Stachybotrys microspora triprenyl phenol-7, a novel fibrinolytic agent, suppresses superoxide production, matrix metalloproteinase-9 expression, and thereby attenuates ischemia/reperfusion injury in rat brain

被引:37
作者
Akamatsu, Yosuke [2 ]
Saito, Atsushi [3 ]
Fujimura, Miki [1 ]
Shimizu, Hiroaki [3 ]
Mekawy, Moataz [2 ]
Hasumi, Keiji [4 ]
Tominaga, Teiji [2 ]
机构
[1] Natl Hosp Org Sendai Med Ctr, Dept Neurosurg, Sendai, Miyagi 9838520, Japan
[2] Tohoku Univ, Dept Neurosurg, Grad Sch Med, Sendai, Miyagi 980, Japan
[3] Kohnan Hosp, Dept Neurosurg, Taihaku Ku, Sendai, Miyagi 9828523, Japan
[4] Tokyo Univ Agr & Technol, Dept Appl Biol Sci, Tokyo 1838538, Japan
关键词
Matrix metalloproteinase-9; Reactive oxygen species; Stachybotrys microspora triprenyl phenol-7; Transient focal cerebral ischemia (tFCI); FOCAL CEREBRAL-ISCHEMIA; TISSUE-PLASMINOGEN ACTIVATOR; MATRIX METALLOPROTEINASES; BARRIER DISRUPTION; STROKE; MICE; INHIBITION; STAPLABIN; NEUROTOXICITY; HYDROETHIDINE;
D O I
10.1016/j.neulet.2011.08.018
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Stachybotrys microspora triprenyl phenol-7 (SMTP-7) is a novel fibrinolytic agent with anti-inflammatory effect. Previous study demonstrated that SMTP-7 further ameliorated infarction volume in a mouse embolic stroke model compared with tissue type plasminogen activator (tPA), but the reason SMTP-7 has more beneficial effect than tPA has not yet been determined. In the present study, we investigated whether SMTP-7 has an intrinsic neuroprotective effect against transient focal cerebral ischemia (tFCI). Sprague-Dawley rats were subjected to tFCI by intraluminal middle cerebral artery occlusion for 2 h. Following induction of tFCI, rats were randomized into two groups based on the agent administered: SMTP-7 group and vehicle group. We examined cerebral infarction volume 24 h after reperfusion, and evaluated superoxide production, the expressions of nitrotyrosine and matrix metalloproteinase-9 (MMP-9), which play major roles in secondary brain injury and hemorrhagic transformation. The findings showed that SMTP-7 significantly suppressed superoxide production, the expression of nitrotyrosine and MMP-9 after tFCI, and consequently attenuated ischemic neuronal damage. These results suggest that SMTP-7 has an intrinsic neuroprotective effect on ischemia/reperfusion injury through the suppression of oxidative stress and MMP-9 activation. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:110 / 114
页数:5
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