Food- and light-entrainable oscillators control feeding and locomotor activity rhythms, respectively, in the Japanese catfish, Plotosus japonicus
Tóm tắt
Feeding and locomotor activities of the Japanese catfish Plotosus japonicus under solitary condition were recorded to identify mechanisms controlling these behaviours. In the absence of food, the catfish showed nocturnal locomotor activity, but no feeding activity. Under ad libitum food conditions, both feeding and locomotor activities occurred during the dark period and were synchronized with light/dark (LD) cycles. Feeding activity lasted for 11–24 days when food was stopped after ad libitum food availability. Restricted food during the light phase produced both food-anticipatory and light-entrainable feeding activity. Furthermore, this condition produced weak food-anticipatory and light-entrainable locomotor activity. Under the light/light (LL) condition, restricted food produced food-anticipatory feeding and locomotor activities, suggesting that a food-entrainable oscillator controls both feeding and locomotor activities. However, under the LL condition, light-entrainable feeding and locomotor activities were not observed, suggesting that a light-entrainable oscillator controls both feeding and locomotor activities. During a restricted food schedule, LD cycle shifts resulted in disrupted synchronization of feeding activity onset in three of the four fish, but one fish showed synchronized feeding activity. These results suggest that the food- and the light-entrainable oscillator may control feeding and locomotor activities, respectively.
Tài liệu tham khảo
Akashi M, Nishida E (2000) Involvement of the MAP kinase cascade in resetting of the mammalian circadian clock. Genes Dev 14:645–649
Balsalobre A, Damiola F, Schibler U (1998) A serum shock induces circadian gene expression in mammalian tissue culture cells. Cell 93:929–937
Balsalobre A, Brown SA, Marcacci L, Tronche F, Kellendonk C, Reichardt HM, Schütz G, Schibler U (2000) Resetting of circadian time in peripheral tissues by glucocorticoid signaling. Science 289:2344–2347
Bolliet V, Aranda A, Boujard T (2001) Demand-feeding rhythm in rainbow trout and European catfish: synchronisation by photoperiod and food availability. Physiol Behav 73:625–633
Boulos Z, Terman M (1980) Food availability and daily biological rhythms. Neurosci Biobehav Rev 4:119–131
Cahill GM (1996) Circadian regulation of melatonin production in cultured zebrafish pineal and retina. Brain Res 708:177–181
Chou TC, Scammel TE, Gooley JJ, Gaus SE, Saper CB, Lu J (2003) Critical role of dorsomedial hypothalamic nucleus in a wide range of behavioral circadian rhythms. J Neurosci 23:10691–10702
Comperatore CA, Stephan FK (1987) Entrainment of duodenal activity to periodic feeding. J Biol Rhythms 2:227–242
Damiola F, Minh NL, Preitner N, Kornmann B, Fleury-Olela F, Schibler U (2000) Restricted feeding uncouples circadian oscillators in peripheral tissues from the central pacemaker in the suprachiasmatic nucleus. Genes Dev 14:2950–2961
Davis RE, Bardach JE (1965) Time-co-ordinated prefeeding activity in fish. Anim Behav 13:154–162
Ekström P, Meissl H (1988) Intracellular staining of physiologically identified photoreceptor cells and hyperpolarizing interneurons in the teleost pineal organ. Neurosci 25:1061–1070
Emery IF, Noveral JM, Jamison CF, Siwicki KK (1997) Rhythms of Drosophila period gene expression in culture. Proc Natl Acad Sci USA 94:4092–4096
Eriksson LO (1978) Nocturnalism versus diurnalism: dualism within fish individuals. In: Thorpe JE (ed) Rhythmic activity of fishes. Academic Press, London, pp 69–90
Eriksson LO, van Veen T (1980) Circadian rhythms in the brown bullhead, Ictalurus nebulosus (Teleostei). Evidence for an endogenous rhythm in feeding, locomotor and reaction time behavior. Can J Zool 58:1899–1907
Fraser NHC, Heggenes J, Metcalfe NB, Thorpe JE (1995) Low summer temperatures cause juvenile Atlantic salmon to become nocturnal. Can J Zool 73:446–451
Fuller PM, Lu J, Saper CB (2008) Differential rescue of light- and food-entrainable circadian rhythms. Science 320:1074–1077
Garg SK, Sundararaj BI (1986) Role of pineal in the regulation of some aspects of circadian rhythmicity in the catfish. Heteropneustes fossilis (bloch). Chronobiol 13:1–11
Giebultowicz JM, Stanewsky R, Hall JC, Hege DM (2000) Transplanted Drosophila excretory tubules maintain circadian clock cycling out of phase with the host. Curr Biol 10:107–110
Gooley JJ, Schomer A, Saper CB (2006) The dorsomedial hypothalamic nucleus is critical for the expression of food-entrainable circadian rhythms. Nature Neurosci 9:398–407
Goudie CA, Davis KB, Simco BA (1983) Influence of the eyes and pineal gland on locomotor activity patterns of channel catfish Ictalurus punctatus. Physiol Zool 56:10–17
Heggenes J, Krog OMW, Lindås OR, Dokk JG, Bremnes T (1993) Homeostatic behavioural responses in a changing environment: brown trout (Salmo trutta) become nocturnal during winter. J Anim Ecol 62:295–308
Herrero MJ, Pascual M, Madrid JA, Sánchez-Vázqueza FJ (2005) Demand-feeding rhythms and feeding-entrainment of locomotor activity rhythms in tench (Tinca tinca). Physiol Behav 84:595–605
Honma KI, Honma S, Hiroshige T (1983) Critical role of food amount for prefeeding corticosterone peak in rats. Am J Physiol 245:R339–R344
Iigo M, Tabata M (1996) Circadian rhythms of locomotor activity in the goldfish Carassius auratus. Physiol Behav 60:775–781
Iigo M, Tabata M (1997) Circadian rhythms of locomotor activity in the rainbow trout Oncorhynchus mykiss. Fish Sci 63:77–80
Iigo M, Kezuka H, Aida K, Hanyu I (1991) Circadian rhythms of melatonin secretion from superfused goldfish (Carassius auratus) pineal glands in vitro. Gen Comp Endocrinol 83:152–158
Iigo M, Kezuka H, Suzuki T, Tabata M, Aida K (1994) Melatonin signal transduction in the goldfish, Carassius auratus. Neurosci Biobehav Rev 18:563–569
Iigo M, Mizusawa K, Yokosuka M, Hara M, Ohtani-Kaneko R, Tabata M, Aida K, Hirata K (2003) In vitro photic entrainment of the circadian rhythm in melatonin release from the pineal organ of a teleost, ayu (Plecoglossus altivelis) in flow-through culture. Brain Res 982:131–135
Iigo M, Furukawa K, Nishi G, Tabata M, Aida K (2007) Ocular melatonin rhythms in teleost fish. Brain Behav Evol 69:114–121
Kasai M, Yamamoto T, Kiyohara S (2009a) Circadian locomotor activity in Japanese sea catfish, Plotosus lineatus. Fish Sci 75:81–89
Kasai M, Yamamoto T, Kitasako K, Kiyohara S (2009b) Feeding activity rhythm in Japanese sea catfish, Plotosus japonicus. Fish Sci 75:1125–1132
Kavaliers M (1978) Seasonal changes in the circadian period of the lake chub, Couesius plumbeus. Can J Zool 56:2591–2596
Kavaliers M (1979) The pineal gland and circadian organization of teleosts fish. Rev Can Biol 38:281–292
Kavaliers M (1980) Circadian locomotor activity rhythms of the burbot, Lata lata: seasonal differences in period length and the effect of pinealectomy. J Comp Physiol 136:215–218
Klein DC, Moore RY (1979) Pineal N-acetyltransferase and hydroxyindole-o-methyltransferase: control by the retinohypothalamic tract and suprachiasmatic nucleus. Brain Res 174:245–262
Krieger DT (1974) Food and water restriction shifts corticosterone, temperature, activity and brain amine periodicity. Endocrinol 95:1195–1197
Krieger DT, Hauser H, Krey LC (1977) Suprachiasmatic nuclear lesions do not abolish food-shifted circadian adrenal and temperature rhythmicity. Science 197:398–399
Krishnan B, Dryer SE, Hardin PE (1999) Circadian rhythms in olfactory responses of Drosophila melanogaster. Nature 400:375–378
Lague M, Reebs SG (2000) Phase-shifting the light–dark cycle influences food-anticipatory activity in golden shiners. Physiol Behav 70:55–59
Landless PJ (1976) Demand-feeding behavior of rainbow trout. Aquaculture 7:11–25
López-Olmeda JF, Montoya A, Oliveira C, Sánchez-Vázquez FJ (2009) Synchronization to light and restricted-feeding schedules of behavioral and humoral daily rhythms in gilthead sea bream (Sparus aurata). Chronobiol Int 26:1389–1408
Mistlberger RE (1994) Circadian food-anticipatory activity: formal models and physiological mechanisms. Neurosci Biobehav Rev 18:171–195
Moore RY (1996) Neural control of the pineal gland. Behav Brain Res 73:125–130
Müller K (1978) The flexibility of the circadian system of fish at different latitudes. In: Thorpe JE (ed) Rhythmic activity of fishes. Academic Press, London, pp 91–104
Plautz JD, Kaneko M, Hall JC, Kay SA (1997) Independent photoreceptive circadian clocks throughout Drosophila. Science 278:1632–1635
Randolph KN, Clemens HP (1976) Some factors influencing the feeding behavior of channel catfish in culture ponds. Trans Am Fish Soc 6:718–724
Reebs SG, Lague M (2000) Daily food-anticipatory activity in golden shiners: a test of endogenous timing mechanisms. Physiol Behav 70:35–43
Saito M, Murakami E, Suda M (1976) Circadian rhythms in disaccharidases of rat small intestine and its relation to food intake. Biochim Biophys Acta 421:177–179
Sánchez JA, Sánchez-Vázquez FJ (2009) Feeding entrainment of daily rhythms of locomotor activity and clock gene expression in zebrafish brain. Chronobiol Int 26:1120–1135
Sánchez JA, López-Olmeda JF, Blanco-Vives B, Sánchez-Vázquez FJ (2009) Effects of feeding schedule on locomotor activity rhythms and stress response in sea bream. Physiol Behav 98:125–129
Sánchez-Vázquez FJ, Madrid JA, Zamora S, Madrid JA (1995) Light–dark and food restriction cycles in sea bass: effect of conflicting zeitgebers on demand-feeding rhythms. Physiol Behav 58:705–714
Sánchez-Vázquez FJ, Madrid JA, Zamora S, Iigo M, Tabata M (1996) Demand feeding and locomotor circadian rhythms in the goldfish, Carassius auratus: dual and independent phasing. Physiol Behav 60:665–674
Sánchez-Vázquez FJ, Madrid JA, Zamora S, Tabata M (1997) Feeding entrainment of locomotor activity rhythms in the goldfish is mediated by a feeding-entrainable circadian oscillator. J Comp Physiol A 181:121–132
Sánchez-Vázquez FJ, Azzaydi M, Martinez FJ, Zamora S, Madrid JA (1998) Annual rhythms of demand-feeding activity in sea bass: evidence of a seasonal phase inversion of the diel feeding pattern. Chronobiol Int 15:607–622
Savage GE, Roberts MG (1975) Behavioral effects of electrical stimulation of the hypothalamus of the goldfish (Carassius auratus). Brain Behav Evol 12:42–56
Stephan FK (1989) Entrainment of activity to multiple feeding times in rats. Physiol Behav 46:489–497
Stephan FK, Zucker I (1972) Circadian rhythms in drinking behavior and locomotor activity of rats are eliminated by hypothalamic lesions. Proc Natl Acad Sci USA 69:1583–1586
Stephan FK, Swann JM, Sisk CL (1979) Anticipation of 24-hr feeding schedules in rats with lesions of the suprachiasmatic nucleus. Behav Neural Biol 25:346–363
Sunuma T, Amano M, Iigo M, Yamamori K (2009) Food-entrainable circadian oscillator in goldfish: multiple daily feeding times and food-anticipatory activity. Fish Sci 75:207–214
Tabata M, Suzuki T, Niwa H (1985) Chromophores in the extraretinal photoreceptor (pineal organ) of teleosts. Brain Res 338:173–176
Tabata M, Minh-Nyo M, Niwa H, Oguri M (1989) Circadian rhythm of locomotor activity in a teleost, Silurus asotus. Zool Sci 6:367–375
Thorpe JE (1978) Rhythmic activity of fishes. Academic Press, New York
Vera LM, López-Olmeda JF, Bayarri MJ, Madrid JA, Sánchez-Vázquez FJ (2005) Influence of light intensity on plasma melatonin and locomotor activity rhythms in tench. Chronobiol Int 22:67–78
Vera LM, Madrid JA, Sánchez-Vázquez FJ (2006) Locomotor, feeding and melatonin daily rhythms in sharpsnout seabream (Diplodus puntazzo). Physiol Behav 88:167–172
Vera LM, De Pedro N, Gómez-Milán E, Delgado MJ, Sánchez-Muros MJ, Madrid JA, Sánchez-Vázquez FJ (2007) Feeding entrainment of locomotor activity rhythms, digestive enzymes and neuroendocrine factors in goldfish. Physiol Behav 90:518–524
Vigh-Teichmann I, Korf H-W, Nürnberger F, Okche A, Vigh B, Olsson R (1983) Opsin-immunoreactive outer segments in the pineal and parapineal organs of the lamprey (Lampetra fluviatilis), the eel (Anguilla anguilla), and the rainbow trout (Salmo gairdneri). Cell Tissue Res 230:289–307
Whitmore D, Foulkes NS, Sassone-Corsi P (2000) Light acts directly on organs and cells in culture to set the vertebrate circadian clock. Nature 404:87–91
Yamazaki S, Numano R, Abe M, Hida A, Takahashi R, Ueda M, Block GD, Sakaki Y, Menaker M, Tei H (2000) Resetting central and peripheral circadian oscillators in transgenic rats. Science 288:682–685
Zylka MJ, Shearman LP, Weaver DR, Reppert SM (1998) Three period homologs in mammals: differential light responses in the suprachiasmatic circadian clock and oscillating transcripts outside of brain. Neuron 20:1103–1110