Expression patterns of AMPK and genes associated with lipid metabolism in newly hatched chicks during the metabolic perturbation of fasting and refeeding

Zhang, Xu; Wang, Yuanyuan; Zhao, Hongduo; Zhang, Yanhong; Wang, Li; Ma, Jingyun

doi:10.1016/j.psj.2022.102231

Cited by 2 publications

(1 citation statement)

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“…Using these models, a number of studies have revealed that many genes and pathways are influenced by changes in nutrition and energy levels. For example, using the fasting/refeeding model, Xu et al [10] demonstrated that fasting decreased the expression of fat synthesis genes (Stearoyl-CoA Desaturase (SCD), glucocorticoid receptor (GR) and fatty acid synthase (FAS)) in the liver and increased the expression of lipolytic genes (AMP-activated protein kinase alpha subunit (AMPKα), AMPKβ and AMPKγ) in the hypothalamus. Liver transcriptome analysis indicates that fasting affects the nutrition metabolism in goose liver, especially the signaling pathways related to lipid metabolism.…”

Section: Introductionmentioning

confidence: 99%

Study on the Mechanism of MC5R Participating in Energy Metabolism of Goose Liver

Zhang

Xing

et al. 2023

IJMS

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Nutrition and energy levels have an important impact on animal growth, production performance, disease occurrence and health recovery. Previous studies indicate that melanocortin 5 receptor (MC5R) is mainly involved in the regulations of exocrine gland function, lipid metabolism and immune response in animals. However, it is not clear how MC5R participates in the nutrition and energy metabolism of animals. To address this, the widely used animal models, including the overfeeding model and the fasting/refeeding model, could provide an effective tool. In this study, the expression of MC5R in goose liver was first determined in these models. Goose primary hepatocytes were then treated with nutrition/energy metabolism-related factors (glucose, oleic acid and thyroxine), which is followed by determination of MC5R gene expression. Moreover, MC5R was overexpressed in goose primary hepatocytes, followed by identification of differentially expressed genes (DEGs) and pathways subjected to MC5R regulation by transcriptome analysis. At last, some of the genes potentially regulated by MC5R were also identified in the in vivo and in vitro models, and were used to predict possible regulatory networks with PPI (protein–protein interaction networks) program. The data showed that both overfeeding and refeeding inhibited the expression of MC5R in goose liver, while fasting induced the expression of MC5R. Glucose and oleic acid could induce the expression of MC5R in goose primary hepatocytes, whereas thyroxine could inhibit it. The overexpression of MC5R significantly affected the expression of 1381 genes, and the pathways enriched with the DEGs mainly include oxidative phosphorylation, focal adhesion, ECM–receptor interaction, glutathione metabolism and MAPK signaling pathway. Interestingly, some pathways are related to glycolipid metabolism, including oxidative phosphorylation, pyruvate metabolism, citrate cycle, etc. Using the in vivo and in vitro models, it was demonstrated that the expression of some DEGs, including ACSL1, PSPH, HMGCS1, CPT1A, PACSIN2, IGFBP3, NMRK1, GYS2, ECI2, NDRG1, CDK9, FBXO25, SLC25A25, USP25 and AHCY, was associated with the expression of MC5R, suggesting these genes may mediate the biological role of MC5R in these models. In addition, PPI analysis suggests that the selected downstream genes, including GYS2, ECI2, PSPH, CPT1A, ACSL1, HMGCS1, USP25 and NDRG1, participate in the protein–protein interaction network regulated by MC5R. In conclusion, MC5R may mediate the biological effects caused by changes in nutrition and energy levels in goose hepatocytes through multiple pathways, including glycolipid-metabolism-related pathways.

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Section: Introductionmentioning

confidence: 99%