Moghanlou Abdorreza Eghbal, Yazdanian Mohtaram, Roshani Sajad, Demirli Abdullah, Seydyousefi Mehdi, Metz Gerlinde A S, Faghfoori Zeinab
Department of Coaching Education, Istanbul Esenyurt University, Istanbul, Turkey.
Sanabad Golbahar Institute of Higher Education, Mashhad, Iran.
Brain Res Bull. 2023 Mar;194:54-63. doi: 10.1016/j.brainresbull.2023.01.004. Epub 2023 Jan 13.
Stroke causes irreversible damage, particularly to the hippocampus. Evidence suggests that exercise training may mitigate adverse structural and functional consequences of an ischemic lesion in the brain. The purpose of this study was to investigate the effects of preconditioning exercise on expression of neurotrophic factor genes and proteins in hippocampalCA1 region and their relationship with sensorimotor recovery following global ischemia/reperfusion (Is/Re) injury in a rat model of stroke.
Male Wistar rats were randomly assigned to Exercise+Ischemia/Reperfusion (Ex+Is/Re),Control+Ischemia/Reperfusion (Co+Is/Re), and Sham treatments. Rats in the exercise groups ran on a treadmill for 45 min/d for five days/week for 8 consecutive weeks prior to Is/Re lesion.Ischemia was induced by common carotid artery occlusion (CCAO). The ladder rung walking task was used to assess functional impairments and recovery following ischemic lesion.Tissue from hippocampal area CA1 was inspected for ischemia-induced cell loss and gene and protein expression linked to neurotrophins NT-3, NT-4, and their receptorsTrkB and TrkC.
CCAO caused hippocampal cell death in CA1 and resulted in significant sensori motor impairments in the ladder rung walking task. In contrast, pre-ischemic exercise considerably reduced cell death and supported sensorimotor recovery following CCAO.In addition, NT-3, NT-4,TrkB and TrkC gene expression and their protein levels were significantly increased inthe Ex+Is/Re group compared to Co+Is/Re (p < 0.05).
The findings showed that pre-ischemic exercise can exert neuroprotective effects via NT-3 and NT-4 pathways against ischemia in hippocampal CA1 neurons and promote post-injury sensorimotor recovery.
中风会造成不可逆的损伤,尤其是对海马体。有证据表明,运动训练可能减轻脑部缺血性损伤的不良结构和功能后果。本研究的目的是探讨预处理运动对海马CA1区神经营养因子基因和蛋白表达的影响,以及它们与中风大鼠模型全脑缺血/再灌注(Is/Re)损伤后感觉运动恢复的关系。
将雄性Wistar大鼠随机分为运动+缺血/再灌注组(Ex+Is/Re)、对照+缺血/再灌注组(Co+Is/Re)和假手术组。运动组大鼠在缺血/再灌注损伤前连续8周,每周5天,每天在跑步机上跑45分钟。通过颈总动脉闭塞(CCAO)诱导缺血。采用阶梯行走任务评估缺血性损伤后的功能障碍和恢复情况。检查海马CA1区组织的缺血诱导细胞损失以及与神经营养因子NT-3、NT-4及其受体TrkB和TrkC相关的基因和蛋白表达。
CCAO导致CA1区海马细胞死亡,并在阶梯行走任务中导致明显的感觉运动障碍。相比之下,缺血前运动显著减少了细胞死亡,并支持了CCAO后的感觉运动恢复。此外,与Co+Is/Re组相比,Ex+Is/Re组中NT-3、NT-4、TrkB和TrkC基因表达及其蛋白水平显著增加(p<0.05)。
研究结果表明,缺血前运动可通过NT-3和NT-4途径对海马CA1神经元缺血发挥神经保护作用,并促进损伤后感觉运动恢复。