- About this Journal ·
- Abstracting and Indexing ·
- Aims and Scope ·
- Annual Issues ·
- Article Processing Charges ·
- Articles in Press ·
- Author Guidelines ·
- Bibliographic Information ·
- Citations to this Journal ·
- Contact Information ·
- Editorial Board ·
- Editorial Workflow ·
- Free eTOC Alerts ·
- Publication Ethics ·
- Reviewers Acknowledgment ·
- Submit a Manuscript ·
- Subscription Information ·
- Table of Contents
BioMed Research International
Volume 2014 (2014), Article ID 721968, 13 pages
Vascular Endothelial Growth Factor Increases during Blood-Brain Barrier-Enhanced Permeability Caused by Phoneutria nigriventer Spider Venom
1Department of Pharmacology, Faculty of Medical Sciences, State University of Campinas (UNICAMP), 13084-971 Campinas, SP, Brazil
2Department of Biochemistry and Tissue Biology, Institute of Biology, State University of Campinas (UNICAMP), 13083-970 Campinas, SP, Brazil
3Department of General Biology, Institute of Biological Sciences, Federal University of Minas Gerais (UFMG), 31270-901 Belo Horizonte, MG, Brazil
Received 25 May 2014; Revised 26 July 2014; Accepted 5 August 2014; Published 27 August 2014
Academic Editor: Yoshinori Marunaka
Copyright © 2014 Monique C. P. Mendonça et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Phoneutria nigriventer spider accidental envenomation provokes neurotoxic manifestations, which when critical, results in epileptic-like episodes. In rats, P. nigriventer venom (PNV) causes blood-brain barrier breakdown (BBBb). The PNV-induced excitotoxicity results from disturbances on Na+, K+ and Ca2+ channels and glutamate handling. The vascular endothelial growth factor (VEGF), beyond its angiogenic effect, also, interferes on synaptic physiology by affecting the same ion channels and protects neurons from excitotoxicity. However, it is unknown whether VEGF expression is altered following PNV envenomation. We found that adult and neonates rats injected with PNV showed immediate neurotoxic manifestations which paralleled with endothelial occludin, β-catenin, and laminin downregulation indicative of BBBb. In neonate rats, VEGF, VEGF mRNA, and Flt-1 receptors, glutamate decarboxylase, and calbindin-D28k increased in Purkinje neurons, while, in adult rats, the BBBb paralleled with VEGF mRNA, Flk-1, and calbindin-D28k increases and Flt-1 decreases. Statistically, the variable age had a role in such differences, which might be due to age-related unequal maturation of blood-brain barrier (BBB) and thus differential cross-signaling among components of the glial neurovascular unit. The concurrent increases in the VEGF/Flt-1/Flk-1 system in the cerebellar neuron cells and the BBBb following PNV exposure might imply a cytokine modulation of neuronal excitability consequent to homeostatic perturbations induced by ion channels-acting PNV neuropeptides. Whether such modulation represents neuroprotection needs further investigation.
Accidents with venomous animals have been considered a neglected health public issue. Accidents caused by Phoneutria nigriventer, popularly known as the armed spider, are common in Southeast Brazil. The majority of them only cause pain, intense sudoresis, and local inflammation. However, accidents graded as severe (less than 0.5%) cause in addition cramps, tremors, blurred yellow vision, tachypnea, cardiovascular alterations, priapism, and convulsion and rarely death, those symptoms appearing to be more severe in children [1, 2].
Experimental studies in rats showed that the clinical symptoms of envenomation paralleled those of humans. Our studies have shown that the Phoneutria nigriventer venom induces blood-brain barrier breakdown through increased vesicular transcellular transport  followed by upregulation of the glycoprotein P (P-gp) efflux protein and by impairment of the paracellular pathway due to the displacement and phosphorylation of junctional proteins . Apart from that, the venom induces vasogenic edema in hippocampus  and cytotoxic edema in rat cerebellum , reactive gliosis in the two regions , and neuronal activation (FOS+ induction) in regions associated with stress and motor activity . In the cerebellum gray matter, mainly in the granular layer, PNV upregulates the water channel aquaporin-4 , a protein which regulates edema formation and resolution. All the changes have a pace and tend to be restored with time. The mechanism(s) underlying these effects is unknown, but hypoxia secondary to the respiratory and cardiovascular distress exhibited by animals could be a primary cause.
VEGF, an angiogenic cytokine which mediates vascular permeability , has been reported to protect neurons in adverse conditions by modulation of glutamatergic synaptic excitability and interference on Ca2+, K+, and voltage-gated Na+ channels physiology [11–13]. In hippocampus, the cytokine is considered an endogenous anti-convulsing factor to preserve pyramidal neurons from hyperexcitability . VEGF exerts its action through the binding and activation of two transmembrane tyrosine kinase receptors: VEGFR-1 or Flt-1  and VEGFR-2 or Flk-1 . The receptors, in turn, modulate the VEGF signals that affect different cellular processes, so contributing for counteracting or aggravating the noxious stimuli.
In the light of the above, the current study aimed at determining whether the expression of VEGF, Flt-1, and Flk-1 and respective mRNAs of cerebellar neurons is altered in the course of BBB impairment caused by PNV in rats. Age-related alterations were investigated in neonate and young adult rats. We further analyzed the expression of glutamate decarboxylase (GAD), responsible for the synthesis of gamma-amino butyric acid (GABA) and of the calcium-binding protein calbindin-D28k (CaB), a marker of Purkinje cells. Such events were investigated because postnatal development continues for several months in the cerebellum and blood-brain barrier interface is immature in neonates. Besides, BBB of cerebellum has been already shown to be disrupted by PNV, and our hypothesis is that changes in the expression of VEGF/Flt-1/Flk-1 system may occur in parallel with BBB opening induced by ion channels-acting P. nigriventer venom and those changes could be age dependent.
2. Material and Methods
2.1. Ethics Statement
This study was approved by the Institution’s Committee for Ethics in Animal Use (CEUA/IB/Unicamp, protocol 2403-1) and the experiments were carried out according to the Brazilian Society of Laboratory Animal Science (SBCAL) guidelines for animal use.
PNV was obtained by the electrical stimulation of spiders living in Arachnid Laboratory at the Department of Biology, IBS, UFMG, Belo Horizonte, MG, Brazil, and stored at −20°C until use.
2.3. Animals and Envenoming Procedure
Male Wistar rats (Rattus norvegicus) were obtained from an established colony maintained by the Central Animal House Service at Unicamp (CEMIB/Unicamp) and housed under standard laboratory conditions. Rats aged 14 days (P14 animals—neonate group) and 8–10 weeks (adult group) were used; they received a single intraperitoneal (i.p.) injection of PNV (1.7 mg/kg in 0.5 mL of 0.9% sterile saline solution), while to control groups the same volume of vehicle was given. PNV concentration was selected based on previous laboratory studies [9, 17]. Neonate rats were used for comparison with adult rats, since severe accidents by Phoneutria generally occur in children . Time limits of 2, 5, and 24 hours corresponded to periods of peak of intoxication, beginning of clinical recovery, and no sign of intoxication at all, respectively .
2.4. Evaluation of Blood-Brain Barrier (BBB) Permeability
The integrity of the BBB was determined using Evans blue extravasation method. Briefly, 10 mL/kg of Evans blue (Vetec Química, Duque de Caxias, RJ, Brazil) dye solution (2% in 0.9% saline) was injected into the tail vein of adult rats (i.v.) at 2, 5, and 24 hours after i.p injection of 0.9% saline or PNV (1.7 mg/kg). Fifteen minutes after Evans blue injection, the rats were killed with an overdose of anesthetics and brain and cerebellum were rapidly removed and photographed.
At designated time intervals and after anesthesia, the animals (/time interval, control, and PNV-treated per age) were perfused transcardially with saline solution followed by 4% paraformaldehyde in 0.1 M PBS (phosphate buffered saline), pH 7.4. The cerebella were dissected out and were embedded in paraffin. Antibodies utilized were anti-VEGF (1 : 50, sc-7269), anti-Flt-1 (1 : 500, sc-316), and anti-Flk-1 (1 : 50, sc-315), all from Santa Cruz Biotechnology (Santa Cruz, CA, USA), CaB (1 : 1000, C2724, Sigma-Aldrich, St. Louis, MO, USA), and GAD (1 : 500, AB1511, Millipore, Billerica, MA, USA). Immunohistochemistry was performed in sequential coronal 5 μm thick paraffin sections of the cerebellum as previously described . To avoid procedure differences between control and envenomed groups, the immunohistochemistry for each protein (VEGF/Flt-1/Flk-1 and CaB/GAD) was performed concomitantly. Three images per region (molecular, granular, and Purkinje) of rats, totaling 12 images per time/age/treatment, were captured using a BX51 microscope (Olympus Optical C. Ltd., Tokyo, Japan). Objective (20x), lens aperture, and light intensity were set for all images captured.
2.6. Western Blot (WB)
Standard Western blot analysis  of cerebellum lysates (/time interval, control, and PNV treated per age) was performed using rabbit polyclonal antibody against CaB (1 : 2000, C2724, Sigma-Aldrich, St. Louis, MO, USA), Flt-1 (1 : 500, sc-316), Flk-1 (1 : 250, sc-315), both from Santa Cruz Biotechnology (Santa Cruz, CA, USA), GAD (1 : 1000, AB1511, Millipore, Billerica, MA, USA) and laminin (1 : 500, L9393, Sigma-Aldrich, St. Louis, MO, USA), mouse monoclonal antibody against VEGF (1 : 500, sc-7269) and β-Catenin (1 : 600, sc-7963), both from Santa Cruz Biotechnology (Santa Cruz, CA, USA) and β-actin (1 : 1000, A2228, Sigma-Aldrich, St. Louis, MO, USA) and goat monoclonal antibody against occludin (1 : 500, sc-8144, Santa Cruz Biotechnology, Santa Cruz, CA, USA). Bands were visualized using chemiluminescence reagent (Thermo Scientific, Waltham, MA, USA). For quantification, the density of pixels of each band was determined by the NIH Image J 1.45s software (available at http://rsb.info.nih.gov/nih-image; developed by Wayne Rasband, NIH, Bethesda, MD). For each protein investigated the results were confirmed in three sets of experiments and data were normalized using the respective loading controls. Values were normalized to the corresponding value for β-actin internal control and expressed as a ratio.
2.7. RNA Isolation and Real-Time Quantitative Reverse Transcription-PCR (qPCR)
Total RNA was isolated from the cerebellum of each group (/time interval, control, and PNV treated per age) using Trizol reagent (Life Technologies, Gaithersburg, MD, USA). Primers used in this study and their respective assay identification numbers in the Applied Biosystem catalogue were VEGF: Rn01511601_m1, Flt-1: Rn00570815_m1, Flk-1: Rn00564986_m1. The levels of VEGF, Flt-1, and Flk-1 mRNAs were calculated relative to amplicon-specific standard curves by qPCR using 50 ng total RNA in triplicate and analyzed on an ABI Prism 7500 sequence detector, using a TaqMan Universal Master Mix. The optimal concentrations of cDNA and primers, as well as the maximum efficiency of amplification, were obtained by five-point, twofold dilution curve analysis for each gene. Each PCR contained 3.0 ng of reverse-transcribed RNA, 200 nM of each specific primer, SYBR SAFE PCR master mix, and RNAse-free water to a final volume of 20 μL. All samples were run in triplicate with water as a no-template control and GAPDH as an endogenous control. Real-time data were analyzed using the Sequence Detection System 1.7 (Applied Biosystems).
Data were assessed by a three-way ANOVA to compare the variables: treatment (saline treated and PNV treated), age (P14 and 8–10 weeks), and time (2, 5, and 24 hours). Groups’ comparison was done using unpaired Student’s t-test. The results were expressed as the mean ± SEM. Values of indicate significance.
Animals of both ages injected with saline solution were alive and exhibited no sign of discomfort. Animals injected with PNV showed neurotoxic manifestation as described elsewhere . P14 rat excitotoxic effects were more precocious than in adult rats, but the recovery was delayed relative to adults. Nevertheless, signs of recovery of intoxication started 5 hours after envenoming; one adult and one neonate rat died.
3.1. Blood-Brain Barrier Permeability
Control rats (saline injected) that received i.v. infusion of Evans blue showed absence of any blue color on the brain surface or in the interior of cerebellum hemispheres which indicaes that there is no extravasation of Evans blue dye from microvasculature circulation (Figures 1(a) and 1(b)). On the contrary, PNV-treated rats showed brain and cerebellum surface and cerebellum interior shaded blue which indicates disruption of microvascular blood bed and leakage of Evans blue (Figures 1(c) and 1(d)). The leakage of Evans blue was detected at 2 hours, but not at 5 and 24 hours suggesting BBB return to integrity (not shown).
3.2. BBB Assessment: PNV Decreased Transiently Occludin, β-Catenin, and Laminin
All the three BBB-associated proteins, occludin from tight junction, β-catenin from adhesion junction, and laminin from the endothelial basal membrane, were decreased significantly by 34%, 35%, and 36%, respectively, 2 hours after administration of PNV to neonates. In adult rats, PNV induced a 33% decrease of occludin at 2 hours followed by 23% increase at 24 hours and 60% decrease of β-catenin at 2 hours and did not alter laminin expression (Figures 2(a) to 2(c)). The changes were transitory in animals of both ages.
Age-related changes showed occludin and β-catenin basal level lower in saline-injected neonate rats at 2 hours relative to adult rats. Moreover, baseline expression of laminin was lower in neonates at 5 hours and higher at 24 hours compared to adults. In envenomed rats, occludin was higher in adult rats at 5 hours than in P14 rats.
Immunohistochemistry: PNV Increased the VEGF, Flt-1, and Flk-1 Reactivity. In P14 and adult controls, VEGF immunolabeling was weakly detected in the perikaryum, outlining the cell profile of Purkinje cells (PCs); the nucleus was negative. Some cells in the molecular (ML) and granular layer (GL) were stained (Figure 3(a)). PNV-administered animals induced anti-VEGF staining in the nucleus and increased it in the somata and marginal cytoplasm of PCs (Figure 3(b)). In addition, delicate VEGF+ tangled cell processes were labeled within the ML. Cells in the GL and ML remained VEGF negative. The labeling pattern was fairly similar throughout time; however, the intensity of the reaction was marginally strongest at 24 hours.
In the cerebellum of controls, the anti-Flt-1 and anti-Flk-1 reactivity was seen in the PC nucleus and perikaryum or only in the peripheral perikaryum; a number of stained nuclei were labeled within the ML and GL (Figures 3(c) and 3(e)). PNV upregulated Flt-1 and Flk-1 level at all times in cells throughout the cerebellar cortex such as in the PCs’ nuclei, somata, and peripheral cytoplasm, in nuclei within the GL and ML, and in straight-lined processes present in the ML; in envenomed rats, regions of glomeruli were wider and density of glomerular neurons seemed lower than in controls in some parts of the GL (Figure 3(d)). Flk-1 upregulation was not as intense as for Flt-1 (compare Figures 3(e) and 3(f)). Flt-1 and Flk-1 staining increased with time, but visually no obvious difference in the intensity of the labeling could be perceived between P14 and adults (not shown).
3.3. Western Blot and Real-Time PCR
VEGF, Flt-1, and Flk-1 expressions were higher in neonates than in adult animals, both basally and after envenomation. PNV altered level of the proteins and respective mRNAs but the dynamics of changes differed between neonates and adults.
Throughout the time interval examined, VEGF, Flt-1, and Flk-1 expressions were significantly higher in neonates than in adults, both controls and envenomed (Figures 4(a) to 4(c)). However, Flk-1 mRNA was higher in adults, both controls and envenomed, than in neonates at all three time points (Figure 5(c)).
PNV induced an 18% increase of VEGF expression in P14 animals at 5 hours (Figure 4(a)). VEGF mRNA content was quite similar in control and envenomed neonates and adults (Figure 5(a)), except at 5 and 24 hours when there was a twofold increase for neonates and an 18% increase for adults.
In relation to VEGF receptors, PNV caused an immediate 50% increase in the Flt-1 level in P14 rats (2 hours) that changed to 14% increase at 5 hours and 11% increase at 24 hours above baseline (Figure 4(b)). In contrast, in adult rats PNV promoted decreases in the level of Flt-1, 25% at 2 hours, and 93% at 5 hours followed by recovery to baseline values at 24 hours. In neonate and adult rats, Flt-1 mRNA expression was unaffected by PNV exposure (Figure 5(b)). PNV did not alter the expression of the Flk-1 and its mRNA in neonates (Figures 4(c) and 5(c)) but increased Flk-1 expression in adults at 5 hours.
The three-way analysis of variance showed that variables treatment versus age versus time influenced VEGF mRNA expression () and Flt-1 receptor expression (). In addition, there was interaction between treatment versus age for the Flt-1 receptor () and treatment versus time for VEGF ().
PNV increased CaB in neonate and adult rats while GAD was increased only in neonate rats.
In controls, adult and neonate, the Purkinje cell-specific calcium-binding protein, calbindin-D28k, was expressed in the nucleus, cytosol, and dendritic tree of PCs (Figure 6(a)). Following PNV injection anti-CaB labeling was stronger particularly in PC dendrites extending across the ML (Figure 6(b)). Western blot analyses confirmed that PNV induced a 16% significant upregulation of the protein at 24 hours in neonates and a 9% increase at 5 hours in adult rats (Figure 6(c)). The baseline expression of CaB was significantly higher in neonates than in adults at 2 hours (23%); also the PNV-induced CaB expression was higher in neonates than in adults at 2 hours (25%) and 24 hours (28%). The three-way analysis of variance showed that the variables treatment versus age versus time influenced CaB expression ().
GABA signaling was altered in PNV-administered rats, given the expression of GAD, responsible for GABA synthesis, and was noticeably increased in PCs somata and dendritic tree (Figures 6(e) and 6(f)). Immunoblots showed that the GAD protein expression of treated P14 rats was 10% upregulated at 2 hours and remained practically unchanged thereafter (Figure 6(g)). In adult rats exposed to PNV, GAD remained unchanged compared to baselines values (Figure 6(h)). There was an age-related difference at 24 hours with GAD expression of PNV-treated neonate rats surpassing by 15% that of PNV-treated adults. The three-way analysis of variance showed interaction only between treatment versus age ().
The present findings show that prominent increases of VEGF and receptor Flt-1 in cerebellar neurons course with neurotoxic effects caused by PNV in P14 rats. This is accompanied by upregulations of VEGF mRNA, CaB, and GAD. The data suggest that, upon systemic presence of PNV, endogenous signaling mechanisms may have activated transcription factors and promote proteins translational regulation in newborn rats.
The alterations involving the VEGF-Flt-1 binding in neonate rats were concurrent with prominent decreases of the proteins associated with BBB endothelium: occludin, β-catenin, and laminin. The data corroborate previous studies showing PNV-induced BBB permeation in adult rats [3–6], now reaffirmed by the extravasation of Evans blue injected peripherally. Herein, the time course data over a period of 2 hours to 24 hours revealed that expressional decreases of occludin, β-catenin, and laminin (at 2 hours) were simultaneous with the peak of Flt-1 upregulation (50%) but preceded the PNV-induced significant increases of VEGF and VEGF mRNA, which occurred later at 5 hours after PNV. Also, at 5 hours, occludin, β-catenin, and laminin levels were recovered markedly relative to corresponding control levels, which paralleled with content of VEGF and Flt-1 significantly above baseline. Such data disclose what seems to be a coordinated sequence of molecular events, which began with the BBB breakdown, and proceeded with increases of Flt-1, VEGF, and VEGF mRNA. The transient disturbance of BBB-associated proteins in P14 rats might be due to the fact that VEGF receptors once activated trigger signals directed to endothelial cells  and neuron cell , either to accentuate permeability [20–22] and/or to restore homeostasis.
Curiously, in contrast to neonates, PNV induced decreases over time of Flt-1 in adult rats reaching ~93% downregulation at 5 hours, which though was transient and shows great capacity for recovery since at 24 hours the baseline level had been already reached. Consistent with this, at the same 24 hours, VEGF mRNA was significantly increased. However, PNV increased cerebellar Flk-1 and CaB at 5 hours, a time point in which BBB functionality had been restored as indicated by absence of extravasation of Evans blue dye. Interestingly, 5-hour time coincides with the beginning of the adult animals’ recovery from neurotoxic manifestations caused by PNV [4, 6].
VEGF, Flt-1, and Flk-1 protein expressions were also detected by immunohistochemistry. The three proteins were constitutively present in Purkinje neurons and their dendritic processes extended across the ML in control animals. The exposure to PNV induced visible increases in the Purkinje neurons’ immunoreactivity over a period of 2 to 24 hours; interestingly, nonuniformly dispersed cells within the GL and ML also showed increases in the Flt-1 and Flk-1 reactivity in envenomed P14 and adult rats. We do not know whether such cells are astrocytes and/or neurons. Studies have shown that VEGF and Flk-1 can be expressed by granule neurons during postnatal development of cerebellum [23–25] and by astrocytes under normal or pathological conditions [26–29]. Astrocytes also express Flt-1, but as far as we know there is no mention in the literature on Flt-1 expression by cerebellar granule cells. Since the ML is characterized by extensive synaptic contacts between granule neurons, interneurons, Begmann glia, and Purkinje neurons , it is conceivable that activation of a given cell may elicit a chain of stimuli in the others. The induction of VEGF and receptors in neurons and probably in astrocytes supports previous evidence showing these cells as targets of PNV concurrently with BBB dysfunction [3–9, 17].
VEGF family members, traditionally known as potent inducers of angiogenesis, have been recently recognized to exert various nonangiogenic effects on different cell types, among which there are neuron cells . VEGF and receptors have been recognized as an important element for neuron survival and maintenance of endothelium in adults. It acts in the nervous system both through vascular and neuronal mechanisms. Molecules that dually affect both neural and vascular (neurovascular) functions are referred to as angioneurins; their action includes regulation of angiogenesis, BBB integrity, vascular perfusion, neuroprotection, neurodegeneration, and synaptic plasticity . The protection of neurons by VEGF is exerted by interference on Ca2+, K+, and voltage-gated Na+ channels physiology and modulation of glutamatergic synaptic excitability [11–13]. VEGF inhibits outward delayed K+ currents and reduces Ca2+ influx through the high-voltage-activated Ca2+ channels; the cytokine also inhibits Na+ currents in cultured rat hippocampal neurons, thus modulating neuron excitability. In hippocampus, the cytokine is considered an endogenous anticonvulsing factor to preserve pyramidal neurons from hyperexcitability . The interference of PNV peptides in calcium homeostasis and glutamate handling have been well-documented [32–36]. Herein, we found signs that PNV disturbed calcium buffering in Purkinje neurons. P14 and adult rats treated with PNV increased CaB immunoreactivity in the PC’s nucleus, perikaryum, and dendritic ramification, which was confirmed by the WB data showing upregulation of the protein. Because PCs are the only output cell of the cerebellar cortex and because CaB functions as a calcium buffer, the changes in the PC’s immunoreactivity and level of the protein in the cerebellum lysates suggests implication on PC functional changes related with PNV effect.
PNV induced an immediate, but transient, increase of GAD expression in neonate rats, while in adults it was unaffected. The key synthesizing isoforms for GABA, GAD types 65 and 67, were decreased in the Purkinje cells of neonate rats but not in adult rats treated with PNV. This suggests that the decarboxylation of glutamate to the major inhibitory neurotransmitter GABA supports the view that synaptic inhibition is vital for the control of neuron excitability in the central nervous system and a dynamic mechanism to restore brain homeostasis, when disturbed by neurotoxic peptides of PNV. The increase of GAD in neonate rats in response to PNV is in accordance with the major level of VEGF both basically and after PNV treatment in neonate than in adult rats (see Figure 4). Whether the increase of VEGF promoted by PNV, mainly seen in neonate rats, was a way to preserve neurons [11, 12] against the glutamate toxicity generated by PNV is uncertain. Nevertheless, it is well-known that the postnatal development of cerebellum continues during months after birth , which requires active angiogenesis, neurogenesis, and cell migration. These cell processes are regulated by angioneurins, that is, growth factors that act both in neural an vascular cells, like VEGF and receptors [10, 13, 19]. In contrast, angiogenesis, neurogenesis, and cell migration are very discrete or switched off in adult animals. This might explain the relative lower expression of VEGF and receptors of cerebellum in adult animals, what could imply a mature BBB able to better stand the toxic effects. In addition, the BBB in neonate rats is undergoing postnatal development , what could explain why junctional proteins remains below baseline at 24 h in P14 rats whereas it is above baseline in adult rats. It could be the reason why systemic PNV increases even more the expression of VEGF and its mRNA (at 5 hours) and the receptors Flt-1 (from 2 to 24 hours) for neonates and transiently decreases Flt-1 expression but does not alter VEGF and only increases VEGF mRNA at 24 h in adults. Interestingly, PNV causes release of kallikrein , and kallikrein causes BBB breakdown . VEGF and kallikrein share a series of effects such as enhancing the survival and migration of neuronal and glial cells, promoting angiogenesis, protecting against ischemia, apoptosis, and glutamate-induced neurotoxicity . However, we do not know if kallikrein released by PNV is able to increase VEGF.
VEGF and PNV have in common to act on BBB-enhanced permeability, interfere in ion channels physiology, affect synaptic plasticity, and disturb glutamatergic transmission. Here, we found that the evolution of the toxic manifestations exhibited by rats injected with PNV seems to be time-related to the dynamics of immunochemical content of VEGF, Flt-1, and Flk-1 and respective mRNAs and CaB and GAD in the cerebellum. Age-related differences with neonate rats apparently were also found more susceptible to PNV than adult rats. Future studies are needed to determine whether VEGF and tyrosine kinase intracellular domains changes in Purkinje cells underlie BBB disturbances as a consequence of venom effect or a causal factor mediating the venom’s homeostatic perturbations. Ionic and glutamate disturbances, induced by PNV, affect synaptic extracellular compartments and neuronal signaling and could underlie the neurotoxic manifestations of animals. Whether the increase of VEGF in neurons represents protective modulation of synaptic excitability and of Ca2+, K+, and Na+ channels functioning is a matter to be elucidated.
Conflict of Interests
The authors declare that there is no conflict of interests regarding the publication of this paper.
The authors gratefully acknowledge Dr. L. Sodek for English revision, Dr. Licio Augusto Velloso for providing some laboratory facilities, Ms. Stephanie Souto Maior for technical assistance, and Mr. Miguel Silva for excellent animal care. MCPM was supported by studentship from Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES); ESS and LMS were supported by studentships of Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq). The work received Grants from CNPq (no. 481316/2008-6 and no. 305099/2011-6) and Fundação de Amparo à Pesquisa do Estado de São Paulo (no. 2012/24782-5).
- F. Bucaretchi, C. R. de Deus Reinaldo, S. Hyslop, P. R. Madureira, E. M. De Capitani, and R. J. Vleira, “A clinico-epidemiological study of bites by spiders of the genus phoneutrla,” Revista do Instituto de Medicina Tropical de Sao Paulo, vol. 42, no. 1, pp. 17–21, 2000.
- F. Bucaretchi, S. M. Mello, R. J. Vieira et al., “Systemic envenomation caused by the wandering spider Phoneutria nigriventer, with quantification of circulating venom,” Clinical Toxicology, vol. 46, no. 9, pp. 885–889, 2008.
- L. P. Le Sueur, C. B. Collares-Buzato, and M. A. da Cruz-Höfling, “Mechanisms involved in the blood-brain barrier increased permeability induced by Phoneutria nigriventer spider venom in rats,” Brain Research, vol. 1027, no. 1-2, pp. 38–47, 2004.
- C. Rapôso, P. A. M. Odorissi, A. L. R. Oliveira et al., “Effect of Phoneutria nigriventer venom on the expression of junctional protein and P-gp efflux pump function in the blood-brain barrier,” Neurochemical Research, vol. 37, no. 9, pp. 1967–1981, 2012.
- L. le Sueur, E. Kalapothakis, and M. A. da Cruz-Höfling, “Breakdown of the blood-brain barrier and neuropathological changes induced by Phoneutria nigriventer spider venom,” Acta Neuropathologica, vol. 105, no. 2, pp. 125–134, 2003.
- C. Rapôso, G. M. Zago, G. H. da Silva, and M. A. da Cruz Höfling, “Acute blood-brain barrier permeabilization in rats after systemic Phoneutria nigriventer venom,” Brain Research, vol. 1149, no. 1, pp. 18–29, 2007.
- M. A. da Cruz-Höfling, C. Rapôso, L. Verinaud, and G. M. Zago, “Neuroinflammation and astrocytic reaction in the course of Phoneutria nigriventer (armed-spider) blood-brain barrier (BBB) opening,” NeuroToxicology, vol. 30, no. 4, pp. 636–646, 2009.
- M. A. da Cruz-Höfling, G. M. Zago, L. L. Melo, and C. Rapôso, “C-FOS and n-NOS reactive neurons in response to circulating Phoneutria nigriventer spider venom,” Brain Research Bulletin, vol. 73, no. 1–3, pp. 114–126, 2007.
- L. M. Stavale, E. S. Soares, M. C. P. Mendonça, S. P. Irazusta, and M. A. da Cruz Höfling, “Temporal relationship between aquaporin-4 and glial fibrillary acidic protein in cerebellum of neonate and adult rats administered a BBB disrupting spider venom,” Toxicon, vol. 66, pp. 37–46, 2013.
- J. A. Nagy, L. Benjamin, H. Zeng, A. M. Dvorak, and H. F. Dvorak, “Vascular permeability, vascular hyperpermeability and angiogenesis,” Angiogenesis, vol. 11, no. 2, pp. 109–119, 2008.
- F. Sun and X. Guo, “Molecular and cellular mechanisms of neuroprotection by vascular endothelial growth factor,” Journal of Neuroscience Research, vol. 79, no. 1-2, pp. 180–184, 2005.
- J. M. Rosenstein, J. M. Krum, and C. Ruhrberg, “VEGF in the nervous system,” Organogenesis, vol. 6, no. 2, pp. 107–114, 2010.
- G. Sun and Y. Ma, “Vascular endothelial growth factor modulates voltage-gated Na+ channel properties and depresses action potential firing in cultured rat hippocampal neurons,” Biological and Pharmaceutical Bulletin, vol. 36, no. 4, pp. 548–555, 2013.
- M. Cammalleri, D. Martini, C. Ristori, A. M. Timperio, and P. Bagnoli, “Vascular endothelial growth factor up-regulation in the mouse hippocampus and its role in the control of epileptiform activity,” European Journal of Neuroscience, vol. 33, no. 3, pp. 482–498, 2011.
- C. De Vries, J. A. Escobedo, H. Ueno, K. Houck, N. Ferrara, and L. T. Williams, “The fms-like tyrosine kinase, a receptor for vascular endothelial growth factor,” Science, vol. 255, no. 5047, pp. 989–991, 1992.
- B. I. Terman, M. Dougher-Vermazen, M. E. Carrion et al., “Identification of the KDR tyrosine kinase as a receptor for vascular endothelial cell growth factor,” Biochemical and Biophysical Research Communications, vol. 187, no. 3, pp. 1579–1586, 1992.
- M. C. P. Mendonça, E. Siqueira Soares, L. Miguel Stávale, S. Pierre Irazusta, and M. A. da Cruz-Höfling, “Upregulation of the vascular endothelial growth factor, Flt-1, in rat hippocampal neurons after envenoming by Phoneutria nigriventer; age-related modulation,” Toxicon, vol. 60, no. 4, pp. 656–664, 2012.
- I. Zachary and G. Gliki, “Signaling transduction mechanisms mediating biological actions of the vascular endothelial growth factor family,” Cardiovascular Research, vol. 49, no. 3, pp. 568–581, 2001.
- B. Obermeier, R. Daneman, and R. M. Ransohoff, “Development, maintenance and disruption of the blood-brain barrier,” Nature Medicine, vol. 19, no. 12, pp. 1584–1596, 2013.
- W. G. Mayhan, “VEGF increases permeability of the blood-brain barrier via a nitric oxide synthase/cGMP-dependent pathway,” The American Journal of Physiology, vol. 276, no. 5, pp. C1148–C1153, 1999.
- Z. G. Zhang, L. Zhang, Q. Jiang et al., “VEGF enhances angiogenesis and promotes blood-brain barrier leakage in the ischemic brain,” The Journal of Clinical Investigation, vol. 106, no. 7, pp. 829–838, 2000.
- Z. G. Zhang, L. Zhang, W. Tsang, et al., “Correlation of VEGF and angiopoietin expression with disruption of blood-brain barrier and angiogenesis after focal cerebral ischemia,” Journal of Cerebral Blood Flow and Metabolism, vol. 22, no. 4, pp. 379–392, 2002.
- W. T. Monacci, M. J. Merrill, and E. H. Oldfield, “Expression of vascular permeability factor/vascular endothelial growth factor in normal rat tissues,” American Journal of Physiology, vol. 264, no. 4, pp. C995–C1002, 1993.
- C. R. de Almodovar, C. Coulon, P. A. Salin et al., “Matrix-binding vascular endothelial growth factor (VEGF) isoforms guide granule cell migration in the cerebellum via VEGF receptor Flk1,” Journal of Neuroscience, vol. 30, no. 45, pp. 15052–15066, 2010.
- C. Meissirel, C. R. de Almodovar, E. Knevels et al., “VEGF modulates NMDA receptors activity in cerebellar granule cells through src-family kinases before synapse formation,” Proceedings of the National Academy of Sciences of the United States of America, vol. 108, no. 33, pp. 13782–13787, 2011.
- T. Acker, H. Beck, and K. H. Plate, “Cell type specific expression of vascular endothelial growth factor and angiopoietin-1 and -2 suggests an important role of astrocytes in cerebellar vascularization,” Mechanisms of Development, vol. 108, no. 1-2, pp. 45–57, 2001.
- C. Kaur, V. Sivakumar, Y. Zhang, and E. A. Ling, “Hypoxia-induced astrocytic reaction and increased vascular permeability in the rat cerebellum,” Glia, vol. 54, no. 8, pp. 826–839, 2006.
- S. Y. Leung, A. S. Y. Chan, M. P. Wong, S. T. Yuen, N. Cheung, and L. P. Chung, “Expression of vascular endothelial growth factor and its receptors in pilocytic astrocytoma,” The American Journal of Surgical Pathology, vol. 21, no. 8, pp. 941–950, 1997.
- E. Papavassiliou, N. Gogate, M. Proescholdt, et al., “Vascular endothelial growth factor (vascular permeability factor) expression in injured rat brain,” Journal of Neuroscience Research, vol. 49, no. 4, pp. 451–460, 1997.
- K. Matsui and C. E. Jahr, “Differential control of synaptic and ectopic vesicular release of glutamate,” The Journal of Neuroscience, vol. 24, no. 41, pp. 8932–8939, 2004.
- S. Zacchigna, D. Lambrechts, and P. Carmeliet, “Neurovascular signalling defects in neurodegeneration,” Nature Reviews Neuroscience, vol. 9, no. 3, pp. 169–181, 2008.
- S. Love and M. A. Cruz-Hofling, “Acute swelling of nodes of Ranvier caused by venoms which slow inactivation of sodium channels,” Acta Neuropathologica, vol. 70, no. 1, pp. 1–9, 1986.
- M. V. Gomez, E. Kalapothakis, C. Guatimosim, and M. A. M. Prado, “Phoneutria nigriventer venom: a cocktail of toxins that affect ion channels,” Cellular and Molecular Neurobiology, vol. 22, no. 5-6, pp. 579–588, 2002.
- R. A. Mafra, S. G. Figueiredo, C. R. Diniz, M. N. Cordeiro, J. Dos Santos Cruz, and M. E. de Lima, “Phtx4, a new class of toxins from Phoneutria nigriventer spider venom, inhibits the glutamate uptake in rat brain synaptosomes,” Brain Research, vol. 831, no. 1-2, pp. 297–300, 1999.
- M. A. M. Prado, C. Guatimosim, M. V. Gomez, C. R. Diniz, M. N. Cordeiro, and M. A. Romano-Silva, “A novel tool for the investigation of glutamate release from rat cerebrocortical synaptosomes: the toxin Tx3-3 from the venom of the spider Phoneutria nigriventer,” The Biochemical Journal, vol. 314, no. 1, pp. 145–150, 1996.
- A. C. N. Pinheiro, R. S. Gomez, A. R. Massensini et al., “Neuroprotective effect on brain injury by neurotoxins from the spider Phoneutria nigriventer,” Neurochemistry International, vol. 49, no. 5, pp. 543–547, 2006.
- J. Altman and S. A. Bayer, Development of the Cerebellar System in Relation to Its Evolution, Structure and Functions, CRC Press, New York, NY, USA, 1997.
- W. Risau, S. Esser, and B. Engelhardt, “Differentiation of blood-brain barrier endothelial cells,” Pathologie Biologie, vol. 46, no. 3, pp. 171–175, 1998.
- C. Gewehr, S. M. Oliveira, M. F. Rossato et al., “Mechanisms involved in the nociception triggered by the venom of the armed spider Phoneutria nigriventer,” PLoS Neglected Tropical Diseases, vol. 7, no. 4, Article ID e2198, 2013.
- M. Kunz, J. Nussberger, M. Holtmannspätter, H. Bitterling, N. Plesnila, and S. Zausinger, “Bradykinin in blood and cerebrospinal fluid after acute cerebral lesions: correlations with cerebral edema and intracranial pressure,” Journal of Neurotrauma, vol. 30, no. 19, pp. 1638–1644, 2013.
- C. Emanueli, P. Schratzberger, R. Kirchmair, and P. Madeddu, “Paracrine control of vascularization and neurogenesis by neurotrophins,” British Journal of Pharmacology, vol. 140, no. 4, pp. 614–619, 2003.