Loading...
Please wait, while we are loading the content...
Similar Documents
Resveratrol Promotes Hypertrophy in Wildtype Skeletal Muscle and Reduces Muscle Necrosis and Gene Expression of Inflammatory Markers in Mdx Mice
| Content Provider | MDPI |
|---|---|
| Author | Shireen, Lamandé Woodman, Keryn Coles, Chantal White, Jason |
| Copyright Year | 2021 |
| Description | Duchenne muscular dystrophy (DMD) is a progressive fatal neuromuscular disorder with no cure. Therapies to restore dystrophin deficiency have been approved in some jurisdictions but long-term effectiveness is yet to be established. There is a need to develop alternative strategies to treat DMD. Resveratrol is a nutraceutical with anti-inflammatory properties. Previous studies have shown high doses (100–400 mg/kg bodyweight/day) benefit mdx mice. We treated 4-week-old mdx and wildtype mice with a lower dose of resveratrol (5 mg/kg bodyweight/day) for 15 weeks. Voluntary exercise was used to test if a lower dosage than previously tested could reduce exercise-induced damage where a greater inflammatory infiltrate is present. We found resveratrol promoted skeletal muscle hypertrophy in wildtype mice. In dystrophic muscle, resveratrol reduced exercise-induced muscle necrosis. Gene expression of immune cell markers, CD86 and CD163 were reduced; however, signalling targets associated with resveratrol’s mechanism of action including Sirt1 and NF-κB were unchanged. In conclusion, a lower dose of resveratrol compared to the dosage used by other studies reduced necrosis and gene expression of inflammatory cell markers in dystrophic muscle suggesting it as a therapeutic candidate for treating DMD. |
| Starting Page | 853 |
| e-ISSN | 14203049 |
| DOI | 10.3390/molecules26040853 |
| Journal | Molecules |
| Issue Number | 4 |
| Volume Number | 26 |
| Language | English |
| Publisher | MDPI |
| Publisher Date | 2021-02-06 |
| Access Restriction | Open |
| Subject Keyword | Molecules Cell Tissue Engineering Muscle Muscular Dystrophy Mdx Resveratrol Nutraceuticals Duchenne Inflammation |
| Content Type | Text |
| Resource Type | Article |