PMID- 25045713 OWN - NLM STAT- MEDLINE DCOM- 20150312 LR - 20211021 IS - 2314-6141 (Electronic) IS - 2314-6133 (Print) VI - 2014 DP - 2014 TI - Gradually increased training intensity benefits rehabilitation outcome after stroke by BDNF upregulation and stress suppression. PG - 925762 LID - 10.1155/2014/925762 [doi] LID - 925762 AB - Physical training is necessary for effective rehabilitation in the early poststroke period. Animal studies commonly use fixed training intensity throughout rehabilitation and without adapting it to the animals' recovered motor ability. This study investigated the correlation between training intensity and rehabilitation efficacy by using a focal ischemic stroke rat model. Eighty male Sprague-Dawley rats were induced with middle cerebral artery occlusion/reperfusion surgery. Sixty rats with successful stroke were then randomly assigned into four groups: control (CG, n = 15), low intensity (LG, n = 15), gradually increased intensity (GIG, n = 15), and high intensity (HG, n = 15). Behavioral tests were conducted daily to evaluate motor function recovery. Stress level and neural recovery were evaluated via plasma corticosterone and brain-derived neurotrophic factor (BDNF) concentration, respectively. GIG rats significantly (P < 0.05) recovered motor function and produced higher hippocampal BDNF (112.87 +/- 25.18 ng/g). GIG and LG rats exhibited similar stress levels (540.63 +/- 117.40 nM/L and 508.07 +/- 161.30 nM/L, resp.), which were significantly lower (P < 0.05) than that (716.90 +/- 156.48 nM/L) of HG rats. Training with gradually increased intensity achieved better recovery with lower stress. Our observations indicate that a training protocol that includes gradually increasing training intensity should be considered in both animal and clinical studies for better stroke recovery. FAU - Sun, Jing AU - Sun J AUID- ORCID: 0000-0001-9847-3372 AD - Interdisciplinary Division of Biomedical Engineering, The Hong Kong Polytechnic University, Hong Kong. FAU - Ke, Zheng AU - Ke Z AD - Interdisciplinary Division of Biomedical Engineering, The Hong Kong Polytechnic University, Hong Kong. FAU - Yip, Shea Ping AU - Yip SP AUID- ORCID: 0000-0002-2170-8185 AD - Department of Health Technology and Informatics, The Hong Kong Polytechnic University, Hong Kong. FAU - Hu, Xiao-ling AU - Hu XL AUID- ORCID: 0000-0003-3188-3005 AD - Interdisciplinary Division of Biomedical Engineering, The Hong Kong Polytechnic University, Hong Kong. FAU - Zheng, Xiao-xiang AU - Zheng XX AD - College of Biomedical Engineering and Instrument Science, Zhejiang University, Hangzhou 310027, China. FAU - Tong, Kai-yu AU - Tong KY AUID- ORCID: 0000-0003-4375-653X AD - Interdisciplinary Division of Biomedical Engineering, The Hong Kong Polytechnic University, Hong Kong. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20140619 PL - United States TA - Biomed Res Int JT - BioMed research international JID - 101600173 RN - 0 (Brain-Derived Neurotrophic Factor) RN - 7171WSG8A2 (BDNF protein, human) SB - IM MH - Animals MH - Brain Ischemia/metabolism/pathology/*rehabilitation MH - Brain-Derived Neurotrophic Factor/*metabolism MH - Disease Models, Animal MH - Humans MH - Infarction, Middle Cerebral Artery/pathology MH - Male MH - *Physical Conditioning, Animal MH - Rats MH - Rats, Sprague-Dawley MH - Stress, Physiological MH - Stroke/metabolism/pathology MH - *Stroke Rehabilitation MH - Treatment Outcome PMC - PMC4090448 EDAT- 2014/07/22 06:00 MHDA- 2015/03/13 06:00 PMCR- 2014/06/19 CRDT- 2014/07/22 06:00 PHST- 2014/02/28 00:00 [received] PHST- 2014/05/14 00:00 [revised] PHST- 2014/05/21 00:00 [accepted] PHST- 2014/07/22 06:00 [entrez] PHST- 2014/07/22 06:00 [pubmed] PHST- 2015/03/13 06:00 [medline] PHST- 2014/06/19 00:00 [pmc-release] AID - 10.1155/2014/925762 [doi] PST - ppublish SO - Biomed Res Int. 2014;2014:925762. doi: 10.1155/2014/925762. Epub 2014 Jun 19.