Combination Treatment With VELCADE and Low-Dose Tissue Plasminogen Activator Provides Potent Neuroprotection in Aged Rats After Embolic Focal Ischemia

被引:50
作者
Zhang, Li [1 ]
Zhang, Zheng Gang [1 ]
Buller, Ben [1 ,3 ]
Jiang, James [1 ]
Jiang, Yanting [1 ]
Zhao, Danping [1 ]
Liu, Xianshuang [1 ]
Morris, Dan [2 ]
Chopp, Michael [1 ,3 ]
机构
[1] Henry Ford Hlth Syst, Dept Neurol, Detroit, MI 48202 USA
[2] Henry Ford Hlth Syst, Dept Emergency Med, Detroit, MI 48202 USA
[3] Oakland Univ, Dept Phys, Rochester, MI USA
关键词
embolic stroke; thrombolysis; BLOOD-BRAIN-BARRIER; CEREBRAL-ISCHEMIA; FUNCTIONAL RECOVERY; REDUCES INFARCTION; UP-REGULATION; IN-VIVO; STROKE; INHIBITOR; THROMBOLYSIS; MODEL;
D O I
10.1161/STROKEAHA.109.577288
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose-Treatment with a selective proteasome inhibitor, VELCADE, in combination with tissue plasminogen activator (tPA) extended the therapeutic window to 6 hours in young rats after stroke. However, stroke is a major cause of death and disability in the elderly. The present study investigated the effect of VELCADE in combination with a low-dose tPA on aged rats after embolic stroke. Methods-Male Wistar rats at the age of 18 to 20 months were treated with VELCADE (0.2 mg/kg) alone, a low-dose tPA (5 mg/kg) alone, combination of VELCADE and tPA, or saline 2 hours after embolic middle cerebral artery occlusion. To test the contribution of endothelial nitric oxide synthase to VELCADE-mediated neuroprotection, endothelial nitric oxide synthase knockout and wild-type mice were treated with VELCADE (0.5 mg/kg) 2 hours after embolic stroke. Results-Treatment with VELCADE significantly reduced infarct volume, whereas tPA alone did not reduce infarct volume and aggravated blood-brain barrier disruption in aged rats compared with saline-treated rats. However, the combination treatment significantly enhanced the reduction of infarct volume, which was associated with an increase in endothelial nitric oxide synthase activity compared with saline-treated rats. Additionally, the combination treatment promoted thrombolysis and did not increase the incidence of hemorrhage transformation. VELCADE significantly reduced lesion volume in wild-type mice but failed to significantly reduce lesion volume in endothelial nitric oxide synthase knockout mice. Conclusions-Treatment with VELCADE exerts a neuroprotective effect in aged rats after stroke. The combination of VELCADE with the low-dose tPA further amplifies the neuroprotective effect. Endothelial nitric oxide synthase at least partly contributes to VELCADE-mediated neuroprotection after stroke. (Stroke. 2010;41:1001-1007.)
引用
收藏
页码:1001 / 1007
页数:7
相关论文
共 25 条
[1]   AGE-RELATED-CHANGES IN THE HEMOSTATIC SYSTEM [J].
ABBATE, R ;
PRISCO, D ;
ROSTAGNO, C ;
BODDI, M ;
GENSINI, GF .
INTERNATIONAL JOURNAL OF CLINICAL & LABORATORY RESEARCH, 1993, 23 (01) :1-3
[2]  
[Anonymous], 1995, N. Engl J Med, V333, P1581, DOI DOI 10.1056/NEJM199512143332401
[3]   Effects of matrix metalloproteinase-9 gene knock-out on the proteolysis of blood-brain barrier and white matter components after cerebral ischemia [J].
Asahi, M ;
Wang, XY ;
Mori, T ;
Sumii, T ;
Jung, JC ;
Moskowitz, MA ;
Fini, ME ;
Lo, EH .
JOURNAL OF NEUROSCIENCE, 2001, 21 (19) :7724-7732
[4]   Therapeutic benefit of intravenous administration of bone marrow stromal cells after cerebral ischemia in rats [J].
Chen, JL ;
Li, Y ;
Wang, L ;
Zhang, ZG ;
Lu, DY ;
Lu, M ;
Chopp, M .
STROKE, 2001, 32 (04) :1005-1011
[5]   Structure and functions of the 20S and 26S proteasomes [J].
Coux, O ;
Tanaka, K ;
Goldberg, AL .
ANNUAL REVIEW OF BIOCHEMISTRY, 1996, 65 :801-847
[6]   Early disruptions of the blood-brain barrier may contribute to exacerbated neuronal damage and prolonged functional recovery following stroke in aged rats [J].
DiNapoli, Vincent A. ;
Huber, Jason D. ;
Houser, Kimberly ;
Li, Xinlan ;
Rosen, Charles L. .
NEUROBIOLOGY OF AGING, 2008, 29 (05) :753-764
[7]   Early intravenous thrombolysis for acute ischemic stroke in a community-based approach [J].
Grond, M ;
Stenzel, C ;
Schmülling, S ;
Rudolf, J ;
Neveling, M ;
Lechleuthner, A ;
Schneweis, S ;
Heiss, WD .
STROKE, 1998, 29 (08) :1544-1549
[8]   eNOS gene transfer inhibits smooth muscle cell migration and MMP-2 and MMP-9 activity [J].
Gurjar, MV ;
Sharma, RV ;
Bhalla, RC .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1999, 19 (12) :2871-2877
[9]   The proteasome inhibitor VELCADE® reduces infarction in rat models of focal cerebral ischemia [J].
Henninger, N ;
Sicard, KM ;
Bouley, J ;
Fisher, M ;
Stagliano, NE .
NEUROSCIENCE LETTERS, 2006, 398 (03) :300-305
[10]   Predictors of in-hospital mortality in patients with acute ischemic stroke treated with thrombolytic therapy [J].
Heuschmann, PU ;
Kolominsky-Rabas, PL ;
Roether, J ;
Misselwitz, B ;
Lowitzsch, K ;
Heidrich, J ;
Hermanek, P ;
Leffmann, C ;
Sitzer, M ;
Biegler, M ;
Buecker-Nott, HJ ;
Berger, K .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2004, 292 (15) :1831-1838