R-phycocyanin from porphyra haitanensis influences drosophila melanogaster lifespan in a sex-specific manner

Int J Biol Macromol. 2023 Sep 1:248:125914. doi: 10.1016/j.ijbiomac.2023.125914. Epub 2023 Jul 21.

Abstract

Aging has become a major global public health challenge. Our previous research showed that R-phycocyanin (R-PC) possessed anti-aging activity. Notably, studies already revealed that gender may affect the responses to the anti-aging drug. Therefore, it is worth investigating whether the anti-aging effects and their underlying molecular mechanisms of R-PC differ between genders. Firstly, R-PC was isolated from porphyra haitanensis and its anti-aging mechanisms were explored using the nature aging male and female drosophila melanogaster as model. Next, the regulation pathway of longevity was analyzed by KEGG pathway analysis. The longevity pathways-associated molecules were also examined to explore anti-aging mechanisms of R-PC. The results showed that R-PC increased AMPK activity, thus enhanced the key regulatory factors of autophagy (Atg1, Atg8, Atg5), and consequently induced autophagy. Hence, the longevity activity of R-PC life was related with AMPK/mTOR/S6K autophagic signaling pathways in aging female drosophila melanogaster. Meanwhile, R-PC significantly down-regulated TNF-α, MMP3, IL-1β, IL-6, IL-8 expression levels, and the anti-inflammatory and longevity was associated with R-PC-induced regulation of pI3k/AKT/FOXO3 signaling pathway in aging male drosophila melanogaster. These finding showed that R-PC from porphyra haitanensis might exert the anti-aging actions via different mechanisms in male and female drosophila melanogaste.

Keywords: Anti-aging; Drosophila melanogaster; Porphyra haitanensis; R-phycocyanin; Sex-specific manner.

MeSH terms

  • AMP-Activated Protein Kinases
  • Animals
  • Drosophila melanogaster
  • Female
  • Longevity*
  • Male
  • Phosphatidylinositol 3-Kinases
  • Phycocyanin / pharmacology
  • Porphyra*

Substances

  • Phycocyanin
  • AMP-Activated Protein Kinases
  • Phosphatidylinositol 3-Kinases