Characterization and variations of organic parameters in teleost fish endolymph during day-night cycle, starvation and stress conditions

Comparative Biochemistry and Physiology - A Molecular and Integrative Physiology

Volumn 145, Issue 1, 2006, Pages 99-107

  Guibbolini, Marielle ^a   Borelli, Gil ^a   Mayer Gostan, Nicole ^a   Priouzeau, Fabrice ^a   De Pontual, Hélène ^b   Allemand, Denis ^a,c   Payan, Patrick ^a  

^a UNIVERSITÉ CÔTE D'AZUR   (France)

^b IFREMER   (France)

^c CENTRE SCIENTIFIQUE DE MONACO   (Monaco)

Author keywords

Day night cycle; Endolymph; In vitro crystallization; Organic matrix; Otolith calcification; Starvation; Stress; Trout; Turbot

Indexed keywords

CALCIUM CARBONATE;

ANIMAL EXPERIMENT; ANTIBODY LABELING; ARTICLE; CALCIFICATION; CONTROLLED STUDY; CRYSTALLIZATION; ELECTROPHORESIS; ENDOLYMPH; ENVIRONMENTAL FACTOR; GEL ELECTROPHORESIS; MOLECULAR WEIGHT; NONHUMAN; OTOLITH; STARVATION; STRESS; TELEOST; TROUT; WESTERN BLOTTING;

SALMONIDAE; TELEOSTEI;

EID: 33747177902     PISSN: 10956433     EISSN: 15314332     Source Type: Journal    
DOI: 10.1016/j.cbpa.2006.05.003     Document Type: Article

References (53)

1. Addadi I., and Weiner S. Interactions between acidic proteins and crystals: stereochemical requirements in biomineralization. Proc. Natl. Acad. Sci. 82 (1985) 4110-4114
2. Asano M., and Mugiya Y. Biochemical and calcium-binding properties of water-soluble proteins isolated from otolith of the Tilapia, Oreochromis niloticus. Comp. Biochem. Physiol. 104B (1993) 201-205
3. Bass M.L., and Heath A.G. Cardiovascular and respiratory changes in rainbow trout (Salmo gairdneri) exposed intermittently to chlorine. Water Res. 11 (1977) 497-502
4. Belcher A.M., Wu X.H., Christensen R.J., Hansma P.K., Stuky G.D., and Morse D.E. Control of crystal switching and orientation by soluble mollusc-shell proteins. Nature 381 (1996) 56-58
5. Berghahm R., and Karakiri M. Experimental induction of biological tags in otoliths of 0-group plaice Pleuronectes platessa by starvation, temperature, and UV-B radiation. Mar. Ecol., Prog. Ser. 67 (1990) 227-233
6. Booth N.H., and Mc Donald L.E. Veterinary Pharmacology and Therapeutics. 6th ed. (1988), Iowa State University Press, Ames, Iowa 774-777
7. Borelli G., Mayer-Gostan N., De Pontual H., Bœuf G., and Payan P. Biochemical relationships between endolymph and otolith matrix in the trout (Oncorhynchus mykiss) and the turbot (Psetta maxima). Calcif. Tissue Int. 69 (2001) 356-364
8. Borelli G., Mayer-Gostan N., Merle P.L., De Pontual H., Bœuf G., Allemand D., and Payan P. Composition of biomineral organic matrices with special emphasis on turbot (Psetta maxima) otolith and endolymph. Calcif. Tissue Int. 72 (2003) 717-725
9. Borelli G., Guibbolini M.E., Mayer-Gostan N., Priouzeau F., De Pontual H., Allemand D., Puverel S., Tambutté E., and Payan P. Daily variations of endolymph composition: relationship with otolith calcification process in trout. J. Exp. Biol. 206 (2003) 2685-2892
10. Campana S.E. Calcium deposition and otolith check formation during periods of stress in Coho salmon Oncorhynchus kisutch. Comp. Biochem. Physiol. 75A (1983) 215-220
11. Carlstom D. A crystallographic study of vertebrate otoliths. Biol. Bull. 125 (1963) 441-463
12. Degens E.T., Deuser W.G., and Haedrich R.L. Molecular structure and composition of fish otoliths. Int. J. Life Oceans Coast. Waters 2 (1969) 105-113
13. Edeyer A., de Pontual H., Payan P., Troadec H., Severe A., and Mayer-Gostan N. Daily variations of the saccular endolymph and plasma compositions in the turbot Psetta maxima: relationship with the diurnal rhythm in otolith formation. Mar. Ecol., Prog. Ser. 192 (2000) 287-294
14. Elsdon T.S., and Gillanders B.M. Interactive effects of temperature and salinity on otolith chemistry: challenges for determining environmental histories of fish. Can. J. Fish. Aquat. Sci. 59 (2002) 1796-1808
15. Enger P.R. Ionic composition of the cranial and labyrinth fluids and saccular D.C. potentials in fish. Comp. Biochem. Physiol. 11 (1964) 131-137
16. Falini G., Albeck S., Weiner S., and Addadi L. Control of aragonite or calcite polymorphism by mollusk shell macromolecules. Science 271 (1996) 67-69
17. Fay R.R. The Goldfish Ear codes the axis of acoustic particle motion in three dimensions. Science 225 (1984) 951-953
18. Gauldie R.W., and Nelson D.G.A. Aragonite twinning and neuroprotein secretion are the cause of daily growth rings in fish otoliths. Comp. Biochem. Physiol. 90A (1988) 501-509
19. Gautron J., Bain M., Solomon S., and Nys Y. Soluble matrix of hen's eggshell extracts changes in vitro the rate of calcium carbonate precipitation and crystal morphology. Br. Poult. Sci. 37 (1996) 853-866
20. Gautron J., Hincke M.T., and Nys Y. Precursor matrix proteins in the uterine fluid change with stages of eggshell formation in hens. Connect. Tissue Res. 36 (1997) 195-210
21. Kalish J.M. Determinants of otolith chemistry: seasonal variation in the composition of blood plasma, endolymph and otoliths of bearded rock cod, Pseudophycis barbatus. Mar. Ecol., Prog. Ser. 74 (1991) 137-159
22. Laemmli U.K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227 (1970) 680-685
23. Marin F., Corstjens P., de Gaulejac B., de Vrind-De-Jong E., and Westbrœk P. Mucins and molluscan calcification. J. Biol. Chem. 275 (2000) 20667-20675
24. Mayer-Gostan N., Kossmann H., Watrin A., Payan P., and Bœuf G. Distribution of ionocytes in the saccular epithelium of the inner ear of two teleosts (Oncorhynchus mykiss and Scophthalmus maximus). Cell Tissue Res. 289 (1997) 53-61
25. Molony B.W. Episodes of starvation are recorded in the otoliths of juvenile (Ambassis vachelli Chandidae), a tropical estuarine fish. Mar. Biol. 125 (1996) 439-446
26. Molony B.W., and Choat J.H. Otolith increment widths and somatic growth rate: the presence of a time lag. J. Fish Biol. 37 (1990) 541-551
27. Morales-Nin B. Ultrastructure of the organic and inorganic constituents of the otoliths of the sea bass. In: Summerfelt R.C., and Hall G.E. (Eds). The Age and Growth of Fish (1987), Iowa State University Press, Ames, Iowa 331-344
28. Morris C.C. Statocyst fluid composition and its effects on calcium carbonate precipitation in the squid Alloteuthis subulata; towards a model for biomineralization. Bull. Mar. Sci. 49 (1991) 379-388
29. Mugiya Y., and Takahashi T. Chemical properties of the saccular endolymph in the rainbow trout, Salmo gairdneri. Bull. Faculty Fish. Hokkaido Univ. 36 (1985) 57-63
30. Mugiya Y., and Oka H. Chemical relationship between otolith and somatic growth in the Rainbow trout Onchorhynchus mykiss: consequence of starvation, resumed feeding, and diel variations. Fish Bull. 89 (1991) 239-245
31. Murayama E., Okuno A., Ohira T., Takagi Y., and Nagasawa H. Molecular cloning and expression of an otolith matrix protein cDNA from the rainbow trout, Oncorhynchus mykiss. Comp. Biochem. Physiol. 126B (2000) 511-520
32. Murayama E., Takagi Y., Ohira T., Davis J.G., Greene M.I., and Nagasawa H. Fish otolith contains a unique structural protein, otolin-1. Eur. J. Biochem. 269 (2002) 688-696
33. Murayama E., Takagi Y., and Nagasawa H. Immunohistochemical localization of two otolith matrix proteins in the otolith and inner ear of the rainbow trout, Oncorhynchus mykiss: comparative aspects between the adult inner ear and embryonic otocysts. Histochem. Cell Biol. 121 (2004) 155-166
34. Okazaki M., Sato T., Mutho N., Wada N., and Umegaki T. Calcified scales (coccoliths) of pleurochrysis carterae (Haptophyta): structure, crystallography, and acid polysaccharides. J. Mar. Biotechnol. 6 (1998) 16-21
35. Pannella G. Growth pattern in fish sagittae. In: Rhoads D.C., and Lutz R.A. (Eds). Skeletal growth of aquatic organisms: biological records of environmental change (1980), Plenum Press, New York and London 519-560
36. Payan P., Kossman H., Watrin A., Mayer-Gostan N., and Boeuf G. Ionic composition of endolymph in teleosts: origin and importance of endolymph alkalinity. J. Exp. Biol. 200 (1997) 1905-1912
37. Payan P., Borelli G., Boeuf G., and Mayer-Gostan N. Relationship between otolith and somatic growth: consequence of starvation on acid-base balance in plasma and endolymph in the rainbow trout Oncorhynchus mykiss. Fish Physiol. Biochem. 19 (1998) 35-41
38. Payan P., Edeyer A., De Pontual H., Borelli G., Boeuf G., and Mayer-Gostan N. Heterogeneity of endolymph and otolith chemistry of inner ear in teleost fish. Am. J. Physiol. 46 (1999) R123-R131
39. Payan P., De Pontual H., Edeyer A., Borelli G., Bœuf G., and Mayer-Gostan N. Effects of stress on plasma homeostasis, endolymph chemistry and check formation during otolith growth in trout (Oncorhynchus mykiss). Can. J. Fish. Aquat. Sci. 61 (2004) 1247-1255
40. Pisam M., Payan P., Le Moal C., Edeyer A., Boeuf G., and Mayer-Gostan N. Ultrastructural study of the saccular epithelium of the inner ear of two teleosts (Oncorhynchus mykiss and Psetta maxima). Cell Tissue Res. 294 (1998) 261-270
41. Popper A.N., and Fay R.R. Sound detection and processing by fish: critical review and major research questions. Brain Behav. Evol. 41 (1993) 14-38
42. Romanek C.S., and Gauldie R.W. A predictive model of otolith growth in fish based on the chemistry of the endolymph. Comp. Biochem. Physiol. 114A (1996) 71-79
43. Sasagawa T., and Mugiya Y. Biochemical properties of water-soluble otolith proteins and the immunobiochemical detection of the proteins in serum and various tissues in the tilapia, Oreochromis niloticus. Fish. Sci. 62 (1996) 970-976
44. Söllner C., Burghammer M., Busch-Nentwich E., Berger J., Schwarz H., Riekel C., and Nicolson E. Control of crystal size and lattice formation by Starmaker in otolith biomineralization. Science 302 (2003) 282-286
45. +-ATPase-rich cell in the saccular epithelium of rainbow trout (Oncorhynchus mykiss) inner ear. Anat. Rec. 248 (1997) 483-489
46. Takagi Y., and Takahashi A. Characterization of otolith soluble-matrix producing cells in the saccular epithelium of rainbow trout (Oncorhynchus mykiss) inner ear. Anat. Rec. 254 (1999) 322-329
47. Takagi Y., Toshe H., Murayama E., Ohira T., and Nagasawa H. Diel changes in endolymph aragonite saturation rate and mRNA expression of otolith matrix proteins in the trout otolith organ. Mar. Ecol., Prog. Ser. 294 (2005) 249-256
48. Towbin H., Staehelin T., and Gordon J. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. Proc. Natl. Acad. Sci. U. S. A. 76 (1979) 4350-4354
49. Wheeler A.P., and Sikes C.S. Regulation of carbonate calcification by organic matrix. Am. Zool. 24 (1984) 933-944
50. Wheeler A.P., George J.W., and Evans C.A. Control of carbonate nucleation and crystal growth by soluble matrix of oyster shell. Science 212 (1981) 1392-1398
51. 3 crystallization by fractions of oyster shell organic matrix. Mar. Biol. 98 (1988) 71-80
52. Wright P.J. Calcium binding by soluble matrix of the otoliths of atlantic salmon, Salmo salar L. J. Fish Biol. 38 (1991) 625-627
53. Wright P.J., Talbot C., and Thorpe J.E. Otolith calcification in Atlantic salmon parr (Salmo salar L.) and its relation to photoperiod and calcium metabolism. J. Fish Biol. 40 (1992) 779-790