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

被引:2
|
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
  • [1] Matrix Metalloproteinase-9 in the Ventricular Cerebrospinal Fluid Correlated with the Prognosis of Traumatic Brain Injury
    Liu, Chun-Lin
    Chen, Chun-Chang
    Lee, Han-Chung
    Cho, Der-Yang
    [J]. TURKISH NEUROSURGERY, 2014, 24 (03) : 363 - 368
  • [2] Matrix metalloproteinase-9, its inhibitor-1 and interleukines in experimental traumatic brain injury
    Ziablitsev, S. V.
    Yuzkiv, Ya. S.
    [J]. PATHOLOGIA, 2016, (03): : 20 - 24
  • [3] Matrix metalloproteinase-9 regulates the blood brain barrier via the hedgehog pathway in a rat model of traumatic brain injury
    Wu, Mu-Yao
    Gao, Fan
    Yang, Xiao-Mei
    Qin, Xia
    Chen, Guo-Zhao
    Li, Di
    Dang, Bao-Qi
    Chen, Gang
    [J]. BRAIN RESEARCH, 2020, 1727
  • [4] Ablation of Matrix Metalloproteinase-9 Mitigates Caveolar Transcytosis in Cerebral Vessels After Mild Traumatic Brain Injury
    Muradashvili, Nino
    Tyagi, Reeta
    Benton, Richard L.
    Lominadze, David
    [J]. CIRCULATION, 2013, 128 (22)
  • [5] Hyperbaric oxygen therapy reduces neuroinflammation and expression of matrix metalloproteinase-9 in the rat model of traumatic brain injury
    Vlodavsky, E
    Palzur, E
    Soustiel, JF
    [J]. NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 2006, 32 (01) : 40 - 50
  • [6] Selective Inhibition of Matrix Metalloproteinase-9 Attenuates Secondary Damage Resulting from Severe Traumatic Brain Injury
    Hadass, Orr
    Tomlinson, Brittany N.
    Gooyit, Major
    Chen, Shanyan
    Purdy, Justin J.
    Walker, Jennifer M.
    Zhang, Chunyang
    Giritharan, Andrew B.
    Purnell, Whitley
    Robinson, Christopher R., II
    Shin, Dmitriy
    Schroeder, Valerie A.
    Suckow, Mark A.
    Simonyi, Agnes
    Sun, Grace Y.
    Mobashery, Shahriar
    Cui, Jiankun
    Chang, Mayland
    Gu, Zezong
    [J]. PLOS ONE, 2013, 8 (10):
  • [7] Matrix metalloproteinase-9 potentiates early brain injury after subarachnoid hemorrhage
    Guo, Zongduo
    Sun, Xiaochuan
    He, Zhaohui
    Jiang, Yong
    Zhang, Xiaodong
    Zhang, John H.
    [J]. NEUROLOGICAL RESEARCH, 2010, 32 (07) : 715 - 720
  • [8] Tissue Inhibitors of Metalloproteinase 1 and 2 and Matrix Metalloproteinase-9 in Prediabetes
    Chen, Junping
    Fu, Dongxu
    Stoner, Julie A.
    Wu, Mingyuan
    Lyons, Timothy J.
    [J]. DIABETES, 2011, 60 : A156 - A156
  • [9] Structures of Matrix Metalloproteinase-9 in Complex with Pharmacological Inhibitors
    Tochowicz, Anna
    Goettig, Peter
    Bode, Wolfram
    Maskos, Klaus
    [J]. ACTA CRYSTALLOGRAPHICA A-FOUNDATION AND ADVANCES, 2005, 61 : C217 - C217
  • [10] Effects of matrix metalloproteinase-9 gene knock-out on morphological and motor outcomes after traumatic brain injury
    Wang, XY
    Jung, JC
    Asahi, M
    Chwang, W
    Russo, L
    Moskowitz, MA
    Dixon, CE
    Fini, ME
    Lo, EH
    [J]. JOURNAL OF NEUROSCIENCE, 2000, 20 (18): : 7037 - 7042