Beneficial Effects of Exercise Pretreatment in a Sporadic Alzheimer's Rat Model

Med Sci Sports Exerc. 2018 May;50(5):945-956. doi: 10.1249/MSS.0000000000001519.

Abstract

Purpose: This study aimed to examine the effects of swimming exercise pretreatment on a streptozotocin (STZ)-induced sporadic Alzheimer's disease (AD) rat model and provide an initial understanding of related molecular mechanisms.

Methods: Male 2.5-month-old Sprague-Dawley rats were divided into the following four groups: (a) control, (b) swim + vehicle, (c) STZ without swim, and (d) swim + STZ. The Barnes maze task and novel object recognition test were used to measure hippocampus-dependent spatial learning and working memory, respectively. Immunofluorescence staining, Western blot analysis, enzyme-linked immunosorbent assay (ELISA) analysis, and related assay kits were used to assess synaptic proteins, inflammatory cytokines, total antioxidant capacity, antioxidant enzymes, amyloid-beta production, and tau hyperphosphorylation.

Results: Behavioral tests revealed that exercise pretreatment could significantly inhibit STZ-induced cognitive dysfunction (P < 0.05). STZ animals displayed significant loss of presynaptic/postsynaptic markers in the hippocampal CA1 that was reversed by exercise pretreatment (P < 0.05). STZ rats also displayed increased reactive gliosis, release of proinflammatory cytokines, and oxidative damage, effects attenuated by preexercise (P < 0.05, between-treatment changes). Likewise, preexercise significantly induced protein expression (P < 0.001) and DNA-binding activity (P = 0.015) of Nrf2 and downstream antioxidant gene expression in the hippocampal CA1 region (P < 0.05). STZ rats had increased levels of amyloid-beta (1-42) and tau hyperphosphorylation that were significantly ameliorated by exercise (P < 0.05). Histological studies showed that exercise imparted substantial neuroprotection (P < 0.001), suppressing neuronal apoptosis-like cell death in the hippocampal CA1 compared with the STZ control group (P < 0.001).

Conclusions: Exercise pretraining exerts multifactorial benefits on AD that support its use as a promising new therapeutic option for prevention of neurodegeneration in the elderly and/or AD population.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alzheimer Disease / therapy*
  • Animals
  • Antioxidants / metabolism
  • Apoptosis
  • CA1 Region, Hippocampal / cytology
  • CA1 Region, Hippocampal / pathology
  • Cognitive Dysfunction / prevention & control
  • Cytokines / metabolism
  • Disease Models, Animal
  • Inflammation / prevention & control
  • Male
  • Memory, Short-Term
  • NF-E2-Related Factor 2 / metabolism
  • Neurons / cytology
  • Neurons / pathology
  • Oxidative Stress
  • Physical Conditioning, Animal*
  • Protein Carbonylation
  • Rats, Sprague-Dawley
  • Swimming

Substances

  • Antioxidants
  • Cytokines
  • NF-E2-Related Factor 2
  • Nfe2l2 protein, rat