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肌肉发育
AQUACULTURE · 2024 · IF 3.9

The effects of phospholipids (PL) addition in the high fat diet on growth performance, oxidative stress, lipid and protein metabolism, and muscle development in yellow catfish Pelteobagrus fulvidraco

Qing-Lin Li,Biao Wang,Hua Zheng,Li-Xiang Wu,Peng-Cheng Xu,Xiao-Ying Tan

This present study was undertaken to explore the influences of phospholipids (PL) addition in the high-fat diet (HFD) on growth performance, nutritional composition, oxidative stress, lipid and protein metabolism in the muscle tissue of yellow catfish Pelteobagrus fulvidraco. The five experimental diets were formulated, which included the control (10.31 % normal dietary lipid without PL addition), high-fat dietary group (HFD, 14.99 % dietary lipid without PL addition), 0.1 % PL group (PL1,10.83 % dietary lipid with 0.1 % PL addition), high-fat diet +0.1 % PL group (HFD + PL1, 14.93 % dietary lipid with 0.1 % PL addition) and high-fat diet +0.2 % PL group (HFD + PL2, 14.76 % dietary lipid with 0.2 % PL addition). The feeding experiment continued for 10wk, and then the muscle samples were taken. Compared to the control, HFD reduced growth performance, feed utilization, muscle crude protein and total PL content, induced oxidative stress, lipogenesis and caused muscle lipid accumulation, and PL addition alleviated the HFD-induced changes above. HFD group had the smaller (100-249 μm) myofiber areas, while other groups showed a higher proportion of greater myofiber areas (>350 μm). Additionally, HFD suppressed the expression of muscle regulatory factors and protein synthesis, triggered protein degradation, whereas the PL addition in the diet mitigated the suppressive effects induced by HFD. Furthermore, the HFD inhibited the expression of muscle regulatory factors and protein synthesis, induced protein degradation; PL addition alleviated the HFD-induced inhibition of muscle regulatory factors and protein synthesis, and alleviated the HFD-induced protein degradation. Mechanistically, HFD enhanced the MYOG/FOXO3 binding with the atrogin-1/murf-1 promoters and increased their expression, and PL addition alleviated these effects induced by HFD. Taken together, our research demonstrated that dietary phospholipids could alleviate the adverse effects induced by HFD, and accordingly are beneficial additives for aquatic feeds. Our results also provided innovative insights into the regulatory mechanism of muscle development and growth in the vertebrates. Statement of relevance Our results indicated that dietary PL alleviated adverse effects of HFD on growth performance, oxidative stress, lipid and protein metabolism in the muscle of fish, and accordingly was a good additive in the aquafeeds.

CAS / MDL: 97281-47-5
研究领域: 水产养殖学 · 营养学 · 分子生物学
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Genes & Diseases · 2020 · IF 4.803

MiR-743a-5p regulates differentiation of myoblast by targeting Mob1b in skeletal muscle development and regeneration

YongSheng Zhang,YiLong Yao,ZiShuai Wang,Dan Lu,YuanYuan Zhang,Adeyinka Abiola Adetula,SiYuan Liu,Min Zhu,YaLan Yang,XinHao Fan,MuYa Chen,YiJie Tang,Yun Chen,YuWen Liu,GuoQiang Yi,ZhongLin Tang

The microRNAs (miRNAs) play an important role in regulating myogenesis by targeting mRNA. However, the understanding of miRNAs in skeletal muscle development and diseases is unclear. In this study, we firstly performed the transcriptome profiling in differentiating C2C12 myoblast cells. Totally, we identified 187 miRNAs and 4260 mRNAs significantly differentially expressed that were involved in myoblast differentiation. We carried out validation of microarray data based on 5 mRNAs and 5 miRNAs differentially expressed and got a consistent result. Then we constructed and validated the significantly up- and down-regulated mRNA-miRNA interaction networks. Four interaction pairs (miR-145a-5p- Fscn1, miR-200c-5p- Tmigd1, miR-27a-5p- Sln and miR-743a-5p- Mob1b ) with targeted relationships in differentiated myoblast cells were demonstrated. They are all closely related to myoblast development. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis indicated cell cycle signals important for exploring skeletal muscle development and disease. Functionally, we discovered that miR-743a targeting gene Mps One Binder Kinase Activator-Like 1B ( Mob1b ) gene in differentiated C2C12. The up-regulated miR-743a can promote the differentiation of C2C12 myoblast. While the down-regulated Mob1b plays a negative role in differentiation. In addition, the expression profile of miR-743a and Mob1b are consistent with skeletal muscle recovery after Cardiotoxin (CTX) injury. Our study revealed that miR-743a-5p regulates myoblast differentiation by targeting Mob1b involved in skeletal muscle development and regeneration. Our findings made a further exploration for mechanisms in myogenesis and might provide potential possible miRNA-based target therapies for skeletal muscle regeneration and disease in the near future.

研究领域: 分子生物学 · 肌肉发育 · 再生医学 · 基因调控
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