Gut-brain and brain-gut axis in Parkinson's disease models: Effects of a uridine and fish oil diet

Nutr Neurosci. 2018 Jul;21(6):391-402. doi: 10.1080/1028415X.2017.1294555. Epub 2017 Mar 9.

Abstract

Recent investigations have focused on the potential role of gastrointestinal (GI) abnormalities in the pathogenesis of Parkinson's disease (PD). The 'dual-hit' hypothesis of PD speculates that a putative pathogen enters the brain via two routes: the olfactory system and the GI system. Here, we investigated (1) whether local exposures of the neurotoxin rotenone in the gut or the brain of mice could induce PD-like neurological and GI phenotypes as well as a characteristic neuropathology in accordance with this 'dual-hit hypothesis' and (2) the effects of a diet containing uridine and fish oil providing docosahexaenoic acid (DHA), in both models. Mice were given rotenone either orally or by an injection in the striatum. Dietary interventions were started 1 week before rotenone exposures. We found that (1) both oral and intrastriatal administration of rotenone induced similar PD-like motor deficits, dopaminergic cell loss, delayed intestinal transit, inflammation, and alpha-synuclein accumulation in the colon; (2) the uridine and DHA containing diet prevented rotenone-induced motor and GI dysfunctions in both models. The models suggest possible bidirectional communication between the gut and the brain for the genesis of PD-like phenotype and pathology. The dietary intervention may provide benefits in the prevention of motor and non-motor symptoms in PD.

Keywords: Docosahexaenoic acid; GI dysfunction; Gut–brain and brain–gut axis; Rotenone Parkinson's model; Uridine.

MeSH terms

  • Animals
  • Brain / drug effects*
  • Brain / metabolism
  • Diet
  • Docosahexaenoic Acids / administration & dosage
  • Docosahexaenoic Acids / blood
  • Fish Oils / administration & dosage*
  • Fish Oils / blood
  • Gastrointestinal Tract / drug effects*
  • Gastrointestinal Tract / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Parkinson Disease / blood
  • Parkinson Disease / pathology*
  • Rotenone / toxicity
  • Uridine / administration & dosage*
  • Uridine / blood
  • alpha-Synuclein / metabolism

Substances

  • Fish Oils
  • alpha-Synuclein
  • Rotenone
  • Docosahexaenoic Acids
  • Uridine