Injectable Hydrogels Providing Sustained Delivery of Vascular Endothelial Growth Factor are Neuroprotective in a Rat Model of Huntington's Disease

被引:27
作者
Emerich, Dwaine F. [1 ]
Mooney, David J. [2 ,3 ]
Storrie, Hannah [2 ]
Babu, Rangasamy Suresh [4 ]
Kordower, Jeffrey H. [4 ]
机构
[1] InCytu Inc, Lincoln, RI 02865 USA
[2] Harvard Univ, Sch Engn & Appl Sci, Cambridge, MA 02138 USA
[3] Wyss Inst Biologically Inspired Engn, Cambridge, MA 02138 USA
[4] Rush Univ, Med Ctr, Dept Neurol Sci, Chicago, IL 60612 USA
关键词
VEGF; Huntington's disease; Hydrogel; Alginate; Neuroprotection; CILIARY NEUROTROPHIC FACTOR; PARKINSONS-DISEASE; RODENT MODEL; NEUROCHEMICAL DEFICITS; HIPPOCAMPAL-NEURONS; GENE-TRANSFER; VEGF; SURVIVAL; CELLS; EXCITOTOXICITY;
D O I
10.1007/s12640-009-9079-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Vascular endothelial growth factor (VEGF) is a potent peptide with well-documented pro-angiogenic effects. Recently, it has also become clear that exogenous administration of VEGF is neuroprotective in animal models of central nervous system diseases. In the present study, VEGF was incorporated into a sustained release hydrogel delivery system to examine its potential benefits in a rat model of Huntington's disease (HD). The VEGF-containing hydrogel was stereotaxically injected into the striatum of adult rats. Three days later, quinolinic acid (QA; 225 nmol) was injected into the ipsilateral striatum to produce neuronal loss and behavioral deficits that mimic those observed in HD. Two weeks after surgery, animals were tested for motor function using the placement and cylinder tests. Control animals received either QA alone or QA plus empty hydrogel implants. Behavioral testing confirmed that the QA lesion resulted in significant deficits in the ability of the control animals to use their contralateral forelimb. In contrast, the performance of those animals receiving VEGF was significantly improved relative to controls with only modest motor impairments observed. Stereological counts of NeuN-positive neurons throughout the striatum demonstrated that VEGF implants significantly protected against the loss of striatal neurons induced by QA. These data are the first to demonstrate that VEGF can be used to protect striatal neurons from excitotoxic damage in a rat model of HD.
引用
收藏
页码:66 / 74
页数:9
相关论文
共 65 条
[1]   Neurotrophic factors in Huntington's disease [J].
Alberch, J ;
Pérez-Navarro, E ;
Canals, JM .
NGF AND RELATED MOLECULES IN HEALTH AND DISEASE, 2004, 146 :195-229
[2]  
[Anonymous], NEURODEGENERATIVE DI
[3]  
Araujo DM, 1998, NEUROSCIENCE, V82, P117
[4]   Glial cell line-derived neurotrophic factor attenuates the excitotoxin-induced behavioral and neurochemical deficits in a rodent model of Huntington's disease [J].
Araujo, DM ;
Hilt, DC .
NEUROSCIENCE, 1997, 81 (04) :1099-1110
[5]   Neuroprotective gene therapy for Huntington's disease, using polymer-encapsulated cells engineered to secrete human ciliary neurotrophic factor:: Results of a phase I study [J].
Bloch, J ;
Bachoud-Lévi, AC ;
Déglon, N ;
Lefaucheur, JP ;
Winkel, L ;
Palfi, S ;
Nguyen, JP ;
Bourdet, C ;
Gaura, V ;
Remy, P ;
Brugières, P ;
Boisse, MF ;
Baudic, S ;
Cesaro, P ;
Hantraye, P ;
Aebischer, P ;
Peschanski, M .
HUMAN GENE THERAPY, 2004, 15 (10) :968-975
[6]  
Bogaert E, 2009, NEUROBIOL AGING 0128
[7]  
Cavalieri B, 1966, GEOMETRIA INDIVISIBI, P1
[8]   Nurr1 in Parkinson's disease and related disorders [J].
Chu, YP ;
Le, WD ;
Kompoliti, K ;
Jankovic, J ;
Mufson, EJ ;
Kordower, JH .
JOURNAL OF COMPARATIVE NEUROLOGY, 2006, 494 (03) :495-514
[9]  
CONNEALLY P M, 1984, Genetic Epidemiology, V1, P81, DOI 10.1002/gepi.1370010110
[10]   Vascular growth factors in cerebral ischemia [J].
Croll, SD ;
Wiegand, SJ .
MOLECULAR NEUROBIOLOGY, 2001, 23 (2-3) :121-135