Treatment of motoneuron degeneration by intracerebroventricular delivery of VEGF in a rat model of ALS

Neurotrophin treatment has so far failed to prolong the survival of individuals affected with amyotrophic lateral sclerosis (ALS), an incurable motoneuron degenerative disorder. Here we show that intracerebroventricular (i.c.v.) delivery of recombinant vascular endothelial growth factor (Vegf) in a...

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Published inNature neuroscience Vol. 8; no. 1; pp. 85 - 92
Main Authors Carmeliet, Peter, Storkebaum, Erik, Lambrechts, Diether, Dewerchin, Mieke, Moreno-Murciano, Maria-Paz, Appelmans, Saskia, Oh, Hideyasu, Van Damme, Philip, Rutten, Bart, Man, Wing Yan, De Mol, Maria, Wyns, Sabine, Manka, David, Vermeulen, Kristel, Van Den Bosch, Ludo, Mertens, Nico, Schmitz, Christoph, Robberecht, Wim, Conway, Edward M, Collen, Désiré, Moons, Lieve
Format Journal Article
LanguageEnglish
Published United States Nature Publishing Group 01.01.2005
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Abstract Neurotrophin treatment has so far failed to prolong the survival of individuals affected with amyotrophic lateral sclerosis (ALS), an incurable motoneuron degenerative disorder. Here we show that intracerebroventricular (i.c.v.) delivery of recombinant vascular endothelial growth factor (Vegf) in a SOD1(G93A) rat model of ALS delays onset of paralysis by 17 d, improves motor performance and prolongs survival by 22 d, representing the largest effects in animal models of ALS achieved by protein delivery. By protecting cervical motoneurons, i.c.v. delivery of Vegf is particularly effective in rats with the most severe form of ALS with forelimb onset. Vegf has direct neuroprotective effects on motoneurons in vivo, because neuronal expression of a transgene expressing the Vegf receptor prolongs the survival of SOD1(G93A) mice. On i.c.v. delivery, Vegf is anterogradely transported and preserves neuromuscular junctions in SOD1(G93A) rats. Our findings in preclinical rodent models of ALS may have implications for treatment of neurodegenerative disease in general.
AbstractList Neurotrophin treatment has so far failed to prolong the survival of individuals affected with amyotrophic lateral sclerosis (ALS), an incurable motoneuron degenerative disorder. Here we show that intracerebroventricular (i.c.v.) delivery of recombinant vascular endothelial growth factor (Vegf) in a SOD1(G93A) rat model of ALS delays onset of paralysis by 17 d, improves motor performance and prolongs survival by 22 d, representing the largest effects in animal models of ALS achieved by protein delivery. By protecting cervical motoneurons, i.c.v. delivery of Vegf is particularly effective in rats with the most severe form of ALS with forelimb onset. Vegf has direct neuroprotective effects on motoneurons in vivo, because neuronal expression of a transgene expressing the Vegf receptor prolongs the survival of SOD1(G93A) mice. On i.c.v. delivery, Vegf is anterogradely transported and preserves neuromuscular junctions in SOD1(G93A) rats. Our findings in preclinical rodent models of ALS may have implications for treatment of neurodegenerative disease in general.
Neurotrophin treatment has so far failed to prolong the survival of individuals affected with amyotrophic lateral sclerosis (ALS), an incurable motoneuron degenerative disorder. Here we show that intracerebroventricular (i.c.v.) delivery of recombinant vascular endothelial growth factor (Vegf) in a SOD1 super(G93A) rat model of ALS delays onset of paralysis by 17 d, improves motor performance and prolongs survival by 22 d, representing the largest effects in animal models of ALS achieved by protein delivery. By protecting cervical motoneurons, i.c.v. delivery of Vegf is particularly effective in rats with the most severe form of ALS with forelimb onset. Vegf has direct neuroprotective effects on motoneurons in vivo, because neuronal expression of a transgene expressing the Vegf receptor prolongs the survival of SOD1 super(G93A) mice. On i.c.v. delivery, Vegf is anterogradely transported and preserves neuromuscular junctions in SOD1 super(G93A) rats. Our findings in preclinical rodent models of ALS may have implications for treatment of neurodegenerative disease in general.
Audience Academic
Author Wyns, Sabine
Van Damme, Philip
De Mol, Maria
Mertens, Nico
Collen, Désiré
Robberecht, Wim
Van Den Bosch, Ludo
Dewerchin, Mieke
Appelmans, Saskia
Oh, Hideyasu
Man, Wing Yan
Storkebaum, Erik
Moreno-Murciano, Maria-Paz
Rutten, Bart
Schmitz, Christoph
Lambrechts, Diether
Manka, David
Carmeliet, Peter
Vermeulen, Kristel
Moons, Lieve
Conway, Edward M
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/15568021$$D View this record in MEDLINE/PubMed
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Snippet Neurotrophin treatment has so far failed to prolong the survival of individuals affected with amyotrophic lateral sclerosis (ALS), an incurable motoneuron...
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StartPage 85
SubjectTerms Amyotrophic lateral sclerosis
Amyotrophic Lateral Sclerosis - genetics
Amyotrophic Lateral Sclerosis - physiopathology
Animals
Axonal Transport
Cell Survival - drug effects
Diagnosis
Disease Models, Animal
Humans
Injections, Intraventricular
Motor neurons
Motor Neurons - drug effects
Nerve Degeneration - physiopathology
Neuromuscular Junction - drug effects
Neuroprotective Agents - administration & dosage
Neuroprotective Agents - pharmacokinetics
Neuroprotective Agents - pharmacology
Physiological aspects
Rats
Rats, Sprague-Dawley
Rats, Wistar
Recombinant Proteins - administration & dosage
Recombinant Proteins - pharmacology
Risk factors
Superoxide Dismutase - genetics
Vascular endothelial growth factor
Vascular Endothelial Growth Factor A - administration & dosage
Vascular Endothelial Growth Factor A - pharmacokinetics
Vascular Endothelial Growth Factor A - pharmacology
Title Treatment of motoneuron degeneration by intracerebroventricular delivery of VEGF in a rat model of ALS
URI http://dx.doi.org/10.1038/nn1360
https://www.ncbi.nlm.nih.gov/pubmed/15568021
https://www.proquest.com/docview/274823448
https://search.proquest.com/docview/17825119
https://search.proquest.com/docview/67335893
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