DOI QR코드

DOI QR Code

급격한 염분변화에 따른 담수어 3종의 프로락틴 및 성장호르몬 유전자 발현변화

Changes in Prolactin and Growth Hormone Gene Expression in Three Freshwater Teleosts with Rapid Changes in Salinity

  • 박우동 (강릉대학교 해양생명공학부) ;
  • 이철호 (국립수산과학원 영동내수면연구소) ;
  • 김대중 (국립수산과학원 양식연구본부 양식관리팀) ;
  • 손영창 (강릉대학교 해양생명공학부)
  • Park, Woo-Dong (Division of Marine Molecular Biotechnology, Faculty of Marine Bioscience and Technolohy, Kangnung National University) ;
  • Lee, Cheul-Ho (Yeongdong Inland Fisheries Research Institute, National Fisheries Research and Development Institute) ;
  • Kim, Dae-Jung (Aquaculture Research Team, Headquarters for Aquaculture, National Fisheries Research and Development Institute) ;
  • Sohn, Young-Chang (Division of Marine Molecular Biotechnology, Faculty of Marine Bioscience and Technolohy, Kangnung National University)
  • 발행 : 2008.02.29

초록

The changes in osmolality and the gene expression profiles of prolactin (PRL) and growth hormone (GH) with rapid changes in salinity were compared in the eel (Anguilla japonica), crucian carp (Carassius carassius), and masu salmon (Oncorhynchus masou). Fish stocked in freshwater (FW) were abruptly transferred to experimental tanks containing FW, 50% seawater (50% SW), or 100% SW (SW). Blood samples and pituitary glands were collected 2 and 24 hrs after the exposure. No mortality was observed in SW eel (n=6), whereas all of the crucian carp (n=6) and two masu salmon (n=6) exposed to SW died after land 24 hrs, respectively. The PRL mRNA levels of the eel and masu salmon decreased in 50% SW and SW compared to those of the fish kept in FW after 24 hrs, whereas the PRL levels of crucian carp were higher in 50% SW than in FW. Unlike the PRL mRNA levels, the GH mRNA levels of the eel did not differ significantly among three different salinities, while the GH mRNA levels of crucian carp and masu salmon increased significantly in 50% SW and SW after 24 hrs. The serum osmolalities increased marginally in the eel and masu salmon in 50% SW at 24 hrs (19% and 9%, respectively), whereas those of crucian carp increased abruptly in 50% SW (50% increase). These results suggest that the synthesis of PRL and GH is important in relation to the osmoregulatory system with environmental changes in salinity.

키워드

참고문헌

  1. Auperin, B., F. Rentier-Delrue, lA. Martial and P. Prunet. 1994. Evidence that two tilapia (Oreochromis niloticus) prolactins have different osmoregulatory functions during adaptation to a hyperosmotic environment. J. Mol. Endocrinol., 12, 13-24 https://doi.org/10.1677/jme.0.0120013
  2. Ayson, F.G., T. Kaneko, M. Tagawa, S. Hasegawa, E.G. Grau, R.S. Nishioka, S.K. David, H.A. Bern and T. Hirano. 1993. Effects of acclimation to hypertonic environment on plasma and pituitary levels of two prolactins and growth ormone in two species of tilapia, Oreochromis mossambicus and Oreochromis iloticus. Gen. Compo Endocrinol., 89, 138-148 https://doi.org/10.1006/gcen.1993.1017
  3. Boeuf, G. and P. Payan. 2001. How should salinity influence fish growth? Compo Biochem. Physiol. C Toxicol. Pharmacol., 130, 411-423 https://doi.org/10.1016/S1532-0456(01)00268-X
  4. Chang, Y.J., B.H. Min, H.J. Chang and J.W Hur. 2002. Comparison of blood physiology in juvenile black seabream (Acanthopagrus schlegeli) reared in converted freshwater from seawater and seawater from freshwater. J. Kor. Fish. Soc., 35, 595-600 https://doi.org/10.5657/kfas.2002.35.6.595
  5. Chang, YJ. and J.W. Hur. 1999. Physiological responses of grey mullet (Mugil cephalus) and nile ti1apia (Oreochromis niloticus) by rapid changes in salinity of rearing water. J. Kor. Fish. Soc., 32, 310-316
  6. Cho, Y.M., J. Shin and Y.C. Sohn, 2006. Gene expression levels of growth hormone, prolactin and their receptors of olive flounder (Paralichthys olivaceus) by salinity changes. J. Kor. Fish. Soc., 39, 326-332 https://doi.org/10.5657/kfas.2006.39.4.326
  7. Helms, L.M., E.G. Grau and R.J. Borski. 1991. Effects of osmotic pressure and somatostatin on the cAMP messenger system of the osmosensitive prolactin cell of a teleost fish, the tilapia (Oreochromis mossambi¬cus). Gen. Compo Endocrinol., 83, 111-117 https://doi.org/10.1016/0016-6480(91)90111-I
  8. Hirano, T. 1986. The spectrum of prolactin action in teleosts. Prog. Clin. Biol. Res., 205, 53-74
  9. Jarvis, P.L. and J.S. Ballantyne. 2003. Metabolic responses to salinity acclimation in juvenile shotnose sturgeon Acipenser brevirostrum. Aquaculture, 219, 891-909 https://doi.org/10.1016/S0044-8486(03)00063-2
  10. Kawauchi, H. and S.A. Sower. 2006. The dawn and evolution of hormones in the adenohypophysis. Gen. Comp. Endocrinol., 148, 3-14 https://doi.org/10.1016/j.ygcen.2005.10.011
  11. Lee, Y.C., Y.J. Chang and B.K. Lee. 1997, Osmoregulation capability of juvenile grey mullets (Mugil cephalus) with the different salinities. J. Kor. Fish. Soc., 30, 216-224
  12. Lee, K.M., T. Kaneko and K. Aida. 2006. Prolactin and prolactin receptor expressions in a marine teleost, pufferfish Takifugu rubripes. Gen. Comp. Endocrinol., 146, 318-328 https://doi.org/10.1016/j.ygcen.2005.12.003
  13. Madsen, S.S. and H.A. Bern. 1992. Antagonism of prolactin and growth hormone: impact on seawater adaptation in two salmonids, Salmo trutta and Oncrohynchus. Zool. Sci., 9, 775-784
  14. Madsen, S.S. and E.T. Naamansen. 1989. Plasma ionic regulation and gill $Na^+/k^+$-ATPase changes during rapid trasfer to sea water of yearling rainbow trout, Salmo gairdneri: time course and seasonal variation. J. Fish Biol., 34, 829-840 https://doi.org/10.1111/j.1095-8649.1989.tb03367.x
  15. Maina, J.N. 1990. A study of the morphology of the gills of an extreme alkalinity and hypersomotic adapted teleost Oreochromis alcalicus grahami (Boulenger) with particular emphasis on the ultrastructure of the chloride cells and their modifications with water dilution. A SEM and TEM study. Anat. Embryol., 181, 83-98
  16. Manzon, L.A. 2002. The role of prolactin in fish osmoregulation: a review. Gen. Comp. Endocrinol., 125, 291-310 https://doi.org/10.1006/gcen.2001.7746
  17. Morgan, J.D. and G.K. Iwama. 1991. Effects of salinity on growth, metabolism, and ion regulation in juvenile rainbow trout and steelhead trout (Oncorhynchus mykiss) and fall chinook salmon (Oncorhynchus kisutch). Can. J. Fish. Aquat. Sci., 48, 2083-2094 https://doi.org/10.1139/f91-247
  18. Partridge, G.J. and G.I. Jenkins. 2002. The effect of salinity on growth and survival of juvenile black bream (Acanthopagrus butcheri). Aquaculture, 210, 219-230 https://doi.org/10.1016/S0044-8486(01)00817-1
  19. Seale, A.P., L.G. Riley, T.A. Leedom, S. Kajimura, R.M. Dores, T. Hirano and E.G. Grau. 2002. Effects of environmental osmolality on release of prolactin, growth hormone and ACTH from the tilapia pituitary. Gen. Comp. Endocrinol., 128, 91-101 https://doi.org/10.1016/S0016-6480(02)00027-8
  20. Toften, H., A.M. Arne sen and M. Obling. 2003, Feed intake, growth and ionoregulation in Atlantic salmon (Salmo salar L.) smolts in relation to dietary addition of a feeding stimulant and time of seawater transfer. Aquaculture, 217, 647-662 https://doi.org/10.1016/S0044-8486(02)00404-0
  21. Tsuzuki, M.Y., K. Ogawa, C.A. Strussmann, M. Maita and F. Takashima. 2001. Physiological responses during stress and subsequent recovery at different salinities in adults in adult pejerrey Odontesthes bonariensis. Aquaculture, 200, 349-362 https://doi.org/10.1016/S0044-8486(00)00573-1
  22. Yada, T., T. Hirano and E.G. Grau. 1994. Changes in plasma levels of the two prolactins and growth hormone during adaptation to different salinities in the euryhaline tilapia, Oreochromis mossambicus. Gen. Comp. Endocrinol., 93, 214-223 https://doi.org/10.1006/gcen.1994.1025

피인용 문헌

  1. Physiological mechanism of osmoregulatory adaptation in anguillid eels 2018, https://doi.org/10.1007/s10695-018-0464-6