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Distinct Effects of Tissue-Type Plasminogen Activator and SMTP-7 on Cerebrovascular Inflammation Following Thrombolytic Reperfusion
Author(s) -
Takuro Miyazaki,
Yuji Kimura,
Hisayuki Ohata,
Terumasa Hashimoto,
Keita Shibata,
Keiji Hasumi,
Kazuo Honda
Publication year - 2011
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.110.598359
Subject(s) - medicine , inflammation , tissue plasminogen activator , plasminogen activator , stroke (engine) , cardiology , fibrinolytic agent , thrombolysis , fibrinolysis , pharmacology , myocardial infarction , mechanical engineering , engineering
Thrombolysis therapy using tissue-type plasminogen activator (t-PA) is occasionally accompanied by harmful outcomes, including intracerebral hemorrhage. We have reported that Stachybotrys microspora triprenyl phenol-7 (SMTP-7), a candidate thrombolytic drug, has excellent therapeutic effect on cerebral infarction in embolic stroke model in mice; however, little is known regarding whether this agent influences cerebrovascular inflammation following thrombolytic reperfusion. The current study aimed to compare the effects of recombinant t-PA (rt-PA) and SMTP-7 on cerebrovascular inflammation.

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