Adropin Slightly Modulates Lipolysis, Lipogenesis and Expression of Adipokines but Not Glucose Uptake in Rodent Adipocytes.


Journal

Genes
ISSN: 2073-4425
Titre abrégé: Genes (Basel)
Pays: Switzerland
ID NLM: 101551097

Informations de publication

Date de publication:
13 06 2021
Historique:
received: 19 04 2021
revised: 04 06 2021
accepted: 11 06 2021
entrez: 2 7 2021
pubmed: 3 7 2021
medline: 15 12 2021
Statut: epublish

Résumé

Adropin is a peptide hormone which modulates energy homeostasis and metabolism. In animals with diet-induced obesity, adropin attenuates adiposity and improves lipid and glucose homeostasis. Adropin promotes the proliferation of rodent white preadipocytes and suppresses their differentiation into adipocytes. By contrast, the effects of adropin on mature white adipocytes are unknown. Therefore, we aimed to evaluate the effects of adropin on lipolysis, lipogenesis and glucose uptake in white rodent adipocytes. We assessed the effects of adropin on the mRNA expression of adiponectin, resistin and visfatin. White preadipocytes were isolated from male Wistar rats. Differentiated 3T3-L1 cells were used as a surrogate model of white adipocytes. Lipolysis was measured by the evaluation of glycerol and free fatty acid secretion using colorimetric kits. The effects of adropin on lipogenesis and glucose uptake were measured using radioactive-labelled glucose. The expression of adipokine mRNA was studied using real-time PCR. Our results show that adropin slightly promotes lipolysis in rat adipocytes and 3T3-L1 cells. Adropin suppresses lipogenesis in rat adipocytes without influencing glucose uptake. In addition, adropin stimulates adiponectin mRNA expression and suppresses the expression of resistin and visfatin. These results indicate that adropin may be involved in controlling lipid metabolism and adipokine expression in white rodent adipocytes.

Identifiants

pubmed: 34199277
pii: genes12060914
doi: 10.3390/genes12060914
pmc: PMC8231953
pii:
doi:

Substances chimiques

Adipokines 0
Fatty Acids 0
Intercellular Signaling Peptides and Proteins 0
Peptides 0
Glucose IY9XDZ35W2
Glycerol PDC6A3C0OX

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Mariami Jasaszwili (M)

Department of Animal Physiology, Biochemistry and Biostructure, Poznan University of Life Sciences, 60-637 Poznan, Poland.

Ewa Pruszyńska-Oszmałek (E)

Department of Animal Physiology, Biochemistry and Biostructure, Poznan University of Life Sciences, 60-637 Poznan, Poland.

Tatiana Wojciechowicz (T)

Department of Animal Physiology, Biochemistry and Biostructure, Poznan University of Life Sciences, 60-637 Poznan, Poland.

Mathias Z Strowski (MZ)

Department of Hepatology and Gastroenterology, Charité-University Medicine Berlin, 13353 Berlin, Germany.
Department of Internal Medicine-Gastroenterology & Oncology, Park-Klinik Weissensee, 13086 Berlin, Germany.

Krzysztof W Nowak (KW)

Department of Animal Physiology, Biochemistry and Biostructure, Poznan University of Life Sciences, 60-637 Poznan, Poland.

Marek Skrzypski (M)

Department of Animal Physiology, Biochemistry and Biostructure, Poznan University of Life Sciences, 60-637 Poznan, Poland.

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Classifications MeSH