Evidence for the presence of novel β-melatonin receptors along with classical α-melatonin receptors in the fish Rasbora daniconius (Ham.)

References

• Bartness TJ, Goldman BD. Mammalian pineal melatonin: a clock for all seasons. Experientia 1989;45:939–45
   PubMedGoogle Scholar
• P’evet P. Melatonin and biological rhythms. Biol Signals Recept 2000;9:203–12
   PubMedGoogle Scholar
• Lerner AB, Case JD, Takahashi Y. Isolation of melatonin and 5-methoxyindole-3-acetic acid from bovine pineal glands. J Cell Biol 1960;235:1992–7
   Google Scholar
• Fujii R. Demonstration of the adrenergic nature of transmission at the junction between melanophores concentrating nerve and melanophores in bony fishes. J Fac Sci Univ Tokyo Sect 1961;4:171–96
   Google Scholar
• Fujii R. The regulation of motile activity in fish chromatophores. Pigment Cell Res 2000;13:300–19
   PubMedGoogle Scholar
• Aspengren S, Hedberg D, Skold HN, Wallin M. New insights into melanosome transport in vertebrate pigment cell. Int Rev Cell Mol Biol 2009;272:245–302
   PubMed Web of Science ®Google Scholar
• Fujii R, Miyashita Y. Receptor mechanism in fish chromatophores – IV. Effects of melatonin and related substances on dermal and epidermal melanophores of the siluroid, Parasilurus asotus. Comp Biochem Physiol 1978;59C:59–63
   Google Scholar
• Reppert SM, Weaver DR, Cassone VM, et al. Melatonin receptors are for the birds: molecular analysis of two receptor subtypes differentially expressed in chick brain. Neuron 1995;15:1003–15
   PubMed Web of Science ®Google Scholar
• Vanecek J. Cellular mechanisms of melatonin action. Physiol Rev 1998;78:687–721
   PubMed Web of Science ®Google Scholar
• Dubocovich ML, Cardinali DP, Delagrange PRM, et al. Melatonin receptors. In: Girdlestone D, ed. The IUPHAR compendium of receptor characterization and classification. 2nd ed. London: IUPHAR Media; 2000:270–7
   Google Scholar
• Masana MI, Dubocovich ML. Melatonin receptor signaling: finding the path through the dark. Sci STKE 2001;2001:39
   Google Scholar
• Aspengren S, Skold HN, Martennsson LGE, et al. Nor-adrenaline and melatonin- mediated regulation of pigment aggregation in fish melanophores. Pigment Cell Res 2003;16:59–64
   PubMedGoogle Scholar
• Karlsson AM, Bjuhr K, Testorf MF, et al. Biosensing of opioids using frog melanophores. Biosens Bioelectron 2002;17:331–5
   PubMed Web of Science ®Google Scholar
• Fujii R, Oshima N. Control of chromatophore movements in teleost fishes. Zool Sci 1986;3:13–47
   Web of Science ®Google Scholar
• Leander NJ, Shen K-N, Chen R-T, Tzeng W-N. Species composition and seasonal occurrence of recruiting glass eels (Anguilla spp.) in the Hsiukuluan River, eastern Taiwan. Zool Stud 2012;51:59–71
   Web of Science ®Google Scholar
• Sköld HN, Aspengren S, Wallin M. Rapid color change in fish and amphibians – function, regulation, and emerging applications. Pigment Cell Melanoma Res 2013;26:29–38
   PubMed Web of Science ®Google Scholar
• Spaeth RA. The physiology of the chromatophores of fishes. J Exp Zool 1913;15:527–85
   Google Scholar
• Bhattacharya SK, Parikh AK, Das PK. Effects of catecholamines on the melanophores of Rana tigrina. Indian J Expt Biol 1976;14:486–8
   PubMed Web of Science ®Google Scholar
• Ovais M, Gaur A, Praveen S. Effect of Lithium ions on the innervated and denervated melanophores of a carps, Cirrhinus mrigala (Ham.). Zool J Physiol 1993;97:284–92
   Google Scholar
• Mubashshir M, Ahmed F, Sumoona S, Ovais M. Analyzing the responses of saccharin in context with melatonin receptors on the melanophores of the fish Labeo rohita (Ham.). J Recept Signal Transduct 2012;32:114–19
   PubMed Web of Science ®Google Scholar
• Lewis AE. Biostatistics. New Delhi: Affiliated East-West Press Pvt. Ltd; 1971
   Google Scholar
• Katayama H, Morishita F, Matushima O, Yamada K. Co-existence of beta1 and beta2 adrenoceptor in the melanophore of the Goby Tridentiger obscurus. Pigment Cell Res 1990;3:192–9
   PubMedGoogle Scholar
• Takabatake I, Matsuura M, Iga T. Seasonal variation in sensitivity of fish melanophores to melatonin. Zool Sci 1986;3:379–81
   Web of Science ®Google Scholar
• Bagnara JT, Hadley ME, eds. Chromatophores and color change. In: The comparative physiology of animal pigmentation. Englewood Cliffs: Prentice-Hall; 1973:202
   Google Scholar
• Fujii R. Chromatophore and pigments. In: Hoar WH, Randall DJ, eds. Fish physiology, Vol. 3. New York: Academic Press;1969:307–53
   Google Scholar
• Nicholus J, Schncebeck C, Hadley ME. Comparative in vivo response of embryonic larval and adult melanophores of Fundulus hetroclitus to melatonin. Am Zool 1966;6:576
   Google Scholar
• Fain WB, Hadley ME. In vitro response of melanophores of Fundulus hetroclitus to melatonin, adrenaline and nor-adrenaline. Am Zool 1966;6:596
   Google Scholar
• Reed BL. The control of circadian pigment changes in the pencil fish: a proposed role for melatonin. Life Sci 1968;7:961–73
   PubMed Web of Science ®Google Scholar
• Masagaki A, Fujii R. Differential actions of melatonin on melanophores of three line pencil fish, Nannostomus trifasciatus. Zool Sci 1999;16:35–42
   Web of Science ®Google Scholar
• Hajare S. Studies on the responses of Rasbora daniconius (Ham.) Melanophores in vitro to adrenergic, cholinergic and histaminergic drugs. Ph.D. Thesis, Biosciences, Barkatullah University, Bhopal, India; 2009
   Google Scholar
• Sumoona S. Studies on the effects of MSH and MCH on the isolated scale melanophores of a tropical fish Rasbora daniconius (Ham.). Ph.D. Thesis, Biosciences, Barkatullah University, Bhopal, India; 2008
   Google Scholar
• Martensson LGE, Andersson RGG. Denervation of pigment cells lead to a receptor that is ultrasensitive to melatonin and noradrenaline. Life Sci 1997;60:1575–82
   PubMed Web of Science ®Google Scholar
• Iga T, Takabatake I. Action of melanophores stimulating hormone on melanophores of the cyprinid fish Zacco temmincki. Comp Biochem Physiol 1982;73C:51–5
   Google Scholar
• Abbot FS. The effects of certain drugs and biogenic substances on the melanophores of Fundulus heteroclitus. Can J Zool 1968;46:1149–61
   PubMed Web of Science ®Google Scholar
• Nishi H, Fujii R. Novel receptors for melatonin that mediate pigment dispersion are present in some melanophores of the pencil fish (Nannostomus). Comp Biochem Physiol 1992;103C:263–8
   Google Scholar
• Boehm S, Kubista H. Fine tuning of sympathetic transmitter release via ionotropic and metabotropic presynaptic receptors. Pharmacol Rev 2002;54:43–99
   PubMed Web of Science ®Google Scholar
• Fujii R. Mechanism of ionic action in the melanophore system I. Melanophores concentrating action of potassium and some other ions. Annot Zool Jpn 1959;32:47–58
   Google Scholar
• Messenger EA, Warner AE. Action of melatonin on single amphibian cells in tissue culture. British J Pharmacol 1977;61:607–14
   PubMed Web of Science ®Google Scholar
• Singh R. Studies on the effect of melatonin on the melanophores of O. mossambica in vitro. M. Phil. Dissertation, Biosciences, Barkatullah University, Bhopal, India; 2001
   Google Scholar
• Sheikh IA, Ovais M. Melatonin mediated regulation of pigment aggregation in lizard melanophores. J Exp Zool India 2010;13:247–55
   Google Scholar
• Teh M-T, Sugden D. An endogenous 5-HT7 receptor mediates pigment granule dispersion in Xenopus laevis melanophores. Br J Pharmacol 2001;132:1799–808
   PubMed Web of Science ®Google Scholar
• Mubashshir M, Ahmed F, Acharya LSK, et al. Effects of melatonin on the isolated scale melanophores of an Indian major carp Labeo rohita (Ham.). Global J Pharmacol 2011;5:122–9
   Google Scholar