Does dietary restriction of amino acids other than methionine have any effect on peroxide and superoxide production rates, oxidative protein and DNA damage in the liver and heart mitochondria of aging rats?


Ademoglu E., Kucuk S. T.

International Journal of Medical Biochemistry, cilt.5, sa.1, ss.1-7, 2022 (Scopus) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 5 Sayı: 1
  • Basım Tarihi: 2022
  • Doi Numarası: 10.14744/ijmb.2021.29981
  • Dergi Adı: International Journal of Medical Biochemistry
  • Derginin Tarandığı İndeksler: Scopus, TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.1-7
  • Anahtar Kelimeler: Mitotic tissue, peroxide production, postmitotic tissue, protein carbonyl, protein restriction, superoxide production
  • İstanbul Üniversitesi Adresli: Evet

Özet

© 2022, Kare Publishing. All rights reserved.Objectives: The objective of this study was to evaluate the long-term effects of amino acids other than methionine in mitotic and postmitotic tissue of rats by measuring mitochondrial peroxide and superoxide production as well as oxidative protein and DNA damage in the liver and heart of rats fed with either a normal diet (ND) or a protein-restricted diet (PREMD). Methods: The study group comprised 4-and 12-month-old rats fed with either a ND or a PREMD for 4 months. The rate of mitochondrial peroxide and superoxide production, and the protein carbonyl (PC) and mitochondrial DNA (mtDNA) 8-hydroxy-2'-deoxyguanosine (8-OHdG) levels in the liver and heart mitochondria were measured. Results: The mitochondrial peroxide and superoxide production rates of the liver and heart mitochondria of rats did not demonstrate any significant difference based on the diet provided. Similarly, diet did not have a significant effect on the PC level in the liver and heart mitochondria of either age group. In the 16-month-old rats, the mtDNA 8-OHdG level was significantly higher in the heart than the liver, regardless of the diet. Conclusion: Mitochondrial reactive oxygen species production, and oxidative protein and DNA damage increased in mitotic and postmitotic tissue with age; however, the increment was more prominent in the heart than the liver. Long-term PREMD consumption did not decelerate oxidative damage in the heart or in the liver with age.