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

被引:7
|
作者
Sunny, Angel [1 ]
James, Raisa Rani [2 ]
Menon, Swathi Radhakrishnan [3 ]
Rayaroth, Swetha [4 ]
Daniel, Abhijith [5 ]
Thompson, Namita Ann [5 ]
Tharakan, Binu [6 ,7 ]
机构
[1] Icahn Sch Med Mt Sinai, Elmhurst, NY USA
[2] Govt Med Coll, Kozhikode, India
[3] Kashibai Navale Med Coll, Pune, India
[4] JSS Med Coll, Mysore, Karnataka, India
[5] Pushpagiri Inst Med Sci & Res Ctr, Thiruvalla, India
[6] Morehouse Sch Med, Dept Surg, Atlanta, GA USA
[7] Morehouse Sch Med, Dept Surg, 720 Westview Dr, Atlanta, GA 30310 USA
基金
美国国家卫生研究院;
关键词
Traumatic brain injury; Matrix Metalloproteinase-9; Microvascular hyperpermeability; Blood-brain barrier; Cerebral edema; CANNABINOID RECEPTOR AGONIST; FOCAL CEREBRAL-ISCHEMIA; MATRIX METALLOPROTEINASES; BARRIER DISRUPTION; MELATONIN; EDEMA; ESTROGEN; MMP-9; NEUROPROTECTION; PROGESTERONE;
D O I
10.1016/j.neuint.2023.105642
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页数:11
相关论文
共 50 条
  • [21] Role of Matrix Metalloproteinases in the Pathogenesis of Traumatic Brain Injury
    Abdul-Muneer, P. M.
    Pfister, Bryan J.
    Haorah, James
    Chandra, Namas
    MOLECULAR NEUROBIOLOGY, 2016, 53 (09) : 6106 - 6123
  • [22] Plasma matrix metalloproteinase-9 levels predict intensive care unit mortality early after severe traumatic brain injury
    Simon, Daniel
    Evaldt, Joice
    Nabinger, Debora Dreher
    Fontana, Mariano Feraboli
    Klein, Mirelli Gabardo
    Gomes, Julia do Amaral
    Regner, Andrea
    BRAIN INJURY, 2017, 31 (03) : 390 - 395
  • [23] Blood-Brain Barrier Disruption in Humans Is Independently Associated With Increased Matrix Metalloproteinase-9
    Barr, Taura L.
    Latour, Lawrence L.
    Lee, Kyung-Yul
    Schaewe, Timothy J.
    Luby, Marie
    Chang, George S.
    El-Zammar, Ziad
    Alam, Shaista
    Hallenbeck, John M.
    Kidwell, Chelsea S.
    Warach, Steven
    STROKE, 2010, 41 (03) : E123 - E128
  • [24] Role of VEGF and matrix metalloproteinase-9 in peritumoral brain edema associated with supratentorial benign meningiomas
    Iwado, Eiji
    Ichikawa, Tomotsugu
    Kosaka, Hiroshi
    Otsuka, Shinji
    Kambara, Hirokazu
    Tamiya, Takashi
    Kondo, Seiji
    Date, Isao
    NEUROPATHOLOGY, 2012, 32 (06) : 638 - 646
  • [25] Matrix Metalloproteinase-9 Mediates the Deleterious Effects of α2-Antiplasmin on Blood-Brain Barrier Breakdown and Ischemic Brain Injury in Experimental Stroke
    Singh, Satish
    Houng, Aiilyan K.
    Reed, Guy L.
    NEUROSCIENCE, 2018, 376 : 40 - 47
  • [26] Astaxanthin reduces matrix metalloproteinase-9 expression and activity in the brain after experimental subarachnoid hemorrhage in rats
    Zhang, Xiang-Sheng
    Zhang, Xin
    Zhang, Qing-Rong
    Wu, Qi
    Li, Wei
    Jiang, Tian-Wei
    Hang, Chun-Hua
    BRAIN RESEARCH, 2015, 1624 : 113 - 124
  • [27] Increase of tumor necrosis factor-α in the blood induces early activation of matrix metalloproteinase-9 in the brain
    Tsuge, Mitsuru
    Yasui, Kozo
    Ichiyawa, Takashi
    Saito, Yukie
    Nagaoka, Yoshiharu
    Yashiro, Masato
    Yamashita, Nobuko
    Morishima, Tsuneo
    MICROBIOLOGY AND IMMUNOLOGY, 2010, 54 (07) : 417 - 424
  • [28] Role of matrix metalloproteinase-9 in apoptosis of hippocampal neurons in rats during early brain injury after subarachnoid hemorrhage
    Guo, Zongduo
    Sun, Xiaochuan
    He, Zhaohui
    Jiang, Yong
    Zhang, Xiaodong
    NEUROLOGICAL SCIENCES, 2010, 31 (02) : 143 - 149
  • [29] Methamphetamine transiently increases the blood-brain barrier permeability in the hippocampus: Role of tight junction proteins and matrix metalloproteinase-9
    Martins, Tania
    Baptista, Sofia
    Goncalves, Joana
    Leal, Ermelindo
    Milhazes, Nuno
    Borges, Fernanda
    Ribeiro, Carlos F.
    Quintela, Oscar
    Lendoiro, Elena
    Lopez-Rivadulla, Manuel
    Ambrosio, Antonio F.
    Silva, Ana P.
    BRAIN RESEARCH, 2011, 1411 : 28 - 40
  • [30] Sulforaphane Attenuates Matrix Metalloproteinase-9 Expression Following Spinal Cord Injury in Mice
    Mao, Lei
    Wang, Han Dong
    Wang, Xiao Liang
    Qiao, Liang
    Yin, Hong Xia
    ANNALS OF CLINICAL AND LABORATORY SCIENCE, 2010, 40 (04) : 354 - 360