Combination therapy for ischemic stroke: Novel approaches to lengthen therapeutic window of tissue plasminogen activator

被引:42
|
作者
Knecht, Talia [1 ]
Borlongan, Cesar [2 ]
dela Pena, Ike [1 ]
机构
[1] Loma Linda Univ, Sch Pharm, Dept Pharmaceut & Adm Sci, Loma Linda, CA 92350 USA
[2] Univ S Florida, Coll Med, Ctr Excellence Aging & Brain Repair, Dept Neurosurg & Brain Repair, Tampa, FL 33620 USA
关键词
Blood-brain barrier; hemorrhage; matrix metalloproteinase; stem cell; tissue plasminogen activator;
D O I
10.4103/bc.bc_21_18
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Tissue plasminogen activator (tPA) thrombolysis continues to be the gold standard therapy for ischemic stroke. Due to the time-limited treatment window, within 4.5 h of stroke onset, and a variety of potentially deadly complications related to delayed administration, particularly hemorrhagic transformation (HT), clinical use of tPA is limited. Combination therapies with other interventions, drug or nondrug, have been hypothesized as a logical approach to enhancing tPA effectiveness. Here, we discuss various potential pharmacological and nondrug treatments to minimize adverse effects, primarily HT, associated with delayed tPA administration. Pharmacological interventions include many that support the integrity of the blood-brain barrier (i.e., atorvastatin, batimastat, candesartan, cilostazol, fasudil, and minocycline), promote vascularization and preserve cerebrovasculature (i.e., coumarin derivative IMM-H004 and granulocyte-colony stimulating factor), employing other mechanisms of action (i.e., oxygen transporters and ascorbic acid). Nondrug treatments are comprised of stem cell transplantation and gas therapies with multi-faceted approaches. Combination therapy with tPA and the aforementioned treatments demonstrated promise for mitigating the adverse complications associated with delayed tPA treatment and rescuing stroke-induced behavioral deficits. Therefore, the conjunctive therapy method is a novel therapeutic approach that can attempt to minimize the limitations of tPA treatment and possibly increase the therapeutic window for ischemic stroke treatment.
引用
收藏
页码:99 / 108
页数:10
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