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Bromelain has Antioxidant Effect on Methotrexate Hepatotoxicity and Nephrotoxicity

Yıl 2022, , 37 - 42, 30.04.2022
https://doi.org/10.52976/vansaglik.982411

Öz

Objective: The goal of this study was to look into whether bromelain (BRM) could protect against methotrexate (MTX)-induced kidney and liver damage.
Material and Method: The rats were divided into four groups (n=7); the control group was given distilled water by gavage for 14 days and intraperitoneal (i.p.) physiological saline (%0.9 NaCI) on the third day; the BRM group was given 200 mg/kg BRM by gavage for 14 days and i.p. physiological saline (%0.9 NaCI) on third day; the MTX group was given distilled water by gavage for 14 days and i.p. single dose of 20 mg/kg MTX on the third day; the MTX+BRM group was given 200 mg/kg BRM by gavage for 14 days and i.p. single dose of 20 mg/kg MTX on the third day. Rats were decapitated at the end of the experiment, kidney and liver tissues were kept at -80°C, and biochemical analyzes were performed on the supernatants obtained from tissue homo-gentates.
Results: With the administration of MTX, oxidation indicator thiobarbituric acid reactive substance (TBARS) levels increased in comparison with the control group; antioxidants- glutathione peroxidase (GPx), glutathione (GSH), superoxide dismutase (SOD), and catalase (CAT) activities were decreased compared to the control group. Co-administration of BRM with MTX resulted in reduction in TBARS level and increase in GSH, CAT, SOD, and GPx activities.
Conclusion: In this study, it was determined that MTX caused oxidative damage in kidney and liver tissues and BRM prevented this damage.

Kaynakça

  • 1. Hafez HM, Ibrahim MA, Ibrahim SA, Amin EF, Goma W, Abdelrahman AM. Potential protective effect of etanercept and aminoguanidine in methotrexate-induced hepatotoxicity and nephrotoxicity in rats. Eur J Pharmacol 2015;768:1–12.
  • 2. Bernsen EC, Hagleitner MM, Kouwenberg TW, Hanff LM. Pharmacogenomics as a Tool to Limit Acute and Long-Term Adverse Effects of Chemotherapeutics: An Update in Pediatric Oncology. Front Pharmacol. 2020;11:1–19.
  • 3. El Demerdash FM, Baghdadi HH, Ghanem NF, Mhanna ABA. Nephroprotective role of bromelain against oxidative injury induced by aluminium in rats. Environ Toxicol Pharmacol 2020;80:103509.
  • 4. Pavan R, Jain S, Shraddha, Kumar A. Properties and therapeutic application of bromelain: a review. Biotechnol Res Int 2012;2012:1-6.
  • 5. White RR, Crawley FE, Vellini M, Rovati LA. Bioavailability of 125I bromelain after oral administration to rats. Biopharm Drug Dispos 1988;9:397-403.
  • 6. Castell JV, Friedrich G, Kuhn CS, Poppe GE. Intestinal absorption of undegraded proteins in men: presence of bromelain in plasma after oral intake. Am J Physiol 1997;273:139-146.
  • 7. Ataide JA, De Carvalho NM, Rebelo MDA, Chaud MV, Grotto D, Gerenutti M. Bacterial nanocellulose loaded with bromelain: assessment of antimicrobial, antioxidant and physical-chemical properties. Sci Rep 2017;7:2-10.
  • 8. Jebur AB, El Demerdash FM, Kang W. Bromelain from Ananas comosus stem attenuates oxidative toxicity and testicular dysfunction caused by aluminum in rats. J Trace Elem Med Biol 2020;62:126631.
  • 9. Yagi K. Simple assay for the level of total lipid peroxides in serum or plasma. Methods Mol Biol. 1998;108:101–106.
  • 10. Ighodaro OM, Akinloye OA. First line defence antioxidants-superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPX): Their fundamental role in the entire antioxidant defence grid. Alexandria J Med 2018;54(4):287–293.
  • 11. Sun Y, Oberley LW, Li Y. A simple method for clinical assay of superoxide dismutase. Clin Chem. 1988;34(3):497–500.
  • 12. Aebi H. Catalase. Methods Enzym Anal. 1974;673–684.
  • 13. Paglia DE, Valentine WN. Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. J Lab Clin Med. 1967;70(1):158–169.
  • 14. Sedlak J, Lindsay RH. Estimation of total, protein-bound, and nonprotein sulfhydryl groups in tissue with Ellman’s reagent. Anal Biochem. 1968;25(C):192–205.
  • 15. Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. The folin by oliver. Readings. 1951;193(1):265–275.
  • 16. Wang W, Zhou H, Liu L. Side effects of methotrexate therapy for rheumatoid arthritis: A systematic review. Eur J Med Chem 2018;158:502–516.
  • 17. Campbell JM, Bateman E, Peters MDJ, Bowen JM, Keefe DM, Stephenson MD. Fluoropyrimidine and platinum toxicity pharmacogenetics: An umbrella review of systematic reviews and meta-analyses. Pharmacogenomics 2016;17(4):435–451.
  • 18. Yalçın A, Gürel A. Theraupeutic potency of benfotiamine against methotrexate-induced kidney injury and irisin immunoreactivity. Journal of Ankara Health Sciences (JAHS) 2020, 9(2): 244-253.
  • 19. Vardi N, Parlakpinar H, Cetin A, Erdogan A, Cetin OI. 2010. Protective effect of β-carotene on methotrexate– induced oxidative liver damage. Toxicol Pathol. 38(4):592-597.
  • 20. Agarwal S, Chaudhary B, Bist R. Bacoside a and bromelain relieve dichlorvos induced changes in oxidative responses in mice serum. Chem Biol Interact 2016;254:173-178.

Bromelain Metotreksat Hepatotoksisitesi ve Nefrotoksisitesi Üzerine Antioksidan Etkilidir

Yıl 2022, , 37 - 42, 30.04.2022
https://doi.org/10.52976/vansaglik.982411

Öz

Amaç: Bu çalışmada bromelainin (BRM) metotreksat (MTX) kaynaklı böbrek ve karaciğer hasarına karşı potansiyel koruyucu etkilerinin araştırılması amaçlandı.
Materyal ve Metot: Dört gruba ayrılan sıçanlarda (n=7); kontrol grubuna 14 gün gavaj yoluyla distile su ve üçüncü gün intraperitoneal (i.p.) fizyolojik salin (%0.9 NaCI) verildi; BRM grubuna 14 gün boyunca gavaj yol-uyla 200 mg/kg BRM ve üçüncü gün i.p fizyolojik salin (%0.9 NaCI); MTX grubuna 14 gün boyunca gavaj yolu-yla distile su ve üçüncü günde i.p. tek doz 20 mg/kg MTX; BRM+MTX grubuna 14 gün boyunca gavaj yoluyla 200 mg/kg BRM ve üçüncü günde i.p. tek doz 20 mg/kg MTX uygulandı. Deney sonunda sıçanlar dekapite edildi, böbrek ve karaciğer dokuları -80 °C'de muhafaza edilerek, doku homojentlarından elde edilen superna-tantlarda biyokimyasal analizler gerçekleştirildi.
Bulgular: MTX uygulaması ile oksidasyon belirteci tiyobarbitürik asit reaktif madde (TBARS) seviyeleri kontrol grubuna kıyasla arttı; antioksidanlar süperoksit dismutaz (SOD), glutatyon (GSH), glutatyon peroksidaz (GPx) ve katalaz (CAT) aktiviteleri kontrol grubuna göre azaldı. BRM'nin MTX ile birlikte uygulanması, TBARS se-viyesinde azalmaya ve GSH, CAT, SOD ve GPx aktivitelerinde artışa neden oldu.
Sonuç: Bu çalışmada MTX'in böbrek ve karaciğer dokularında oksidatif hasara neden olduğu ve BRM'nin bu hasarı önlediği belirlenmiştir.

Kaynakça

  • 1. Hafez HM, Ibrahim MA, Ibrahim SA, Amin EF, Goma W, Abdelrahman AM. Potential protective effect of etanercept and aminoguanidine in methotrexate-induced hepatotoxicity and nephrotoxicity in rats. Eur J Pharmacol 2015;768:1–12.
  • 2. Bernsen EC, Hagleitner MM, Kouwenberg TW, Hanff LM. Pharmacogenomics as a Tool to Limit Acute and Long-Term Adverse Effects of Chemotherapeutics: An Update in Pediatric Oncology. Front Pharmacol. 2020;11:1–19.
  • 3. El Demerdash FM, Baghdadi HH, Ghanem NF, Mhanna ABA. Nephroprotective role of bromelain against oxidative injury induced by aluminium in rats. Environ Toxicol Pharmacol 2020;80:103509.
  • 4. Pavan R, Jain S, Shraddha, Kumar A. Properties and therapeutic application of bromelain: a review. Biotechnol Res Int 2012;2012:1-6.
  • 5. White RR, Crawley FE, Vellini M, Rovati LA. Bioavailability of 125I bromelain after oral administration to rats. Biopharm Drug Dispos 1988;9:397-403.
  • 6. Castell JV, Friedrich G, Kuhn CS, Poppe GE. Intestinal absorption of undegraded proteins in men: presence of bromelain in plasma after oral intake. Am J Physiol 1997;273:139-146.
  • 7. Ataide JA, De Carvalho NM, Rebelo MDA, Chaud MV, Grotto D, Gerenutti M. Bacterial nanocellulose loaded with bromelain: assessment of antimicrobial, antioxidant and physical-chemical properties. Sci Rep 2017;7:2-10.
  • 8. Jebur AB, El Demerdash FM, Kang W. Bromelain from Ananas comosus stem attenuates oxidative toxicity and testicular dysfunction caused by aluminum in rats. J Trace Elem Med Biol 2020;62:126631.
  • 9. Yagi K. Simple assay for the level of total lipid peroxides in serum or plasma. Methods Mol Biol. 1998;108:101–106.
  • 10. Ighodaro OM, Akinloye OA. First line defence antioxidants-superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPX): Their fundamental role in the entire antioxidant defence grid. Alexandria J Med 2018;54(4):287–293.
  • 11. Sun Y, Oberley LW, Li Y. A simple method for clinical assay of superoxide dismutase. Clin Chem. 1988;34(3):497–500.
  • 12. Aebi H. Catalase. Methods Enzym Anal. 1974;673–684.
  • 13. Paglia DE, Valentine WN. Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. J Lab Clin Med. 1967;70(1):158–169.
  • 14. Sedlak J, Lindsay RH. Estimation of total, protein-bound, and nonprotein sulfhydryl groups in tissue with Ellman’s reagent. Anal Biochem. 1968;25(C):192–205.
  • 15. Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. The folin by oliver. Readings. 1951;193(1):265–275.
  • 16. Wang W, Zhou H, Liu L. Side effects of methotrexate therapy for rheumatoid arthritis: A systematic review. Eur J Med Chem 2018;158:502–516.
  • 17. Campbell JM, Bateman E, Peters MDJ, Bowen JM, Keefe DM, Stephenson MD. Fluoropyrimidine and platinum toxicity pharmacogenetics: An umbrella review of systematic reviews and meta-analyses. Pharmacogenomics 2016;17(4):435–451.
  • 18. Yalçın A, Gürel A. Theraupeutic potency of benfotiamine against methotrexate-induced kidney injury and irisin immunoreactivity. Journal of Ankara Health Sciences (JAHS) 2020, 9(2): 244-253.
  • 19. Vardi N, Parlakpinar H, Cetin A, Erdogan A, Cetin OI. 2010. Protective effect of β-carotene on methotrexate– induced oxidative liver damage. Toxicol Pathol. 38(4):592-597.
  • 20. Agarwal S, Chaudhary B, Bist R. Bacoside a and bromelain relieve dichlorvos induced changes in oxidative responses in mice serum. Chem Biol Interact 2016;254:173-178.
Toplam 20 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Klinik Tıp Bilimleri
Bölüm Orijinal Araştırma Makaleleri
Yazarlar

Ali Gürel 0000-0001-8087-8814

Kürşat Kaya Bu kişi benim 0000-0002-6353-7791

Yayımlanma Tarihi 30 Nisan 2022
Gönderilme Tarihi 13 Ağustos 2021
Yayımlandığı Sayı Yıl 2022

Kaynak Göster

APA Gürel, A., & Kaya, K. (2022). Bromelain has Antioxidant Effect on Methotrexate Hepatotoxicity and Nephrotoxicity. Van Sağlık Bilimleri Dergisi, 15(1), 37-42. https://doi.org/10.52976/vansaglik.982411

ISSN 

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