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基质金属蛋白酶-9 抑制剂作为创伤性脑损伤的治疗药物。

Matrix Metalloproteinase-9 inhibitors as therapeutic drugs for traumatic brain injury.

机构信息

Icahn School of Medicine at Mount Sinai, Elmhurst, NY, USA.

Government Medical College, Kozhikode, India.

出版信息

Neurochem Int. 2024 Jan;172:105642. doi: 10.1016/j.neuint.2023.105642. Epub 2023 Nov 24.

Abstract

Traumatic brain injury (TBI) is one of the leading causes of morbidity and mortality among young adults and the elderly. In the United States, TBI is responsible for around 30 percent of all injuries brought on by injuries in general. Vasogenic cerebral edema due to blood-brain barrier (BBB) dysfunction and the associated elevation of intracranial pressure (ICP) are some of the major causes of secondary injuries following traumatic brain injury. Matrix metalloproteinase-9 (MMP-9) is a therapeutic target for being an enzyme that degrades the proteins that make up a part of the microvascular basal lamina as well as inter-endothelial tight junctions of the blood-brain barrier. MMP-9-mediated BBB dysfunctions and the compromise of the BBB is a major pathway that leads the development of vasogenic cerebral edema, elevation of ICP, poor cerebral perfusion and brain herniation following traumatic brain injury. That makes MMP-9 an effective therapeutic target and endogenous or exogenous MMP-9 inhibitors as therapeutic drugs for preventing secondary brain damage after traumatic brain injury. Although our understanding of the mechanisms that underlie the primary and secondary stages of damage following a TBI has significantly improved in recent years, such information has not yet resulted in the successful development of novel pharmacological treatment options for traumatic brain injury. Recent pre-clinical and/or clinical studies have demonstrated that there are several compounds with specific or non-specific MMP-9 inhibitory properties either directly binding and inhibiting MMP-9 or by indirectly inhibiting MMP-9, with potential as therapeutic agents for traumatic brain injury. This article reviews the efficacy of several such medications and potential agents that include endogenous and exogeneous compounds that are at various levels of research and development. MMP-9-based therapeutic drug development has enormous potential in the pharmacological treatment of cerebral edema and/or neuronal injury resulting from traumatic brain injury.

摘要

创伤性脑损伤(TBI)是导致年轻人和老年人发病率和死亡率的主要原因之一。在美国,TBI 约占所有因受伤导致的损伤的 30%。血脑屏障(BBB)功能障碍导致的血管源性脑水肿和相关颅内压(ICP)升高是创伤性脑损伤后继发性损伤的主要原因之一。基质金属蛋白酶-9(MMP-9)是一种治疗靶点,因为它是一种能够降解构成微血管基底膜和血脑屏障内皮细胞紧密连接的一部分的蛋白质的酶。MMP-9 介导的 BBB 功能障碍和 BBB 的损害是导致血管源性脑水肿、ICP 升高、脑灌注不良和创伤性脑损伤后脑疝形成的主要途径。这使得 MMP-9 成为一种有效的治疗靶点,内源性或外源性 MMP-9 抑制剂作为治疗创伤性脑损伤后继发性脑损伤的药物。尽管近年来我们对 TBI 后原发性和继发性损伤阶段的机制有了更深入的了解,但这些信息尚未导致新的创伤性脑损伤治疗药物的成功开发。最近的临床前和/或临床研究表明,有几种具有特定或非特异性 MMP-9 抑制特性的化合物,要么直接结合并抑制 MMP-9,要么间接抑制 MMP-9,具有作为创伤性脑损伤治疗剂的潜力。本文综述了几种此类药物的疗效和潜在药物,包括内源性和外源性化合物,它们处于不同的研究和开发阶段。基于 MMP-9 的治疗药物开发在创伤性脑损伤引起的脑水肿和/或神经元损伤的药理学治疗方面具有巨大潜力。

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