l-Cysteine and Vitamin D Co-Supplementation Alleviates Markers of Musculoskeletal Disorders in Vitamin D-Deficient High-Fat Diet-Fed Mice.
Study Design
- अध्ययन प्रकार
- animal study (controlled preclinical)
- अवधि
- 16 weeks
- हस्तक्षेप
- l-Cysteine and Vitamin D Co-Supplementation Alleviates Markers of Musculoskeletal Disorders in Vitamin D-Deficient High-Fat Diet-Fed Mice. not specified; LC alone, VD alone, or LC + VD for 8 weeks
- तुलनित्र
- Placebo
- प्रभाव की दिशा
- Positive
- पूर्वाग्रह का जोखिम
- Moderate
Abstract
Vitamin D (VD) deficiency is associated with musculoskeletal disorders. This study examines whether co-supplementation of l-cysteine (LC) and VD is better than monotherapy with LC or VD at alleviating musculoskeletal dyshomeostasis in the skeletal muscle of VD-deficient high-fat diet (HFD-VD-) fed mice. Mice were fed a healthy diet or an HFD; for VD-deficient animals, the mice were maintained on a HFD-VD-diet (16 weeks); after the first 8 weeks, the HFD-VD-diet-fed mice were supplemented for another 8 weeks with LC, VD-alone, or the same doses of LC + VD by oral gavage. Saline and olive oil served as controls. Myotubes were exposed with high-glucose, palmitate, Monocyte Chemoattractant Protein 1 (MCP-1), and Tumor Necrosis Factor (TNF), to mimic the in vivo microenvironment. In vitro deficiencies of glutathione and hydrogen sulfide were induced by knockdown of GCLC and CSE genes. Relative gene expression of biomarkers (myogenic: MyoD, Mef2c, Csrp3; muscle dystrophy: Atrogin1, Murf1, and Myostatin; bone modeling and remodeling: RANK, RANKL, OPG) were analyzed using qRT-PCR. Co-supplementatoin with LC + VD showed beneficial effects on gene expression of myogenic markers and OPG but reduced markers of dystrophy, RANK/RANKL in comparison to LC or VD alone-supplementation. In vitro myotubes treated with glutathione (GSH) precursors also showed a positive effect on OPG and the myogenesis genes, and inhibited RANK/RANKL and muscle-dystrophy markers. This study reveals that the co-supplementation of LC with VD significantly alleviates the markers of musculoskeletal disorders in the skeletal muscle better than monotherapy with LC or VD in HFD-VD-fed mice.
Full Text
Figures
Tables
Table 1
| Atrogin1/Fbxo32 | skeletal muscle-specific F-box protein |
| CSE/CTH | Cystathionine Gamma-Lyase |
| GCLC/ γ-GCSc | Glutamate-Cysteine Ligase Catalytic Subunit |
| GSH | Glutathione |
| H2S | Hydrogen sulfide |
| LC | |
| HFD-VD- | VD-deficient high-fat diet-fed |
| MCP-1 | Monocyte Chemoattractant Protein 1 |
| TNF | Tumor Necrosis Factor |
| MuRF1/Trim63 | Muscle RING-finger protein-1 |
| Mstn | Myostatin |
| MyoD | Myoblast determination protein 1 |
| Mef2c | Myocyte enhancer factor 2C |
| Csrp3 | Cysteine and glycine-rich protein 3 |
| Rank/Tnfrsf11a | Receptor activator of nuclear factor-kB |
| RANKL | Receptor activator of nuclear factor-kB ligand |
| OPG | Osteoprotegerin |
| VD | Vitamin D |
References
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