Effect of Proline-Containing Oligopeptides PGP and RGP on Proliferative and Protein-Synthesizing Activity of Cultured

I V Tolstenok1, M Yu Fleishman2, E N Sazonova1

  • 1Central Research Laboratory, Far-Eastern State Medical University, Khabarovsk, Russia.

Insights

Gly-Pro peptides Pro-Gly-Pro (PGP) and Arg-Gly-Pro (RGP) did not affect normal pulmonary fibroblast cell division. However, these peptides protected cells against hydrogen peroxide-induced oxidative stress, improving DNA synthesis and reducing oxidative markers.

Area of Science:

  • Cell Biology
  • Biochemistry
  • Toxicology

Background:

  • Pulmonary fibroblasts are crucial for lung tissue maintenance.
  • Oxidative stress can impair fibroblast function and contribute to lung disease.
  • Gly-proline peptides are known for their potential biological activities.

Purpose of the Study:

  • To investigate the effects of Pro-Gly-Pro (PGP) and Arg-Gly-Pro (RGP) on rat pulmonary fibroblasts.
  • To determine the protective potential of PGP and RGP against oxidative stress induced by hydrogen peroxide.
  • To assess the impact of these peptides on cell division, protein synthesis, and oxidative status.

Main Methods:

  • Primary culture of pulmonary fibroblasts from newborn albino rats.
  • Treatment with Pro-Gly-Pro (PGP) and Arg-Gly-Pro (RGP) under normal and oxidative stress conditions.
  • Assessment of cell division parameters, protein-synthesizing function, and lucigenin-dependent chemiluminescence.

Main Results:

  • PGP and RGP showed no effect on cell division under physiological conditions.
  • Hydrogen peroxide induced significant oxidative stress, suppressing protein synthesis.
  • Co-administration of PGP and RGP with hydrogen peroxide corrected oxidative status, activated DNA synthesis, and inhibited chemiluminescence.

Conclusions:

  • Pro-Gly-Pro (PGP) and Arg-Gly-Pro (RGP) do not influence normal pulmonary fibroblast proliferation.
  • These gly-proline peptides exhibit protective effects against hydrogen peroxide-induced oxidative stress in pulmonary fibroblasts.
  • PGP and RGP demonstrate potential as therapeutic agents for mitigating oxidative damage in lung tissue.