在小儿猪创伤性脑损伤模型中,CMX-2043治疗限制神经损伤病理生理并促进神经和认知恢复。

IF 3.8 2区 医学 Q1 CLINICAL NEUROLOGY
Sarah L Schantz, Taylor H LePage, Stephanie T Dubrof, Sydney E Sneed, Savannah R Cheek, Hea Jin Park, Deborah A Barany, Holly A Kinder, Kylee J Duberstein, David A DeWahl, Alexander B Baguisi, Jerry O Stern, Erin E Kaiser, Franklin D West
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引用次数: 0

摘要

创伤性脑损伤(TBI)是造成严重残疾和死亡率的一个重大全球健康问题。脑外伤引起的继发性损伤级联,以神经炎症、神经细胞死亡和组织损伤为特征,可导致终身功能缺陷。α - n -[(R)- 1,2 -二硫代烷-3-戊烷]l-谷氨酰-l-丙氨酸(CMX-2043)是一种新型的基于α硫辛酸(ALA)的治疗药物,具有神经保护、抗凋亡和抗炎特性,可减轻TBI后的细胞、组织和功能缺陷。在本研究中,我们在临床相关的猪TBI模型中评估了CMX-2043对神经损伤程度和功能恢复的治疗效果。CMX-2043在颅脑损伤后1小时皮下注射(SQ;n = 8)或静脉注射(IV;N = 8),共5天。对照仔猪(安慰剂;N = 11)皮下注射生理盐水。磁共振成像(MRI)、免疫组织化学分析、改良兰金量表(mRS)神经学评估和社会识别测试(SRT)在脑损伤后42天进行评估。MRI显示SQ和IV CMX-2043减少了半球肿胀和萎缩、病变体积、中线移位和脑出血,并保持了弥漫性、脑血流量和白质完整性。SQ和IV给药后,cmx -2043介导的神经保护和再生表明神经细胞密度增加,神经炎症减少,神经发生增强。这些细胞和组织水平的变化分别与mRS和SRT结果的改善所表明的神经功能缺陷的减少和认知能力的快速恢复相对应。总的来说,这些在转译的大型动物猪模型中观察到的结果表明,CMX-2043在缓解TBI病理生理和促进功能恢复方面具有重要的临床价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CMX-2043 Treatment Limits Neural Injury Pathophysiology and Promotes Neurological and Cognitive Recovery in a Pediatric Porcine Traumatic Brain Injury Model.

Traumatic brain injury (TBI) represents a major global health issue contributing to significant disability and mortality. The TBI-induced secondary injury cascade, characterized by neuroinflammation, neural cell death, and tissue damage, results in lifelong functional deficits. Alpha-N-[(R)-1, 2-dithiolane-3-pentanoyl]l-glutamyl-l-alanine (CMX-2043) is a novel alpha lipoic acid (ALA)-based therapeutic that has neuroprotective, anti-apoptotic, and anti-inflammatory properties that mitigate cellular, tissue, and functional deficits following TBI. In this study, we evaluated the therapeutic efficacy of CMX-2043 on neural injury severity and functional recovery in a clinically relevant porcine TBI model. CMX-2043 was administered 1-h post-TBI subcutaneously (SQ; n = 8) or intravenously (IV; n = 8) for a total of 5 days. Control piglets (placebo; n = 11) received saline subcutaneously. Magnetic resonance imaging (MRI), immunohistochemistry analysis, modified Rankin Scale (mRS) neurological evaluation, and social recognition testing (SRT) were evaluated up to 42 days post-TBI. MRI revealed that SQ and IV CMX-2043 administration reduced hemispheric swelling and atrophy, lesion volume, midline shift, and intracerebral hemorrhage and preserved diffusivity, cerebral blood flow, and white matter integrity. CMX-2043-mediated neuroprotection and regeneration were indicated by increased neural cell density, decreased neuroinflammation, and enhanced neurogenesis following SQ and IV administration. These cellular and tissue-level changes corresponded with reduced neurological deficits and rapid cognitive recovery as indicated by improved mRS and SRT results, respectively. Collectively, these results observed in a translational large animal porcine model suggest that CMX-2043 holds significant clinical value to potentially mitigate TBI pathophysiology and promote functional recovery.

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来源期刊
Journal of neurotrauma
Journal of neurotrauma 医学-临床神经学
CiteScore
9.20
自引率
7.10%
发文量
233
审稿时长
3 months
期刊介绍: Journal of Neurotrauma is the flagship, peer-reviewed publication for reporting on the latest advances in both the clinical and laboratory investigation of traumatic brain and spinal cord injury. The Journal focuses on the basic pathobiology of injury to the central nervous system, while considering preclinical and clinical trials targeted at improving both the early management and long-term care and recovery of traumatically injured patients. This is the essential journal publishing cutting-edge basic and translational research in traumatically injured human and animal studies, with emphasis on neurodegenerative disease research linked to CNS trauma.
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