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创伤性脑损伤后普罗布考治疗激活 BDNF/TrkB 通路,促进神经再生,改善小鼠的功能缺陷。

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

机构信息

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

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

出版信息

Br J Pharmacol. 2023 Oct;180(20):2605-2622. doi: 10.1111/bph.16157. Epub 2023 Jun 26.

Abstract

BACKGROUND AND PURPOSE

Traumatic 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 APPROACH

Male 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 RESULTS

Probucol 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 IMPLICATIONS

Probucol 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.

摘要

背景与目的

创伤性脑损伤(TBI)是全球范围内导致死亡和发病的主要原因,但目前缺乏 TBI 的药物治疗方法。神经再生对于脑修复和功能恢复很重要。在这项研究中,普罗布考作为一种具有明确安全性的降胆固醇药物,研究了其在 TBI 中的治疗效果和神经再生作用。

实验方法

雄性小鼠接受皮质撞击模型 TBI,随后每天给予普罗布考治疗。评估神经和认知功能。对新皮层和海马进行组织学分析,以检测损伤、树突变性(微管相关蛋白 2)、突触密度(突触素)、神经发生(双皮质素)、脑源性神经营养因子(BDNF)和原肌球蛋白受体激酶 B(TrkB)的激活。在皮质神经元原代培养物中检测 BDNF/TrkB 途径在普罗布考介导作用中的作用。

主要结果

普罗布考可减少脑损伤体积,促进 TBI 后身体对称性恢复、运动功能改善和记忆功能障碍减轻。同时,普罗布考促进损伤后树突生长和突触形成,并增加海马增殖性神经前体细胞,形成和存活新生神经元。此外,普罗布考增强 BDNF 表达和 TrkB 激活。在体外,普罗布考促进神经突生长,而选择性 TrkB 拮抗剂 ANA-12 则抑制其生长。

结论和意义

普罗布考通过促进损伤后神经元重塑和神经发生,增强 TBI 后的功能恢复并改善认知障碍。普罗布考增加 BDNF/TrkB 途径的激活,至少部分导致了普罗布考的神经再生作用。总之,重新利用普罗布考治疗 TBI 可能具有广阔前景。

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