron and boron compounds have benefical effects on health of human and animals.This study was designed to determine the protective effect of borax (BX) in doxorubicin (DXR) induced cardiotoxicity in rats.
📊
Key Findings & Data:In this study, 20 Wistar-Albino male rats were used.
💡
Conclusion & Impact:According to the results, MDA levels increased significantly in doxorubucin induced group (p
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Boraks · Bor bileşikleri · Doksorubisin

Abstract

Boron and boron compounds have benefical effects on health of human and animals.This study was designed to determine the protective effect of borax (BX) in doxorubicin (DXR) induced cardiotoxicity in rats. In this study, 20 Wistar-Albino male rats were used. The rats were divided into four groups including 5 rats in each one; control group (standard pellet food + water + normal saline), doxorubicin (3.75 mg/kg/ip, single dose in a week), doxorubicin + borax (3,75 mg/kg/ip + 25 mg/kg/oral/ respectively), and borax (25 mg/kg/oral, single dose in a week). At the end of the experiment, to evaluate antioxidant activity MDA, GSH, CAT, SOD levels determined in blood samples of rats. Besides, CK levels were investigated to determine the effect of doxorubucine on heart tissue. According to the results, MDA levels increased significantly in doxorubucin induced group (p

Özet

Boron and boron compounds have benefical effects on health of human and animals.This study was designed to determine the protective effect of borax (BX) in doxorubicin (DXR) induced cardiotoxicity in rats. In this study, 20 Wistar-Albino male rats were used. The rats were divided into four groups including 5 rats in each one; control group (standard pellet food + water + normal saline), doxorubicin (3.75 mg/kg/ip, single dose in a week), doxorubicin + borax (3,75 mg/kg/ip + 25 mg/kg/oral/ respectively), and borax (25 mg/kg/oral, single dose in a week). At the end of the experiment, to evaluate antioxidant activity MDA, GSH, CAT, SOD levels determined in blood samples of rats. Besides, CK levels were investigated to determine the effect of doxorubucine on heart tissue. According to the results, MDA levels increased significantly in doxorubucin induced group (p

🔖

Cite This Article

ÇELİKEZEN, B., TANYILDIZI, S., OTO, G. (2021). The Protective Effects of Borax on Doxorubicin Induced Cardiotoxicity In Rats. Bitlis Eren Üniversitesi Fen Bilimleri Dergisi, Cilt: 10 - Sayı: 3, 692–702. https://ajindex.com/articles/477402

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (11)

  1. Baker S.D., Pharm D. 1997. Drug interaction with the taxanes. Pharmacotherapy, 17: 126-132.
  2. Muggia F.M., Green M.D. 1991. New anthracycline antitumor antibiotics. Critical Reviews oncology/ Hematology, 11: 43-64.
  3. Hideg K., Kálai T. 2007. Novel antioxidants in anthracycline cardiotoxicity. Cardiovascular Toxicology, 7: 160-164. Ferrans V.J. 1983. Anthracycline cardiotoxicity. Advances in Experimental Medicine and Biology, 161: 519-532.
  4. Childs A.C., Phaneuf S.L., Dirks A.J., Phillips T., Leeuweburgh C. 2002. Doxorubicin treatment in vivo causes cytochrome C release and cardiomyocyte apoptosis, as well as increased mitochondrial efficiency, superoxide dismutase activity and Bcl2. Cancer Research, 62: 4592-4598.
  5. Menna P., Salvatorelli E., Minotti G. 2008. Cardiotoxicity of antitumor drugs. Chemical Research in Toxicology, 21: 978-989.
  6. Pizzino G., Irrera N., Cucinotta M., Pallio G., Mannino F., Arcoraci V., Squadrito F., Altavilla D., Bitto A. 2017. Oxidative stress: harms and benefits for human health. Oxidative Medicine and Cellular Longevity, 8416763. doi: 10.1155/2017/8416763 Zhang H., Davies K.J.A., Forman H.J. 2015. Oxidative stress response and Nrf2 signaling in aging. Free Radical Biology and Medicine, 88: 314-336.
  7. El-Kenawi A., Ruffel B. 2017.
  8. Inflamattion, ROS, and mutagenesis. Cancer Cell, 32: 727-729. Ren J. 2007. Influence of gender on oxidative stress, lipid peroxidation, protein damage and apoptosis in hearts and brains from spontaneously hypertensive rats. Clinical and Experimental Pharmacology and Physiology, 34: 432-438.
  9. Hosseini A., Bakhtiari E., Mousavi S.H. 2017. Protective effect of hibiscus sabdariffa on doxorubicin-induced cytotoxicity in H9c2 cardiomyoblast cells. Iranian Journal of Pharmaceutical Research, 16: 708-713.
  10. Capasso I., Esposito E., Maurea N., Montella M., Crispo A., De Laurentiis M., D'Aiuto M., Frasci G., Botti G., Grimaldi M., Cavalcanti E., Esposito G., Fucito A., Brillante G., D'Aiuto G., Ciliberto G. 2013. Combination of inositol and alpha lipoic acid in metabolic syndrome-affected women: a randomized placebo-controlled trial. Trials, 14 (1): 273 Møller P., Loft S., Lundby C., Olsen N.V. 2001. Acute hypoxia and hypoxic exercise induce DNA strand breaks and oxidative DNA damage in humans. The FASEB Journal, 15 (7): 1181-1186.
  11. Nakamura K., Fushimi K., Kouchi H., Mihara K., Masahiro M, Ohe T., Namba M.1998. Inhibitory effects of antioxidants on neonatal rat cardiac myocyte hypertrophy induced by tumor necrosis factor-alph