摘要

Prothymosin alpha (ProT alpha) suppresses stress-induced necrosis of cultured cortical neurons. As neuroprotection alone could not explain the long-lasting protective actions against cerebral ischemia by ProT alpha, we further examined whether ProT alpha, in addition to neuroprotective effects, has other anti-ischemic activities. When recombinant mouse ProT alpha (rmProT alpha) at 0.3 mg/kg was intravenously (i.v.) given 2 h after the start of tMCAO, all mice survived for more than 14 days. In evaluation of CD31- and tomato lectin-labeling as well as IgG and Evans blue leakage, rmProTa treatment (0.1 mg/kg) largely blocked ischemia-induced vascular damages. Therefore, rmProT alpha has novel beneficial effects against ischemia-induced brain damage through vascular mechanisms.

  • 出版日期2016-9