Features of the Spectra of Medium-Molecular Peptides of the Liver with Protein-Deficient Nutrition


Askerov F., ÇAKMAK G., KARADAĞ H.

Van Veterinary Journal, cilt.34, sa.1, ss.18-24, 2023 (Hakemli Dergi) identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 34 Sayı: 1
  • Basım Tarihi: 2023
  • Doi Numarası: 10.36483/vanvetj.1192729
  • Dergi Adı: Van Veterinary Journal
  • Derginin Tarandığı İndeksler: TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.18-24
  • Van Yüzüncü Yıl Üniversitesi Adresli: Evet

Özet

With this study, the determination of three spectra of medium molecular peptides (SMP) in liver tissue can provide a basis for ideas about the relationship between exogenous and endogenous proteins, the degree of damage to nucleotides and proteins, and enable certain judgments to be made. The work was carried out on 45 outbred white rats against the background of full-fledged protein-vitamin nutrition and under conditions of 60% protein deficiency in the diet. The experimental animals were divided into 3 groups, 15 rats in each group. The first group (Group I) of rats in all subgroups served as controls, kept in a vivarium; rats of the 2nd group (Group II) received a complete protein-vitamin diet; Group III received the same diet, but with a 60% protein (casein) deficiency in the diet. Experimental animals of groups II and III received food for 20, 30 and 40 days. The results of studies on the background of a monthly feeding of animals with a protein-vitamin complex with a deficiency of 60% protein in the recipe showed that the content of medium molecular peptides (MMP) fractions at a wavelength of 230 nm significantly increases compared with the control group and is 124%. The results of these studies indicate that 40-day feeding of animals with a full-fledged protein-vitamin diet and 60% protein deficiency causes significant changes in the MMP content at 254 and 280nm wavelengths, and in the MMP subfractions at 230nm wavelength, there is a moderate increase in the MMP subfractions, which is possibly due to the peculiarities of the substitution of the genetic apparatus of hepatocytes.