TY - JOUR
T1 - The benefits of voluntary physical exercise after traumatic brain injury on rat's object recognition memory
T2 - A comparison of different temporal schedules
AU - Amorós-Aguilar, Laura
AU - Portell-Cortés, Isabel
AU - Costa-Miserachs, David
AU - Torras-Garcia, Meritxell
AU - Riubugent-Camps, Èlia
AU - Almolda, Beatriz
AU - Coll-Andreu, Margalida
N1 - Copyright © 2020 Elsevier Inc. All rights reserved.
PY - 2020/4/1
Y1 - 2020/4/1
N2 - Physical exercise can reduce the cognitive decline associated with traumatic brain injury, yet little is known about the optimal administration schedules. Here, different protocols of voluntary wheel running were evaluated for their effects on object recognition memory (ORM), neuroprotection (NeuN+ cells), microglial reactivity (Iba1 staining) and neurogenesis (DCX+ cells) after controlled cortical impact injury (CCI). CCI-lesioned rats were divided into a sedentary group and three exercise groups: early discontinued exercise (3 weeks of exercise initiated 4 days post-injury, followed by 4 weeks in a sedentary state); delayed exercise (3 weeks of exercise initiated 4 weeks post-injury), and early continuous exercise (7 weeks of exercise starting 4 days post-injury). The deficits induced by CCI in a 24 h ORM test were reversed in the delayed exercise group and reduced in the early discontinued and early continuous groups. The early discontinued protocol also reduced the loss of NeuN+ cells in the hilus, while attenuated microglial reactivity was found in the dorsal hippocampus of both the early exercising groups. Running at the end of the experiment increased the number of DCX+ cells in the early continuous and delayed groups, and an inverted U-shaped relationship was found between the mean daily exercise time and the amount of neurogenesis. Thus, exercise had benefits on memory both when it was commenced soon and later after injury, although the neural mechanisms implicated differed. Accordingly, the effects of exercise on memory and neurogenesis appear to not only depend on the specific temporal schedule but also, they may be influenced by the amount of daily exercise.
AB - Physical exercise can reduce the cognitive decline associated with traumatic brain injury, yet little is known about the optimal administration schedules. Here, different protocols of voluntary wheel running were evaluated for their effects on object recognition memory (ORM), neuroprotection (NeuN+ cells), microglial reactivity (Iba1 staining) and neurogenesis (DCX+ cells) after controlled cortical impact injury (CCI). CCI-lesioned rats were divided into a sedentary group and three exercise groups: early discontinued exercise (3 weeks of exercise initiated 4 days post-injury, followed by 4 weeks in a sedentary state); delayed exercise (3 weeks of exercise initiated 4 weeks post-injury), and early continuous exercise (7 weeks of exercise starting 4 days post-injury). The deficits induced by CCI in a 24 h ORM test were reversed in the delayed exercise group and reduced in the early discontinued and early continuous groups. The early discontinued protocol also reduced the loss of NeuN+ cells in the hilus, while attenuated microglial reactivity was found in the dorsal hippocampus of both the early exercising groups. Running at the end of the experiment increased the number of DCX+ cells in the early continuous and delayed groups, and an inverted U-shaped relationship was found between the mean daily exercise time and the amount of neurogenesis. Thus, exercise had benefits on memory both when it was commenced soon and later after injury, although the neural mechanisms implicated differed. Accordingly, the effects of exercise on memory and neurogenesis appear to not only depend on the specific temporal schedule but also, they may be influenced by the amount of daily exercise.
KW - Animals
KW - Antigens, Nuclear/genetics
KW - Brain Injuries, Traumatic/pathology
KW - Calcium-Binding Proteins/genetics
KW - Dentate Gyrus/pathology
KW - Hippocampus/pathology
KW - Male
KW - Memory
KW - Microfilament Proteins/genetics
KW - Microglia/pathology
KW - Microtubule-Associated Proteins/genetics
KW - Nerve Tissue Proteins/genetics
KW - Neurogenesis
KW - Neuropeptides/genetics
KW - Neuroprotection
KW - Physical Conditioning, Animal/methods
KW - Psychomotor Performance
KW - Rats
KW - Rats, Sprague-Dawley
KW - Recognition, Psychology
KW - Running
KW - Time Factors
UR - http://www.scopus.com/inward/record.url?scp=85077753154&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/e765befa-ec8e-3eb1-85c0-cdf83586974e/
U2 - 10.1016/j.expneurol.2020.113178
DO - 10.1016/j.expneurol.2020.113178
M3 - Artículo
C2 - 31926165
AN - SCOPUS:85077753154
SN - 0014-4886
VL - 326
JO - Experimental Neurology
JF - Experimental Neurology
M1 - 113178
ER -