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EFFECTS OF β-HYDROXY-β-METHYLBUTYRATE SUPPLEMENTATION ON MUSCLE MASS AND STRENGTH IN ONABOTULINUMTOXIN TYPE-A-INJECTED AND CONTRALATERAL QUADRICEPS FEMORIS IN RABBITS
OBJECTIVE: To determine the effects of the leucine metabolite β-hydroxy-β-methylbutyrate (HMB) on strength, muscle mass, and contractile material in muscle wasting induced by onabotulinumtoxin type-A (BoNT-A) injection into the quadriceps femoris muscles of New Zealand white rabbits. METHODS: A tota...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Foundation for Rehabilitation Information
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8638725/ https://www.ncbi.nlm.nih.gov/pubmed/34430979 http://dx.doi.org/10.2340/16501977-2866 |
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author | FORTUNA, Rafael SAWATSKY, Andrew FULLER, John C. HERZOG, Walter |
author_facet | FORTUNA, Rafael SAWATSKY, Andrew FULLER, John C. HERZOG, Walter |
author_sort | FORTUNA, Rafael |
collection | PubMed |
description | OBJECTIVE: To determine the effects of the leucine metabolite β-hydroxy-β-methylbutyrate (HMB) on strength, muscle mass, and contractile material in muscle wasting induced by onabotulinumtoxin type-A (BoNT-A) injection into the quadriceps femoris muscles of New Zealand white rabbits. METHODS: A total of 21, female rabbits were divided into 3 groups (n = 7, each). Group 1 (Control) received intramuscular injection of saline. Groups 2 and 3 received intramuscular injection of BoNT-A (3.5 units/kg), with group 3 receiving supplementation with HMB (120 mg/kg-BW/day). Muscle morphology, mass, and strength were assessed 8 weeks later in both injected and non-injected contralateral limbs. RESULTS: Injected muscle strength of group 2 (BoNT-A) and group 3 (BoNT-A+HMB) was reduced by 63% and 60%, respectively, compared with Controls (p < 0.0001). Strength in contralateral muscles of group 2 was reduced by 23% vs Controls (p <0.002), while in group 3, strength was similar to Controls. Muscle mass in the injected muscles of the BoNT-A and BoNT-A+HMB groups was significantly reduced, by 46% and 48%, respectively. CONCLUSION: While HMB did not prevent loss of muscle strength and mass in the BoNT-A-injected musculature, it prevented significant loss of contractile material in the injected musculature and strength loss in the contralateral non-injected musculature. |
format | Online Article Text |
id | pubmed-8638725 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Foundation for Rehabilitation Information |
record_format | MEDLINE/PubMed |
spelling | pubmed-86387252022-02-08 EFFECTS OF β-HYDROXY-β-METHYLBUTYRATE SUPPLEMENTATION ON MUSCLE MASS AND STRENGTH IN ONABOTULINUMTOXIN TYPE-A-INJECTED AND CONTRALATERAL QUADRICEPS FEMORIS IN RABBITS FORTUNA, Rafael SAWATSKY, Andrew FULLER, John C. HERZOG, Walter J Rehabil Med Original Report OBJECTIVE: To determine the effects of the leucine metabolite β-hydroxy-β-methylbutyrate (HMB) on strength, muscle mass, and contractile material in muscle wasting induced by onabotulinumtoxin type-A (BoNT-A) injection into the quadriceps femoris muscles of New Zealand white rabbits. METHODS: A total of 21, female rabbits were divided into 3 groups (n = 7, each). Group 1 (Control) received intramuscular injection of saline. Groups 2 and 3 received intramuscular injection of BoNT-A (3.5 units/kg), with group 3 receiving supplementation with HMB (120 mg/kg-BW/day). Muscle morphology, mass, and strength were assessed 8 weeks later in both injected and non-injected contralateral limbs. RESULTS: Injected muscle strength of group 2 (BoNT-A) and group 3 (BoNT-A+HMB) was reduced by 63% and 60%, respectively, compared with Controls (p < 0.0001). Strength in contralateral muscles of group 2 was reduced by 23% vs Controls (p <0.002), while in group 3, strength was similar to Controls. Muscle mass in the injected muscles of the BoNT-A and BoNT-A+HMB groups was significantly reduced, by 46% and 48%, respectively. CONCLUSION: While HMB did not prevent loss of muscle strength and mass in the BoNT-A-injected musculature, it prevented significant loss of contractile material in the injected musculature and strength loss in the contralateral non-injected musculature. Foundation for Rehabilitation Information 2021-08-25 /pmc/articles/PMC8638725/ /pubmed/34430979 http://dx.doi.org/10.2340/16501977-2866 Text en © 2021 Journal of Rehabilitation Medicine https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Original Report FORTUNA, Rafael SAWATSKY, Andrew FULLER, John C. HERZOG, Walter EFFECTS OF β-HYDROXY-β-METHYLBUTYRATE SUPPLEMENTATION ON MUSCLE MASS AND STRENGTH IN ONABOTULINUMTOXIN TYPE-A-INJECTED AND CONTRALATERAL QUADRICEPS FEMORIS IN RABBITS |
title | EFFECTS OF β-HYDROXY-β-METHYLBUTYRATE SUPPLEMENTATION ON MUSCLE MASS AND STRENGTH IN ONABOTULINUMTOXIN TYPE-A-INJECTED AND CONTRALATERAL QUADRICEPS FEMORIS IN RABBITS |
title_full | EFFECTS OF β-HYDROXY-β-METHYLBUTYRATE SUPPLEMENTATION ON MUSCLE MASS AND STRENGTH IN ONABOTULINUMTOXIN TYPE-A-INJECTED AND CONTRALATERAL QUADRICEPS FEMORIS IN RABBITS |
title_fullStr | EFFECTS OF β-HYDROXY-β-METHYLBUTYRATE SUPPLEMENTATION ON MUSCLE MASS AND STRENGTH IN ONABOTULINUMTOXIN TYPE-A-INJECTED AND CONTRALATERAL QUADRICEPS FEMORIS IN RABBITS |
title_full_unstemmed | EFFECTS OF β-HYDROXY-β-METHYLBUTYRATE SUPPLEMENTATION ON MUSCLE MASS AND STRENGTH IN ONABOTULINUMTOXIN TYPE-A-INJECTED AND CONTRALATERAL QUADRICEPS FEMORIS IN RABBITS |
title_short | EFFECTS OF β-HYDROXY-β-METHYLBUTYRATE SUPPLEMENTATION ON MUSCLE MASS AND STRENGTH IN ONABOTULINUMTOXIN TYPE-A-INJECTED AND CONTRALATERAL QUADRICEPS FEMORIS IN RABBITS |
title_sort | effects of β-hydroxy-β-methylbutyrate supplementation on muscle mass and strength in onabotulinumtoxin type-a-injected and contralateral quadriceps femoris in rabbits |
topic | Original Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8638725/ https://www.ncbi.nlm.nih.gov/pubmed/34430979 http://dx.doi.org/10.2340/16501977-2866 |
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