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Voluntary wheel running complements microdystrophin gene therapy to improve muscle function in mdx mice

We tested the hypothesis that voluntary wheel running would complement microdystrophin gene therapy to improve muscle function in young mdx mice, a model of Duchenne muscular dystrophy. mdx mice injected with a single dose of AAV9-CK8-microdystrophin or vehicle at age 7 weeks were assigned to three...

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Autores principales: Hamm, Shelby E., Fathalikhani, Daniel D., Bukovec, Katherine E., Addington, Adele K., Zhang, Haiyan, Perry, Justin B., McMillan, Ryan P., Lawlor, Michael W., Prom, Mariah J., Vanden Avond, Mark A., Kumar, Suresh N., Coleman, Kirsten E., Dupont, J.B., Mack, David L., Brown, David A., Morris, Carl A., Gonzalez, J. Patrick, Grange, Robert W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8020351/
https://www.ncbi.nlm.nih.gov/pubmed/33850950
http://dx.doi.org/10.1016/j.omtm.2021.02.024
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author Hamm, Shelby E.
Fathalikhani, Daniel D.
Bukovec, Katherine E.
Addington, Adele K.
Zhang, Haiyan
Perry, Justin B.
McMillan, Ryan P.
Lawlor, Michael W.
Prom, Mariah J.
Vanden Avond, Mark A.
Kumar, Suresh N.
Coleman, Kirsten E.
Dupont, J.B.
Mack, David L.
Brown, David A.
Morris, Carl A.
Gonzalez, J. Patrick
Grange, Robert W.
author_facet Hamm, Shelby E.
Fathalikhani, Daniel D.
Bukovec, Katherine E.
Addington, Adele K.
Zhang, Haiyan
Perry, Justin B.
McMillan, Ryan P.
Lawlor, Michael W.
Prom, Mariah J.
Vanden Avond, Mark A.
Kumar, Suresh N.
Coleman, Kirsten E.
Dupont, J.B.
Mack, David L.
Brown, David A.
Morris, Carl A.
Gonzalez, J. Patrick
Grange, Robert W.
author_sort Hamm, Shelby E.
collection PubMed
description We tested the hypothesis that voluntary wheel running would complement microdystrophin gene therapy to improve muscle function in young mdx mice, a model of Duchenne muscular dystrophy. mdx mice injected with a single dose of AAV9-CK8-microdystrophin or vehicle at age 7 weeks were assigned to three groups: mdxRGT (run, gene therapy), mdxGT (no run, gene therapy), or mdx (no run, no gene therapy). Wild-type (WT) mice were assigned to WTR (run) and WT (no run) groups. WTR and mdxRGT performed voluntary wheel running for 21 weeks; remaining groups were cage active. Robust expression of microdystrophin occurred in heart and limb muscles of treated mice. mdxRGT versus mdxGT mice showed increased microdystrophin in quadriceps but decreased levels in diaphragm. mdx final treadmill fatigue time was depressed compared to all groups, improved in mdxGT, and highest in mdxRGT. Both weekly running distance (km) and final treadmill fatigue time for mdxRGT and WTR were similar. Remarkably, mdxRGT diaphragm power was only rescued to 60% of WT, suggesting a negative impact of running. However, potential changes in fiber type distribution in mdxRGT diaphragms could indicate an adaptation to trade power for endurance. Post-treatment in vivo maximal plantar flexor torque relative to baseline values was greater for mdxGT and mdxRGT versus all other groups. Mitochondrial respiration rates from red quadriceps fibers were significantly improved in mdxGT animals, but the greatest bioenergetic benefit was observed in the mdxRGT group. Additional assessments revealed partial to full functional restoration in mdxGT and mdxRGT muscles relative to WT. These data demonstrate that voluntary wheel running combined with microdystrophin gene therapy in young mdx mice improved whole-body performance, affected muscle function differentially, mitigated energetic deficits, but also revealed some detrimental effects of exercise. With microdystrophin gene therapy currently in clinical trials, these data may help us understand the potential impact of exercise in treated patients.
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spelling pubmed-80203512021-04-12 Voluntary wheel running complements microdystrophin gene therapy to improve muscle function in mdx mice Hamm, Shelby E. Fathalikhani, Daniel D. Bukovec, Katherine E. Addington, Adele K. Zhang, Haiyan Perry, Justin B. McMillan, Ryan P. Lawlor, Michael W. Prom, Mariah J. Vanden Avond, Mark A. Kumar, Suresh N. Coleman, Kirsten E. Dupont, J.B. Mack, David L. Brown, David A. Morris, Carl A. Gonzalez, J. Patrick Grange, Robert W. Mol Ther Methods Clin Dev Original Article We tested the hypothesis that voluntary wheel running would complement microdystrophin gene therapy to improve muscle function in young mdx mice, a model of Duchenne muscular dystrophy. mdx mice injected with a single dose of AAV9-CK8-microdystrophin or vehicle at age 7 weeks were assigned to three groups: mdxRGT (run, gene therapy), mdxGT (no run, gene therapy), or mdx (no run, no gene therapy). Wild-type (WT) mice were assigned to WTR (run) and WT (no run) groups. WTR and mdxRGT performed voluntary wheel running for 21 weeks; remaining groups were cage active. Robust expression of microdystrophin occurred in heart and limb muscles of treated mice. mdxRGT versus mdxGT mice showed increased microdystrophin in quadriceps but decreased levels in diaphragm. mdx final treadmill fatigue time was depressed compared to all groups, improved in mdxGT, and highest in mdxRGT. Both weekly running distance (km) and final treadmill fatigue time for mdxRGT and WTR were similar. Remarkably, mdxRGT diaphragm power was only rescued to 60% of WT, suggesting a negative impact of running. However, potential changes in fiber type distribution in mdxRGT diaphragms could indicate an adaptation to trade power for endurance. Post-treatment in vivo maximal plantar flexor torque relative to baseline values was greater for mdxGT and mdxRGT versus all other groups. Mitochondrial respiration rates from red quadriceps fibers were significantly improved in mdxGT animals, but the greatest bioenergetic benefit was observed in the mdxRGT group. Additional assessments revealed partial to full functional restoration in mdxGT and mdxRGT muscles relative to WT. These data demonstrate that voluntary wheel running combined with microdystrophin gene therapy in young mdx mice improved whole-body performance, affected muscle function differentially, mitigated energetic deficits, but also revealed some detrimental effects of exercise. With microdystrophin gene therapy currently in clinical trials, these data may help us understand the potential impact of exercise in treated patients. American Society of Gene & Cell Therapy 2021-03-03 /pmc/articles/PMC8020351/ /pubmed/33850950 http://dx.doi.org/10.1016/j.omtm.2021.02.024 Text en © 2021 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Hamm, Shelby E.
Fathalikhani, Daniel D.
Bukovec, Katherine E.
Addington, Adele K.
Zhang, Haiyan
Perry, Justin B.
McMillan, Ryan P.
Lawlor, Michael W.
Prom, Mariah J.
Vanden Avond, Mark A.
Kumar, Suresh N.
Coleman, Kirsten E.
Dupont, J.B.
Mack, David L.
Brown, David A.
Morris, Carl A.
Gonzalez, J. Patrick
Grange, Robert W.
Voluntary wheel running complements microdystrophin gene therapy to improve muscle function in mdx mice
title Voluntary wheel running complements microdystrophin gene therapy to improve muscle function in mdx mice
title_full Voluntary wheel running complements microdystrophin gene therapy to improve muscle function in mdx mice
title_fullStr Voluntary wheel running complements microdystrophin gene therapy to improve muscle function in mdx mice
title_full_unstemmed Voluntary wheel running complements microdystrophin gene therapy to improve muscle function in mdx mice
title_short Voluntary wheel running complements microdystrophin gene therapy to improve muscle function in mdx mice
title_sort voluntary wheel running complements microdystrophin gene therapy to improve muscle function in mdx mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8020351/
https://www.ncbi.nlm.nih.gov/pubmed/33850950
http://dx.doi.org/10.1016/j.omtm.2021.02.024
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