PubMed:27729412
Annnotations
LitCoin-entities
{"project":"LitCoin-entities","denotations":[{"id":"11603","span":{"begin":8,"end":19},"obj":"GeneOrGeneProduct"},{"id":"11604","span":{"begin":97,"end":104},"obj":"GeneOrGeneProduct"},{"id":"11605","span":{"begin":117,"end":139},"obj":"GeneOrGeneProduct"},{"id":"11606","span":{"begin":169,"end":180},"obj":"GeneOrGeneProduct"},{"id":"11607","span":{"begin":205,"end":214},"obj":"GeneOrGeneProduct"},{"id":"11608","span":{"begin":246,"end":258},"obj":"DiseaseOrPhenotypicFeature"},{"id":"11609","span":{"begin":347,"end":356},"obj":"DiseaseOrPhenotypicFeature"},{"id":"11610","span":{"begin":366,"end":378},"obj":"DiseaseOrPhenotypicFeature"},{"id":"11611","span":{"begin":385,"end":408},"obj":"DiseaseOrPhenotypicFeature"},{"id":"11612","span":{"begin":422,"end":433},"obj":"GeneOrGeneProduct"},{"id":"11613","span":{"begin":445,"end":454},"obj":"ChemicalEntity"},{"id":"11614","span":{"begin":467,"end":476},"obj":"ChemicalEntity"},{"id":"11615","span":{"begin":603,"end":614},"obj":"GeneOrGeneProduct"},{"id":"11616","span":{"begin":669,"end":678},"obj":"ChemicalEntity"},{"id":"11617","span":{"begin":693,"end":697},"obj":"OrganismTaxon"},{"id":"11618","span":{"begin":713,"end":724},"obj":"GeneOrGeneProduct"},{"id":"11619","span":{"begin":771,"end":796},"obj":"GeneOrGeneProduct"},{"id":"11620","span":{"begin":798,"end":805},"obj":"GeneOrGeneProduct"},{"id":"11621","span":{"begin":832,"end":845},"obj":"ChemicalEntity"},{"id":"11622","span":{"begin":908,"end":912},"obj":"OrganismTaxon"},{"id":"11623","span":{"begin":926,"end":935},"obj":"ChemicalEntity"},{"id":"11624","span":{"begin":960,"end":971},"obj":"GeneOrGeneProduct"},{"id":"11625","span":{"begin":1011,"end":1015},"obj":"OrganismTaxon"},{"id":"11626","span":{"begin":1027,"end":1036},"obj":"ChemicalEntity"},{"id":"11627","span":{"begin":1105,"end":1134},"obj":"GeneOrGeneProduct"},{"id":"11628","span":{"begin":1140,"end":1144},"obj":"GeneOrGeneProduct"},{"id":"11629","span":{"begin":1188,"end":1207},"obj":"GeneOrGeneProduct"},{"id":"11630","span":{"begin":1237,"end":1248},"obj":"GeneOrGeneProduct"},{"id":"11631","span":{"begin":1269,"end":1276},"obj":"GeneOrGeneProduct"},{"id":"11632","span":{"begin":1308,"end":1311},"obj":"GeneOrGeneProduct"},{"id":"11633","span":{"begin":1347,"end":1358},"obj":"GeneOrGeneProduct"},{"id":"11634","span":{"begin":1433,"end":1440},"obj":"GeneOrGeneProduct"},{"id":"11635","span":{"begin":1501,"end":1514},"obj":"ChemicalEntity"},{"id":"11636","span":{"begin":1534,"end":1537},"obj":"GeneOrGeneProduct"},{"id":"11637","span":{"begin":1579,"end":1592},"obj":"ChemicalEntity"},{"id":"11638","span":{"begin":1637,"end":1640},"obj":"GeneOrGeneProduct"},{"id":"11639","span":{"begin":1671,"end":1682},"obj":"GeneOrGeneProduct"},{"id":"11640","span":{"begin":1852,"end":1863},"obj":"GeneOrGeneProduct"},{"id":"11641","span":{"begin":1941,"end":1948},"obj":"GeneOrGeneProduct"},{"id":"11642","span":{"begin":1961,"end":1983},"obj":"GeneOrGeneProduct"}],"attributes":[{"id":"A1","pred":"db_id","subj":"11603","obj":"NCBIGene:11450"},{"id":"A2","pred":"db_id","subj":"11604","obj":"NCBIGene:11668"},{"id":"A3","pred":"db_id","subj":"11605","obj":"NCBIGene:19401"},{"id":"A4","pred":"db_id","subj":"11605","obj":"NCBIGene:19411"},{"id":"A5","pred":"db_id","subj":"11605","obj":"NCBIGene:20181"},{"id":"A6","pred":"db_id","subj":"11606","obj":"NCBIGene:11450"},{"id":"A7","pred":"db_id","subj":"11607","obj":"NCBIGene:11450"},{"id":"A8","pred":"db_id","subj":"11608","obj":"MESH:D007249"},{"id":"A9","pred":"db_id","subj":"11609","obj":"MESH:D009765"},{"id":"A10","pred":"db_id","subj":"11610","obj":"MESH:D007249"},{"id":"A11","pred":"db_id","subj":"11611","obj":"MESH:D002318"},{"id":"A12","pred":"db_id","subj":"11612","obj":"NCBIGene:11450"},{"id":"A13","pred":"db_id","subj":"11613","obj":"MESH:D014801"},{"id":"A14","pred":"db_id","subj":"11614","obj":"MESH:D012176"},{"id":"A15","pred":"db_id","subj":"11615","obj":"NCBIGene:11450"},{"id":"A16","pred":"db_id","subj":"11616","obj":"MESH:D014801"},{"id":"A17","pred":"db_id","subj":"11617","obj":"NCBITaxon:10090"},{"id":"A18","pred":"db_id","subj":"11618","obj":"NCBIGene:11450"},{"id":"A19","pred":"db_id","subj":"11619","obj":"NCBIGene:11668"},{"id":"A20","pred":"db_id","subj":"11620","obj":"NCBIGene:11668"},{"id":"A21","pred":"db_id","subj":"11621","obj":"MESH:D014212"},{"id":"A22","pred":"db_id","subj":"11622","obj":"NCBITaxon:10090"},{"id":"A23","pred":"db_id","subj":"11623","obj":"MESH:D014801"},{"id":"A24","pred":"db_id","subj":"11624","obj":"NCBIGene:11450"},{"id":"A25","pred":"db_id","subj":"11625","obj":"NCBITaxon:10090"},{"id":"A26","pred":"db_id","subj":"11626","obj":"MESH:D014801"},{"id":"A27","pred":"db_id","subj":"11627","obj":"NCBIGene:19401"},{"id":"A28","pred":"db_id","subj":"11628","obj":"NCBIGene:19411"},{"id":"A29","pred":"db_id","subj":"11629","obj":"NCBIGene:20181"},{"id":"A30","pred":"db_id","subj":"11630","obj":"NCBIGene:11450"},{"id":"A31","pred":"db_id","subj":"11631","obj":"NCBIGene:11668"},{"id":"A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adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue.\nAdiponectin is an adipocyte-derived adipokine with potent antidiabetic, anti-inflammatory, and antiatherogenic activity. Long-term, high-fat diet results in gain of body weight, adiposity, further inflammatory-based cardiovascular diseases, and reduced adiponectin secretion. Vitamin A derivatives/retinoids are involved in several of these processes, which mainly take place in white adipose tissue (WAT). In this study, we examined adiponectin expression as a function of dietary high-fat and high-vitamin A conditions in mice. A decrease of adiponectin expression in addition to an up-regulation of aldehyde dehydrogenase A1 (ALDH1A1), retinoid signaling, and retinoic acid response element signaling was selectively observed in WAT of mice fed a normal-vitamin A, high-fat diet. Reduced adiponectin expression in WAT was also observed in mice fed a high-vitamin A diet. Adipocyte cell culture revealed that endogenous and synthetic retinoic acid receptor (RAR)α- and RARγ-selective agonists, as well as a synthetic retinoid X receptor agonist, efficiently reduced adiponectin expression, whereas ALDH1A1 expression only increased with RAR agonists. We conclude that reduced adiponectin expression under high-fat dietary conditions is dependent on 1) increased ALDH1A1 expression in adipocytes, which does not increase all-trans-retinoic acid levels; 2) further RAR ligand-induced, WAT-selective, increased retinoic acid response element-mediated signaling; and 3) RAR ligand-dependent reduction of adiponectin expression.-Landrier, J.-F., Kasiri, E., Karkeni, E., Mihály, J., Béke, G., Weiss, K., Lucas, R., Aydemir, G., Salles, J., Walrand, S., de Lera, A. R., Rühl, R. Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue."}
LitCoin-entities-OrganismTaxon-PD
{"project":"LitCoin-entities-OrganismTaxon-PD","denotations":[{"id":"T1","span":{"begin":693,"end":697},"obj":"OrganismTaxon"},{"id":"T3","span":{"begin":908,"end":912},"obj":"OrganismTaxon"},{"id":"T5","span":{"begin":1011,"end":1015},"obj":"OrganismTaxon"}],"attributes":[{"id":"A1","pred":"db_id","subj":"T1","obj":"NCBItxid:10095"},{"id":"A2","pred":"db_id","subj":"T1","obj":"NCBItxid:10088"},{"id":"A3","pred":"db_id","subj":"T3","obj":"NCBItxid:10095"},{"id":"A4","pred":"db_id","subj":"T3","obj":"NCBItxid:10088"},{"id":"A5","pred":"db_id","subj":"T5","obj":"NCBItxid:10095"},{"id":"A6","pred":"db_id","subj":"T5","obj":"NCBItxid:10088"}],"text":"Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue.\nAdiponectin is an adipocyte-derived adipokine with potent antidiabetic, anti-inflammatory, and antiatherogenic activity. Long-term, high-fat diet results in gain of body weight, adiposity, further inflammatory-based cardiovascular diseases, and reduced adiponectin secretion. Vitamin A derivatives/retinoids are involved in several of these processes, which mainly take place in white adipose tissue (WAT). In this study, we examined adiponectin expression as a function of dietary high-fat and high-vitamin A conditions in mice. A decrease of adiponectin expression in addition to an up-regulation of aldehyde dehydrogenase A1 (ALDH1A1), retinoid signaling, and retinoic acid response element signaling was selectively observed in WAT of mice fed a normal-vitamin A, high-fat diet. Reduced adiponectin expression in WAT was also observed in mice fed a high-vitamin A diet. Adipocyte cell culture revealed that endogenous and synthetic retinoic acid receptor (RAR)α- and RARγ-selective agonists, as well as a synthetic retinoid X receptor agonist, efficiently reduced adiponectin expression, whereas ALDH1A1 expression only increased with RAR agonists. We conclude that reduced adiponectin expression under high-fat dietary conditions is dependent on 1) increased ALDH1A1 expression in adipocytes, which does not increase all-trans-retinoic acid levels; 2) further RAR ligand-induced, WAT-selective, increased retinoic acid response element-mediated signaling; and 3) RAR ligand-dependent reduction of adiponectin expression.-Landrier, J.-F., Kasiri, E., Karkeni, E., Mihály, J., Béke, G., Weiss, K., Lucas, R., Aydemir, G., Salles, J., Walrand, S., de Lera, A. R., Rühl, R. Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue."}
LitCoin-sentences
{"project":"LitCoin-sentences","denotations":[{"id":"T1","span":{"begin":0,"end":168},"obj":"Sentence"},{"id":"T2","span":{"begin":169,"end":289},"obj":"Sentence"},{"id":"T3","span":{"begin":290,"end":444},"obj":"Sentence"},{"id":"T4","span":{"begin":445,"end":575},"obj":"Sentence"},{"id":"T5","span":{"begin":576,"end":698},"obj":"Sentence"},{"id":"T6","span":{"begin":699,"end":951},"obj":"Sentence"},{"id":"T7","span":{"begin":952,"end":1042},"obj":"Sentence"},{"id":"T8","span":{"begin":1043,"end":1321},"obj":"Sentence"},{"id":"T9","span":{"begin":1322,"end":1830},"obj":"Sentence"},{"id":"T10","span":{"begin":1831,"end":1843},"obj":"Sentence"},{"id":"T11","span":{"begin":1844,"end":2012},"obj":"Sentence"}],"text":"Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue.\nAdiponectin is an adipocyte-derived adipokine with potent antidiabetic, anti-inflammatory, and antiatherogenic activity. Long-term, high-fat diet results in gain of body weight, adiposity, further inflammatory-based cardiovascular diseases, and reduced adiponectin secretion. Vitamin A derivatives/retinoids are involved in several of these processes, which mainly take place in white adipose tissue (WAT). In this study, we examined adiponectin expression as a function of dietary high-fat and high-vitamin A conditions in mice. A decrease of adiponectin expression in addition to an up-regulation of aldehyde dehydrogenase A1 (ALDH1A1), retinoid signaling, and retinoic acid response element signaling was selectively observed in WAT of mice fed a normal-vitamin A, high-fat diet. Reduced adiponectin expression in WAT was also observed in mice fed a high-vitamin A diet. Adipocyte cell culture revealed that endogenous and synthetic retinoic acid receptor (RAR)α- and RARγ-selective agonists, as well as a synthetic retinoid X receptor agonist, efficiently reduced adiponectin expression, whereas ALDH1A1 expression only increased with RAR agonists. We conclude that reduced adiponectin expression under high-fat dietary conditions is dependent on 1) increased ALDH1A1 expression in adipocytes, which does not increase all-trans-retinoic acid levels; 2) further RAR ligand-induced, WAT-selective, increased retinoic acid response element-mediated signaling; and 3) RAR ligand-dependent reduction of adiponectin expression.-Landrier, J.-F., Kasiri, E., Karkeni, E., Mihály, J., Béke, G., Weiss, K., Lucas, R., Aydemir, G., Salles, J., Walrand, S., de Lera, A. R., Rühl, R. Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue."}
LitCoin_Mondo
{"project":"LitCoin_Mondo","denotations":[{"id":"T1","span":{"begin":385,"end":408},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"0004995"}],"text":"Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue.\nAdiponectin is an adipocyte-derived adipokine with potent antidiabetic, anti-inflammatory, and antiatherogenic activity. Long-term, high-fat diet results in gain of body weight, adiposity, further inflammatory-based cardiovascular diseases, and reduced adiponectin secretion. Vitamin A derivatives/retinoids are involved in several of these processes, which mainly take place in white adipose tissue (WAT). In this study, we examined adiponectin expression as a function of dietary high-fat and high-vitamin A conditions in mice. A decrease of adiponectin expression in addition to an up-regulation of aldehyde dehydrogenase A1 (ALDH1A1), retinoid signaling, and retinoic acid response element signaling was selectively observed in WAT of mice fed a normal-vitamin A, high-fat diet. Reduced adiponectin expression in WAT was also observed in mice fed a high-vitamin A diet. Adipocyte cell culture revealed that endogenous and synthetic retinoic acid receptor (RAR)α- and RARγ-selective agonists, as well as a synthetic retinoid X receptor agonist, efficiently reduced adiponectin expression, whereas ALDH1A1 expression only increased with RAR agonists. We conclude that reduced adiponectin expression under high-fat dietary conditions is dependent on 1) increased ALDH1A1 expression in adipocytes, which does not increase all-trans-retinoic acid levels; 2) further RAR ligand-induced, WAT-selective, increased retinoic acid response element-mediated signaling; and 3) RAR ligand-dependent reduction of adiponectin expression.-Landrier, J.-F., Kasiri, E., Karkeni, E., Mihály, J., Béke, G., Weiss, K., Lucas, R., Aydemir, G., Salles, J., Walrand, S., de Lera, A. R., Rühl, R. Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue."}
LitCoin-GeneOrGeneProduct-v0
{"project":"LitCoin-GeneOrGeneProduct-v0","denotations":[{"id":"T1","span":{"begin":0,"end":7},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":8,"end":19},"obj":"GeneOrGeneProduct"},{"id":"T3","span":{"begin":37,"end":41},"obj":"GeneOrGeneProduct"},{"id":"T4","span":{"begin":83,"end":93},"obj":"GeneOrGeneProduct"},{"id":"T5","span":{"begin":97,"end":104},"obj":"GeneOrGeneProduct"},{"id":"T6","span":{"begin":126,"end":130},"obj":"GeneOrGeneProduct"},{"id":"T7","span":{"begin":131,"end":139},"obj":"GeneOrGeneProduct"},{"id":"T8","span":{"begin":153,"end":160},"obj":"GeneOrGeneProduct"},{"id":"T9","span":{"begin":169,"end":180},"obj":"GeneOrGeneProduct"},{"id":"T10","span":{"begin":280,"end":288},"obj":"GeneOrGeneProduct"},{"id":"T11","span":{"begin":290,"end":294},"obj":"GeneOrGeneProduct"},{"id":"T12","span":{"begin":295,"end":299},"obj":"GeneOrGeneProduct"},{"id":"T13","span":{"begin":301,"end":305},"obj":"GeneOrGeneProduct"},{"id":"T14","span":{"begin":334,"end":345},"obj":"GeneOrGeneProduct"},{"id":"T15","span":{"begin":347,"end":356},"obj":"GeneOrGeneProduct"},{"id":"T16","span":{"begin":379,"end":384},"obj":"GeneOrGeneProduct"},{"id":"T17","span":{"begin":414,"end":421},"obj":"GeneOrGeneProduct"},{"id":"T18","span":{"begin":422,"end":433},"obj":"GeneOrGeneProduct"},{"id":"T19","span":{"begin":434,"end":443},"obj":"GeneOrGeneProduct"},{"id":"T20","span":{"begin":510,"end":519},"obj":"GeneOrGeneProduct"},{"id":"T21","span":{"begin":527,"end":533},"obj":"GeneOrGeneProduct"},{"id":"T22","span":{"begin":548,"end":553},"obj":"GeneOrGeneProduct"},{"id":"T23","span":{"begin":554,"end":561},"obj":"GeneOrGeneProduct"},{"id":"T24","span":{"begin":603,"end":614},"obj":"GeneOrGeneProduct"},{"id":"T25","span":{"begin":651,"end":655},"obj":"GeneOrGeneProduct"},{"id":"T26","span":{"begin":664,"end":668},"obj":"GeneOrGeneProduct"},{"id":"T27","span":{"begin":693,"end":697},"obj":"GeneOrGeneProduct"},{"id":"T28","span":{"begin":713,"end":724},"obj":"GeneOrGeneProduct"},{"id":"T29","span":{"begin":751,"end":756},"obj":"GeneOrGeneProduct"},{"id":"T30","span":{"begin":757,"end":767},"obj":"GeneOrGeneProduct"},{"id":"T31","span":{"begin":771,"end":793},"obj":"GeneOrGeneProduct"},{"id":"T32","span":{"begin":794,"end":796},"obj":"GeneOrGeneProduct"},{"id":"T33","span":{"begin":798,"end":805},"obj":"GeneOrGeneProduct"},{"id":"T34","span":{"begin":841,"end":845},"obj":"GeneOrGeneProduct"},{"id":"T35","span":{"begin":908,"end":912},"obj":"GeneOrGeneProduct"},{"id":"T36","span":{"begin":913,"end":918},"obj":"GeneOrGeneProduct"},{"id":"T37","span":{"begin":937,"end":941},"obj":"GeneOrGeneProduct"},{"id":"T38","span":{"begin":952,"end":959},"obj":"GeneOrGeneProduct"},{"id":"T39","span":{"begin":960,"end":971},"obj":"GeneOrGeneProduct"},{"id":"T40","span":{"begin":1011,"end":1015},"obj":"GeneOrGeneProduct"},{"id":"T41","span":{"begin":1016,"end":1021},"obj":"GeneOrGeneProduct"},{"id":"T42","span":{"begin":1022,"end":1026},"obj":"GeneOrGeneProduct"},{"id":"T43","span":{"begin":1053,"end":1057},"obj":"GeneOrGeneProduct"},{"id":"T44","span":{"begin":1114,"end":1118},"obj":"GeneOrGeneProduct"},{"id":"T45","span":{"begin":1119,"end":1127},"obj":"GeneOrGeneProduct"},{"id":"T46","span":{"begin":1129,"end":1132},"obj":"GeneOrGeneProduct"},{"id":"T47","span":{"begin":1140,"end":1143},"obj":"GeneOrGeneProduct"},{"id":"T48","span":{"begin":1188,"end":1207},"obj":"GeneOrGeneProduct"},{"id":"T49","span":{"begin":1229,"end":1236},"obj":"GeneOrGeneProduct"},{"id":"T50","span":{"begin":1237,"end":1248},"obj":"GeneOrGeneProduct"},{"id":"T51","span":{"begin":1269,"end":1276},"obj":"GeneOrGeneProduct"},{"id":"T52","span":{"begin":1308,"end":1311},"obj":"GeneOrGeneProduct"},{"id":"T53","span":{"begin":1339,"end":1346},"obj":"GeneOrGeneProduct"},{"id":"T54","span":{"begin":1347,"end":1358},"obj":"GeneOrGeneProduct"},{"id":"T55","span":{"begin":1376,"end":1380},"obj":"GeneOrGeneProduct"},{"id":"T56","span":{"begin":1433,"end":1440},"obj":"GeneOrGeneProduct"},{"id":"T57","span":{"begin":1491,"end":1500},"obj":"GeneOrGeneProduct"},{"id":"T58","span":{"begin":1510,"end":1514},"obj":"GeneOrGeneProduct"},{"id":"T59","span":{"begin":1534,"end":1537},"obj":"GeneOrGeneProduct"},{"id":"T60","span":{"begin":1545,"end":1552},"obj":"GeneOrGeneProduct"},{"id":"T61","span":{"begin":1588,"end":1592},"obj":"GeneOrGeneProduct"},{"id":"T62","span":{"begin":1610,"end":1618},"obj":"GeneOrGeneProduct"},{"id":"T63","span":{"begin":1630,"end":1635},"obj":"GeneOrGeneProduct"},{"id":"T64","span":{"begin":1637,"end":1640},"obj":"GeneOrGeneProduct"},{"id":"T65","span":{"begin":1671,"end":1682},"obj":"GeneOrGeneProduct"},{"id":"T66","span":{"begin":1770,"end":1775},"obj":"GeneOrGeneProduct"},{"id":"T67","span":{"begin":1844,"end":1851},"obj":"GeneOrGeneProduct"},{"id":"T68","span":{"begin":1852,"end":1863},"obj":"GeneOrGeneProduct"},{"id":"T69","span":{"begin":1881,"end":1885},"obj":"GeneOrGeneProduct"},{"id":"T70","span":{"begin":1927,"end":1937},"obj":"GeneOrGeneProduct"},{"id":"T71","span":{"begin":1941,"end":1948},"obj":"GeneOrGeneProduct"},{"id":"T72","span":{"begin":1970,"end":1974},"obj":"GeneOrGeneProduct"},{"id":"T73","span":{"begin":1975,"end":1983},"obj":"GeneOrGeneProduct"},{"id":"T74","span":{"begin":1997,"end":2004},"obj":"GeneOrGeneProduct"}],"text":"Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue.\nAdiponectin is an adipocyte-derived adipokine with potent antidiabetic, anti-inflammatory, and antiatherogenic activity. Long-term, high-fat diet results in gain of body weight, adiposity, further inflammatory-based cardiovascular diseases, and reduced adiponectin secretion. Vitamin A derivatives/retinoids are involved in several of these processes, which mainly take place in white adipose tissue (WAT). In this study, we examined adiponectin expression as a function of dietary high-fat and high-vitamin A conditions in mice. A decrease of adiponectin expression in addition to an up-regulation of aldehyde dehydrogenase A1 (ALDH1A1), retinoid signaling, and retinoic acid response element signaling was selectively observed in WAT of mice fed a normal-vitamin A, high-fat diet. Reduced adiponectin expression in WAT was also observed in mice fed a high-vitamin A diet. Adipocyte cell culture revealed that endogenous and synthetic retinoic acid receptor (RAR)α- and RARγ-selective agonists, as well as a synthetic retinoid X receptor agonist, efficiently reduced adiponectin expression, whereas ALDH1A1 expression only increased with RAR agonists. We conclude that reduced adiponectin expression under high-fat dietary conditions is dependent on 1) increased ALDH1A1 expression in adipocytes, which does not increase all-trans-retinoic acid levels; 2) further RAR ligand-induced, WAT-selective, increased retinoic acid response element-mediated signaling; and 3) RAR ligand-dependent reduction of adiponectin expression.-Landrier, J.-F., Kasiri, E., Karkeni, E., Mihály, J., Béke, G., Weiss, K., Lucas, R., Aydemir, G., Salles, J., Walrand, S., de Lera, A. R., Rühl, R. Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue."}
LitCoin-GeneOrGeneProduct-v2
{"project":"LitCoin-GeneOrGeneProduct-v2","denotations":[{"id":"T1","span":{"begin":0,"end":7},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":8,"end":19},"obj":"GeneOrGeneProduct"},{"id":"T3","span":{"begin":37,"end":41},"obj":"GeneOrGeneProduct"},{"id":"T4","span":{"begin":97,"end":104},"obj":"GeneOrGeneProduct"},{"id":"T5","span":{"begin":126,"end":130},"obj":"GeneOrGeneProduct"},{"id":"T6","span":{"begin":131,"end":139},"obj":"GeneOrGeneProduct"},{"id":"T7","span":{"begin":153,"end":160},"obj":"GeneOrGeneProduct"},{"id":"T8","span":{"begin":169,"end":180},"obj":"GeneOrGeneProduct"},{"id":"T9","span":{"begin":295,"end":299},"obj":"GeneOrGeneProduct"},{"id":"T10","span":{"begin":301,"end":305},"obj":"GeneOrGeneProduct"},{"id":"T11","span":{"begin":334,"end":345},"obj":"GeneOrGeneProduct"},{"id":"T12","span":{"begin":414,"end":421},"obj":"GeneOrGeneProduct"},{"id":"T13","span":{"begin":422,"end":433},"obj":"GeneOrGeneProduct"},{"id":"T14","span":{"begin":548,"end":553},"obj":"GeneOrGeneProduct"},{"id":"T15","span":{"begin":554,"end":561},"obj":"GeneOrGeneProduct"},{"id":"T16","span":{"begin":603,"end":614},"obj":"GeneOrGeneProduct"},{"id":"T17","span":{"begin":651,"end":655},"obj":"GeneOrGeneProduct"},{"id":"T18","span":{"begin":664,"end":668},"obj":"GeneOrGeneProduct"},{"id":"T19","span":{"begin":713,"end":724},"obj":"GeneOrGeneProduct"},{"id":"T20","span":{"begin":771,"end":793},"obj":"GeneOrGeneProduct"},{"id":"T21","span":{"begin":798,"end":805},"obj":"GeneOrGeneProduct"},{"id":"T22","span":{"begin":841,"end":845},"obj":"GeneOrGeneProduct"},{"id":"T23","span":{"begin":913,"end":918},"obj":"GeneOrGeneProduct"},{"id":"T24","span":{"begin":937,"end":941},"obj":"GeneOrGeneProduct"},{"id":"T25","span":{"begin":952,"end":959},"obj":"GeneOrGeneProduct"},{"id":"T26","span":{"begin":960,"end":971},"obj":"GeneOrGeneProduct"},{"id":"T27","span":{"begin":1016,"end":1021},"obj":"GeneOrGeneProduct"},{"id":"T28","span":{"begin":1022,"end":1026},"obj":"GeneOrGeneProduct"},{"id":"T29","span":{"begin":1053,"end":1057},"obj":"GeneOrGeneProduct"},{"id":"T30","span":{"begin":1114,"end":1118},"obj":"GeneOrGeneProduct"},{"id":"T31","span":{"begin":1119,"end":1127},"obj":"GeneOrGeneProduct"},{"id":"T32","span":{"begin":1188,"end":1207},"obj":"GeneOrGeneProduct"},{"id":"T33","span":{"begin":1229,"end":1236},"obj":"GeneOrGeneProduct"},{"id":"T34","span":{"begin":1237,"end":1248},"obj":"GeneOrGeneProduct"},{"id":"T35","span":{"begin":1269,"end":1276},"obj":"GeneOrGeneProduct"},{"id":"T36","span":{"begin":1339,"end":1346},"obj":"GeneOrGeneProduct"},{"id":"T37","span":{"begin":1347,"end":1358},"obj":"GeneOrGeneProduct"},{"id":"T38","span":{"begin":1376,"end":1380},"obj":"GeneOrGeneProduct"},{"id":"T39","span":{"begin":1433,"end":1440},"obj":"GeneOrGeneProduct"},{"id":"T40","span":{"begin":1491,"end":1500},"obj":"GeneOrGeneProduct"},{"id":"T41","span":{"begin":1510,"end":1514},"obj":"GeneOrGeneProduct"},{"id":"T42","span":{"begin":1588,"end":1592},"obj":"GeneOrGeneProduct"},{"id":"T43","span":{"begin":1671,"end":1682},"obj":"GeneOrGeneProduct"},{"id":"T44","span":{"begin":1844,"end":1851},"obj":"GeneOrGeneProduct"},{"id":"T45","span":{"begin":1852,"end":1863},"obj":"GeneOrGeneProduct"},{"id":"T46","span":{"begin":1881,"end":1885},"obj":"GeneOrGeneProduct"},{"id":"T47","span":{"begin":1941,"end":1948},"obj":"GeneOrGeneProduct"},{"id":"T48","span":{"begin":1970,"end":1974},"obj":"GeneOrGeneProduct"},{"id":"T49","span":{"begin":1975,"end":1983},"obj":"GeneOrGeneProduct"},{"id":"T50","span":{"begin":1997,"end":2004},"obj":"GeneOrGeneProduct"}],"text":"Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue.\nAdiponectin is an adipocyte-derived adipokine with potent antidiabetic, anti-inflammatory, and antiatherogenic activity. Long-term, high-fat diet results in gain of body weight, adiposity, further inflammatory-based cardiovascular diseases, and reduced adiponectin secretion. Vitamin A derivatives/retinoids are involved in several of these processes, which mainly take place in white adipose tissue (WAT). In this study, we examined adiponectin expression as a function of dietary high-fat and high-vitamin A conditions in mice. A decrease of adiponectin expression in addition to an up-regulation of aldehyde dehydrogenase A1 (ALDH1A1), retinoid signaling, and retinoic acid response element signaling was selectively observed in WAT of mice fed a normal-vitamin A, high-fat diet. Reduced adiponectin expression in WAT was also observed in mice fed a high-vitamin A diet. Adipocyte cell culture revealed that endogenous and synthetic retinoic acid receptor (RAR)α- and RARγ-selective agonists, as well as a synthetic retinoid X receptor agonist, efficiently reduced adiponectin expression, whereas ALDH1A1 expression only increased with RAR agonists. We conclude that reduced adiponectin expression under high-fat dietary conditions is dependent on 1) increased ALDH1A1 expression in adipocytes, which does not increase all-trans-retinoic acid levels; 2) further RAR ligand-induced, WAT-selective, increased retinoic acid response element-mediated signaling; and 3) RAR ligand-dependent reduction of adiponectin expression.-Landrier, J.-F., Kasiri, E., Karkeni, E., Mihály, J., Béke, G., Weiss, K., Lucas, R., Aydemir, G., Salles, J., Walrand, S., de Lera, A. R., Rühl, R. Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue."}
LitCoin-Disease-MeSH
{"project":"LitCoin-Disease-MeSH","denotations":[{"id":"T1","span":{"begin":246,"end":258},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":334,"end":345},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":366,"end":378},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":385,"end":408},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"originalLabel","subj":"T1","obj":"DISEASE"},{"id":"A2","pred":"originalLabel","subj":"T2","obj":"D001835"},{"id":"A3","pred":"originalLabel","subj":"T3","obj":"DISEASE"},{"id":"A4","pred":"originalLabel","subj":"T4","obj":"D002318"}],"text":"Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue.\nAdiponectin is an adipocyte-derived adipokine with potent antidiabetic, anti-inflammatory, and antiatherogenic activity. Long-term, high-fat diet results in gain of body weight, adiposity, further inflammatory-based cardiovascular diseases, and reduced adiponectin secretion. Vitamin A derivatives/retinoids are involved in several of these processes, which mainly take place in white adipose tissue (WAT). In this study, we examined adiponectin expression as a function of dietary high-fat and high-vitamin A conditions in mice. A decrease of adiponectin expression in addition to an up-regulation of aldehyde dehydrogenase A1 (ALDH1A1), retinoid signaling, and retinoic acid response element signaling was selectively observed in WAT of mice fed a normal-vitamin A, high-fat diet. Reduced adiponectin expression in WAT was also observed in mice fed a high-vitamin A diet. Adipocyte cell culture revealed that endogenous and synthetic retinoic acid receptor (RAR)α- and RARγ-selective agonists, as well as a synthetic retinoid X receptor agonist, efficiently reduced adiponectin expression, whereas ALDH1A1 expression only increased with RAR agonists. We conclude that reduced adiponectin expression under high-fat dietary conditions is dependent on 1) increased ALDH1A1 expression in adipocytes, which does not increase all-trans-retinoic acid levels; 2) further RAR ligand-induced, WAT-selective, increased retinoic acid response element-mediated signaling; and 3) RAR ligand-dependent reduction of adiponectin expression.-Landrier, J.-F., Kasiri, E., Karkeni, E., Mihály, J., Béke, G., Weiss, K., Lucas, R., Aydemir, G., Salles, J., Walrand, S., de Lera, A. R., Rühl, R. Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue."}
LitCoin-GeneOrGeneProduct-v3
{"project":"LitCoin-GeneOrGeneProduct-v3","denotations":[{"id":"T1","span":{"begin":8,"end":19},"obj":"GeneOrGeneProduct"},{"id":"T2","span":{"begin":97,"end":104},"obj":"GeneOrGeneProduct"},{"id":"T3","span":{"begin":169,"end":180},"obj":"GeneOrGeneProduct"},{"id":"T4","span":{"begin":422,"end":433},"obj":"GeneOrGeneProduct"},{"id":"T5","span":{"begin":548,"end":553},"obj":"GeneOrGeneProduct"},{"id":"T6","span":{"begin":603,"end":614},"obj":"GeneOrGeneProduct"},{"id":"T7","span":{"begin":713,"end":724},"obj":"GeneOrGeneProduct"},{"id":"T8","span":{"begin":771,"end":793},"obj":"GeneOrGeneProduct"},{"id":"T9","span":{"begin":798,"end":805},"obj":"GeneOrGeneProduct"},{"id":"T10","span":{"begin":832,"end":854},"obj":"GeneOrGeneProduct"},{"id":"T11","span":{"begin":960,"end":971},"obj":"GeneOrGeneProduct"},{"id":"T12","span":{"begin":1188,"end":1207},"obj":"GeneOrGeneProduct"},{"id":"T13","span":{"begin":1237,"end":1248},"obj":"GeneOrGeneProduct"},{"id":"T14","span":{"begin":1269,"end":1276},"obj":"GeneOrGeneProduct"},{"id":"T15","span":{"begin":1347,"end":1358},"obj":"GeneOrGeneProduct"},{"id":"T16","span":{"begin":1433,"end":1440},"obj":"GeneOrGeneProduct"},{"id":"T17","span":{"begin":1491,"end":1500},"obj":"GeneOrGeneProduct"},{"id":"T18","span":{"begin":1579,"end":1601},"obj":"GeneOrGeneProduct"},{"id":"T19","span":{"begin":1671,"end":1682},"obj":"GeneOrGeneProduct"},{"id":"T20","span":{"begin":1852,"end":1863},"obj":"GeneOrGeneProduct"},{"id":"T21","span":{"begin":1941,"end":1948},"obj":"GeneOrGeneProduct"}],"text":"Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue.\nAdiponectin is an adipocyte-derived adipokine with potent antidiabetic, anti-inflammatory, and antiatherogenic activity. Long-term, high-fat diet results in gain of body weight, adiposity, further inflammatory-based cardiovascular diseases, and reduced adiponectin secretion. Vitamin A derivatives/retinoids are involved in several of these processes, which mainly take place in white adipose tissue (WAT). In this study, we examined adiponectin expression as a function of dietary high-fat and high-vitamin A conditions in mice. A decrease of adiponectin expression in addition to an up-regulation of aldehyde dehydrogenase A1 (ALDH1A1), retinoid signaling, and retinoic acid response element signaling was selectively observed in WAT of mice fed a normal-vitamin A, high-fat diet. Reduced adiponectin expression in WAT was also observed in mice fed a high-vitamin A diet. Adipocyte cell culture revealed that endogenous and synthetic retinoic acid receptor (RAR)α- and RARγ-selective agonists, as well as a synthetic retinoid X receptor agonist, efficiently reduced adiponectin expression, whereas ALDH1A1 expression only increased with RAR agonists. We conclude that reduced adiponectin expression under high-fat dietary conditions is dependent on 1) increased ALDH1A1 expression in adipocytes, which does not increase all-trans-retinoic acid levels; 2) further RAR ligand-induced, WAT-selective, increased retinoic acid response element-mediated signaling; and 3) RAR ligand-dependent reduction of adiponectin expression.-Landrier, J.-F., Kasiri, E., Karkeni, E., Mihály, J., Béke, G., Weiss, K., Lucas, R., Aydemir, G., Salles, J., Walrand, S., de Lera, A. R., Rühl, R. Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue."}
LitCoin_Mondo_095
{"project":"LitCoin_Mondo_095","denotations":[{"id":"T1","span":{"begin":385,"end":408},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":570,"end":573},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":901,"end":904},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":913,"end":916},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":986,"end":989},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T6","span":{"begin":1016,"end":1019},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T7","span":{"begin":1554,"end":1557},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"mondo_id","subj":"T1","obj":"0004995"},{"id":"A2","pred":"mondo_id","subj":"T2","obj":"0004255"},{"id":"A3","pred":"mondo_id","subj":"T3","obj":"0004255"},{"id":"A4","pred":"mondo_id","subj":"T4","obj":"0007620"},{"id":"A5","pred":"mondo_id","subj":"T5","obj":"0004255"},{"id":"A6","pred":"mondo_id","subj":"T6","obj":"0007620"},{"id":"A7","pred":"mondo_id","subj":"T7","obj":"0004255"}],"text":"Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue.\nAdiponectin is an adipocyte-derived adipokine with potent antidiabetic, anti-inflammatory, and antiatherogenic activity. Long-term, high-fat diet results in gain of body weight, adiposity, further inflammatory-based cardiovascular diseases, and reduced adiponectin secretion. Vitamin A derivatives/retinoids are involved in several of these processes, which mainly take place in white adipose tissue (WAT). In this study, we examined adiponectin expression as a function of dietary high-fat and high-vitamin A conditions in mice. A decrease of adiponectin expression in addition to an up-regulation of aldehyde dehydrogenase A1 (ALDH1A1), retinoid signaling, and retinoic acid response element signaling was selectively observed in WAT of mice fed a normal-vitamin A, high-fat diet. Reduced adiponectin expression in WAT was also observed in mice fed a high-vitamin A diet. Adipocyte cell culture revealed that endogenous and synthetic retinoic acid receptor (RAR)α- and RARγ-selective agonists, as well as a synthetic retinoid X receptor agonist, efficiently reduced adiponectin expression, whereas ALDH1A1 expression only increased with RAR agonists. We conclude that reduced adiponectin expression under high-fat dietary conditions is dependent on 1) increased ALDH1A1 expression in adipocytes, which does not increase all-trans-retinoic acid levels; 2) further RAR ligand-induced, WAT-selective, increased retinoic acid response element-mediated signaling; and 3) RAR ligand-dependent reduction of adiponectin expression.-Landrier, J.-F., Kasiri, E., Karkeni, E., Mihály, J., Béke, G., Weiss, K., Lucas, R., Aydemir, G., Salles, J., Walrand, S., de Lera, A. R., Rühl, R. Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue."}
LitCoin-NCBITaxon-2
{"project":"LitCoin-NCBITaxon-2","denotations":[{"id":"T1","span":{"begin":693,"end":697},"obj":"OrganismTaxon"},{"id":"T2","span":{"begin":908,"end":912},"obj":"OrganismTaxon"},{"id":"T3","span":{"begin":1011,"end":1015},"obj":"OrganismTaxon"},{"id":"T4","span":{"begin":1095,"end":1104},"obj":"OrganismTaxon"},{"id":"T5","span":{"begin":1178,"end":1187},"obj":"OrganismTaxon"}],"text":"Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue.\nAdiponectin is an adipocyte-derived adipokine with potent antidiabetic, anti-inflammatory, and antiatherogenic activity. Long-term, high-fat diet results in gain of body weight, adiposity, further inflammatory-based cardiovascular diseases, and reduced adiponectin secretion. Vitamin A derivatives/retinoids are involved in several of these processes, which mainly take place in white adipose tissue (WAT). In this study, we examined adiponectin expression as a function of dietary high-fat and high-vitamin A conditions in mice. A decrease of adiponectin expression in addition to an up-regulation of aldehyde dehydrogenase A1 (ALDH1A1), retinoid signaling, and retinoic acid response element signaling was selectively observed in WAT of mice fed a normal-vitamin A, high-fat diet. Reduced adiponectin expression in WAT was also observed in mice fed a high-vitamin A diet. Adipocyte cell culture revealed that endogenous and synthetic retinoic acid receptor (RAR)α- and RARγ-selective agonists, as well as a synthetic retinoid X receptor agonist, efficiently reduced adiponectin expression, whereas ALDH1A1 expression only increased with RAR agonists. We conclude that reduced adiponectin expression under high-fat dietary conditions is dependent on 1) increased ALDH1A1 expression in adipocytes, which does not increase all-trans-retinoic acid levels; 2) further RAR ligand-induced, WAT-selective, increased retinoic acid response element-mediated signaling; and 3) RAR ligand-dependent reduction of adiponectin expression.-Landrier, J.-F., Kasiri, E., Karkeni, E., Mihály, J., Béke, G., Weiss, K., Lucas, R., Aydemir, G., Salles, J., Walrand, S., de Lera, A. R., Rühl, R. Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue."}
LitCoin-MeSH-Disease-2
{"project":"LitCoin-MeSH-Disease-2","denotations":[{"id":"T1","span":{"begin":246,"end":258},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":334,"end":345},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T3","span":{"begin":347,"end":356},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T4","span":{"begin":366,"end":378},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T5","span":{"begin":385,"end":408},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"ID:","subj":"T1","obj":"DISEASE"},{"id":"A2","pred":"ID:","subj":"T2","obj":"D001835"},{"id":"A3","pred":"ID:","subj":"T3","obj":"DISEASE"},{"id":"A4","pred":"ID:","subj":"T4","obj":"DISEASE"},{"id":"A5","pred":"ID:","subj":"T5","obj":"D002318"}],"text":"Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue.\nAdiponectin is an adipocyte-derived adipokine with potent antidiabetic, anti-inflammatory, and antiatherogenic activity. Long-term, high-fat diet results in gain of body weight, adiposity, further inflammatory-based cardiovascular diseases, and reduced adiponectin secretion. Vitamin A derivatives/retinoids are involved in several of these processes, which mainly take place in white adipose tissue (WAT). In this study, we examined adiponectin expression as a function of dietary high-fat and high-vitamin A conditions in mice. A decrease of adiponectin expression in addition to an up-regulation of aldehyde dehydrogenase A1 (ALDH1A1), retinoid signaling, and retinoic acid response element signaling was selectively observed in WAT of mice fed a normal-vitamin A, high-fat diet. Reduced adiponectin expression in WAT was also observed in mice fed a high-vitamin A diet. Adipocyte cell culture revealed that endogenous and synthetic retinoic acid receptor (RAR)α- and RARγ-selective agonists, as well as a synthetic retinoid X receptor agonist, efficiently reduced adiponectin expression, whereas ALDH1A1 expression only increased with RAR agonists. We conclude that reduced adiponectin expression under high-fat dietary conditions is dependent on 1) increased ALDH1A1 expression in adipocytes, which does not increase all-trans-retinoic acid levels; 2) further RAR ligand-induced, WAT-selective, increased retinoic acid response element-mediated signaling; and 3) RAR ligand-dependent reduction of adiponectin expression.-Landrier, J.-F., Kasiri, E., Karkeni, E., Mihály, J., Béke, G., Weiss, K., Lucas, R., Aydemir, G., Salles, J., Walrand, S., de Lera, A. R., Rühl, R. Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue."}
LitCoin-MONDO_bioort2019
{"project":"LitCoin-MONDO_bioort2019","denotations":[{"id":"T1","span":{"begin":347,"end":356},"obj":"DiseaseOrPhenotypicFeature"},{"id":"T2","span":{"begin":385,"end":408},"obj":"DiseaseOrPhenotypicFeature"}],"attributes":[{"id":"A1","pred":"#label","subj":"T1","obj":"DISEASE"},{"id":"A2","pred":"#label","subj":"T2","obj":"D002318"}],"text":"Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue.\nAdiponectin is an adipocyte-derived adipokine with potent antidiabetic, anti-inflammatory, and antiatherogenic activity. Long-term, high-fat diet results in gain of body weight, adiposity, further inflammatory-based cardiovascular diseases, and reduced adiponectin secretion. Vitamin A derivatives/retinoids are involved in several of these processes, which mainly take place in white adipose tissue (WAT). In this study, we examined adiponectin expression as a function of dietary high-fat and high-vitamin A conditions in mice. A decrease of adiponectin expression in addition to an up-regulation of aldehyde dehydrogenase A1 (ALDH1A1), retinoid signaling, and retinoic acid response element signaling was selectively observed in WAT of mice fed a normal-vitamin A, high-fat diet. Reduced adiponectin expression in WAT was also observed in mice fed a high-vitamin A diet. Adipocyte cell culture revealed that endogenous and synthetic retinoic acid receptor (RAR)α- and RARγ-selective agonists, as well as a synthetic retinoid X receptor agonist, efficiently reduced adiponectin expression, whereas ALDH1A1 expression only increased with RAR agonists. We conclude that reduced adiponectin expression under high-fat dietary conditions is dependent on 1) increased ALDH1A1 expression in adipocytes, which does not increase all-trans-retinoic acid levels; 2) further RAR ligand-induced, WAT-selective, increased retinoic acid response element-mediated signaling; and 3) RAR ligand-dependent reduction of adiponectin expression.-Landrier, J.-F., Kasiri, E., Karkeni, E., Mihály, J., Béke, G., Weiss, K., Lucas, R., Aydemir, G., Salles, J., Walrand, S., de Lera, A. R., Rühl, R. Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue."}
LitCoin-Chemical-MeSH-CHEBI
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Long-term, high-fat diet results in gain of body weight, adiposity, further inflammatory-based cardiovascular diseases, and reduced adiponectin secretion. Vitamin A derivatives/retinoids are involved in several of these processes, which mainly take place in white adipose tissue (WAT). In this study, we examined adiponectin expression as a function of dietary high-fat and high-vitamin A conditions in mice. A decrease of adiponectin expression in addition to an up-regulation of aldehyde dehydrogenase A1 (ALDH1A1), retinoid signaling, and retinoic acid response element signaling was selectively observed in WAT of mice fed a normal-vitamin A, high-fat diet. Reduced adiponectin expression in WAT was also observed in mice fed a high-vitamin A diet. Adipocyte cell culture revealed that endogenous and synthetic retinoic acid receptor (RAR)α- and RARγ-selective agonists, as well as a synthetic retinoid X receptor agonist, efficiently reduced adiponectin expression, whereas ALDH1A1 expression only increased with RAR agonists. We conclude that reduced adiponectin expression under high-fat dietary conditions is dependent on 1) increased ALDH1A1 expression in adipocytes, which does not increase all-trans-retinoic acid levels; 2) further RAR ligand-induced, WAT-selective, increased retinoic acid response element-mediated signaling; and 3) RAR ligand-dependent reduction of adiponectin expression.-Landrier, J.-F., Kasiri, E., Karkeni, E., Mihály, J., Béke, G., Weiss, K., Lucas, R., Aydemir, G., Salles, J., Walrand, S., de Lera, A. R., Rühl, R. Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue."}
LitCoin-training-merged
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adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue.\nAdiponectin is an adipocyte-derived adipokine with potent antidiabetic, anti-inflammatory, and antiatherogenic activity. Long-term, high-fat diet results in gain of body weight, adiposity, further inflammatory-based cardiovascular diseases, and reduced adiponectin secretion. Vitamin A derivatives/retinoids are involved in several of these processes, which mainly take place in white adipose tissue (WAT). In this study, we examined adiponectin expression as a function of dietary high-fat and high-vitamin A conditions in mice. A decrease of adiponectin expression in addition to an up-regulation of aldehyde dehydrogenase A1 (ALDH1A1), retinoid signaling, and retinoic acid response element signaling was selectively observed in WAT of mice fed a normal-vitamin A, high-fat diet. Reduced adiponectin expression in WAT was also observed in mice fed a high-vitamin A diet. Adipocyte cell culture revealed that endogenous and synthetic retinoic acid receptor (RAR)α- and RARγ-selective agonists, as well as a synthetic retinoid X receptor agonist, efficiently reduced adiponectin expression, whereas ALDH1A1 expression only increased with RAR agonists. We conclude that reduced adiponectin expression under high-fat dietary conditions is dependent on 1) increased ALDH1A1 expression in adipocytes, which does not increase all-trans-retinoic acid levels; 2) further RAR ligand-induced, WAT-selective, increased retinoic acid response element-mediated signaling; and 3) RAR ligand-dependent reduction of adiponectin expression.-Landrier, J.-F., Kasiri, E., Karkeni, E., Mihály, J., Béke, G., Weiss, K., Lucas, R., Aydemir, G., Salles, J., Walrand, S., de Lera, A. R., Rühl, R. Reduced adiponectin expression after high-fat diet is associated with selective up-regulation of ALDH1A1 and further retinoic acid receptor signaling in adipose tissue."}