Spermidine and spermine delay brain aging by inducing autophagy in SAMP8 mice

Aging (Albany NY). 2020 Apr 8;12(7):6401-6414. doi: 10.18632/aging.103035. Epub 2020 Apr 8.

Abstract

The natural polyamine spermidine and spermine have been reported to ameliorate aging and aging-induced dementia. However, the mechanism is still confused. An aging model, the senescence accelerated mouse-8 (SAMP8), was used in this study. Novel object recognition and the open field test results showed that oral administration of spermidine, spermine and rapamycin increased discrimination index, modified number, inner squares distance and times. Spermidine and spermine increased the activity of SOD, and decreased the level of MDA in the aging brain. Spermidine and spermine phosphorylate AMPK and regulate autophagy proteins (LC3, Beclin 1 and p62). Spermidine and spermine balanced mitochondrial and maintain energy for neuron, with the regulation of MFN1, MFN2, DRP1, COX IV and ATP. In addition, western blot results (Bcl-2, Bax and Caspase-3, NLRP3, IL-18, IL-1β) showed that spermidine and spermine prevented apoptosis and inflammation, and elevate the expression of neurotrophic factors, including NGF, PSD95and PSD93 and BDNF in neurons of SAMP8 mice. These results indicated that the effect of spermidine and spermine on anti-aging is related with improving autophagy and mitochondrial function.

Keywords: aging; autophagy; mitochondrial dysfunction; polyamine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autophagy* / drug effects
  • Autophagy* / physiology
  • Brain / metabolism*
  • Cellular Senescence* / drug effects
  • Cellular Senescence* / physiology
  • Dementia / metabolism
  • Disease Models, Animal
  • Mice
  • Mitochondria* / drug effects
  • Mitochondria* / physiology
  • Oxidative Stress
  • Spermidine* / metabolism
  • Spermidine* / pharmacology
  • Spermine* / metabolism
  • Spermine* / pharmacology

Substances

  • Spermine
  • Spermidine