Retinoic acid receptors move in time with the clock in the hippocampus. Effect of a vitamin-A-deficient diet

Journal of Nutritional Biochemistry

Volumn 24, Issue 5, 2013, Pages 859-867

  Navigatore Fonzo, Lorena S ^a   Golini, Rebeca L ^a   Ponce, Ivana T ^a   Delgado, Silvia M ^a   Plateo Pignatari, Maria G ^a   Gimenez, María S ^a   Anzulovich, Ana C ^a  

^a UNIVERSIDAD NACIONAL DE SAN LUIS   (Argentina)

Author keywords

BMAL1; Circadian rhythm; Hippocampus; PER; RAR; RXR; Vitamin A

Indexed keywords

RETINOIC ACID RECEPTOR; RETINOID X RECEPTOR; RETINOID X RECEPTOR ALPHA; RETINOID X RECEPTOR BETA;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CIRCADIAN RHYTHM; CONTROLLED STUDY; GENE CONTROL; HIPPOCAMPUS; NONHUMAN; NUTRITIONAL DEFICIENCY; PROTEIN CONTENT; PROTEIN EXPRESSION; RAT; RETINOL DEFICIENCY;

ANIMALS; ARNTL TRANSCRIPTION FACTORS; CIRCADIAN RHYTHM; DIET; GENE EXPRESSION REGULATION; HIPPOCAMPUS; MALE; PERIOD CIRCADIAN PROTEINS; POLYMERASE CHAIN REACTION; RATS; RATS, SPRAGUE-DAWLEY; RECEPTORS, RETINOIC ACID; RETINOID X RECEPTOR BETA; RNA, MESSENGER; VITAMIN A DEFICIENCY;

ANIMALIA; MAMMALIA; RATTUS;

EID: 84876796956     PISSN: 09552863     EISSN: 18734847     Source Type: Journal    
DOI: 10.1016/j.jnutbio.2012.05.006     Document Type: Article

References (65)

1. Cailotto C., van Heijningen C., van der Vliet J., van der Plasse G., Habold C., Kalsbeek A., et al. Daily rhythms in metabolic liver enzymes and plasma glucose require a balance in the autonomic output to the liver. Endocrinology 2007, 149:1914-1925.
2. Lamia K.A., Storch K.F., Weitz C.J. Physiological significance of a peripheral tissue circadian clock. Proc Natl Acad Sci USA 2008, 105:15172-15177.
3. Froy O. The circadian clock and metabolism. Clin Sci (Lond) 2011, 120:65-72.
4. Chaudhury D., Wang L.M., Colwell C.S. Circadian regulation of hippocampal long-term potentiation. J Biol Rhythm 2005, 20:225-236.
5. Golombek D.A., Rosenstein R.E. Physiology of circadian entrainment. Physiol Rev 2010, 90:1063-1102.
6. Aschoff J. Circadian rhythms in man. Science 1965, 148:1427-1432.
7. Aschoff J., Wever R. Human circadian rhythms: a multioscillatory system. Federation Proc 1976, 35:232-236.
8. Sangoram A.M., Saez L., Antoch M.P., Gekakis N., Staknis D., Whiteley A., et al. Mammalian circadian autoregulatory loop: a timeless ortholog and mPer1 interact and negatively regulate CLOCK-BMAL1-induced transcription. Neuron 1998, 21:1101-1113.
9. Reppert S.M., Weaver D.R. Coordination of circadian timing in mammals. Nature 2002, 418:935-941.
10. Panda S., Hogenesch J.B., Kay S.A. Circadian light input in plants, flies and mammals. Novartis Found Symp 2003, 253:73-82.
11. Schibler U., Sassone-Corsi P. A web of circadian pacemakers. Cell 2002, 111:919-922.
12. Hirota T., Fukada Y. Resetting mechanism of central and peripheral circadian clocks in mammals. Zoolog Sci 2004, 21:359-368.
13. Panda S., Hogenesch J.B. It's all in the timing: many clocks, many outputs. J Biol Rhythms 2004, 19:374-387.
14. Gekakis N., Staknis D., Nguyen H.B., Davis F.C., Wilsbacher L.D., King D.P., et al. Role of the CLOCK protein in the mammalian circadian mechanism. Science 1998, 280:1564-1569.
15. Hogenesch J.B., Gu Y.Z., Jain S., Bradfield C.A. The basic-helix-loop-helix-PAS orphan MOP3 forms transcriptionally active complexes with circadian and hypoxia factors. Proc Natl Acad Sci USA 1998, 95:5474-5479.
16. King D.P., Takahashi J.S. Molecular genetics of circadian rhythms in mammals. Annu Rev Neurosci 2000, 23:713-742.
17. Lee C., Weaver D.R., Reppert S.M. Direct association between mouse PERIOD and CKIε is critical for a functioning circadian clock. Mol Cell Biol 2004, 24:584-594.
18. Vanselow K., Kramer A. Role of phosphorylation in the mammalian circadian clock. Cold Spring Harb Symp Quant Biol 2007, 72:167-176.
19. Sato T.K., Yamada R.G., Ukai H., Baggs J.E., Miraglia L.J., Kobayashi T.J., et al. Feedback repression is required for mammalian circadian clock function. Nat Genet 2006, 38:312-319.
20. Preitner N., Damiola F., Lopez-Molina L., Zakany J., Duboule D., Albrecht U., et al. The orphan nuclear receptor REV-ERBa controls circadian transcription within the positive limb of the mammalian circadian oscillator. Cell 2002, 110:251-260.
21. Sato T.K., Panda S., Miraglia L.J., Reyes T.M., Rudic R.D., McNamara P., et al. A functional genomics strategy reveals Rora as a component of the mammalian circadian clock. Neuron 2004, 43:527-537.
22. Akashi M., Takumi T. The orphan nuclear receptor RORa regulates circadian transcription of the mammalian core-clock Bmal1. Nat Struct Mol Biol 2005, 12:441-448.
23. Guillaumond F., Dardente H., Giguere V., Cermakian N. Differential control of Bmal1 circadian transcription by REV-ERB and ROR nuclear receptors. J Biol Rhythms 2005, 20:391-403.
24. Johnson R.F., Moore R.Y., Morin L.P. Loss of entrainment and anatomical plasticity after lesions of the hamster retinohypothalamic tract. Brain Res 1998, 460:297-313.
25. Gooley J.J., Lu J., Chou T.C., Scammell T.E., Saper C.B. Melanopsin in cells of origin of the retinohypothalamic tract. Nat Neurosci 2001, 4:1165.
26. Palmer J.D. The clocks controlling the tide-associated rhythms of intertidal animals. Bioessays 2000, 22:32-37.
27. Feillet C.A., Albrecht U., Challet E. "Feeding time" for the brain: a matter of clocks. J Physiol 2006, 100:252-260.
28. Mendoza J. Circadian clocks: setting time by food. J Neuroendocrinol 2007, 19:127-137.
29. Damiola F., Le Minh N., Preitner N., Kornmann B., Fleury-Olela F., Schibler U. Restricted feeding uncouples circadian oscillators in peripheral tissues from the central pacemaker in the suprachiasmatic nucleus. Genes Dev 2000, 14:2950-2961.
30. Cassone V.M., Stephan F.K. Central and peripheral regulation of feeding and nutrition by the mammalian circadian clock: implications for nutrition during manned space flight. Nutrition 2002, 18:814-819.
31. Heyman R.A., Mangelsdorf D.J., Dyck J.A., Stein R.B., Eichele G., Evans R.M., et al. 9-Cis retinoic acid is a high affinity ligand for the retinoid X receptor. Cell 1992, 68:397-406.
32. Mangelsdorf D.J., Thummel C., Beato M., Herrlich P., Schutz G., Umesono K., et al. The nuclear receptor superfamily: the second decade. Cell 1995, 83:835-839.
33. Soprano D.R., Qin P., Soprano K.J. Retinoic acid receptors and cancers. Annu Rev Nutr 2004, 24:201-221.
34. McNamara P., Seo S.P., Rudic R.D., Sehgal A., Chakravarti D., FitzGerald G.A. Regulation of CLOCK and MOP4 by nuclear hormone receptors in the vasculature: a humoral mechanism to reset a peripheral clock. Cell 2001, 105:877-889.
35. Misner D.L., Jacobs S., Shimizu Y., de Urquiza A.M., Solomin L., Perlmann T., et al. Vitamin A deprivation results in reversible loss of hippocampal long-term synaptic plasticity. Proc Natl Acad Sci USA 2001, 98:11714-11719.
36. Cocco S., Diaz G., Stancampiano R., Diana A., Carta M., Curreli R., et al. Vitamin A deficiency produces spatial learning and memory impairment in rats. Neuroscience 2002, 115:475-482.
37. McCaffery P., Zhang J., Crandall J.E. Retinoic acid signaling and function in the adult hippocampus. J Neurobiol 2006, 66:780-791.
38. Chiang M.-Y., Misner D., Kempermann G., Schikorski T., Giguere V., Sucov H.M., et al. An essential role for retinoid receptors RARb and RXRg in long-term potentiation and depression. Neuron 1998, 21:1353-1361.
39. Etchamendy N., Enderlin V., Marighetto A., Pallet V., Higueret P., Jaffard R. Vitamin A deficiency and relational memory deficit in adult mice: relationships with changes in brain retinoid signalling. Behav Brain Res 2003, 145:37-49.
40. Winocur G., Hasher L. Aging and time-of-day effects on cognition in rats. Behav Neurosci 1999, 113:991-997.
41. Winocur G., Hasher L. Circadian rhythms and memory in aged humans and animals. Neuropsychology of memory 2002, 273-285. Guilford Press, New York. 3rd ed. L.R. Squire, D.L. Schacter (Eds.).
42. Winocur G., Hasher L. Age and time-of-day effects on learning and memory in a non-matching-to-sample test. Neurobiol Aging 2004, 25:1107-1115.
43. Valentinuzzi V.S., Neto S.P., Carneiro B.T., Santana K.S., Araújo J.F., Ralph M.R. Memory for time of training modulates performance on a place conditioning task in marmosets. Neurobiol Learn Mem 2008, 89:604-607.
44. Fonzo L.S., Golini R., Delgado S.M., Bonomi M.R., Rezza I.G., Gimenez M.S., et al. Temporal patterns of lipoperoxidation and antioxidant enzymes are modified in the hippocampus of vitamin A-deficient rats. Hippocampus 2009, 19:869-880.
45. Vega V.A., Anzulovich A.C., Varas S.M., Bonomi M.R., Giménez M.S., Oliveros L.B. Effect of nutritional vitamin A deficiency on lipid metabolism in the rat heart: Its relation to PPAR gene expression. Nutrition 2009, 25:828-838.
46. Ponce I.T., Rezza I.G., Delgado S.M., Navigatore L.S., Bonomi M.R., Golini R., et al. Daily oscillation of glutathione redox cycle is dampened in the nutricional vitamin A deficiency. Biol Rhythm Res. 2011, In Press.
47. Reeves P.G., Nielsen F.H., Fahey G.C. AIN-purified diets for laboratory rodents: final report of the American Institute of Nutrition ad hoc writing committee on the reformulation of the AIN-76A rodent diet. J Nutr 1993, 123:1939-1951.
48. Babu H., Claasen J.H., Kannan S., Rünker A.E., Palmer T., Kempermann G. A protocol for isolation and enriched monolayer cultivation of neural precursor cells from mouse dentate gyrus. Front Neurosci. 2011, 5:89.
49. Quandt K., Frech K.K., Karas H., Wingender E., Werner T. MatInd and MatInspector: new fast and versatile tools for detection of consensus matches in nucleotide sequence data. Nucleic Acids Res 1995, 23:4878-4884.
50. Halberg F. Chronobiology. Ann Rev Physiol 1969, 31:675-725.
51. Bingham C., Arbogast B., Cornelissen-Guillaume G., Lee J.K., Halberg F. Inferential statistical methods for estimating and comparing cosinor parameters. Chronobiologia 1982, 9:397-439.
52. Thaela M.J., Jensen M.S., Cornélissen G., Halberg F., Nöddegaard F., Jakobsen K., et al. Circadian and ultradian variation in pancreatic secretion of meal-fed pigs after weaning. J Anim Sci 1998, 76:1131-1139.
53. Yang X., Downes M., Yu R.T., Bookout A.L., He W., Straume M., et al. Nuclear receptor expression links the circadian clock to metabolism. Cell 2006, 126:801-810.
54. Pando M.P., Sassone-Corsi P. Signaling to the mammalian circadian clocks: in pursuit of the primary mammalian circadian photoreceptor. Science STKE 2001, 6:re16.
55. Reppert S.M., Weaver D.R. Molecular analysis of mammalian circadian rhythms. Annu Rev Physiol 2001, 63:647-676.
56. Nakahata Y., Yoshida M., Takano A., Soma H., Yamamoto T., Yasuda A., et al. A direct repeat of E-box-like elements is required for cell-autonomous circadian rhythm of clock genes. BMC Mol Biol 2008, 4(9):1.
57. Matsui T. Transcriptional regulation of a Purkinje cell-specific gene through a functional interaction between ROR alpha and RAR. Genes Cells 1997, 2:263-272.
58. Ueda H.R., Hayashi S., Chen W.B., Sano M., Machida M., Shigeyoshi Y., et al. System level identification of transcriptional circuits underlying mammalian circadian clocks. Nat Genet 2005, 37:187-192.
59. Crumbley C., Wang Y., Kojetin D.J., Burris T.P. Characterization of the core mammalian clock component, NPAS2, as a REV-ERBalpha/RORalpha target gene. J Biol Chem 2010, 285:35386-35392.
60. Golini R.S., Delgado S.M., Navigatore-Fonzo L.S., Ponce I.T., Lacoste M.G., Anzulovich A.C. Daily patterns of clock and cognition-related factors are modified in the hippocampus of vitamin a-deficient rats. Hippocampus 2011, In Press.
61. Nakahata Y., Akashi M., Trcka D., Yasuda A., Takumi T. The in vitro real-time oscillation monitoring system identifies potential entrainment factors for circadian clocks. BMC Mol Biol 2006, 7:5.
62. Garcia J.A., Zhang D., Estill S.J., Michnoff C., Rutter J., Reick M., et al. Impaired cued and contextual memory in NPAS2-deficient mice. Science 2000, 288:2226-2230.
63. Abarca C., Albrecht U., Spanagel R. Cocaine sensitization and reward are under the influence of circadian genes and rhythm. Proc Natl Acad Sci USA 2002, 99:9026-9030.
64. Hampp G., Albrecht U. The circadian clock and mood-related behavior. Commun Integr Biol. 2008, 1:1-3.
65. Jilg A., Lesny S., Peruzki N., Schwegler H., Selbach O., Dehghani F., et al. Temporal dynamics of mouse hippocampal clock gene expression support memory processing. Hippocampus 2010, 20:377-388.