Effect of intracortical vascular endothelial growth factor infusion and blockade during the critical period in the rat visual cortex

被引:5
作者
Argandona, Enrike G. [1 ]
Bengoetxea, Harkaitz [2 ]
Bulnes, Susana [2 ]
Rico-Barrio, Irantzu [2 ]
Ortuzar, Naiara [2 ]
Lafuente, Jose V. [2 ]
机构
[1] Univ Fribourg, Dept Med, Unit Anat, CH-1700 Fribourg, Switzerland
[2] Univ Basque Country UPV EHU, Dept Neurosci, Lab Expt Neurosci LaNCE, E-48940 Leioa, Spain
关键词
Neurovascular unit; Diaschisis; VEGF; Neuroprotection; Neurorestoration; TRAUMATIC BRAIN-INJURY; POSTNATAL-DEVELOPMENT; CEREBRAL-ISCHEMIA; FACTOR EXPRESSION; PLASTICITY MECHANISMS; BARRIER PERMEABILITY; NEUROVASCULAR UNIT; FACTOR RECEPTOR; FOCAL ISCHEMIA; TISSUE-DAMAGE;
D O I
10.1016/j.brainres.2012.07.008
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
VEGF is the major angiogenic and vascular permeability factor in health and disease. Vascular development depends on function, and in sensory areas is experience-dependent. Our aim was to investigate, qualitatively and quantitatively, the effects of intracortical infusion and neutralisation of VEGF during the first days of the critical visual period, when peak levels of endogenous VEGF secretion are reached. VEGF was intracortically delivered into middle cortical layers of P18 Long-Evans rats. Another cohort received anti-VEGF. Vehicle (PBS)-infused and non-operated animals were used as controls. Various immunopathological analyses were performed: Endothelial Barrier Antigen (EBA) for the BBB integrity and GFAP for astroglial response. Vascular density was measured by Butyryl Cholinesterase Histochemistry, neuronal density by NeuN immunohistochemistry and apoptosis by TUNEL staining. VEGF levels were measured by Western Blot. Decreased vascular permeability was evoked in VEGF-infused rats whilst EBA expression remained constant, suggesting a preserved BBB function. When VEGF was blocked, tissue showed a higher degree of extravasation and a decreased number of EBA-positive vessels surrounding the injury. Lesion induced by cannula implantation annulled the normal increase in vascular density and the decrease in neuronal density during this time. VEGF rescued in part the vascular increase, and also prevented physiological and pathological neuronal death. VEGF blockade induced a higher amount of neural loss and lower astrocytic reaction. Our results support the role of VEGF as extending beyond vascularization, preventing physiological and pathological neuronal death, not only in the injured hemisphere but also in the intact one suggesting a process of transhemispheric diaschisis. (C) 2012 Elsevier By. All rights reserved.
引用
收藏
页码:141 / 154
页数:14
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