Butyric Acid Precursor Tributyrin Modulates Hippocampal Synaptic Plasticity and Prevents Spatial Memory Deficits: Role of PPARγ and AMPK

Int J Neuropsychopharmacol. 2022 Jun 21;25(6):498-511. doi: 10.1093/ijnp/pyac015.

Abstract

Background: Short chain fatty acids (SCFA), such as butyric acid (BA), derived from the intestinal fermentation of dietary fiber and contained in dairy products, are gaining interest in relation to their possible beneficial effects on neuropsychological disorders.

Methods: C57BL/6J male mice were used to investigate the effect of tributyrin (TB), a prodrug of BA, on hippocampus (HIP)-dependent spatial memory, HIP synaptic transmission and plasticity mechanisms, and the expression of genes and proteins relevant to HIP glutamatergic transmission.

Results: Ex vivo studies, carried out in HIP slices, revealed that TB can transform early-LTP into late-LTP (l-LTP) and to rescue LTP-inhibition induced by scopolamine. The facilitation of l-LTP induced by TB was blocked both by GW9662 (a PPARγ antagonist) and C-Compound (an AMPK inhibitor), suggesting the involvement of both PPARγ and AMPK on TB effects. Moreover, 48-hour intake of a diet containing 1% TB prevented, in adolescent but not in adult mice, scopolamine-induced impairment of HIP-dependent spatial memory. In the adolescent HIP, TB upregulated gene expression levels of Pparg, leptin, and adiponectin receptors, and that of the glutamate receptor subunits AMPA-2, NMDA-1, NMDA-2A, and NMDA-2B.

Conclusions: Our study shows that TB has a positive influence on LTP and HIP-dependent spatial memory, which suggests that BA may have beneficial effects on memory.

Keywords: LTP; Tributyrin; hippocampus; spatial memory; synaptic transmission.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AMP-Activated Protein Kinases / metabolism
  • AMP-Activated Protein Kinases / pharmacology
  • Animals
  • Butyric Acid / metabolism
  • Butyric Acid / pharmacology
  • Hippocampus
  • Long-Term Potentiation / physiology
  • Male
  • Memory Disorders / metabolism
  • Mice
  • Mice, Inbred C57BL
  • N-Methylaspartate / metabolism
  • Neuronal Plasticity
  • PPAR gamma* / metabolism
  • PPAR gamma* / pharmacology
  • Receptors, N-Methyl-D-Aspartate / metabolism
  • Scopolamine Derivatives / metabolism
  • Scopolamine Derivatives / pharmacology
  • Spatial Memory* / physiology
  • Triglycerides

Substances

  • PPAR gamma
  • Receptors, N-Methyl-D-Aspartate
  • Scopolamine Derivatives
  • Triglycerides
  • Butyric Acid
  • N-Methylaspartate
  • AMP-Activated Protein Kinases
  • tributyrin