Effects of intraventricular infusion of vascular endothelial growth factor on cerebral blood flow, edema, and infarct volume

被引:82
作者
Harrigan, MR [1 ]
Ennis, SR [1 ]
Sullivan, SE [1 ]
Keep, RF [1 ]
机构
[1] Univ Michigan Hlth Syst, Dept Neurosurg, Ann Arbor, MI 48109 USA
关键词
angiogenesis; vascular endothelial growth factor; brain edema; cerebral ischemia;
D O I
10.1007/s00701-002-1035-1
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background. Therapeutic cerebral angiogenesis, utilizing angiogenic factors to enhance collateral vessel formation within the central nervous system, is a potential method for cerebral revascularization. A prior dose-response study determined that intracerebroventricular infusion of vascular endothelial growth factor (VEGF) increases vascular density with minimal associated brain edema at a concentration of 5 mug/ml. The purpose of this study was to assess effects of intracerebroventricular infusion of VEGF (5 mug/ml) on cerebral blood flow, infarct volume. and brain edema after ischemia. Methods. Recombinant human VEGF(165) was infused into the right lateral ventricle of rats with an osmotic minipump at a rate of 1 mul/hr for 7 days. Control animals received vehicle only. Ischemia was produced by transient (2 hours) middle cerebral artery occlusion (MCAO). After MCAO, cerebral blood flow was determined with the indicator fractionation technique: infarct volume was assessed with 2,3,5-triphenlytetrazolium chloride staining. and brain edema was determined by measuring brain water content. Findings. Cerebral blood flow was not significantly different in animals treated with VEGF compared to controls. There was a significant reduction in total infarct volume after temporary MCAO in VEGF-treated animals compared to controls (163 +/- 37 mm(3) vs. 309 +/- 54 mm(3), P < 0.05). Brain water content after transient MCAO was also significantly reduced in VEGF-treated animals compared to controls (80.9 +/- 0.7% vs. 83.3 +/- 0.65, P < 0.05). Interpretation. Intracerebroventricular infusion of VEGF(165) (5 mug/ml) decreases infarct volume and brain edema after temporary MCAO without a significant increase in cerebral blood flow. These results indicate that VEGF may have a direct neuroprotective effect in cerebral ischemia.
引用
收藏
页码:49 / 53
页数:5
相关论文
共 21 条
[1]  
Bao WL, 1999, ACTA PHARMACOL SIN, V20, P313
[2]   Constitutive expression of phVEGF165 after intramuscular gene transfer promotes collateral vessel development in patients with critical limb ischemia [J].
Baumgartner, I ;
Pieczek, A ;
Manor, O ;
Blair, R ;
Kearney, M ;
Walsh, K ;
Isner, JM .
CIRCULATION, 1998, 97 (12) :1114-1123
[3]   Therapeutic angiogenesis for ischemic cardiovascular disease [J].
Freedman, SB ;
Isner, JM .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2001, 33 (03) :379-393
[4]   Intraventricular infusion of vascular endothelial growth factor promotes cerebral angiogenesis with minimal brain edema [J].
Harrigan, MR ;
Ennis, SR ;
Masada, T ;
Keep, RF .
NEUROSURGERY, 2002, 50 (03) :589-598
[5]   Reduction of ischemic damage by application of vascular endothelial growth factor in rat brain after transient ischemia [J].
Hayashi, T ;
Abe, K ;
Itoyama, Y .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1998, 18 (08) :887-895
[6]   Vascular endothelial growth factor rescues HN33 neural cells from death induced by serum withdrawal [J].
Jin, KL ;
Mao, XO ;
Greenberg, DA .
JOURNAL OF MOLECULAR NEUROSCIENCE, 2000, 14 (03) :197-203
[7]   REVERSIBLE MIDDLE CEREBRAL-ARTERY OCCLUSION WITHOUT CRANIECTOMY IN RATS [J].
LONGA, EZ ;
WEINSTEIN, PR ;
CARLSON, S ;
CUMMINS, R .
STROKE, 1989, 20 (01) :84-91
[8]   Gene therapy for myocardial angiogenesis -: Initial clinical results with direct myocardial injection of phVEGF165 as sole therapy for myocardial ischemia [J].
Losordo, DW ;
Vale, PR ;
Symes, JF ;
Dunnington, CH ;
Esakof, DD ;
Maysky, M ;
Ashare, AB ;
Lathi, K ;
Isner, JM .
CIRCULATION, 1998, 98 (25) :2800-2804
[9]   CONTRIBUTIONS OF IONS AND ALBUMIN TO THE FORMATION AND RESOLUTION OF ISCHEMIC BRAIN EDEMA [J].
MENZIES, SA ;
BETZ, AL ;
HOFF, JT .
JOURNAL OF NEUROSURGERY, 1993, 78 (02) :257-266
[10]   Deletion of the hypoxia-response element in the vascular endothelial growth factor promoter causes motor neuron degeneration [J].
Oosthuyse, B ;
Moons, L ;
Storkebaum, E ;
Beck, H ;
Nuyens, D ;
Brusselmans, K ;
Van Dorpe, J ;
Hellings, P ;
Gorselink, M ;
Heymans, S ;
Theilmeier, G ;
Dewerchin, M ;
Laudenbach, V ;
Vermylen, P ;
Raat, H ;
Acker, T ;
Vleminckx, V ;
Van den Bosch, L ;
Cashman, N ;
Fujisawa, H ;
Drost, MR ;
Sciot, R ;
Bruyninckx, F ;
Hicklin, DJ ;
Ince, C ;
Gressens, P ;
Lupu, F ;
Plate, KH ;
Robberecht, W ;
Herbert, JM ;
Collen, D ;
Carmeliet, P .
NATURE GENETICS, 2001, 28 (02) :131-138