Daily rhythms in activity and mRNA abundance of enzymes involved in glucose and lipid metabolism in liver of rainbow trout, Oncorhynchus mykiss. Influence of light and food availability

References

• Akhtar RA, Reddy AB, Maywood ES, et al. (2002). Circadian cycling of the mouse liver transcriptome, as revealed by cDNA microarray, is driven by the suprachiasmatic nucleus. Curr Biol. 12:540–50
   PubMed Web of Science ®Google Scholar
• Aranda A, Madrid JA, Sánchez-Vázquez FJ. (2001). Influence of light on feeding anticipatory activity in goldfish. J Biol Rhythms. 16:50–7
   PubMed Web of Science ®Google Scholar
• Bailey SM, Udoh US, Young ME. (2014). Circadian regulation of metabolism. J Endocrinol. 222:75–96
   PubMed Web of Science ®Google Scholar
• Bayarri MJ, Muñoz-Cueto JA, López-Olmeda JF, et al. (2004). Daily locomotor activity and melatonin rhythms in Senegal sole (Solea senegalensis). Physiol Behav. 81:577–83
   PubMed Web of Science ®Google Scholar
• Betancor MB, McStay E, Minghetti M, et al. (2014). Daily rhythms in expression of genes of hepatic lipid metabolism in Atlantic salmon (Salmo salar L.). PLoS One. 9:e106739
   PubMed Web of Science ®Google Scholar
• Boujard T, Leatherland JF. (1992b). Circadian rhythm and feeding time in fishes. Environ Biol Fishes. 35:109–31
   Web of Science ®Google Scholar
• Cailotto C, van Heijningen C, van der Vliet J, et al. (2008). Daily rhythms in metabolic liver enzymes and plasma glucose require a balance in the autonomic output to the liver. Endocrinology. 149:1914–25
   PubMed Web of Science ®Google Scholar
• Canaple L, Rambaud J, Dkhissi-Benyahya O, et al. (2006). Reciprocal regulation of brain and muscle arnt-like protein 1 and peroxisome proliferator-activated receptor alpha defines a novel positive feedback loop in the rodent liver circadian clock. Mol Endocrinol. 20:1715–27
   PubMed Web of Science ®Google Scholar
• Cermakian N, Whitmore D, Foulkes NS, Sassone-Corsi P. (2000). Asynchronous oscillations of two zebrafish CLOCK partners reveal differential clock control and function. PNAS. 97:4339–44
   PubMed Web of Science ®Google Scholar
• Chang HC, Guarente L. (2014). SIRT1 and other sirtuins in metabolism. Trends Endocrinol Metab. 25:138–45
   PubMed Web of Science ®Google Scholar
• Damiola F, Le Minh N, Preitner N, et al. (2000). Restricted feeding uncouples circadian oscillators in peripheral tissues from the central pacemaker in the suprachiasmatic nucleus. Genes Dev. 14:2950–61
   PubMed Web of Science ®Google Scholar
• De Pedro N, Delgado MJ, Pinillos ML, et al. (1998). Daily rhythms in NAT activity, cortisol, glucose, glycogen, and catecholamines in tench (Tinca tinca (L.). Pol Arch Hydrobiol. 45:321–9
   Google Scholar
• De Pedro N, Guijarro AI, López-Patiño MA, et al. (2005). Daily and seasonal variations in haematological and blood biochemical parameters in the tench, Tinca tinca Linnaeus, 1758. Aquac Res. 36:1185–96
   Web of Science ®Google Scholar
• Desvergne B, Michalik L, Wahli W. (2006). Transcriptional regulation of metabolism. Physiol Rev. 86:465–514
   PubMed Web of Science ®Google Scholar
• Eckel-Mahan K, Sassone-Corsi P. (2013). Metabolism and the circadian clock converge. Physiol Rev. 93:107–35
   PubMed Web of Science ®Google Scholar
• Engeland WC, Arnhold MM. (2005). Neural circuitry in the regulation of adrenal corticosterone rhythmicity. Endocrine. 28:325–32
   PubMed Web of Science ®Google Scholar
• Figueroa RI, Rodríguez-Sabarís R, Aldegunde M, Soengas JL. (2000). Effects of food deprivation on 24 h-changes in brain and liver carbohydrate and ketone body metabolism of rainbow trout. J. Fish Biol. 57:631–46
   Web of Science ®Google Scholar
• Gervois P, Chopin-Delannoy S, Fadel A, et al. (1999). Fibrates increase human REV-ERBalpha expression in liver via a novel peroxisome proliferator-activated receptor response element. Mol Endocrinol. 13:400–9
   PubMed Web of Science ®Google Scholar
• Gómez-Milán E, Sánchez-Muros Lozano MJ. (2007). Daily and annual variations of the hepatic glucose 6-phosphate dehydrogenase activity and seasonal changes in the body fats of the gilthead seabream Sparus aurata. J Exp Zool A Ecol Genet Physiol. 307:516–26
   PubMed Web of Science ®Google Scholar
• Hara R, Wan KK, Wakamatsu H, et al. (2001). Restricted feeding entrains liver clock without participation of the suprachiasmatic nucleus. Genes Cells. 6:269–78
   PubMed Web of Science ®Google Scholar
• Hardin PE, Panda S. (2013). Circadian timekeeping and output mechanisms in animals. Curr Opin Neurobiol. 23:724–31
   PubMed Web of Science ®Google Scholar
• Haus E. (2007). Chronobiology in the endocrine system. Adv Drug Deliv Rev. 59:985–1014
   PubMed Web of Science ®Google Scholar
• Huang W, Ramsey KM, Marcheva B, Bass J. (2011). Circadian rhythms, sleep and metabolism. J Clin Invest. 121:2133–41
   PubMed Web of Science ®Google Scholar
• Kirchner S, Seixas P, Kaushik S, Panserat S. (2005). Effects of low protein intake on extra-hepatic gluconeogenic enzyme expression and peripheral glucose phosphorylation in rainbow trout (Oncorhynchus mykiss). Comp Biochem Physiol B. 140:333–40
   PubMed Web of Science ®Google Scholar
• Ko CH, Takahashi JS. (2006). Molecular components of the mammalian circadian clock. Hum Mol Gen. 15:R271–7
   PubMed Web of Science ®Google Scholar
• Kornmann B, Schaad O, Reinke H, et al. (2007). Regulation of circadian gene expression in liver by systemic signals and hepatocyte oscillators. Cold Spring Harbor Symp Quant Biol. 72:319–30
   PubMedGoogle Scholar
• Laidley CW, Leatherland JF. (1988). Circadian studies of plasma cortisol, thyroid hormone, protein, glucose and ion concentration, liver glycogen concentration and liver and spleen weight in rainbow trout, Salmo gairdneri Richardson. Comp Biochem Physiol A 89:495–502
   PubMed Web of Science ®Google Scholar
• Le Martelot G, Claudel T, Gatfield D, et al. (2009). REV-ERB alpha participates in circadian SREBP signaling and bile acid homeostasis. PLoS Biol. 7:e1000181
   PubMed Web of Science ®Google Scholar
• Librán-Pérez M, Polakof S, López-Patiño MA, et al. (2012). Evidence of a metabolic fatty acid-sensing system in the hypothalamus and Brockmann bodies of rainbow trout: implications in food intake regulation. Am J Physiol Regul Integr Comp Physiol. 302:R1340–50
   PubMed Web of Science ®Google Scholar
• López-Olmeda JF, Blanco-Vives B, Pujante M, et al. (2013). Daily rhythms in the Hypothalamus-Pituitary-Interrenal axis and acute stress responses in a teleost flatfish, Solea senegalensis. Chronobiol Int. 30:530–9
   PubMed Web of Science ®Google Scholar
• López-Olmeda JF, Sánchez-Vázquez FJ. (2010). Feeding rhythms in fish: from behavioral to molecular approach. In Kulczykowska E, Popek W, Kapoor BG, eds. Biological clock in fish. Enfield, USA: Science Publishers, pp. 154–84
   Google Scholar
• López-Patiño MA, Rodríguez-Illamola A, Conde-Sieira M, et al. (2011). Daily rhythmic expression patterns of Clock1a, Bmal1, and Per1 genes in retina and hypothalamus of the rainbow trout, Oncorhynchus mykiss. Chronobiol Int. 27:381–9
   Web of Science ®Google Scholar
• Meijer HJ, Rietveld WJ. (1989). Neurophysiology of the suprachiasmatic circadian pacemaker in rodents. Physiol Rev. 69:671–707
   PubMed Web of Science ®Google Scholar
• Nogueiras R, Habegger KM, Chaudhary N, et al. (2012). Sirtuin 1 and sirtuin 3: Physiological modulators of metabolism. Physiol Rev 92:1479–514
   PubMed Web of Science ®Google Scholar
• Paredes JF, Vera LM, Martínez-López FJ, et al. (2014). Circadian rhythms of gene expression of lipid metabolism in gilthead sea ream liver: Synchronisation to light and feeding time. Chronobiol Int. 5:613–26
   Web of Science ®Google Scholar
• Pfaffl MW. (2001). A new mathematical model for relative quantification in real-time RTPCR. Nucleic Acids Res. 29:2002–7
   Web of Science ®Google Scholar
• Polakof S, Ceinos RM, Fernández-Durán B, et al. (2007a). Daily changes in parameters of energy metabolism in brain of rainbow trout: Dependence on feeding. Comp Biochem Physiol A. 146:265–73
   PubMed Web of Science ®Google Scholar
• Polakof S, Míguez JM, Soengas JL. (2007b). Daily changes in parameters of energy metabolism in liver, white muscle, and gills of rainbow trout: Dependence on feeding. Comp Biochem Physiol A. 147:363–74
   PubMed Web of Science ®Google Scholar
• Polakof S, Míguez JM, Soengas JL. (2008a). Changes in food intake and glucosensing function of hypothalamus and hindbrain in rainbow trout subjected to hyperglycemic or hypoglycemic conditions. J Comp Physiol A. 194:829–39
   Web of Science ®Google Scholar
• Polakof S, Míguez JM, Soengas JL. (2008b). Dietary carbohydrates induce changes in glucosensing capacity and food intake in rainbow trout. Am J Physiol Regul Integr Comp Physiol. 295:R478–89
   PubMed Web of Science ®Google Scholar
• Portaluppi F, Smolensky MH, Touitou Y. (2010). Ethics and methods for biological rhythm research on animals and human beings. Chronobiol Int 27:1911–29
   PubMed Web of Science ®Google Scholar
• Sage D, Maurel D, Bosler O. (2002). Corticosterone-dependent driving influence of the suprachiasmatic nucleus on adrenal sensitivity to ACTH. Am J Physiol Endocrinol Metab. 282:E458–65
   PubMed Web of Science ®Google Scholar
• Sánchez-Vázquez FJ, Aranda A, Madrid JA. (2001). Differential effects of meal size and food energy density on feeding entrainment in goldfish. J Biol Rhythms. 16:58–65
   PubMed Web of Science ®Google Scholar
• Sánchez-Vázquez FJ, Madrid JA, Zamora S, et al. (1997). Feeding entrainment of locomotor activity rhythms in the goldfish is mediated by feeding-entrainable circadian oscillator. J Comp Physiol A. 181:121–32
   Web of Science ®Google Scholar
• Sangiao-Alvarellos S, Guzmán JM, Laiz-Carrión R, et al. (2005). Interactive effects of high stocking density and food deprivation on carbohydrate metabolism in several tissues of gilthead sea bream Sparus auratus. J Exp Zool. 303A:761–75
   Google Scholar
• Scheer FA, Hilton MF, Mantzoros CS, Shea SA. (2009). Adverse metabolic and cardiovascular consequences of circadian misalignment. PNAS. 106:4453–8
   PubMed Web of Science ®Google Scholar
• Schibler U. (2009). The 2008 Pittendrigh/Aschoff lecture: Peripheral phase coordination in the mammalian circadian timing system. J Biol Rhythm. 24:3–15
   PubMed Web of Science ®Google Scholar
• Schibler U, Asher G, Saini C, et al. (2010). Hepatic clocks. In Dufour JF, Clavien PA, eds. Signaling pathways in liver diseases. Berlin: Springer-Verlag. pp. 501–12
   Google Scholar
• Shimba S, Ogawa T, Hitosugi S, et al. (2011). Deficient of a Clock gene, brain and muscle Arnt-like protein-1 (BMAL1), induces dyslipidemia and ectopic fat formation. PLoS One. 6:e25231
   PubMed Web of Science ®Google Scholar
• Soengas JL, Polakof S, Chen X, et al. (2006). Glucokinase and hexokinase expression and activities in rainbow trout tissues: changes with food deprivation and refeeding. Am J Physiol Regul Integr Comp Physiol. 291:R810–21
   PubMed Web of Science ®Google Scholar
• Stokkan KA, Yamazaki S, Tei H, et al. (2001). Entrainment of the circadian clock in the liver by feeding. Science. 291:490–3
   PubMed Web of Science ®Google Scholar
• Vera LM, Negrini P, Zagatti C, et al. (2013). Light and feeding entrainment of the molecular circadian clock in a marine teleost (Sparus aurata). Chronobiol Int. 30:649–61
   PubMed Web of Science ®Google Scholar
• Volkoff H, Hoskins LJ, Tuziak SM. (2010). Influence of intrinsic and environmental cues on the endocrine control of feeding in fish: Potential application in aquaculture. Gen Comp Endocrinol. 167:352–9
   PubMed Web of Science ®Google Scholar
• Vollmers C, Gill S, DiTacchio L, et al. (2009). Time of feeding and the intrinsic circadian clock drive rhythms in hepatic gene expression. Proc Natl Acad Sci USA. 106:21453–8
   PubMed Web of Science ®Google Scholar
• Yang X, Downes M, Yu RT, et al. (2006). Nuclear receptor expression links the circadian clock to metabolism. Cell. 126:801–10
   PubMed Web of Science ®Google Scholar