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 in | Nature neuroscience Vol. 8; no. 1; pp. 85 - 92 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Nature Publishing Group
01.01.2005
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Subjects | |
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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. |
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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 |
Author_xml | – sequence: 1 givenname: Peter surname: Carmeliet fullname: Carmeliet, Peter organization: The Center for Transgene Technology and Gene Therapy, Flanders Interuniversity Institute for Biotechnology (VIB), KU Leuven – sequence: 2 givenname: Erik surname: Storkebaum fullname: Storkebaum, Erik organization: The Center for Transgene Technology and Gene Therapy, Flanders Interuniversity Institute for Biotechnology (VIB), KU Leuven – sequence: 3 givenname: Diether surname: Lambrechts fullname: Lambrechts, Diether organization: The Center for Transgene Technology and Gene Therapy, Flanders Interuniversity Institute for Biotechnology (VIB), KU Leuven – sequence: 4 givenname: Mieke surname: Dewerchin fullname: Dewerchin, Mieke organization: The Center for Transgene Technology and Gene Therapy, Flanders Interuniversity Institute for Biotechnology (VIB), KU Leuven – sequence: 5 givenname: Maria-Paz surname: Moreno-Murciano fullname: Moreno-Murciano, Maria-Paz organization: The Center for Transgene Technology and Gene Therapy, Flanders Interuniversity Institute for Biotechnology (VIB), KU Leuven – sequence: 6 givenname: Saskia surname: Appelmans fullname: Appelmans, Saskia organization: The Center for Transgene Technology and Gene Therapy, Flanders Interuniversity Institute for Biotechnology (VIB), KU Leuven – sequence: 7 givenname: Hideyasu surname: Oh fullname: Oh, Hideyasu organization: The Center for Transgene Technology and Gene Therapy, Flanders Interuniversity Institute for Biotechnology (VIB), KU Leuven – sequence: 8 givenname: Philip surname: Van Damme fullname: Van Damme, Philip organization: Department of Neurology, Faculty of Medicine, KU Leuven – sequence: 9 givenname: Bart surname: Rutten fullname: Rutten, Bart organization: Department of Psychiatry and Neuropsychology, Division of Cellular Neuroscience, Maastricht University, and European Graduate School of Neuroscience (EURON) – sequence: 10 givenname: Wing Yan surname: Man fullname: Man, Wing Yan organization: The Center for Transgene Technology and Gene Therapy, Flanders Interuniversity Institute for Biotechnology (VIB), KU Leuven – sequence: 11 givenname: Maria surname: De Mol fullname: De Mol, Maria organization: The Center for Transgene Technology and Gene Therapy, Flanders Interuniversity Institute for Biotechnology (VIB), KU Leuven – sequence: 12 givenname: Sabine surname: Wyns fullname: Wyns, Sabine organization: The Center for Transgene Technology and Gene Therapy, Flanders Interuniversity Institute for Biotechnology (VIB), KU Leuven – sequence: 13 givenname: David surname: Manka fullname: Manka, David organization: The Center for Transgene Technology and Gene Therapy, Flanders Interuniversity Institute for Biotechnology (VIB), KU Leuven – sequence: 14 givenname: Kristel surname: Vermeulen fullname: Vermeulen, Kristel organization: The Center for Transgene Technology and Gene Therapy, Flanders Interuniversity Institute for Biotechnology (VIB), KU Leuven – sequence: 15 givenname: Ludo surname: Van Den Bosch fullname: Van Den Bosch, Ludo organization: Department of Neurology, Faculty of Medicine, KU Leuven – sequence: 16 givenname: Nico surname: Mertens fullname: Mertens, Nico organization: Department of Molecular Biomedical Research, Flanders Interuniversity Institute for Biotechnology, University of Ghent – sequence: 17 givenname: Christoph surname: Schmitz fullname: Schmitz, Christoph organization: Department of Psychiatry and Neuropsychology, Division of Cellular Neuroscience, Maastricht University, and European Graduate School of Neuroscience (EURON) – sequence: 18 givenname: Wim surname: Robberecht fullname: Robberecht, Wim organization: Department of Neurology, Faculty of Medicine, KU Leuven – sequence: 19 givenname: Edward M surname: Conway fullname: Conway, Edward M organization: The Center for Transgene Technology and Gene Therapy, Flanders Interuniversity Institute for Biotechnology (VIB), KU Leuven – sequence: 20 givenname: Désiré surname: Collen fullname: Collen, Désiré organization: The Center for Transgene Technology and Gene Therapy, Flanders Interuniversity Institute for Biotechnology (VIB), KU Leuven – sequence: 21 givenname: Lieve surname: Moons fullname: Moons, Lieve organization: The Center for Transgene Technology and Gene Therapy, Flanders Interuniversity Institute for Biotechnology (VIB), KU Leuven |
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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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 |
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