A neuroprotective tetrapeptide for treatment of acute traumatic brain injury.

IF 8.3 1区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
Aman P Mann, Sazid Hussain, Pablo Scodeller, Hope N B Moore, Elan Sherazee, Rachel M Russo, Erkki Ruoslahti
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Abstract

Traumatic brain injury (TBI) is a major clinical problem because of the high incidence and the severity of the subsequent sequelae. Despite extensive efforts, there are no therapeutic drugs clinically approved for treating acute TBI patients. To address this unmet need, we assessed the activity of the tetrapeptide, CAQK, in mice. When administered intravenously shortly after moderate or severe TBI, CAQK accumulates in the injured brain in mice and pigs. CAQK binds to an extracellular matrix glycoprotein complex that is upregulated in injured brain. Treatment of TBI mice with CAQK resulted in reduction in the size of the injury compared to control mice. There was reduced upregulation of the glycoprotein complex, less apoptosis, and lower expression of inflammatory markers in the injured area, indicating that CAQK alleviates neuroinflammation and the ensuing secondary injury. CAQK treatment also improved functional deficit in TBI mice, with no overt toxicity. Our findings suggest that CAQK may have therapeutic applications in TBI.

一种治疗急性创伤性脑损伤的神经保护四肽。
外伤性脑损伤(Traumatic brain injury, TBI)因其发病率高、后遗症严重而成为一个重要的临床问题。尽管做出了广泛的努力,但目前还没有临床批准的治疗急性TBI患者的药物。为了解决这一未满足的需求,我们评估了小鼠体内四肽CAQK的活性。当在中度或重度脑外伤后不久静脉注射CAQK时,小鼠和猪的损伤脑中会积累CAQK。CAQK与细胞外基质糖蛋白复合物结合,该复合物在损伤脑中上调。与对照组小鼠相比,用CAQK治疗TBI小鼠导致损伤大小减小。损伤区糖蛋白复合物上调减少,细胞凋亡减少,炎症标志物表达降低,表明CAQK减轻了神经炎症和随后的继发性损伤。CAQK治疗也改善了TBI小鼠的功能缺陷,没有明显的毒性。我们的研究结果表明,CAQK可能在TBI中具有治疗应用。
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来源期刊
EMBO Molecular Medicine
EMBO Molecular Medicine 医学-医学:研究与实验
CiteScore
17.70
自引率
0.90%
发文量
105
审稿时长
4-8 weeks
期刊介绍: EMBO Molecular Medicine is an open access journal in the field of experimental medicine, dedicated to science at the interface between clinical research and basic life sciences. In addition to human data, we welcome original studies performed in cells and/or animals provided they demonstrate human disease relevance. To enhance and better specify our commitment to precision medicine, we have expanded the scope of EMM and call for contributions in the following fields: Environmental health and medicine, in particular studies in the field of environmental medicine in its functional and mechanistic aspects (exposome studies, toxicology, biomarkers, modeling, and intervention). Clinical studies and case reports - Human clinical studies providing decisive clues how to control a given disease (epidemiological, pathophysiological, therapeutic, and vaccine studies). Case reports supporting hypothesis-driven research on the disease. Biomedical technologies - Studies that present innovative materials, tools, devices, and technologies with direct translational potential and applicability (imaging technologies, drug delivery systems, tissue engineering, and AI)
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