Publication: Weekend warrior exercise model for protection from chronic mild stress‑induced depression and ongoing cognitive impairment
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Abstract
We aim to investigate the role and biological mechanisms of the weekend warrior (WW) exercise model on depression‑induced
rats in comparison to the continuous exercise (CE) model. Sedentary, WW, and CE rats were subjected to chronic mild stress
(CMS) procedure. CMS and exercise protocols continued for six weeks. Anhedonia was evaluated by sucrose preference,
depressive behavior by Porsolt, cognitive functions by object recognition and passive avoidance, and anxiety levels by open
field and elevated plus maze. After behavioral assessments, brain tissue myeloperoxidase (MPO) activity, malondialdehyde
(MDA) levels, superoxide dismutase and catalase activities and GSH content, tumor necrosis factor‑α (TNF‑α), interleukin‑6 (IL‑6),
IL‑1β, cortisol and brain‑derived neurotrophic factor levels and histological damage was assessed. CMS‑induced depression‑like
outcomes with increases in anhedonia and decreases in cognitive measures that are rescued with both exercise models. The
increased immobilization time in the Porsolt test was decreased with only WW. Exercise also normalized the suppression of
antioxidant capacity and MPO increase induced by CMS in both exercise models. MDA levels also declined with both exercise
models. Anxiety‑like behavior, cortisol levels, and histological damage scores were exacerbated with depression and improved
by both exercise models. TNF‑α levels were depleted with both exercise models, and IL‑6 only with WW. WW was as protective
as CE in CMS‑induced depression‑like cognitive and behavioral changes via suppressing inflammatory processes and improving
antioxidant capacity.
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Öztürk Ç. Ç., Ataoğlu S. N., Arvas A., Tokol H., Yaprak H., Gürel S., Levent H. N., Akakın D., Şahin A., Çakır B., et al., "Weekend warrior exercise model for protection from chronic mild stress‑induced depression and ongoing cognitive impairment.", Acta neurobiologiae experimentalis, cilt.83, sa.1, ss.10-24, 2023
