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Repurposing an Old Drug to Improve the Use and Safety of Tissue Plasminogen Activator for Acute Ischemic Stroke: Minocycline
被引:12
|作者:
Hess, David C.
[1
]
Fagan, Susan C.
[1
,2
]
机构:
[1] Med Coll Georgia, Dept Neurol, Augusta, GA 30912 USA
[2] Univ Georgia, Coll Pharm, Program Clin & Expt Therapeut, Augusta, GA USA
来源:
PHARMACOTHERAPY
|
2010年
/
30卷
/
07期
关键词:
acute ischemic stroke;
tissue plasminogen activator;
minocycline;
MMP-9;
PARP-1;
CEREBRAL-ARTERY OCCLUSION;
MATRIX-METALLOPROTEINASE;
HEMORRHAGIC TRANSFORMATION;
POLY(ADP-RIBOSE) POLYMERASE-1;
DELAYED MINOCYCLINE;
MILD HYPOTHERMIA;
TIME WINDOW;
BRAIN;
REPERFUSION;
THROMBOLYSIS;
D O I:
10.1592/phco.30.pt2.55S
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Tissue plasminogen activator (tPA) is the only drug approved by the United States Food and Drug Administration for treatment of acute ischemic stroke. Because the drug must be used soon after symptom onset and is associated with intracerebral hemorrhage, tPA remains underutilized. Research has therefore focused on identifying other drugs that can be used concomitantly with tPA to improve the odds of a favorable recovery and to reduce the risk of intracerebral hemorrhage. Minocycline is a broad-spectrum antibiotic that has been found to be a neuroprotective agent in preclinical ischemic stroke models. Minocycline inhibits matrix metalloproteinase-9, a biomarker for intracerebral hemorrhage associated with tPA use. Minocycline is also an antiinflammatory agent and inhibits poly(ADP-ribose) polymerase-1. Minocycline has been safe and well tolerated in clinical trials. Additional safety and efficacy data are needed, and a phase III trial of minocycline with tPA in patients experiencing acute ischemic stroke is planned.
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页码:55S / 61S
页数:7
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