Kwon Hyung-Min, Kim YunHee, Yang Seung-In, Kim Yong-Ju, Lee Seung-Hoon, Yoon Byung-Woo
Department of Neurology, Seoul National University Boramae Hospital, Seoul, Korea.
Neurol Res. 2008 Sep;30(7):740-5. doi: 10.1179/174313208X289615. Epub 2008 Jun 3.
Geldanamycin (GA), a benzoquinone ansamycin, binds HSP90, releases heat shock factor 1 and induces heat shock proteins (HSPs). HSP70, a major molecular chaperone, protects the brain against ischemic injury through inhibition of apoptotic pathways in vivo and reduced matrix metalloproteinase 9 (MMP-9) after ischemia in vitro. We hypothesized that GA would protect brain from focal ischemia via induction of HSP70 and MMP suppression in vivo.
GA or vehicle was injected into the lateral cerebral ventricles of adult male Sprague-Dawley rats using the stereotatic frame 24 hours before ischemia. Rats were subjected to 2 hour middle cerebral artery occlusions using the suture technique followed by 22 hour reperfusions. One day after ischemia, we evaluated infarction volume, brain swelling, behavioral scores and immunohistochemistry.
Western blots showed that GA at 2 mug/kg induced HSP70 by 24 hours following administration. GA decreased infarct volumes and brain edema, and improved behavioral outcomes (p<0.05). Immunohistochemistry showed that GA induced HSP70 and decreased MMP-9.
GA protects brain from focal ischemia and reduces edema. This may be due, at least in part, to GA overexpression of HSP70.
格尔德霉素(GA)是一种苯醌安莎霉素,可与热休克蛋白90(HSP90)结合,释放热休克因子1并诱导热休克蛋白(HSPs)。热休克蛋白70(HSP70)是一种主要的分子伴侣,在体内可通过抑制凋亡途径保护大脑免受缺血性损伤,在体外可减少缺血后的基质金属蛋白酶9(MMP-9)。我们推测GA可通过在体内诱导HSP70和抑制MMP来保护大脑免受局灶性缺血损伤。
在缺血前24小时,使用立体定位框架将GA或溶剂注入成年雄性Sprague-Dawley大鼠的侧脑室。采用缝合技术使大鼠大脑中动脉闭塞2小时,随后再灌注22小时。缺血1天后,我们评估梗死体积、脑肿胀、行为评分和免疫组织化学。
蛋白质免疫印迹显示,给予2μg/kg的GA后24小时可诱导HSP70。GA可减少梗死体积和脑水肿,并改善行为结果(p<0.05)。免疫组织化学显示,GA可诱导HSP70并降低MMP-9。
GA可保护大脑免受局灶性缺血损伤并减轻水肿。这可能至少部分归因于GA使HSP70过表达。