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GPR10 gene deletion in mice increases basal neuronal activity, disturbs insulin sensitivity and alters lipid homeostasis
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SYSNO ASEP 0542615 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title GPR10 gene deletion in mice increases basal neuronal activity, disturbs insulin sensitivity and alters lipid homeostasis Author(s) Pražienková, V. (CZ)
Funda, Jiří (FGU-C) ORCID
Pirník, Z. (SK)
Karnošová, A. (CZ)
Hrubá, L. (CZ)
Kořínková, L. (CZ)
Neprašová, B. (CZ)
Janovská, Petra (FGU-C) RID, ORCID
Bencze, Michal (FGU-C) RID, ORCID, SAI
Kadlecová, Michaela (FGU-C) RID
Blahoš, J. (CZ)
Kopecký, Jan (FGU-C) RID, ORCID
Železná, B. (CZ)
Kuneš, Jaroslav (FGU-C) RID, ORCID
Bardová, Kristina (FGU-C) RID, ORCID, SAI
Maletínská, L. (CZ)Article number 145427 Source Title Gene. - : Elsevier - ISSN 0378-1119
Roč. 774, Mar 30 (2021)Number of pages 12 s. Language eng - English Country NL - Netherlands Keywords GPR10 KO mice ; prolactin-releasing peptide ; standard and high-fat diets ; neuronal activity ; gene expression ; energy expenditure Subject RIV FB - Endocrinology, Diabetology, Metabolism, Nutrition OECD category Endocrinology and metabolism (including diabetes, hormones) R&D Projects GA18-10591S GA ČR - Czech Science Foundation (CSF) Method of publishing Limited access Institutional support FGU-C - RVO:67985823 UT WOS 000657683300002 EID SCOPUS 85099637316 DOI 10.1016/j.gene.2021.145427 Annotation G-protein-coupled receptor GPR10 is expressed in brain areas regulating energy metabolism. In this study, the effects of GPR10 gene deficiency on energy homeostasis in mice of both sexes fed either standard chow or a high-fat diet (HFD) were studied, with a focus on neuronal activation of PrRP neurons, and adipose tissue and liver metabolism. GPR10 deficiency in males upregulated the phasic and tonic activity of PrRP neurons in the nucleus of the solitary tract. GPR10 knockout (KO) males on a standard diet displayed a higher body weight than their wild-type (WT) littermates due to an increase in adipose tissue mass, however, HFD feeding did not cause weight differences between genotypes. Expression of lipogenesis genes was suppressed in the subcutaneous adipose tissue of GPR10 KO males. In contrast, GPR10 KO females did not differ in body weight from their WT controls, but showed elevated expression of lipid metabolism genes in the liver and subcutaneous adipose tissue compared to WT controls. An attenuated non-esterified fatty acids change after glucose load compared to WT controls suggested a defect in insulin-mediated suppression of lipolysis in GPR10 KO females. Indirect calorimetry did not reveal any differences in energy expenditure among groups. In conclusion, deletion of GPR10 gene resulted in changes in lipid metabolism in mice of both sexes, however in different extent. An increase in adipose tissue mass observed in only GPR10 KO males may have been prevented in GPR10 KO females owing to a compensatory increase in the expression of metabolic genes. Workplace Institute of Physiology Contact Lucie Trajhanová, lucie.trajhanova@fgu.cas.cz, Tel.: 241 062 400 Year of Publishing 2022 Electronic address https://doi.org/10.1016/j.gene.2021.145427
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