Short-term dietary restriction maintains synaptic plasticity whereas short-term overfeeding alters cellular dynamics in the aged brain: evidence from the zebrafish model organism

Neurobiol Aging. 2021 Oct:106:169-182. doi: 10.1016/j.neurobiolaging.2021.06.010. Epub 2021 Jun 19.

Abstract

Increased caloric intake (OF) impairs quality of life causing comorbidities with other diseases and cognitive deficits, whereas dietary restriction (DR) increases healthspan by preventing age-related deteriorations. To understand the effects of these opposing dietary regimens on the cellular and synaptic dynamics during brain aging, the zebrafish model, which shows gradual aging like mammals, was utilized. Global changes in cellular and synaptic markers with respect to age and a 12 week dietary regimen of OF and DR demonstrated that aging reduces the levels of the glutamate receptor subunits, GLUR2/3, inhibitory synaptic clustering protein, GEP, synaptic vesicle protein, SYP, and early-differentiated neuronal marker, HuC. DR significantly elevates levels of glutamate receptor subunits, GLUR2/3, and NMDA clustering protein, PSD95, levels, while OF subtly increases the level of the neuronal protein, DCAMKL1. These data suggest that decreased caloric intake within the context of aging has more robust effects on synapses than cellular proteins, whereas OF alters cellular dynamics. Thus, patterns like these should be taken into account for possible translation to human subjects.

Keywords: Aging; Dietary restriction; Overfeeding; Synapses; Zebrafish.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging / pathology*
  • Aging / physiology*
  • Animals
  • Brain / cytology*
  • Brain / pathology*
  • Cognitive Dysfunction / etiology*
  • Cognitive Dysfunction / prevention & control*
  • Diet Therapy*
  • Disks Large Homolog 4 Protein / metabolism
  • Doublecortin-Like Kinases / metabolism
  • Energy Intake / physiology*
  • Feeding Behavior / physiology*
  • Healthy Aging
  • Hyperphagia / complications*
  • Hyperphagia / physiopathology*
  • Models, Animal
  • Neuronal Plasticity / physiology*
  • Receptors, AMPA / metabolism
  • Time Factors
  • Zebrafish

Substances

  • Disks Large Homolog 4 Protein
  • Receptors, AMPA
  • Doublecortin-Like Kinases