| First Author | Yang S | Year | 2023 |
| Journal | J Cachexia Sarcopenia Muscle | Volume | 14 |
| Issue | 6 | Pages | 2925-2938 |
| PubMed ID | 37985354 | Mgi Jnum | J:346344 |
| Mgi Id | MGI:7595967 | Doi | 10.1002/jcsm.13377 |
| Citation | Yang S, et al. (2023) MicroRNA-92b in the skeletal muscle regulates exercise capacity via modulation of glucose metabolism. J Cachexia Sarcopenia Muscle 14(6):2925-2938 |
| abstractText | BACKGROUND: Exercise mimetics is a proposed class of therapeutics that specifically mimics or enhances the therapeutic effects of exercise. Muscle glycogen and lactate extrusion are critical for physical performance. The mechanism by which glycogen and lactate metabolism are manipulated during exercise remains unclear. This study aimed to assess the effect of miR-92b on the upregulation of exercise training-induced physical performance. METHODS: Adeno-associated virus (AAV)-mediated skeletal muscle miR-92b overexpression in C57BLKS/J mice, and global knockout of miR-92b mice were used to explore the function of miR-92b in glycogen and lactate metabolism in skeletal muscle. AAV-mediated UGP2 or MCT4 knockdown in WT or miR-92 knockout mice was used to confirm whether miR-92b regulates glycogen and lactate metabolism in skeletal muscle through UGP2 and MCT4. Body weight, muscle weight, grip strength, running time and distance to exhaustion, and muscle histology were assessed. The expression levels of muscle mass-related and function-related proteins were analysed by immunoblotting or immunostaining. RESULTS: Global knockout of miR-92b resulted in normal body weight and insulin sensitivity, but higher glycogen content before exercise exhaustion (0.8538 +/- 0.0417 vs. 1.043 +/- 0.040, **P = 0.0087), lower lactate levels after exercise exhaustion (4.133 +/- 0.2589 vs. 3.207 +/- 0.2511, *P = 0.0279), and better exercise capacity (running distance to exhaustion, 3616 +/- 86.71 vs. 4231 +/- 90.29, ***P = 0.0006; running time to exhaustion, 186.8 +/- 8.027 vs. 220.8 +/- 3.156, **P = 0.0028), as compared with those observed in the control mice. Mice skeletal muscle overexpressing miR-92b (both miR-92b-3p and miR-92b-5p) displayed lower glycogen content before exercise exhaustion (0.6318 +/- 0.0231 vs. 0.535 +/- 0.0194, **P = 0.0094), and higher lactate accumulation after exercise exhaustion (4.5 +/- 0.2394 vs. 5.467 +/- 0.1892, *P = 0.01), and poorer exercise capacity (running distance to exhaustion, 4005 +/- 81.65 vs. 3228 +/- 149.8, ***P<0.0001; running time to exhaustion, 225.5 +/- 7.689 vs. 163 +/- 6.476, **P = 0.001). Mechanistic analysis revealed that miR-92b-3p targets UDP-glucose pyrophosphorylase 2 (UGP2) expression to inhibit glycogen synthesis, while miR-92b-5p represses lactate extrusion by directly target monocarboxylate transporter 4 (MCT4). Knockdown of UGP2 and MCT4 reversed the effects observed in the absence of miR-92b in vivo. CONCLUSIONS: This study revealed regulatory pathways, including miR-92b-3p/UGP2/glycogen synthesis and miR-92b-5p/MCT4/lactate extrusion, which could be targeted to control exercise capacity. |
