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Sökning: WFRF:(Sommer Robert S.) > GPR162 is expressed...

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00003741nam a2200409 4500
001oai:DiVA.org:uu-156816
003SwePub
008110809s2011 | |||||||||||000 ||eng|
024a https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-1568162 URI
040 a (SwePub)uu
041 a engb eng
042 9 SwePub
072 7a vet2 swepub-contenttype
072 7a ovr2 swepub-publicationtype
100a Sreedharan, Smithau Uppsala universitet,Funktionell farmakologi4 aut0 (Swepub:uu)smisr997
2451 0a GPR162 is expressed in the hypothalamus and is involved in food intake related behaviour
264 1c 2011
338 a print2 rdacarrier
520 a The Rhodopsin family of G protein-coupled receptors (GPCRs) includes about 270 non-olfactory receptors and is the largest family of GPCRs. About sixty non-olfactory Rhodopsin GPCRs are still orphans without known ligands, and fairly little is known about their functions. In this study, we present molecular, neuroanatomical, genetic and behavioral data implicating a Rhodopsin family protein, GPR162, in the regulation of food intake-related behaviour and glucose homeostasis. The real-time PCR data show that GPR162 is predominantly expressed in the CNS. The in situ hybridization results confirmed significant expression of GPR162 in several hypothalamic sites, amygdala, substantia nigra and ventral tegmental area, among others regions. In line with the distribution of the GPR162 mRNA in the feeding circuitry, antisense oligo knockdown of GPR162 caused a significant reduction in food intake but no effect was observed towards reduction in body weight in rats. Our human genetics studies suggest that genetic variants of GPR162 affect glucose homeostasis. In conclusion, this study provides evidence linking the orphan GPR162 gene with the regulation of food intake-related behaviour.
700a Carlini, Valeria Pu Departamento de Farmacología, Universidad Nacional de Córdoba, Argentina4 aut
700a Jacobsson, Josefin Au Uppsala universitet,Funktionell farmakologi4 aut0 (Swepub:uu)josja875
700a Olszewski, Pawel Ku Uppsala universitet,Funktionell farmakologi4 aut0 (Swepub:uu)pawol865
700a Haitina, Tatjanau Uppsala universitet,Evolution och utvecklingsbiologi4 aut0 (Swepub:uu)tahai516
700a Hammer, Joannau Uppsala universitet,Genomik4 aut0 (Swepub:uu)joaha488
700a Stephansson, Olgau Uppsala universitet,Funktionell farmakologi4 aut
700a Crona, Filipu Uppsala universitet,Funktionell farmakologi4 aut
700a Sommer, Wolfgang Hu Department of Psychopharmacology, Central institute of Mental Health, Mannheim, Germany4 aut
700a Riserus, Ulfu Uppsala universitet,Klinisk nutrition och metabolism4 aut0 (Swepub:uu)ulfriser
700a Levine, Allen Su Department of Food Science and Nutrition, Minnesota Obesity Center4 aut
700a Lannfelt, Larsu Uppsala universitet,Geriatrik4 aut0 (Swepub:uu)lalan021
700a Marcus, Claudeu Department for Clinical Science, Intervention and Technology, Karolinska Institute4 aut
700a Heilig, Marcusu Laboratory of Clinical and Translational Studies, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, MD, USA4 aut
700a de Barioglio, Susan Ru Departamento de Farmacología, Universidad Nacional de Córdoba, Argentina4 aut
700a Fredriksson, Robertu Uppsala universitet,Funktionell farmakologi4 aut0 (Swepub:uu)rfr20930
700a Schiöth, Helgiu Uppsala universitet,Funktionell farmakologi4 aut0 (Swepub:uu)helgschi
710a Uppsala universitetb Funktionell farmakologi4 org
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-156816

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