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The effect of treadmill exercise on inflammatory responses in rat model of streptozotocin-induced experimental dementia of Alzheimer’s type

[PURPOSE]: The aim of this study was to investigate the effect of treadmill exercise on inflammatory response in streptozotocin (STZ)-induced animal model of Alzheimer’s disease (AD). [METHODS]: To induce the animal model of AD, Sprague-Dawley rats were injected into intracerebroventricular (ICV) in...

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Detalles Bibliográficos
Autores principales: Choi, Dong Hun, Kwon, In Su, Koo, Jung Hoon, Jang, Yong Chul, Kang, Eun Bum, Byun, Jung Eun, Um, Hyun Sub, Park, Hoo Seong, Yeom, Dong Cheol, Cho, In Ho, Cho, Joon Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Exercise Nutrition 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4241920/
https://www.ncbi.nlm.nih.gov/pubmed/25566459
http://dx.doi.org/10.5717/jenb.2014.18.2.225
Descripción
Sumario:[PURPOSE]: The aim of this study was to investigate the effect of treadmill exercise on inflammatory response in streptozotocin (STZ)-induced animal model of Alzheimer’s disease (AD). [METHODS]: To induce the animal model of AD, Sprague-Dawley rats were injected into intracerebroventricular (ICV) injection with 1.5 mg/kg of STZ. Rats were divided into three groups as Sham-con group (n = 7), STZ-con group (n = 7) and STZ-exe group (n = 7). Exercise group ran on the treadmill for 30 min/day, 5 days/week during 6 weeks. [RESULTS]: The results of this study were as follows: First, STZ-exe group was improved on cognitive function when compared to STZ-con group in water maze test. Second, STZ-exe group help reduce the expression level of amyloid-beta (Aβ). In addition, Toll-like receptors-4 (TLR4), Nuclear factor-kB (NF-kB), Tumor necrosis factor-α (TNF-α) and Interleukin-1α (IL-1α) level of STZ-exe group was significantly decreased when compared to STZ-con group. [CONCLUSION]: These results show that treadmill exercise had positive effect on cognitive function and reduced inflammatory response in STZ-induced animal model of AD.