Exercise Plus Pharmacological Neuromodulation of Synaptic Inhibition Enhance Motor Function Recovery After Ischemic Stroke. (15th March 2020)

• Record Type: Journal Article
• Authors: Inoue, Takahiro; Okamura, Misato; Kitahara, Mika; Takamatsu, Yasuyuki; Sakakima, Harutoshi; Maejima, Hiroshi
• Is Part Of: Neuroscience. Volume 430(2020)
• Page Start: 12
• Page End: 24
• Publication Date: 2020-03-15
• Subjects: BDNF -- stroke -- GABA -- exercise -- cortex -- neuromodulation; Neurochemistry -- Periodicals; Neurophysiology -- Periodicals; Neurology -- Periodicals; Neurochimie -- Périodiques; Neurophysiologie -- Périodiques; Neurochemistry; Neurophysiology; Electronic journals; Periodicals; Electronic journals; 612.8
• DOI: 10.1016/j.neuroscience.2020.01.012
• Languages: English
• ISSNs: 0306-4522

Abstract

Highlights: Co-application of exercise and a low-level GABAA antagonist facilitated motor functional recovery after stroke. Co-application of exercise and a low-level GABAA antagonist upregulated BDNF protein levels in the ipsilateral M1. Pharmacological neuromodulation targeting GABA could be a potential treatment modality in stroke rehabilitation. Abstract: The objective of this study was to examine the interactive effects of exercise and low-level inhibition of GABAA receptors on the recovery of motor function and BDNF expression in the primary motor cortex (M1) of a stroke rat model. Male Sprague–Dawley rats were divided into five groups: sham (SHAM), control (CON), exercise (EX), bicuculline (BIC), and bicuculline plus exercise (BICEX) groups. All rats, except those in the SHAM group, underwent middle cerebral artery occlusion (MCAO) surgery to induce an ischemic stroke. GABAA receptor antagonist, bicuculline (0.25 mg/kg, i.p.), was administered to the BIC and BICEX groups. The EX and BICEX groups exercised on a treadmill (11 m/min for 30 min). Each intervention started 3 days after the MCAO surgery and was carried out every day for 2 weeks. Following the intervention, bilateral M1 BDNF mRNA and protein expression levels were assessed using qRT-PCR and ELISA. Marginal recovery was found in the EX and BIC groups, whereas motor function recovery was enhanced with exercise in the presence of BIC administration specifically in the BICEX group. Furthermore, BDNF protein level in the ipsilateral M1 was significantly higher in the BICEX group than in other groups. This study indicated that exercise combined with low-level inhibition of GABAA receptors after stroke could facilitate the recovery of motor function accompanied by BDNF upregulation in the ipsilateral M1. Therefore, this study provides a novel insight of pharmacological neuromodulation into stroke rehabilitation.