Effects of adipokine zinc-α2-glycoprotein on adipose tissue metabolism after dexamethasone treatment
Deutscher übersetzter Titel: | Die Auswirkungen von Adipokin-Zink-α2-Glykoprotein auf den Fettgewebestoffwechsel nach Dexamethason-Behandlung |
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Autor: | Qiao, Yu; Fan, Guoqiang; Guo, Jun; Gao, Shixing; Zhao, Ruqian; Yang, Xiaojing |
Erschienen in: | Applied physiology, nutrition, and metabolism |
Veröffentlicht: | 44 (2019), 1, S. 83-89, Lit. |
Format: | Literatur (SPOLIT) |
Publikationstyp: | Zeitschriftenartikel |
Medienart: | Elektronische Ressource (online) Gedruckte Ressource |
Sprache: | Englisch |
ISSN: | 1715-5312, 1715-5320 |
DOI: | 10.1139/apnm-2018-0165 |
Schlagworte: | |
Online Zugang: | |
Erfassungsnummer: | PU202002001114 |
Quelle: | BISp |
Abstract des Autors
Zinc-α2-glycoprotein (ZAG) has been demonstrated to play a role in stimulating lipid mobilization under normal conditions. However, further studies are required to determine whether ZAG overexpression can alleviate the reduction in plasma lipid levels under stress conditions. In the present study, we investigated the effects of ZAG on lipometabolism in white adipose tissue (WAT) after dexamethasone (DEX) stimulation using C57BL/6 male mice as the experimental models. Transcript and protein levels of genes associated with the β-adrenoreceptor (β-AR)/cyclic adenosine monophosphate/protein kinase a (PKA) pathway, lipid mobilization, and energy metabolism were determined by quantitative real-time polymerase chain reaction and Western blotting. Plasma levels of nonesterified fatty acid (NEFA) were measured using an automatic biochemical analyzer. Results indicated that plasma NEFA levels were decreased in the DEX group, but NEFA levels were rescued by ZAG overexpression. ZAG overexpression resulted in the upregulation of β3-AR and phosphorylated PKA protein relative to those of the DEX group. Analysis of lipometabolism showed that protein levels of phosphorylated hormone-sensitive lipase was reduced upon DEX treatment but were restored by ZAG overexpression. For energy metabolism, ZAG significantly upregulated the protein expression of carnitine palmitoyltransferase1a and cytochrome c oxidase subunit 1 relative to those of the DEX group. In conclusion, ZAG could alleviate DEX-induced decrease in plasma NEFA levels and this could be associated with the promoting lipid mobilization in WAT.