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Activated Protein C Analog Protects From Ischemic Stroke and Extends the Therapeutic Window of Tissue-Type Plasminogen Activator in Aged Female Mice and Hypertensive Rats
Author(s) -
Yaoming Wang,
Zhen Zhao,
Nienwen Chow,
Padmesh S. Rajput,
John H. Griffin,
Patrick D. Lyden,
Berislav V. Zloković
Publication year - 2013
Publication title -
stroke
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.397
H-Index - 319
eISSN - 1524-4628
pISSN - 0039-2499
DOI - 10.1161/strokeaha.113.003350
Subject(s) - medicine , therapeutic window , tissue plasminogen activator , plasminogen activator , stroke (engine) , t plasminogen activator , ischemic stroke , activator (genetics) , ischemia , fibrinolysis , endocrinology , pharmacology , receptor , mechanical engineering , engineering
3K3A-activated protein C (APC) protects young, healthy male rodents after ischemic stroke. 3K3A-APC is currently under development as a neuroprotectant for acute ischemic stroke in humans. Stroke Therapy Academic Industry Roundtable recommends that after initial studies in young, healthy male animals, further studies should be performed in females, aged animals, and animals with comorbid conditions. Here, we studied the effects of delayed 3KA-APC therapy alone and with tissue-type plasminogen activator (tPA) in aged female mice and spontaneously hypertensive rats.

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