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      Orexin system is expressed in avian liver and regulates hepatic lipogenesis via ERK1/2 activation

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          Abstract

          Orexins are originally characterized as orexigenic hypothalamic neuropeptides in mammals. Subsequent studies found orexin to be expressed and perform pleiotropic functions in multiple tissues in mammals. In avian (non-mammalian) species, however, orexin seemed to not affect feeding behavior and its physiological roles are poorly understood. Here, we provide evidence that orexin and its related receptors are expressed in chicken hepatocytes. Double immunofluorescence staining showed that orexin is localized in the ER, Golgi, and in the lysosomes in LMH cells. Brefeldin A treatment reduced orexin levels in the culture media, but increased it in the cell lysates. Administration of recombinant orexins upregulated the expression of orexin system in the liver of 9-day old chicks, but did not affect feed intake. Recombinant orexins increased fatty acid synthase (FASN) protein levels in chicken liver, activated acetyl-CoA carboxylase (ACCα), and increased FASN, ATP citrate lyase(ACLY), and malic enzyme (ME) protein expression in LMH cells. Blockade ERK1/2 activation by PD98059 attenuated these stimulating effects of orexin on lipogenic factors. Overexpression of ERK1/2 increased the expression of lipogenic genes, and orexin treatment induced the phosphorylated levels of ERK1/2 Thr202/Tyr204, but not that of p38 Thr180/Tyr182 or JNK1/2 Thr183/Tyr185 in chicken liver and LMH cells. Taken together, this is the first report evidencing that orexin is expressed and secreted from chicken hepatocytes, and that orexin induced hepatic lipogenesis via activation of ERK1/2 signaling pathway.

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          Analyzing real-time PCR data by the comparative CT method

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            Orexins and Orexin Receptors: A Family of Hypothalamic Neuropeptides and G Protein-Coupled Receptors that Regulate Feeding Behavior

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              Fatty acid synthase and the lipogenic phenotype in cancer pathogenesis.

              There is a renewed interest in the ultimate role of fatty acid synthase (FASN)--a key lipogenic enzyme catalysing the terminal steps in the de novo biogenesis of fatty acids--in cancer pathogenesis. Tumour-associated FASN, by conferring growth and survival advantages rather than functioning as an anabolic energy-storage pathway, appears to necessarily accompany the natural history of most human cancers. A recent identification of cross-talk between FASN and well-established cancer-controlling networks begins to delineate the oncogenic nature of FASN-driven lipogenesis. FASN, a nearly-universal druggable target in many human carcinomas and their precursor lesions, offers new therapeutic opportunities for metabolically treating and preventing cancer.
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                Author and article information

                Contributors
                dridi@uark.edu
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                5 November 2020
                5 November 2020
                2020
                : 10
                : 19191
                Affiliations
                [1 ]GRID grid.411017.2, ISNI 0000 0001 2151 0999, Center of Excellence for Poultry Science, , University of Arkansas, ; 1260 W. Maple Street, Fayetteville, AR 72701 USA
                [2 ]GRID grid.6292.f, ISNI 0000 0004 1757 1758, Dipartimento Di Scienze E Tecnologie Agro-Alimentari, , Alma Mater Studiorum-Università Di Bologna, ; Bologna, Italy
                [3 ]GRID grid.410773.6, ISNI 0000 0000 9949 0476, College of Agriculture, , Ibaraki University, ; Ibaraki, 300-0393 Japan
                Article
                76329
                10.1038/s41598-020-76329-2
                7645691
                33154530
                07c52f37-bb86-42e3-8bb2-30f989ac6847
                © The Author(s) 2020

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 5 February 2020
                : 22 October 2020
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                © The Author(s) 2020

                Uncategorized
                molecular biology,physiology
                Uncategorized
                molecular biology, physiology

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