Probucol treatment after traumatic brain injury activates BDNF/TrkB pathway, promotes neuroregeneration and ameliorates functional deficits in mice

Author:

Chen Chen‐Mei1,Gung Pei‐Yu1,Ho Yen‐Chun12ORCID,Hamdin Candra D.13,Yet Shaw‐Fang14ORCID

Affiliation:

1. Institute of Cellular and System Medicine National Health Research Institutes Zhunan Taiwan

2. Cardiovascular Biology Program Oklahoma Medical Research Foundation Oklahoma City Oklahoma USA

3. National Health Research Institutes & Department of Life Sciences, National Central University Joint Ph.D. Program in Biomedicine Taoyuan City Taiwan

4. Graduate Institute of Biomedical Sciences China Medical University Taichung Taiwan

Abstract

AbstractBackground and PurposeTraumatic brain injury (TBI) is a major cause of mortality and morbidity worldwide, yet pharmacotherapies for TBI are currently lacking. Neuroregeneration is important in brain repair and functional recovery. In this study, probucol, a cholesterol‐lowering drug with established safety profiles, was examined for its therapeutic effects and neuroregenerative actions in TBI.Experimental ApproachMale mice were subjected to the controlled cortical impact model of TBI, followed by daily administration of probucol. Neurological and cognitive functions were evaluated. Histological analyses of the neocortex and hippocampus were performed to detect the lesion, dendritic degeneration (microtubule‐associated protein 2), synaptic density (synaptophysin), neurogenesis (doublecortin), brain‐derived neurotrophic factor (BDNF) and tropomyosin receptor kinase B (TrkB) activation. Involvement of BDNF/TrkB pathway in probucol‐mediated effects was examined in primary cultures of cortical neurons.Key ResultsProbucol reduced brain lesion volume, enhanced the recovery of body symmetry, improved motor function and attenuated memory dysfunction after TBI. Meanwhile, probucol promoted post‐injury dendritic growth and synaptogenesis and increased hippocampal proliferating neuronal progenitor cells, along with the formation as well as the survival of newborn neurons. Moreover, probucol enhances BDNF expression and TrkB activation. In vitro, probucol promoted neurite outgrowth, which was inhibited by a selective TrkB antagonist ANA‐12.Conclusions and ImplicationsProbucol enhanced functional restoration and ameliorated cognitive impairment after TBI by promoting post‐injury neuronal remodelling and neurogenesis. Increased activation of BDNF/TrkB pathway by probucol, at least in part, contributed to the neuroregenerative effects of probucol. Together, it may be promising to repurpose probucol for TBI.

Funder

National Health Research Institutes

Ministry of Science and Technology

Publisher

Wiley

Subject

Pharmacology

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