QRFP-26 enhances insulin's effects on glucose uptake in rat skeletal muscle cells

被引:11
作者
Allerton, Timothy D. [1 ]
Primeaux, Stefany D. [1 ,2 ]
机构
[1] Louisiana State Univ, Dept Physiol, Hlth Sci Ctr New Orleans, New Orleans, LA 70112 USA
[2] Pennington Biomed Res Ctr, Endocrinol & Metab Program, Joint Dis, Baton Rouge, LA 70808 USA
关键词
QRFP-26; QRFP-43; GPR103a; Glucose uptake; L6; cells; FAT FOOD-INTAKE; RFAMIDE PEPTIDES; HYPOTHALAMIC NEUROPEPTIDE; OREXIGENIC ACTIVITY; 26RFA; IDENTIFICATION; SECRETION; FAMILY;
D O I
10.1016/j.peptides.2015.04.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
QRFP is expressed in central and peripheral regions important for nutrient intake and metabolism. Central administration of QRFP-26 and QRFP-43 induces a macronutrient specific increase in the intake of high fat diet in male and female rats. Recently, cell culture models have indicated that QRFP-26 and QRFP-43 are involved in glucose and fatty acid uptake in pancreatic islets and adipocytes. Since skeletal muscle is a major consumer of circulating glucose and a primary contributor to whole body metabolism, the current study examined the effects of QRFP-26 and QRFP-43 on insulin-stimulated uptake of glucose in skeletal muscle using L6 myotubes. The current experiments were designed to test the hypothesis that QRFP and its receptors, GPR103a and GPR103b are expressed in L6 myotubes and that QRFP-26 and QRFP-43 affect insulin-stimulated uptake of glucose in L6 myotubes. The results indicate that prepro-QRFP mRNA and GPR103a mRNA are expressed in L6 cells, though GPR103b mRNA was not detected. Using complementary assays, co-incubation with QRFP-26, increased insulin's ability to induce glycogen synthesis and 2-deoxyglucose uptake in L6 cells. These data suggest that QRFP-26, but not QRFP-43, is involved in the metabolic effects of skeletal muscle and may enhance insulin's effects on glucose uptake in skeletal muscle. These data support a role for QRFP as a modulator of nutrient intake in skeletal muscle. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:77 / 79
页数:3
相关论文
共 14 条
[1]   Identification of 26RFa from frog brain - A novel hypothalamic neuropeptide with orexigenic activity in mammals [J].
Chartrel, N ;
Bruzzone, F ;
Dujardin, C ;
Leprince, J ;
Tollemer, H ;
Anouar, Y ;
Vallarino, M ;
Costentin, J ;
Vaudry, H .
TRENDS IN COMPARATIVE ENDOCRINOLOGY AND NEUROBIOLOGY, 2005, 1040 :80-83
[2]   Identification of 26RFa, a hypothalamic neuropeptide of the RFamide peptide family with orexigenic activity [J].
Chartrel, N ;
Dujardin, C ;
Anouar, Y ;
Leprince, J ;
Decker, A ;
Clerens, S ;
Do-Régo, JC ;
Vandesande, F ;
Llorens-Cortes, C ;
Costentin, J ;
Beauvillain, JC ;
Vaudry, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (25) :15247-15252
[3]   The expanding family of -RFamide peptidesand their effects on feeding behaviour [J].
Dockray, GJ .
EXPERIMENTAL PHYSIOLOGY, 2004, 89 (03) :229-235
[4]   26RFa, a novel orexigenic neuropeptide, inhibits insulin secretion, in the rat pancreas [J].
Egido, Eva M. ;
Hernandez, Raquel ;
Leprince, Jerome ;
Chartrel, Nicolas ;
Vaudry, Hubert ;
Marco, Jose ;
Silvestre, Ramona A. .
PEPTIDES, 2007, 28 (04) :725-730
[5]   Recent advances in mammalian RFamide peptides: The discovery and functional analyses of PrRP, RFRPs and QRFP [J].
Fukusumi, Shoji ;
Fujii, Ryo ;
Hinuma, Shuji .
PEPTIDES, 2006, 27 (05) :1073-1086
[6]   A microassay for measuring glycogen 96-well-cultured cells [J].
GomezLechon, MJ ;
Ponsoda, X ;
Castell, JV .
ANALYTICAL BIOCHEMISTRY, 1996, 236 (02) :296-301
[7]   RFamide Peptides 43RFa and 26RFa Both Promote Survival of Pancreatic β-Cells and Human Pancreatic Islets but Exert Opposite Effects on Insulin Secretion [J].
Granata, Riccarda ;
Settanni, Fabio ;
Trovato, Letizia ;
Gallo, Davide ;
Gesmundo, Iacopo ;
Nano, Rita ;
Gallo, Maria Pia ;
Bergandi, Loredana ;
Volante, Marco ;
Alloatti, Giuseppe ;
Piemonti, Lorenzo ;
Leprince, Jerome ;
Papotti, Mauro ;
Vaudry, Hubert ;
Ong, Huy ;
Ghigo, Ezio .
DIABETES, 2014, 63 (07) :2380-2393
[8]   Identification and characterization of a novel RF-amide peptide ligand for orphan G-protein-coupled receptor SP9155 [J].
Jiang, Y ;
Luo, L ;
Gustafson, EL ;
Yadav, D ;
Laverty, M ;
Murgolo, N ;
Vassileva, G ;
Zeng, M ;
Laz, TM ;
Behan, J ;
Qiu, P ;
Wang, LQ ;
Wang, SK ;
Bayae, M ;
Greene, J ;
Monsma, F ;
Zhang, FL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (30) :27652-27657
[9]   GPR103b Functions in the Peripheral Regulation of Adipogenesis [J].
Mulumba, Mukandila ;
Jossart, Christian ;
Granata, Riccarda ;
Gallo, Davide ;
Escher, Emanuel ;
Ghigo, Ezio ;
Servant, Marc J. ;
Marleau, Sylvie ;
Ong, Huy .
MOLECULAR ENDOCRINOLOGY, 2010, 24 (08) :1615-1625
[10]   Hypothalamic QRFP: Regulation of Food Intake and Fat Selection [J].
Primeaux, S. D. ;
Barnes, M. J. ;
Braymer, H. D. .
HORMONE AND METABOLIC RESEARCH, 2013, 45 (13) :967-974