<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE root>
<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Journal of Ichthyology</journal-id><journal-title-group><journal-title xml:lang="en">Journal of Ichthyology</journal-title><trans-title-group xml:lang="ru"><trans-title>Вопросы ихтиологии</trans-title></trans-title-group></journal-title-group><issn publication-format="print">0042-8752</issn><issn publication-format="electronic">3034-5146</issn><publisher><publisher-name xml:lang="en">The Russian Academy of Sciences</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">650408</article-id><article-id pub-id-type="doi">10.31857/S0042875223030232</article-id><article-id pub-id-type="edn">BZDIYA</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Articles</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Статьи</subject></subj-group><subj-group subj-group-type="article-type"><subject>Unknown</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Effects of Salinity on Lipid Composition in Juvenile Pinc Salmon Oncorhynchus gorbuscha (Salmonidae)</article-title><trans-title-group xml:lang="ru"><trans-title>Влияние солёности на липидный состав молоди горбуши <italic>Oncorhynchus gorbuscha</italic> (Salmonidae)</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Vasileva</surname><given-names>O. B.</given-names></name><name xml:lang="ru"><surname>Васильева</surname><given-names>О. Б.</given-names></name></name-alternatives><email>vasil@krc.karelia.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Efremov</surname><given-names>D. A.</given-names></name><name xml:lang="ru"><surname>Ефремов</surname><given-names>Д. А.</given-names></name></name-alternatives><email>vasil@krc.karelia.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Ruokolainen</surname><given-names>T. R.</given-names></name><name xml:lang="ru"><surname>Руоколайнен</surname><given-names>Т. Р.</given-names></name></name-alternatives><email>vasil@krc.karelia.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Nemova</surname><given-names>N. N.</given-names></name><name xml:lang="ru"><surname>Немова</surname><given-names>Н. Н.</given-names></name></name-alternatives><email>vasil@krc.karelia.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Institute of Biology, Karelian Research Center, Russian Academy of Sciences, Petrozavodsk, Russia</institution></aff><aff><institution xml:lang="ru">Институт биологии Карельского научного центра РАН – ИБ КарНЦ РАН</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2023-05-01" publication-format="electronic"><day>01</day><month>05</month><year>2023</year></pub-date><volume>63</volume><issue>3</issue><fpage>365</fpage><lpage>371</lpage><history><date date-type="received" iso-8601-date="2025-01-31"><day>31</day><month>01</month><year>2025</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2023, О.Б. Васильева, Д.А. Ефремов, Т.Р. Руоколайнен, Н.Н. Немова</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2023, О.Б. Васильева, Д.А. Ефремов, Т.Р. Руоколайнен, Н.Н. Немова</copyright-statement><copyright-year>2023</copyright-year><copyright-holder xml:lang="en">О.Б. Васильева, Д.А. Ефремов, Т.Р. Руоколайнен, Н.Н. Немова</copyright-holder><copyright-holder xml:lang="ru">О.Б. Васильева, Д.А. Ефремов, Т.Р. Руоколайнен, Н.Н. Немова</copyright-holder></permissions><self-uri xlink:href="https://transsyst.ru/0042-8752/article/view/650408">https://transsyst.ru/0042-8752/article/view/650408</self-uri><abstract xml:lang="en"><p>Lipid and fatty acid modifications induced by the effects of various salinity patterns on the juvenile pink salmon Oncorhynchus gorbuscha (the Olkhovka River and the White Sea) within the experiment have been revealed. Concentrations of steroids, saturated fatty acids, and signaling molecules such as phospholipids (phosphatidylserine and phosphatidylinositol) and arachidonic acid under the hyperosmotic stress-related effects (keeping the fish for 1 h in the seawater after the time of transfer from the freswater) tend to increase. Decreases in phosphatidylcholine and n-6 saturated, monounsaturated, and polyunsaturated fatty acids are recorded in the juvenile pink salmon fish kept for 24 h in the seawater after the time of transfer them from the freswater, while the levels of phosphatidylethanolamine and n-3 polyunsaturated fatty acids (especially eicosapentaenoic and docosahexaenoic acids), on the contrary, tend to rise significantly. Lipid composition modifications in the juvenile pink salmon fish kept under the hypoosmotic stress conditions (24 h in freshwater after 24 h in seawater) induce stabilization of functioning the cell membrane structure, since the levels of bioeffectors including phosphatidylserine, phosphatidylinositol, and arachidonic, eicosapentaenoic, and docosahexaenoic acids tend to decrease. A reduced amount of lipids (triacylglycerols) stored as an energy reserve is shown for all the experimental fish groups. The outcomes indicate the high levels of adaptive potential of the juvenile pink salmon fish kept under the effects of abrupt salinity change in the water environments and their readiness for downstream migration not long before leaving the nests.</p></abstract><trans-abstract xml:lang="ru"><p id="idm45181324242624">Выявлены модификации липидов и жирных кислот в эксперименте по влиянию различных режимов солёности на мальков горбуши <italic>Oncorhynchus gorbuscha</italic> (р. Ольховка, бассейн Белого моря). В условиях гиперосмотического шока (1 ч в морской воде после пресной) у молоди увеличивается содержание стероидов, насыщенных жирных кислот и сигнальных молекул – фосфолипидов (фосфатидилсерина и фосфатидилинозитола) и арахидоновой кислоты. Через 24 ч пребывания в морской воде после пресной у мальков горбуши установлено снижение количества фосфатидилхолина, насыщенных, мононенасыщенных и полиненасыщенных <italic>n</italic>-6-жирных кислот, а уровень фосфатидилэтаноламина, полиненасыщенных <italic>n</italic>-3-жирных кислот (особенно эйкозапентаеновой и докозагексаеновой кислот), напротив, значительно возрастает. Изменения липидного состава мальков горбуши в условиях гипоосмотического стресса (24 ч в пресной воде после 24 ч в морской) направлены на стабилизацию функционирования мембранного аппарата клеток – снижается уровень биоэффекторов: фосфатидилсерина, фосфатидилинозитола, арахидоновой, эйкозапентаеновой и докозагексаеновой кислот. Показано снижение уровня энергетических липидов (триацилглицеринов) во всех экспериментальных группах. Результаты свидетельствуют о широком диапазоне адаптивных возможностей организма мальков горбуши в условиях резкой смены солёности среды и их готовности к покатной миграции в море незадолго до выхода из гнёзд.</p></trans-abstract><kwd-group xml:lang="en"><kwd>pink salmon Oncorhynchus gorbuscha</kwd><kwd>salinity of environments</kwd><kwd>lipids</kwd><kwd>fatty acids</kwd><kwd>White Sea</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>горбуша <italic>Oncorhynchus gorbuscha</italic></kwd><kwd>солёность среды</kwd><kwd>липиды</kwd><kwd>жирные кислоты</kwd><kwd>Белое море.</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Богданов М., Доухан В. 1999. Липид-опосредованный фолдинг белка // Журн. биол. химии. Т. 274. С. 827–830.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Елисеева И.И. 2007. Статистика. М.: Высш. образование, 566 с.</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Крепс Е.М. 1981. Липиды клеточных мембран. Л.: Наука, 339 с.</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Немова Н.Н., Кяйвяряйнен Е.И., Рендаков Н.Л. и др. 2021. Содержание кортизола и активность Na+/K+-АТФазы при адаптации молоди горбуши Oncorhynchus gorbuscha (Salmonidae) к изменению солёности среды // Вопр. ихтиологии. Т. 61. № 5. С. 599–606. https://doi.org/10.31857/S0042875221050131</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Сидоров В.С., Лизенко Е.И., Болгова О.М., Нефедова З.А. 1972. Липиды рыб. 1. Методы анализа. Тканевая специфичность ряпушки Coregonus albula L. // Лососёвые (Salmonidae) Карелии. Петрозаводск: Изд-во Карел. фил. АН СССР. С. 152–163.</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Цыганов Э.П. 1971. Метод прямого метилирования липидов после ТСХ без элюирования с силикагеля // Лаб. дело. № 8. С. 490–493.</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Шталь Э. 1965. Хроматография в тонких слоях. М.: Мир, 508 с.</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Allen P.J., McEnroe M., Forostyan T. et al. 2011. Ontogeny of salinity tolerance and evidence for seawater-entry preparation in juvenile green sturgeon, Acipenser medirostris // J. Comp. Physiol. B. V. 181. № 8. P. 1045–1062. https://doi.org/10.1007/s00360-011-0592-0</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Arjona F.J., Vargas-Chacoff L., Ruiz-Jarabo I. 2007. Osmoregulatory response of Senegalese sole (Solea senegalensis, Kaup 1858) to changes in environmental salinity // Comp. Biochem. Physiol. A. V. 148. № 2. P. 413–421. https://doi.org/10.1016/j.cbpa.2007.05.026</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Babili M.E., Brichon G., Zwingelstein G. 1996. Sphingomyelin metabolism is linked to salt transport in the gills of euryhaline fish // Lipids. V. 31. № 4. P. 385–392. https://doi.org/10.1007/BF02522924</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Bell J.G., Tocher D.R., Farndale B.M. et al. 1997. The effect of dietary lipid on polyunsaturated fatty acid metabolism in Atlantic salmon (Salmo salar) undergoing parr-smolt transformation // Ibid. V. 32. № 5. P. 515–525. https://doi.org/10.1007/s11745-997-0066-4</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Daikoku T., Yano I., Masuf M. 1982. Lipid and fatty acid composition and their changes in the different organs and tissues of guppy Poecilia reticulata on sea water adaptation // Comp. Biochem. Physiol. A. V. 73. № 2. P. 167–174. https://doi.org/10.1016/0300-9629(82)90050-0</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Engelbrecht F.M., Mari F., Anderson J.T. 1974. Cholesterol determination in serum. A rapid direction method // S. Afr. Med. J. V. 48. № 2. P. 250–256.</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Folch J., Lees M., Stanley G.H.S. 1957. A simple method for the isolation and purification of total lipides from animal tissues // J. Biol. Chem. V. 226. № 1. P. 497–509. https://doi.org/10.1016/S0021-9258(18)64849-5</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Folmar L.C., Dickhoff W.W. 1980. The parr-smolt transformation (smoltification) and seawater adaptation in salmonids // Aquaculture. V. 21. № 1. P. 1–37. https://doi.org/10.1016/0044-8486(80)90123-4</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Guidelines for the use of fishes in research. 2014. Bethesda: Am. Fish. Soc., 90 p.</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Handeland S.O., Bjornsson B.T., Arnesen A.M., Stefansson S.O. 2003. Seawater adaptation and growth of post-smolt Atlantic salmon (Salmo salar) of wild and fanned strains // Aquaculture. V. 220. № 1–4. P. 367–384. https://doi.org/10.1016/S0044-8486(02)00508-2</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Hansen H.J.M., Kelly S.P., Grosell M., Wood C.M. 2002. Studies on lipid metabolism in trout (Oncorhynchus mykiss) branchial cultures // J. Exp. Zool. V. 293. № 7. P. 683–692. https://doi.org/10.1002/jez.10166</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Harel M., Gavasso S., Leshin J. et al. 2001. The effect of tissue docosahexaenoic and arachidonic acids levels on hypersaline tolerance and leucocyte composition in striped bass (Morone saxatilis) larvae // Fish Physiol. Biochem. V. 24. № 2. P. 113–123. https://doi.org/10.1023/A:1011924704459</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Herrera M., Vargas-Chacoff L., Hachero I. et al. 2009. Osmoregulatory changes in wedge sole (Dicologoglossa cuneata, Moreau, 1881) after acclimation to different environmental salinities // Aquac. Res. V. 40. № 7. P. 762–771. https://doi.org/10.1111/j.1365-2109.2008.02147.x</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Hochachka P.W., Somero G.N. 2002. Biochemical adaptation: mechanism and process in physiological evolution. N.Y.: Oxford Univ. Press, 466 p.</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Hunt A.O., Oxkan F.E., Engin K., Tekelioglu N. 2011. The effects of freshwater rearing on the whole body and muscle tissue fatty acid profile of the European sea bass (Dicentrarchus labrax) // Aquacult. Int. V. 19. № 1. P. 51–61. https://doi.org/10.1007/s10499-010-9340-9</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Jamieson G.R. 1975. GLS identification techniques for long-chain unsaturated fatty acids // J. Chromatogr. Sci. V. 13. № 10. P. 491–497. https://doi.org/10.1093/chromsci/13.10.491</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Jana L., Huang X., Zhang L., Zhuang P. 2006. Hematological parameters of Amur sturgeon, Acipenser schrencki, during different salinity domestication // Mar. Fish. V. 28. P. 177–184.</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Kültz D. 2015. Physiological mechanisms used by fish to cope with salinity stress // J. Exp. Biol. V. 218. № 12. P. 1907–1914. https://doi.org/10.1242/jeb.118695</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>Li H.-O., Yamada J. 1992. Changes of the fatty acid composition in smolts of Masu salmon (Oncorhynchus masou), associated with desmoltification and seawater transfer // Comp. Biochem. Physiol. A. V. 103. № 1. P. 221–226. https://doi.org/10.1016/0300-9629(92)90266-S</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Li S., He F., Wen H. et al. 2017. Low salinity affects cellularity, DNA methylation, and mRNA expression of igf1 in the liver of half smooth tongue sole (Cynoglossus semilaevis) // Fish Physiol. Biochem. V. 43. № 6. P. 1587–1602. https://doi.org/10.1007/s10695-017-0395-7</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>Logue J.A., Howell B.R., Bell J.G., Cossins A.R. 2000. Dietary n-3 long-chain polyunsaturated fatty acid deprivation, tissue lipid composition, ex vivo prostaglandin production, and stress tolerance in juvenile Dover sole (Solea solea L.) // Lipids. V. 35. №. 7. P. 745–755. https://doi.org/10.1007/s11745-000-0581-3</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Mancera J.M., McCormick S.D. 2007. Role of prolactin, growth hormone, insuline-like growth factor and cortisol in teleost osmoregulation // Fish Osmoregulation. N.Y.: Sci. Pub. P. 497–515. https://doi.org/10.1201/9780429063909</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>Marshall W.S. 2002. Na+, Cl−, Ca2+ and Zn2+ transport by fish gills: retrospective review and prospective synthesis // J. Exp. Zool. V. 292. № 3. P. 264–293. https://doi.org/10.1002/jez.10127</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>Martins Y.S., Melo R.M.C., Campos-Junior P.H.A. et al. 2014. Salinity and temperature variations reflecting on cellular PCNA, IGF-I and II expressions, body growth and muscle cellularity of a freshwater fish larvae // Gen. Comp. Endocrinol. V. 202. P. 50–58. https://doi.org/10.1016/j.ygcen.2014.03.047</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>McKenzie D.J., Cataldi E., Romano P. et al. 2001. Effects of acclimation to brackish water on tolerance of salinity challenge by young-of-the-year Adriatic sturgeon (Acipenser naccarii) // Can. J. Fish. Aquat. Sci. V. 58. № 6. P. 1113–1121. https://doi.org/10.1139/f01-058</mixed-citation></ref><ref id="B33"><label>33.</label><mixed-citation>Mustafa T., Srivastava K.C. 1989. Prostaglandins (eicosanoids) and their role in ectothermic organisms // Adv. Comp. Environ. Physiol. V. 5. P. 157–207. https://doi.org/10.1007/978-3-642-74510-2_6</mixed-citation></ref><ref id="B34"><label>34.</label><mixed-citation>Robertson J.C., Hazel J.R. 1999. Influence of temperature and membrane lipid composition on the osmotic water permeability of teleost gills // Physiol. Biochem. Zool. V. 72. № 5. P. 623–632. https://doi.org/10.1086/316699</mixed-citation></ref><ref id="B35"><label>35.</label><mixed-citation>Sangiao-Alvarellos S., Arjona F.J., Martín del Río M.P. et al. 2005. Time course of osmoregulatory and metabolic changes during osmotic acclimation in Sparus auratus // J. Exp. Biol. V. 208. № 22. P. 4291–4304. https://doi.org/10.1242/jeb.01900</mixed-citation></ref><ref id="B36"><label>36.</label><mixed-citation>Sarkheil M., Sorki M.P., Raefipour H. 2017. Effects of acclimation to seawater salinity on some blood parameters in wild Caspian brown trout, Salmo trutta caspius // Comp. Clin. Pathol. V. 26. № 6. P. 1315–1318. https://doi.org/10.1007/s00580-017-2531-2</mixed-citation></ref><ref id="B37"><label>37.</label><mixed-citation>Si Y., Wen H., Li Y. et al. 2018. Liver transcriptome analysis reveals extensive transcriptional plasticity during acclimation to low salinity in Cynoglossus semilaevis // BMC Genomics. V. 19. Article 464. https://doi.org/10.1186/s12864-018-4825-4</mixed-citation></ref><ref id="B38"><label>38.</label><mixed-citation>Soengas J.L., Sangiao-Alvarellos S., Laiz-Carrio’n R., Mancera J.M. 2007. Energy metabolism and osmotic acclimation in teleost fish // Fish osmoregulation. N.Y.: Sci. Pub. P. 277–308. https://doi.org/10.1201/9780429063909</mixed-citation></ref><ref id="B39"><label>39.</label><mixed-citation>Tocher D.R., Sargent J.R. 1987. The effects of calcium ionophore A23187 on the metabolism of arachidonic and eicosapentaenoic acids in neutrophils from a marine teleost fish rich in (n-3) polyunsaturated fatty acids // Comp. Biochem. Physiol. B. V. 87. № 4. P. 733–739. https://doi.org/10.1016/0305-0491(87)90381-6</mixed-citation></ref><ref id="B40"><label>40.</label><mixed-citation>Tocher D.R., Castell J.D., Dick J.R., Sargent J.R. 1995. Effects of salinity on the fatty acid compositions of total lipid and individual glycerophospholipid classes of Atlantic salmon (Salmo salar) and turbot (Scophthalmus maximus) cells in culture // Fish Physiol. Biochem. V. 14. № 2. P. 125–137. https://doi.org/10.1007/BF00002456</mixed-citation></ref><ref id="B41"><label>41.</label><mixed-citation>Tocher D.R., Bendiksen E.A., Campbell P.J., Bell J.G. 2008. The role of phospholipids in nutrition and metabolism of teleost fish // Aquaculture. V. 280. № 1–4. P. 21–34. https://doi.org/10.1016/j.aquaculture.2008.04.034</mixed-citation></ref><ref id="B42"><label>42.</label><mixed-citation>Vargas-Chacoff L., Saavedra E., Oyarzun R. et al. 2015. Effects on the metabolism, growth, digestive capacity and osmoregulation of juvenile of Sub-Antarctic Notothenioid fish Eleginops maclovinus acclimated at different salinities // Fish Physiol. Biochem. V. 41. № 6. P. 1369–1381. https://doi.org/10.1007/s10695-015-0092-3</mixed-citation></ref><ref id="B43"><label>43.</label><mixed-citation>Wedermeyer G.A., Saunders R.L., Clarke W.C. 1980. Environmental factors affecting smoltification and early marine survival of anadromous salmonids // Mar. Fish. Rev. V. 42. № 6. P. 1–14.</mixed-citation></ref><ref id="B44"><label>44.</label><mixed-citation>Zwingelstein G., Bodennec J. 1998. Phospholipid metabolism in euryhaline fish and crustaceans. Effects of environmental salinity and temperature // Recent Res. Dev. Lipids Res. V. 2. P. 39–52.</mixed-citation></ref></ref-list></back></article>
