НЕКОТОРЫЕ АСПЕКТЫ БИОХИМИИ И ФИЗИОЛОГИИ СТЕРОИДНОЙ РЕГУЛЯЦИИ У КОСТИСТЫХ РЫБ

Николай Львович Рендаков, Nikolai Rendakov

Аннотация


Стероидные гормоны – важные регуляторы функций организма, связанных с размножением, стрессом и метаболизмом. В данном обзоре представлены сведения о путях биосинтеза стероидных гормонов у представителей класса костистых рыб в сравнении со стероидогенезом у млекопитающих (на примере человека), а также описана система стероидных рецепторов, при этом более подробно изложены сведения о рецепции кортикостероидов. Pаскрытие минералокортикоидной регуляции у рыб представлено в историческом аспекте. Приведены сведенияоб участии кортикостероидов в осморегуляции костистых рыб, механизмы которой значительно отличаются от таковых у наземных позвоночных. Несмотря на большое сходство в путях биосинтеза стероидных гормонов у рыб и млекопитающих, имеется несколько существенных различий, а именно: 1) отсутствие у костистых рыб способности к биосинтезу альдостерона, 2) возможность синтеза стероидов, индуцирующих созревание (СИС), у костистых рыб и 3) различия в путях биосинтеза андрогенов.


Ключевые слова


стероидные гормоны; глюкокортикоиды; минералокортикоиды; осморегуляция; кортизол; альдостерон.

Полный текст:

PDF

Литература


Adams J. S. “Bound” to work: the free hormone hypothesis revisited. Cell. 2005. Vol. 122, no. 5. P. 647–649. doi: 10.1016/j.cell.2005.08.024

Alsop D., Vijayan M. The zebrafish stress axis: Molecular fallout from the teleost-specific genome duplication event // Gen. Comp. Endocrinol. 2009. Vol. 161. no. 1. P. 62–66. doi: 10.1016/j.ygcen.2008.09.011

Arterbery A. S., Deitcher D. L., Bass A. H. Corticosteroid receptor expression in a teleost fish that displays alternative male reproductive tactics // Gen. Comp. Endocrinol. 2010. Vol. 165. no. 1. P. 83–90. doi: 10.1016/j.ygcen.2009.06.004

Baker M. E. Evolution of glucocorticoid and mineralocorticoid responses: go fish // Endocrinology. 2003. Vol. 144. no. 10. P. 4223–4225. doi: 10.1210/en.2003-0843

Baker M. E., Katsu Y. 30 years of the mineralocorticoid receptor: Evolution of the mineralocorticoid receptor: sequence, structure and function // J. Endocrinol. 2017. Vol. 234. no. 1. P. T1–T16. doi: 10.1530/JOE-16-0661

Beitel S. C., Doering J. A., Patterson S. E., Hecker M. Assessment of the sensitivity of three North American fish species to disruptors of steroidogenesis using in vitro tissue explants // Aquat. Toxicol. 2014. Vol. 152. P. 273–283. doi: 10.1016/j.aquatox.2014.04.013

Bern H. A. Hormones and endocrine glands of fishes. Studies of fish endocrinology reveal major physiologic and evolutionary problems // Science. 1967. Vol. 158. no. 3800. P. 455–462.

Bern H. A., Madsen S. S. A selective survey of the endocrine system of the rainbow trout (Oncorhynchus mykiss) with emphasis on the hormonal regulation of ion balance // Aquaculture. 1992. Vol. 100. no. 1–3. P. 237–262. doi: 10.1016/0044-8486(92)90384-W

Bernier N. J., Flik G., Klaren P. H. M. Regulation and contribution of the corticotropic, melanotropic and thyrotropic axes to the stress response in fishes // Fish Physiology: Fish Neuroendocrinology / Eds. N. J. Bernier, G. Van Der Kraak, A. P. Farrell, C. J. Brauner. London: Academic Press, 2009. P. 235–311. doi: 10.1016/S1546-5098(09)28006-X

Björkblom C., Högfors E., Salste L., Bergelin E., Olsson P. E., Katsiadaki I., Wiklund T. Estrogenic and androgenic effects of municipal wastewater effluent on reproductive endpoint biomarkers in three-spined stickleback (Gasterosteus aculeatus) // Environ. Toxicol. Chem. 2009. Vol. 28. no. 5. P. 1063-1071. doi: 10.1897/08-337.1

Bobe J., Guiguen Y., Fostier A. Diversity and biological significance of sex hormone-binding globulin in fish, an evolutionary perspective // Mol. Cell. Endocrinol. 2010. Vol. 316. no. 1. P. 66–78. doi: 10.1016/j.mce.2009.09.017

Borg B. Androgens in teleost fishes // Comp. Biochem. Physiol. Part C Pharmacol. Toxicol. Endocrinol. 1994. Vol. 109. no. 3. P. 219–245. doi: 10.1016/0742-8413(94)00063-G

Bose M., Whittal R. M., Miller W. L., Bose H. S. Steroidogenic activity of StAR requires contact with mitochondrial VDAC1 and phosphate carrier protein // J. Biol. Chem. 2008. Vol. 283. no. 14. P. 8837–8845. doi: 10.1074/jbc.M709221200

Brann D. W., Hendry L. B., Mahesh V. B. Emerging diversities in the mechanism of action of steroid hormones // J. Steroid Biochem. Mol. Biol. 1995. Vol. 52. no. 2. P. 113–33. doi: 10.1016/0960-0760(94)00160-N

Bridgham J. T. Evolution of hormone-receptor complexity by molecular exploitation // Science. 2006. Vol. 312. no. 5770. P. 97–101. doi: 10.1126/science.1123348

Busby E. R., Roch G. J., Sherwood N. M. Endocrinology of zebrafish: a small fish with a large gene pool // Fish Physiology: Zebrafish / Eds. S. F. Perry, M. Ekker, A. P. Farrell, C. J. Brauner. Amsterdam: Academic Press, 2010. P. 173–247. doi: 10.1016/S1546-5098(10)02905-5

Bystriansky J. S., Frick N. T., Richards J. G., Schulte P. M., Ballantyne J. S. Failure to up-regulate gill Na+,K+-ATPase α-subunit isoform α1b may limit seawater tolerance of land-locked Arctic char (Salvelinus alpinus) // Comp. Biochem. Physiol. Part A Mol. Integr. Physiol. 2007. Vol. 148. no. 2. P. 332–338. doi: 10.1016/j.cbpa.2007.05.007

Carta M. G., Bhat K. M., Preti A. GABAergic neuroactive steroids: a new frontier in bipolar disorders? // Behav. Brain Funct. 2012. Vol. 8. P. 61. doi: 10.1186/1744-9081-8-61

Chaby L. E. Why are there lasting effects from exposure to stress during development? An analysis of current models of early stress // Physiol. Behav. 2016. Vol. 164 (Pt A). P. 164–181. doi: 10.1016/j.physbeh.2016.05.032

Chai C., Liu Y., Chan W.-K. Ff1b is required for the development of steroidogenic component of the zebrafish interrenal organ // Dev. Biol. 2003. Vol. 260. no. 1. P. 226–244. doi: 10.1016/S0012-1606(03)00219-7

Chun R. F., Peercy B. E., Orwoll E. S., Nielson C. M., Adams J. S., Hewison M. Vitamin D and DBP: the free hormone hypothesis revisited // J. Steroid Biochem. Mol. Biol. 2014. Vol. 144 (Pt A). P. 132–137. doi: 10.1016/j.jsbmb.2013.09.012

Chung B. C., Matteson K. J., Voutilainen R., Mohandas T. K., Miller W. L. Human cholesterol side-chain cleavage enzyme, P450scc: cDNA cloning, assignment of the gene to chromosome 15, and expression in the placenta // Proc. Natl. Acad. Sci. U. S. A. 1986. Vol. 83. no. 23. P. 8962–8966.

Chung B. C., Guo I. C., Chou S. J. Transcriptional regulation of the CYP11A1 and ferredoxin genes // Steroids. 1997. Vol. 62. no. 1. P. 37–42. doi: 10.1016/S0039-128X(96)00156-0

Civinini A., Gallo V. P. Degeneration and possible renewal processes related to the interrenal cells in the head kidney of the stickleback Gasterosteus aculeatus // Tissue Cell. 2007. Vol. 39. no. 2. P. 109–122. doi: 10.1016/j.tice.2007.02.002

Clark A. J., Block K. The absence of sterol synthesis in insects // J. Biol. Chem. 1959. Vol. 234. P. 2578–2582.

Clelland E., Peng C. Endocrine/paracrine control of zebrafish ovarian development // Mol. Cell. Endocrinol. 2009. Vol. 312. no. 1–2. P. 42–52. doi: 10.1016/j.mce.2009.04.009

Collomp K., Baillot A., Forget H., Coquerel A., Rieth N., Vibarel-Rebot N. Altered diurnal pattern of steroid hormones in relation to various behaviors, external factors and pathologies: A review // Physiol. Behav. 2016. Vol. 164 (Pt A). P. 68–85. doi: 10.1016/j.physbeh.2016.05.039

Conant G. C., Wolfe K. H. Turning a hobby into a job: How duplicated genes find new functions // Nat. Rev. Genet. 2008. Vol. 9. no. 12. P. 938–950. doi: 10.1038/nrg2482

Cooke B.A., Molen H.J. Van Der, King R.J.B. (eds.) Hormones and their Actions. Amsterdam: Elsevier, 1988. 290 p.

Delville Y. Progesterone-facilitated sexual receptivity: a review of arguments supporting a nongenomic mechanism // Neurosci. Biobehav. Rev. 1991. Vol. 15. no. 3. P. 407–414. doi: 10.1016/S0149-7634(05)80033-8

Diotel N., Do Rego J. L., Anglade I., Vaillant C., Pellegrini E., Gueguen M. M., Mironov S., Vaudry H., Kah O. Activity and expression of steroidogenic enzymes in the brain of adult zebrafish // Eur. J. Neurosci. 2011. Vol. 34. no. 1. P. 45–56. doi: 10.1111/j.1460-9568.2011.07731.x

Dubrovsky B. O. Steroids, neuroactive steroids and neurosteroids in psychopathology // Prog. Neuropsychopharmacol. Biol. Psychiatry. 2005. Vol. 29. no. 2. P. 169–192. doi: 10.1016/j.pnpbp.2004.11.001

Ducouret B. Cloning of a teleost fish glucocorticoid receptor shows that it contains a deoxyribonucleic acid-binding domain different from that of mammals // Endocrinology. 1995. Vol. 136. no. 9. P. 3774–3783. doi: 10.1210/en.136.9.3774

Van Duyse E., Pinxten R., Eens M. Does testosterone affect the trade-off between investment in sexual/territorial behaviour and parental care in male great tits? // Behaviour. 2000. Vol. 137. no. 11. P. 1503–1515. doi: 10.1163/156853900502691

Falkenstein E., Tillmann H. C., Christ M., Feuring M., Wehling M. Multiple actions of steroid hormones–a focus on rapid, nongenomic effects // Pharmacol. Rev. 2000. Vol. 52. no. 4. P. 513–556.

Farman N. Molecular and cellular determinants of mineralocorticoid selectivity // Curr. Opin. Nephrol. Hypertens. 1999. Vol. 8. no. 1. P. 45–51.

Flik G., Perry S. F. Cortisol stimulates whole body calcium uptake and the branchial calcium pump in freshwater rainbow trout // J. Endocrinol. 1989. Vol. 120. no. 1. P. 75–82. doi: 10.1677/joe.0.1200075

Follesa P., Biggio F., Talani G., Murru L., Serra M., Sanna E., Biggio G. Neurosteroids, GABAA receptors, and ethanol dependence // Psychopharmacology (Berl). 2006. Vol. 186. no. 3. P. 267–280. doi: 10.1007/s00213-005-0126-0

Foskett J. K., Bern H. A., Machen T. E., Conner M. Chloride cells and the hormonal control of teleost fish osmoregulation // J. Exp. Biol. 1983. Vol. 106. P. 255–281.

Fuller P. J., Fuller P. J., Yao Y., Yang J., Young M. J. Mechanisms of ligand specificity of the mineralocorticoid receptor // J. Endocrinol. 2012. Vol. 213. no. 1. P. 15–24. doi: 10.1530/JOE-11-0372

Funder J., Pearce P. T., Smith R., Smith A. I. Mineralocorticoid action: target tissue specificity is enzyme, not receptor, mediated // Science. 1988. Vol. 242. no. 4878. P. 583–585. doi: 10.1126/science.2845584

Geering K. Functional roles of Na,K-ATPase subunits // Curr. Opin. Nephrol. Hypertens. 2008. Vol. 17. no. 5. P. 526–532. doi: 10.1097/MNH.0b013e3283036cbf

Gettler L. T., McDade T. W., Feranil A. B., Kuzawa C. W. Longitudinal evidence that fatherhood decreases testosterone in human males // Proc. Natl. Acad. Sci. 2011. Vol. 108. no. 39. P. 16194–16199. doi: 10.1073/pnas.1105403108

Gilmour K. M. Mineralocorticoid receptors and hormones: fishing for answers // Endocrinology. 2005. Vol. 146. no. 1. P. 44–46. doi: 10.1210/en.2004-1390

Glasauer S. M. K., Neuhauss S. C. F. Whole-genome duplication in teleost fishes and its evolutionary consequences // Mol. Genet. Genomics. 2014. Vol. 289. no. 6. P. 1045–1060. doi: 10.1007/s00438-014-0889-2

Greenwood A. K., Butler P. C., White R. B., DeMarco U., Pearce D., Fernald R. D. Multiple corticosteroid receptors in a teleost fish: distinct sequences, expression patterns, and transcriptional activities // Endocrinology. 2003. Vol. 144. no. 10. P. 4226–4236. doi: 10.1210/en.2003-0566

Guillemin R., Rosenberg B. Humoral hypothalamic control of anterior pituitary: a study with combined tissue cultures // Endocrinology. 1955. Vol. 57. no. 5. P. 599–607. doi: 10.1210/endo-57-5-599

Hammes A., Andreassen T. K., Spoelgen R., Raila J., Hubner N., Schulz H., Metzger J., Schweigert F. J., Luppa P. B., Nykjaer A., Willnow T. E. Role of endocytosis in cellular uptake of sex steroids // Cell. 2005. Vol. 122. no. 5. P. 751–762. doi: 10.1016/j.cell.2005.06.032

Hammes S. R., Davis P. J. Overlapping nongenomic and genomic actions of thyroid hormone and steroids // Best Pract. Res. Clin. Endocrinol. Metab. 2015. Vol. 29. no. 4. P. 581–593. doi: 10.1016/j.beem.2015.04.001

Hammes S. R., Levin E. R. Extranuclear steroid receptors: nature and actions // Endocr. Rev. 2007. Vol. 28. no. 7. P. 726–741. doi: 10.1210/er.2007-0022

Harris G. W. Neural control of the pituitary gland // Physiol. Rev. 1948. Vol. 28. no. 2. P. 139–179. doi: 10.1152/physrev.1948.28.2.139

Harris G. W. Humours and hormones // J. Endocrinol. 1972. Vol. 53. no. 2. P. 2–23.

Hsu H.-J., Hsu N. C., Hu M. C., Chung B. C. Steroidogenesis in zebrafish and mouse models // Mol. Cell. Endocrinol. 2006. Vol. 248. no. 1–2. P. 160–163. doi: 10.1016/j.mce.2005.10.011

Huang X., Warren J. T., Gilbert L. I. New players in the regulation of ecdysone biosynthesis // J. Genet. Genomics. 2008. Vol. 35. no. 1. P. 1–10. doi: 10.1016/S1673-8527(08)60001-6

Hughes A. L. The evolution of functionally novel proteins after gene duplication // Proc. R. Soc. B Biol. Sci. 1994. Vol. 256. no. 1346. P. 119–124. doi: 10.1098/rspb.1994.0058

Jiang C.-L., Liu L., Tasker J. G. Why do we need nongenomic glucocorticoid mechanisms? // Front. Neuroendocrinol. 2014. Vol. 35. no. 1. P. 72–75. doi: 10.1016/j.yfrne.2013.09.005

Jiang J., Young G., Kobayashi T., Nagahama Y. Eel (Anguilla japonica) testis 11β-hydroxylase gene is expressed in interrenal tissue and its product lacks aldosterone synthesizing activity // Mol. Cell. Endocrinol. 1998. Vol. 146. no. 1–2. P. 207–211. doi: 10.1016/S0303-7207(98)00147-6

Joss J. M. P., Arnold-Reed D. E., Balment R. J. The steroidogenic response to angiotensin II in the Australian lungfish, Neoceratodus forsteri // J. Comp. Physiol. B. 1994. Vol. 164. no. 5. P. 378–382. doi: 10.1007/BF00302553

Judd S. Na+/K+-ATPase isoform regulation in three-spine stickleback (Gasterosteus aculeatus) during salinity acclimation // A Thesis Degree Master Sci. 2012. 91 p.

Kiilerich P., Milla S., Sturm A., Valotaire C., Chevolleau S., Giton F., Terrien X., Fiet J., Fostier A., Debrauwer L., Prunet P. Implication of the mineralocorticoid axis in rainbow trout osmoregulation during salinity acclimation // J. Endocrinol. 2011. Vol. 209. no. 2. P. 221–235. doi: 10.1530/JOE-10-0371

Kime D. E. «Classical» and «non-classical» reproductive steroids in fish // Rev. Fish Biol. Fish. 1993. Vol. 3. no. 2. P. 160–180. doi: 10.1007/BF00045230

Knapp R., Wingfield J. C., Bass A. H. Steroid hormones and paternal care in the plainfin midshipman fish (Porichthys notatus) // Horm. Behav. 1999. Vol. 35. no. 1. P. 81–89. doi: 10.1006/hbeh.1998.1499

Krozowski Z. S., Funder J. W. Renal mineralocorticoid receptors and hippocampal corticosterone-binding species have identical intrinsic steroid specificity // Proc. Natl. Acad. Sci. U. S. A. 1983. Vol. 80. no. 19. P. 6056–6060.

Kumai Y., Nesan D., Vijayan M. M., Perry S. F. Cortisol regulates Na+ uptake in zebrafish, Danio rerio, larvae via the glucocorticoid receptor // Mol. Cell. Endocrinol. 2012. Vol. 364. no. 1–2. P. 113–125. doi: 10.1016/j.mce.2012.08.017

Laurent P., Perry S. F. Effects of cortisol on gill chloride cell morphology and ionic uptake in the freshwater trout, Salmo gairdneri // Cell Tissue Res. 1990. Vol. 259. no. 3. P. 429–442. doi: 10.1007/BF01740769

Levi L., Pekarski I., Gutman E., Fortina P., Hyslop T., Biran J., Levavi-Sivan B., Lubzens E. Revealing genes associated with vitellogenesis in the liver of the zebrafish (Danio rerio) by transcriptome profiling // BMC Genomics. 2009. Vol. 10. no. 1. P. 141. doi: 10.1186/1471-2164-10-141

Liley N. R., Stacey N. E. Hormones, pheromones, and reproductive behavior in fish // Fish Physiology: Reproduction : behavior and fertility control / Eds. W. S. Hoar, D. J. Randall, E. M. Donaldson. New York: Academic Press, 1983. P. 1–63. doi: 10.1016/S1546-5098(08)60301-5

Liu C., Zhang X., Deng J., Hecker M., Al-Khedhairy A., Giesy J. P., Zhou B. Effects of prochloraz or propylthiouracil on the cross-talk between the HPG, HPA, and HPT axes in zebrafish // Environ. Sci. Technol. 2011. Vol. 45. no. 2. P. 769–775. doi: 10.1021/es102659p

Liu S., Xu X. R., Qi Z. H., Chen H., Hao Q. W., Hu Y. X., Zhao J. L., Ying G. G. Steroid bioaccumulation profiles in typical freshwater aquaculture environments of South China and their human health risks via fish consumption // Environ. Pollut. 2017. Vol. 228. P. 72–81. doi: 10.1016/j.envpol.2017.05.031

Löhr H., Hammerschmidt M. Zebrafish in endocrine systems: recent advances and implications for human disease // Annu. Rev. Physiol. 2011. Vol. 73. P. 183–211. doi: 10.1146/annurev-physiol-012110-142320

Lokman P. M., Harris B., Kusakabe M., Kime D. E., Schulz R. W., Adachi S., Young G. 11-Oxygenated androgens in female teleosts: prevalence, abundance, and life history implications // Gen. Comp. Endocrinol. 2002. Vol. 129. no. 1. P. 1–12. doi: 10.1016/S0016-6480(02)00562-2

Luu-The V. Assessment of steroidogenesis and steroidogenic enzyme functions // J. Steroid Biochem. Mol. Biol. 2013. Vol. 137. P. 176–182. doi: 10.1016/j.jsbmb.2013.05.017

Luu-The V., Labrie F. The intracrine sex steroid biosynthesis pathways // Neuroendocrinology: The Normal Neuroendocrine System / Eds. L. Martini, G. Chrousos, F. Labrie, K. Pacak, D. W. Pfaff. Amsterdam: Elsevier, 2010. P. 177–192. doi: 10.1016/S0079-6123(08)81010-2

Madsen S. S., Kiilerich P., Tipsmark C. K. Multiplicity of expression of Na+,K+-ATPase -subunit isoforms in the gill of Atlantic salmon (Salmo salar): cellular localisation and absolute quantification in response to salinity change // J. Exp. Biol. 2009. Vol. 212. no. 1. P. 78–88. doi: 10.1242/jeb.024612

Maglich J. M. The first completed genome sequence from a teleost fish (Fugu rubripes) adds significant diversity to the nuclear receptor superfamily // Nucleic Acids Res. 2003. Vol. 31. no. 14. P. 4051–4058. doi: 10.1093/nar/gkg444

Margiotta-Casaluci L., Courant F., Antignac J. P., Le Bizec B., Sumpter J. P. Identification and quantification of 5α-dihydrotestosterone in the teleost fathead minnow (Pimephales promelas) by gas chromatography–tandem mass spectrometry // Gen. Comp. Endocrinol. 2013. Vol. 191. P. 202–209. doi: 10.1016/j.ygcen.2013.06.017

Margiotta-Casaluci L., Sumpter J. P. 5α-Dihydrotestosterone is a potent androgen in the fathead minnow (Pimephales promelas) // Gen. Comp. Endocrinol. 2011. Vol. 171. no. 3. P. 309–318. doi: 10.1016/j.ygcen.2011.02.012

Martyniuk C. J., Bissegger S., Langlois V. S. Current perspectives on the androgen 5 alpha-dihydrotestosterone (DHT) and 5 alpha-reductases in teleost fishes and amphibians // Gen. Comp. Endocrinol. 2013. Vol. 194. P. 264–274. doi: 10.1016/j.ygcen.2013.09.019

Marx C. E., Bradford D. W., Hamer R. M., Naylor J. C., Allen T. B., Lieberman J. A., Strauss J. L., Kilts J. D. Pregnenolone as a novel therapeutic candidate in schizophrenia: emerging preclinical and clinical evidence // Neuroscience. 2011. Vol. 191. P. 78–90. doi: 10.1016/j.neuroscience.2011.06.076

McCormick S. D. Endocrine control of osmoregulation in teleost fish // Am. Zool. 2001. Vol. 41. no. 4. P. 781–794. doi: 10.1668/0003-1569(2001)041[0781:ECOOIT]2.0.CO;2

McCormick S. D., Regish A., O'Dea M. F., Shrimpton J. M. Are we missing a mineralocorticoid in teleost fish? Effects of cortisol, deoxycorticosterone and aldosterone on osmoregulation, gill Na+,K+-ATPase activity and isoform mRNA levels in Atlantic salmon // Gen. Comp. Endocrinol. 2008. Vol. 157. no. 1. P. 35–40. doi: 10.1016/j.ygcen.2008.03.024

Mensah-Nyagan A. G., Saredi S., Schaeffer V., Kibaly C., Meyer L., Melcangi R. C., Patte-Mensah C. Assessment of neuroactive steroid formation in diabetic rat spinal cord using high-performance liquid chromatography and continuous flow scintillation detection // Neurochem. Int. 2008. Vol. 52. no. 4–5. P. 554–559. doi: 10.1016/j.neuint.2007.06.010

Meyer A., Van de Peer Y. From 2R to 3R: evidence for a fish-specific genome duplication (FSGD) // BioEssays. 2005. Vol. 27. no. 9. P. 937–945. doi: 10.1002/bies.20293

Miller W. L. Steroid hormone synthesis in mitochondria // Mol. Cell. Endocrinol. 2013. Vol. 379. no. 1–2. P. 62–73. doi: 10.1016/j.mce.2013.04.014

Miller W. L., Auchus R. J. The molecular biology, biochemistry, and physiology of human steroidogenesis and its disorders // Endocr. Rev. 2011. Vol. 32. no. 1. P. 81–151. doi: 10.1210/er.2010-0013

Miller W. L., Bose H. S. Early steps in steroidogenesis: intracellular cholesterol trafficking: Thematic Review Series: Genetics of Human Lipid Diseases // J. Lipid Res. 2011. Vol. 52. no. 12. P. 2111–2135. doi: 10.1194/jlr.R016675

Mindnich R., Haller F., Halbach F., Moeller G., Hrabé de Angelis M., Adamski J. Androgen metabolism via 17 -hydroxysteroid dehydrogenase type 3 in mammalian and non-mammalian vertebrates: comparison of the human and the zebrafish enzyme // J. Mol. Endocrinol. 2005. Vol. 35. no. 2. P. 305–316. doi: 10.1677/jme.1.01853

Moeller G., Adamski J. Integrated view on 17beta-hydroxysteroid dehydrogenases // Mol. Cell. Endocrinol. 2009. Vol. 301. no. 1–2. P. 7–19. doi: 10.1016/j.mce.2008.10.040

Mommsen T. P., Vijayan M. M., Moon T. W. Cortisol in teleosts: dynamics, mechanisms of action, and metabolic regulation // Rev. Fish Biol. Fish. 1999. Vol. 9. no. 3. P. 211–268.

Mooradian A. D., Morley J. E., Korenman S. G. Biological Actions of Androgens // Endocr. Rev. 1987. Vol. 8. no. 1. P. 1–28. doi: 10.1023/A:1008924418720

Moyes C. D., Schulte P. Ion and Water Balance // Principles of Animal Physiology. Edinburgh Gate: Pearson Education Limited, 2014. Second Edition. P. 500–555.

Müller J. Aldosterone: the minority hormone of the adrenal cortex // Steroids. 1995. Vol. 60. no. 1. P. 2–9. doi: 10.1016/0039-128X(94)00021-4

Nagahama Y. Endocrine regulation of gametogenesis in fish // Int. J. Dev. Biol. 1994. Vol. 38. no. 2. P. 217–229.

Nagahama Y., Yamashita M. Regulation of oocyte maturation in fish // Dev. Growth Differ. 2008. Vol. 50 Suppl 1. P. S195-S219. doi: 10.1111/j.1440-169X.2008.01019.x

Nematollahi M. A., van Pelt-Heerschap H., Atsma W., Komen J. High levels of corticosterone, and gene expression of star, cyp17a2, hsd3b, cyp21, hsd11b2 during acute stress in common carp with interrenal hyperplasia // Gen. Comp. Endocrinol. 2012. Vol. 176. no. 2. P. 252–258. doi: 10.1016/j.ygcen.2012.01.023

Norman A. W., Mizwicki M. T., Norman D. P. G. Steroid-hormone rapid actions, membrane receptors and a conformational ensemble model // Nat. Rev. Drug Discov. 2004. Vol. 3. no. 1. P. 27–41. doi: 10.1038/nrd1283

Olsen R. W., Sapp D. W. Neuroactive steroid modulation of GABAA receptors // Adv. Biochem. Psychopharmacol. 1995. Vol. 48. P. 57–74.

Olsson P.-E., Berg A. H., von Hofsten J., Grahn B., Hellqvist A., Larsson A., Karlsson J., Modig C., Borg B., Thomas P. Molecular cloning and characterization of a nuclear androgen receptor activated by 11-ketotestosterone // Reprod. Biol. Endocrinol. 2005. Vol. 3. P. 37. doi: 10.1186/1477-7827-3-37

Oren I., Fleishman S. J., Kessel A., Ben-Tal N. Free diffusion of steroid hormones across biomembranes: a simplex search with implicit solvent model calculations // Biophys. J. 2004. Vol. 87. no. 2. P. 768–779. doi: 10.1529/biophysj.103.035527

Páll M. K., Mayer I., Borg B. Androgen and behavior in the male three-spined stickleback, Gasterosteus aculeatus I.—Changes in 11-ketotestosterone levels during the nesting cycle // Horm. Behav. 2002. Vol. 41. no. 4. P. 377–383. doi: 10.1006/hbeh.2002.1777

Pankhurst N. W., Hilder P. I., Pankhurst P. M. Reproductive condition and behavior in relation to plasma levels of gonadal steroids in the spiny damselfish Acanthochromis polyacanthus // Gen. Comp. Endocrinol. 1999. Vol. 115. no. 1. P. 53–69. doi: 10.1006/gcen.1999.7285

Paul S. M., Purdy R. H. Neuroactive steroids // FASEB J. 1992. Vol. 6. no. 6. P. 2311–22. doi: 10.1096/fasebj.6.6.1347506

Petersen L. H., Hala D., Carty D., Cantu M., Martinović D., Huggett D. B. Effects of progesterone and norethindrone on female fathead minnow (Pimephales promelas) steroidogenesis // Environ. Toxicol. Chem. 2015. Vol. 34. no. 2. P. 379–390. doi: 10.1002/etc.2816

Pickford G. E., Pang P. K. T., Weinstein E., Torretti J., Hendler E., Epstein F. H. The response of the hypophysectomized cyprinodont, Fundulus heteroclitus, to replacement therapy with cortisol: Effects on blood serum and sodium-potassium activated adenosine triphosphatase in the gills, kidney, and intestinal mucosa // Gen. Comp. Endocrinol. 1970. Vol. 14. no. 3. P. 524–534. doi: 10.1016/0016-6480(70)90036-5

Pippal J. B., Cheung C. M., Yao Y. Z., Brennan F. E., Fuller P. J. Characterization of the zebrafish (Danio rerio) mineralocorticoid receptor // Mol. Cell. Endocrinol. 2011. Vol. 332. no. 1–2. P. 58–66. doi: 10.1016/j.mce.2010.09.014

Pittman K., Yúfera M., Pavlidis M., Geffen A. J., Koven W., Ribeiro L., Zambonino-Infante J. L., Tandler A. Fantastically plastic: fish larvae equipped for a new world // Rev. Aquac. 2013. Vol. 5. P. S224–S267. doi: 10.1111/raq.12034

Prunet P., Sturm A., Milla S. Multiple corticosteroid receptors in fish: From old ideas to new concepts // Gen. Comp. Endocrinol. 2006. Vol. 147. no. 1. P. 17–23. doi: 10.1016/j.ygcen.2006.01.015

Raisman G. An urge to explain the incomprehensible: Geoffrey Harris and the discovery of the neural control of the pituitary gland // Annu. Rev. Neurosci. 1997. Vol. 20. no. 1. P. 533–566. doi: 10.1146/annurev.neuro.20.1.533

De Renzis G., Bornancin M. Ion transport and gill ATPases // Gills: Ion and Water Transfer / Eds. W.S. Hoar, D.J. Randall. Orlando: Academic Press, Inc. 1984. P. 65–104. doi: 10.1016/S1546-5098(08)60182-X

Reul J. M. H. M., Gesing A., Droste S., Stec I. S. M., Weber A., Bachmann C., Bilang-Bleuel A., Holsboer F., Linthorst A. C. E. The brain mineralocorticoid receptor: greedy for ligand, mysterious in function // Eur. J. Pharmacol. 2000. Vol. 405. no. 1–3. P. 235–249. doi: 10.1016/S0014-2999(00)00677-4

Richards J. G. Na+/K+-ATPase -isoform switching in gills of rainbow trout (Oncorhynchus mykiss) during salinity transfer // J. Exp. Biol. 2003. Vol. 206. no. 24. P. 4475–4486. doi: 10.1242/jeb.00701

Rosner W. Sex steroids and the free hormone hypothesis. // Cell. 2006. Vol. 124. no. 3. P. 455-456. doi: 10.1016/j.cell.2006.01.026

Rossier B. C., Baker M. E., Studer R. A. Epithelial sodium transport and its control by aldosterone: the story of our internal environment revisited // Physiol. Rev. 2015. Vol. 95. no. 1. P. 297–340. doi: 10.1152/physrev.00011.2014

Rossier N. M., Chew G., Zhang K., Riva F., Fent K. Activity of binary mixtures of drospirenone with progesterone and 17α-ethinylestradiol in vitro and in vivo // Aquat. Toxicol. 2016. Vol. 174. P. 109–122. doi: 10.1016/j.aquatox.2016.02.005

Rove K. O., Crawford E. D., Perachino M., Morote J., Klotz L., Lange P. H., Andriole G. L., Matsumoto A. M., Taneja S. S., Eisenberger M. A., Reis L. O. Maximal testosterone suppression in prostate cancer–free vs total testosterone // Urology. 2014. Vol. 83. no. 6. P. 1217–1222. doi: 10.1016/j.urology.2014.02.001

Schally A. V. Arimura A., Kastin A. J., Matsuo H., Baba Y., Redding T. W., Nair R. M. G., Debeljuk L., White W. F. Gonadotropin-releasing hormone: one polypeptide regulates secretion of luteinizing and follicle-stimulating hormones // Science. 1971. Vol. 173. no. 4001. P. 1036–1038. doi: 10.1126/science.173.4001.1036

Schiffer L., Anderko S., Hannemann F., Eiden-Plach A., Bernhardt R. The CYP11B subfamily // J. Steroid Biochem. Mol. Biol. 2015. Vol. 151. P. 38–51. doi: 10.1016/j.jsbmb.2014.10.011

Schiller C. E., Schmidt P. J., Rubinow D. R. Allopregnanolone as a mediator of affective switching in reproductive mood disorders // Psychopharmacology (Berl). 2014. Vol. 231. no. 17. P. 3557–3567. doi: 10.1007/s00213-014-3599-x

Scholz S., Mayer I. Molecular biomarkers of endocrine disruption in small model fish // Mol. Cell. Endocrinol. 2008. Vol. 293. no. 1–2. P. 57–70. doi: 10.1016/j.mce.2008.06.008

Shen W.-J., Azhar S., Kraemer F. B. Lipid droplets and steroidogenic cells // Exp. Cell Res. 2016. Vol. 340. no. 2. P. 209–214. doi: 10.1016/j.yexcr.2015.11.024

Stein L. R., Trapp R. M., Bell A. M. Do reproduction and parenting influence personality traits? Insights from threespine stickleback // Anim. Behav. 2016. Vol. 112. P. 247–254. doi: 10.1016/j.anbehav.2015.12.002

Stoffel-Wagner B. Neurosteroid metabolism in the human brain // Eur. J. Endocrinol. 2001. Vol. 145. no. 6. P. 669–679. doi: 10.1530/eje.0.1450669

Stolte E. H., de Mazon A. F., Leon-Koosterziel K. M., Jesiak M., Bury N. R., Sturm A., Savelkoul H. F., Verburg van Kemenade B. M. L., Flik G. Corticosteroid receptors involved in stress regulation in common carp, Cyprinus carpio // J. Endocrinol. 2008. Vol. 198. no. 2. P. 403–417. doi: 10.1677/JOE-08-0100

Strous R. D., Maayan R., Weizman A. The relevance of neurosteroids to clinical psychiatry: from the laboratory to the bedside // Eur. Neuropsychopharmacol. 2006. Vol. 16. no. 3. P. 155–169. doi: 10.1016/j.euroneuro.2005.09.005

Sturm A., Bury N., Dengreville L., Fagart J., Flouriot G., Rafestin-Oblin M. E., Prunet P. 11-Deoxycorticosterone is a potent agonist of the rainbow trout (Oncorhynchus mykiss) mineralocorticoid receptor // Endocrinology. 2005. Vol. 146. no. 1. P. 47–55. doi: 10.1210/en.2004-0128

Takahashi H., Sakamoto T. The role of ‘mineralocorticoids’ in teleost fish: Relative importance of glucocorticoid signaling in the osmoregulation and ‘central’ actions of mineralocorticoid receptor // Gen. Comp. Endocrinol. 2013. Vol. 181. P. 223–228. doi: 10.1016/j.ygcen.2012.11.016

Tarkowská D., Strnad M. Plant ecdysteroids: plant sterols with intriguing distributions, biological effects and relations to plant hormones // Planta. 2016. Vol. 244. no. 3. P. 545–555. doi: 10.1007/s00425-016-2561-z

Taylor J. S., Braasch I., Frickey T., Meyer A., Van de Peer Y. Genome duplication, a trait shared by 22000 species of ray-finned fish // Genome Res. 2003. Vol. 13. no. 3. P. 382–390. doi: 10.1101/gr.640303

Thomas P. Rapid steroid hormone actions initiated at the cell surface and the receptors that mediate them with an emphasis on recent progress in fish models // Gen. Comp. Endocrinol. 2012. Vol. 175. no. 3. P. 367–383. doi: 10.1016/j.ygcen.2011.11.032

Tipsmark C. K., Breves J. P., Seale A. P., Lerner D. T., Hirano T., Grau E. G. Switching of Na+, K+-ATPase isoforms by salinity and prolactin in the gill of a cichlid fish // J. Endocrinol. 2011. Vol. 209. no. 2. P. 237–244. doi: 10.1530/JOE-10-0495

Tokarz J., Norton W., Möller G., Hrabé de Angelis M., Adamski J. Zebrafish 20β-hydroxysteroid dehydrogenase type 2 is important for glucocorticoid catabolism in stress response // PLoS One. 2013a. Vol. 8. no. 1. P. e54851. doi: 10.1371/journal.pone.0054851

Tokarz J., Möller G., Hrabé de Angelis M., Adamski J. Zebrafish and steroids: what do we know and what do we need to know? // J. Steroid Biochem. Mol. Biol. 2013b. Vol. 137. P. 165–173. doi: 10.1016/j.jsbmb.2013.01.003

Tokarz J., Möller G., Hrabě de Angelis M., Adamski J. Steroids in teleost fishes: A functional point of view // Steroids. 2015. Vol. 103. P. 123–144. doi: 10.1016/j.steroids.2015.06.011

Ubuka T., Parhar I. Dual actions of mammalian and piscine gonadotropin-inhibitory hormones, RFamide-related peptides and LPXRFamide peptides, in the hypothalamic-pituitary–gonadal axis // Front. Endocrinol. (Lausanne). 2018. Vol. 8. P. 377. doi: 10.3389/fendo.2017.00377

Veillette P. A., Sundell K., Specker J. L. Cortisol mediates the increase in intestinal fluid absorption in Atlantic salmon during parr-smolt transformation // Gen. Comp. Endocrinol. 1995. Vol. 97. no. 2. P. 250–258. doi: 10.1006/gcen.1995.1024

Viero C., Dayanithi G. Neurosteroids are excitatory in supraoptic neurons but inhibitory in the peripheral nervous system: it is all about oxytocin and progesterone receptors // Prog. Brain Res. 2008. Vol. 170. P. 177–192. doi: 10.1016/S0079-6123(08)00416-0

Vos J. G., Dybing E., Greim H. A., Ladefoged O., Lambré C., Tarazona J. V., Brandt I., Vethaak A. D. Health effects of endocrine-disrupting chemicals on wildlife, with special reference to the European situation // Crit. Rev. Toxicol. 2000. Vol. 30. no. 1. P. 71–133. doi: 10.1080/10408440091159176

de Waal P. P., Wang D. S., Nijenhuis W. A., Schulz R. W., Bogerd J. Functional characterization and expression analysis of the androgen receptor in zebrafish (Danio rerio) testis // Reproduction. 2008. Vol. 136. no. 2. P. 225–234. doi: 10.1530/REP-08-0055

Wehling M. Looking beyond the dogma of genomic steroid action: insights and facts of the 1990s // J. Mol. Med. (Berl). 1995. Vol. 73. no. 9. P. 439–447. doi: 10.1007/BF00202262

Willnow T. E., Nykjaer A. Response: Cellular Uptake of Sex Steroid Hormones // Cell. 2006. Vol. 124. no. 3. P. 456–457. doi: 10.1016/j.cell.2006.01.027

Wood C. M., Marshall W. S. Ion balance, acid-base regulation, and chloride cell function in the common killifish, Fundulus heteroclitus—a euryhaline estuarine teleost // Estuaries. 1994. Vol. 17. no. 1. P. 34-52. doi: 10.2307/1352333

Woolston C. ‘Living fossil’ genome unlocked // Nature. 2013. Vol. 496. no. 7445. P. 283–283. doi: 10.1038/496283a

Yu X., Wu L., Xie L., Yang S., Charkraborty T., Shi H., Wang D., Zhou L. Characterization of two paralogous StAR genes in a teleost, Nile tilapia (Oreochromis niloticus) // Mol. Cell. Endocrinol. 2014. Vol. 392. no. 1–2. P. 152–162. doi: 10.1016/j.mce.2014.05.013

Zhang Y., Zhang S., Lu H., Zhang L., Zhang W. Genes encoding aromatases in teleosts: Evolution and expression regulation // Gen. Comp. Endocrinol. 2014. Vol. 205. P. 151–158. doi: 10.1016/j.ygcen.2014.05.008

References in English

Adams J. S. “Bound” to work: the free hormone hypothesis revisited. Cell. 2005. Vol. 122, no. 5. P. 647–649. doi: 10.1016/j.cell.2005.08.024

Alsop D., Vijayan M. The zebrafish stress axis: Molecular fallout from the teleost-specific genome duplication event // Gen. Comp. Endocrinol. 2009. Vol. 161. no. 1. P. 62–66. doi: 10.1016/j.ygcen.2008.09.011

Arterbery A. S., Deitcher D. L., Bass A. H. Corticosteroid receptor expression in a teleost fish that displays alternative male reproductive tactics // Gen. Comp. Endocrinol. 2010. Vol. 165. no. 1. P. 83–90. doi: 10.1016/j.ygcen.2009.06.004

Baker M. E. Evolution of glucocorticoid and mineralocorticoid responses: go fish // Endocrinology. 2003. Vol. 144. no. 10. P. 4223–4225. doi: 10.1210/en.2003-0843

Baker M. E., Katsu Y. 30 years of the mineralocorticoid receptor: Evolution of the mineralocorticoid receptor: sequence, structure and function // J. Endocrinol. 2017. Vol. 234. no. 1. P. T1–T16. doi: 10.1530/JOE-16-0661

Beitel S. C., Doering J. A., Patterson S. E., Hecker M. Assessment of the sensitivity of three North American fish species to disruptors of steroidogenesis using in vitro tissue explants // Aquat. Toxicol. 2014. Vol. 152. P. 273–283. doi: 10.1016/j.aquatox.2014.04.013

Bern H. A. Hormones and endocrine glands of fishes. Studies of fish endocrinology reveal major physiologic and evolutionary problems // Science. 1967. Vol. 158. no. 3800. P. 455–462.

Bern H. A., Madsen S. S. A selective survey of the endocrine system of the rainbow trout (Oncorhynchus mykiss) with emphasis on the hormonal regulation of ion balance // Aquaculture. 1992. Vol. 100. no. 1–3. P. 237–262. doi: 10.1016/0044-8486(92)90384-W

Bernier N. J., Flik G., Klaren P. H. M. Regulation and contribution of the corticotropic, melanotropic and thyrotropic axes to the stress response in fishes // Fish Physiology: Fish Neuroendocrinology / Eds. N. J. Bernier, G. Van Der Kraak, A. P. Farrell, C. J. Brauner. London: Academic Press, 2009. P. 235–311. doi: 10.1016/S1546-5098(09)28006-X

Björkblom C., Högfors E., Salste L., Bergelin E., Olsson P. E., Katsiadaki I., Wiklund T. Estrogenic and androgenic effects of municipal wastewater effluent on reproductive endpoint biomarkers in three-spined stickleback (Gasterosteus aculeatus) // Environ. Toxicol. Chem. 2009. Vol. 28. no. 5. P. 1063-1071. doi: 10.1897/08-337.1

Bobe J., Guiguen Y., Fostier A. Diversity and biological significance of sex hormone-binding globulin in fish, an evolutionary perspective // Mol. Cell. Endocrinol. 2010. Vol. 316. no. 1. P. 66–78. doi: 10.1016/j.mce.2009.09.017

Borg B. Androgens in teleost fishes // Comp. Biochem. Physiol. Part C Pharmacol. Toxicol. Endocrinol. 1994. Vol. 109. no. 3. P. 219–245. doi: 10.1016/0742-8413(94)00063-G

Bose M., Whittal R. M., Miller W. L., Bose H. S. Steroidogenic activity of StAR requires contact with mitochondrial VDAC1 and phosphate carrier protein // J. Biol. Chem. 2008. Vol. 283. no. 14. P. 8837–8845. doi: 10.1074/jbc.M709221200

Brann D. W., Hendry L. B., Mahesh V. B. Emerging diversities in the mechanism of action of steroid hormones // J. Steroid Biochem. Mol. Biol. 1995. Vol. 52. no. 2. P. 113–33. doi: 10.1016/0960-0760(94)00160-N

Bridgham J. T. Evolution of hormone-receptor complexity by molecular exploitation // Science. 2006. Vol. 312. no. 5770. P. 97–101. doi: 10.1126/science.1123348

Busby E. R., Roch G. J., Sherwood N. M. Endocrinology of zebrafish: a small fish with a large gene pool // Fish Physiology: Zebrafish / Eds. S. F. Perry, M. Ekker, A. P. Farrell, C. J. Brauner. Amsterdam: Academic Press, 2010. P. 173–247. doi: 10.1016/S1546-5098(10)02905-5

Bystriansky J. S., Frick N. T., Richards J. G., Schulte P. M., Ballantyne J. S. Failure to up-regulate gill Na+,K+-ATPase α-subunit isoform α1b may limit seawater tolerance of land-locked Arctic char (Salvelinus alpinus) // Comp. Biochem. Physiol. Part A Mol. Integr. Physiol. 2007. Vol. 148. no. 2. P. 332–338. doi: 10.1016/j.cbpa.2007.05.007

Carta M. G., Bhat K. M., Preti A. GABAergic neuroactive steroids: a new frontier in bipolar disorders? // Behav. Brain Funct. 2012. Vol. 8. P. 61. doi: 10.1186/1744-9081-8-61

Chaby L. E. Why are there lasting effects from exposure to stress during development? An analysis of current models of early stress // Physiol. Behav. 2016. Vol. 164 (Pt A). P. 164–181. doi: 10.1016/j.physbeh.2016.05.032

Chai C., Liu Y., Chan W.-K. Ff1b is required for the development of steroidogenic component of the zebrafish interrenal organ // Dev. Biol. 2003. Vol. 260. no. 1. P. 226–244. doi: 10.1016/S0012-1606(03)00219-7

Chun R. F., Peercy B. E., Orwoll E. S., Nielson C. M., Adams J. S., Hewison M. Vitamin D and DBP: the free hormone hypothesis revisited // J. Steroid Biochem. Mol. Biol. 2014. Vol. 144 (Pt A). P. 132–137. doi: 10.1016/j.jsbmb.2013.09.012

Chung B. C., Matteson K. J., Voutilainen R., Mohandas T. K., Miller W. L. Human cholesterol side-chain cleavage enzyme, P450scc: cDNA cloning, assignment of the gene to chromosome 15, and expression in the placenta // Proc. Natl. Acad. Sci. U. S. A. 1986. Vol. 83. no. 23. P. 8962–8966.

Chung B. C., Guo I. C., Chou S. J. Transcriptional regulation of the CYP11A1 and ferredoxin genes // Steroids. 1997. Vol. 62. no. 1. P. 37–42. doi: 10.1016/S0039-128X(96)00156-0

Civinini A., Gallo V. P. Degeneration and possible renewal processes related to the interrenal cells in the head kidney of the stickleback Gasterosteus aculeatus // Tissue Cell. 2007. Vol. 39. no. 2. P. 109–122. doi: 10.1016/j.tice.2007.02.002

Clark A. J., Block K. The absence of sterol synthesis in insects // J. Biol. Chem. 1959. Vol. 234. P. 2578–2582.

Clelland E., Peng C. Endocrine/paracrine control of zebrafish ovarian development // Mol. Cell. Endocrinol. 2009. Vol. 312. no. 1–2. P. 42–52. doi: 10.1016/j.mce.2009.04.009

Collomp K., Baillot A., Forget H., Coquerel A., Rieth N., Vibarel-Rebot N. Altered diurnal pattern of steroid hormones in relation to various behaviors, external factors and pathologies: A review // Physiol. Behav. 2016. Vol. 164 (Pt A). P. 68–85. doi: 10.1016/j.physbeh.2016.05.039

Conant G. C., Wolfe K. H. Turning a hobby into a job: How duplicated genes find new functions // Nat. Rev. Genet. 2008. Vol. 9. no. 12. P. 938–950. doi: 10.1038/nrg2482

Cooke B.A., Molen H.J. Van Der, King R.J.B. (eds.) Hormones and their Actions. Amsterdam: Elsevier, 1988. 290 p.

Delville Y. Progesterone-facilitated sexual receptivity: a review of arguments supporting a nongenomic mechanism // Neurosci. Biobehav. Rev. 1991. Vol. 15. no. 3. P. 407–414. doi: 10.1016/S0149-7634(05)80033-8

Diotel N., Do Rego J. L., Anglade I., Vaillant C., Pellegrini E., Gueguen M. M., Mironov S., Vaudry H., Kah O. Activity and expression of steroidogenic enzymes in the brain of adult zebrafish // Eur. J. Neurosci. 2011. Vol. 34. no. 1. P. 45–56. doi: 10.1111/j.1460-9568.2011.07731.x

Dubrovsky B. O. Steroids, neuroactive steroids and neurosteroids in psychopathology // Prog. Neuropsychopharmacol. Biol. Psychiatry. 2005. Vol. 29. no. 2. P. 169–192. doi: 10.1016/j.pnpbp.2004.11.001

Ducouret B. Cloning of a teleost fish glucocorticoid receptor shows that it contains a deoxyribonucleic acid-binding domain different from that of mammals // Endocrinology. 1995. Vol. 136. no. 9. P. 3774–3783. doi: 10.1210/en.136.9.3774

Van Duyse E., Pinxten R., Eens M. Does testosterone affect the trade-off between investment in sexual/territorial behaviour and parental care in male great tits? // Behaviour. 2000. Vol. 137. no. 11. P. 1503–1515. doi: 10.1163/156853900502691

Falkenstein E., Tillmann H. C., Christ M., Feuring M., Wehling M. Multiple actions of steroid hormones–a focus on rapid, nongenomic effects // Pharmacol. Rev. 2000. Vol. 52. no. 4. P. 513–556.

Farman N. Molecular and cellular determinants of mineralocorticoid selectivity // Curr. Opin. Nephrol. Hypertens. 1999. Vol. 8. no. 1. P. 45–51.

Flik G., Perry S. F. Cortisol stimulates whole body calcium uptake and the branchial calcium pump in freshwater rainbow trout // J. Endocrinol. 1989. Vol. 120. no. 1. P. 75–82. doi: 10.1677/joe.0.1200075

Follesa P., Biggio F., Talani G., Murru L., Serra M., Sanna E., Biggio G. Neurosteroids, GABAA receptors, and ethanol dependence // Psychopharmacology (Berl). 2006. Vol. 186. no. 3. P. 267–280. doi: 10.1007/s00213-005-0126-0

Foskett J. K., Bern H. A., Machen T. E., Conner M. Chloride cells and the hormonal control of teleost fish osmoregulation // J. Exp. Biol. 1983. Vol. 106. P. 255–281.

Fuller P. J., Fuller P. J., Yao Y., Yang J., Young M. J. Mechanisms of ligand specificity of the mineralocorticoid receptor // J. Endocrinol. 2012. Vol. 213. no. 1. P. 15–24. doi: 10.1530/JOE-11-0372

Funder J., Pearce P. T., Smith R., Smith A. I. Mineralocorticoid action: target tissue specificity is enzyme, not receptor, mediated // Science. 1988. Vol. 242. no. 4878. P. 583–585. doi: 10.1126/science.2845584

Geering K. Functional roles of Na,K-ATPase subunits // Curr. Opin. Nephrol. Hypertens. 2008. Vol. 17. no. 5. P. 526–532. doi: 10.1097/MNH.0b013e3283036cbf

Gettler L. T., McDade T. W., Feranil A. B., Kuzawa C. W. Longitudinal evidence that fatherhood decreases testosterone in human males // Proc. Natl. Acad. Sci. 2011. Vol. 108. no. 39. P. 16194–16199. doi: 10.1073/pnas.1105403108

Gilmour K. M. Mineralocorticoid receptors and hormones: fishing for answers // Endocrinology. 2005. Vol. 146. no. 1. P. 44–46. doi: 10.1210/en.2004-1390

Glasauer S. M. K., Neuhauss S. C. F. Whole-genome duplication in teleost fishes and its evolutionary consequences // Mol. Genet. Genomics. 2014. Vol. 289. no. 6. P. 1045–1060. doi: 10.1007/s00438-014-0889-2

Greenwood A. K., Butler P. C., White R. B., DeMarco U., Pearce D., Fernald R. D. Multiple corticosteroid receptors in a teleost fish: distinct sequences, expression patterns, and transcriptional activities // Endocrinology. 2003. Vol. 144. no. 10. P. 4226–4236. doi: 10.1210/en.2003-0566

Guillemin R., Rosenberg B. Humoral hypothalamic control of anterior pituitary: a study with combined tissue cultures // Endocrinology. 1955. Vol. 57. no. 5. P. 599–607. doi: 10.1210/endo-57-5-599

Hammes A., Andreassen T. K., Spoelgen R., Raila J., Hubner N., Schulz H., Metzger J., Schweigert F. J., Luppa P. B., Nykjaer A., Willnow T. E. Role of endocytosis in cellular uptake of sex steroids // Cell. 2005. Vol. 122. no. 5. P. 751–762. doi: 10.1016/j.cell.2005.06.032

Hammes S. R., Davis P. J. Overlapping nongenomic and genomic actions of thyroid hormone and steroids // Best Pract. Res. Clin. Endocrinol. Metab. 2015. Vol. 29. no. 4. P. 581–593. doi: 10.1016/j.beem.2015.04.001

Hammes S. R., Levin E. R. Extranuclear steroid receptors: nature and actions // Endocr. Rev. 2007. Vol. 28. no. 7. P. 726–741. doi: 10.1210/er.2007-0022

Harris G. W. Neural control of the pituitary gland // Physiol. Rev. 1948. Vol. 28. no. 2. P. 139–179. doi: 10.1152/physrev.1948.28.2.139

Harris G. W. Humours and hormones // J. Endocrinol. 1972. Vol. 53. no. 2. P. 2–23.

Hsu H.-J., Hsu N. C., Hu M. C., Chung B. C. Steroidogenesis in zebrafish and mouse models // Mol. Cell. Endocrinol. 2006. Vol. 248. no. 1–2. P. 160–163. doi: 10.1016/j.mce.2005.10.011

Huang X., Warren J. T., Gilbert L. I. New players in the regulation of ecdysone biosynthesis // J. Genet. Genomics. 2008. Vol. 35. no. 1. P. 1–10. doi: 10.1016/S1673-8527(08)60001-6

Hughes A. L. The evolution of functionally novel proteins after gene duplication // Proc. R. Soc. B Biol. Sci. 1994. Vol. 256. no. 1346. P. 119–124. doi: 10.1098/rspb.1994.0058

Jiang C.-L., Liu L., Tasker J. G. Why do we need nongenomic glucocorticoid mechanisms? // Front. Neuroendocrinol. 2014. Vol. 35. no. 1. P. 72–75. doi: 10.1016/j.yfrne.2013.09.005

Jiang J., Young G., Kobayashi T., Nagahama Y. Eel (Anguilla japonica) testis 11β-hydroxylase gene is expressed in interrenal tissue and its product lacks aldosterone synthesizing activity // Mol. Cell. Endocrinol. 1998. Vol. 146. no. 1–2. P. 207–211. doi: 10.1016/S0303-7207(98)00147-6

Joss J. M. P., Arnold-Reed D. E., Balment R. J. The steroidogenic response to angiotensin II in the Australian lungfish, Neoceratodus forsteri // J. Comp. Physiol. B. 1994. Vol. 164. no. 5. P. 378–382. doi: 10.1007/BF00302553

Judd S. Na+/K+-ATPase isoform regulation in three-spine stickleback (Gasterosteus aculeatus) during salinity acclimation // A Thesis Degree Master Sci. 2012. 91 p.

Kiilerich P., Milla S., Sturm A., Valotaire C., Chevolleau S., Giton F., Terrien X., Fiet J., Fostier A., Debrauwer L., Prunet P. Implication of the mineralocorticoid axis in rainbow trout osmoregulation during salinity acclimation // J. Endocrinol. 2011. Vol. 209. no. 2. P. 221–235. doi: 10.1530/JOE-10-0371

Kime D. E. «Classical» and «non-classical» reproductive steroids in fish // Rev. Fish Biol. Fish. 1993. Vol. 3. no. 2. P. 160–180. doi: 10.1007/BF00045230

Knapp R., Wingfield J. C., Bass A. H. Steroid hormones and paternal care in the plainfin midshipman fish (Porichthys notatus) // Horm. Behav. 1999. Vol. 35. no. 1. P. 81–89. doi: 10.1006/hbeh.1998.1499

Krozowski Z. S., Funder J. W. Renal mineralocorticoid receptors and hippocampal corticosterone-binding species have identical intrinsic steroid specificity // Proc. Natl. Acad. Sci. U. S. A. 1983. Vol. 80. no. 19. P. 6056–6060.

Kumai Y., Nesan D., Vijayan M. M., Perry S. F. Cortisol regulates Na+ uptake in zebrafish, Danio rerio, larvae via the glucocorticoid receptor // Mol. Cell. Endocrinol. 2012. Vol. 364. no. 1–2. P. 113–125. doi: 10.1016/j.mce.2012.08.017

Laurent P., Perry S. F. Effects of cortisol on gill chloride cell morphology and ionic uptake in the freshwater trout, Salmo gairdneri // Cell Tissue Res. 1990. Vol. 259. no. 3. P. 429–442. doi: 10.1007/BF01740769

Levi L., Pekarski I., Gutman E., Fortina P., Hyslop T., Biran J., Levavi-Sivan B., Lubzens E. Revealing genes associated with vitellogenesis in the liver of the zebrafish (Danio rerio) by transcriptome profiling // BMC Genomics. 2009. Vol. 10. no. 1. P. 141. doi: 10.1186/1471-2164-10-141

Liley N. R., Stacey N. E. Hormones, pheromones, and reproductive behavior in fish // Fish Physiology: Reproduction : behavior and fertility control / Eds. W. S. Hoar, D. J. Randall, E. M. Donaldson. New York: Academic Press, 1983. P. 1–63. doi: 10.1016/S1546-5098(08)60301-5

Liu C., Zhang X., Deng J., Hecker M., Al-Khedhairy A., Giesy J. P., Zhou B. Effects of prochloraz or propylthiouracil on the cross-talk between the HPG, HPA, and HPT axes in zebrafish // Environ. Sci. Technol. 2011. Vol. 45. no. 2. P. 769–775. doi: 10.1021/es102659p

Liu S., Xu X. R., Qi Z. H., Chen H., Hao Q. W., Hu Y. X., Zhao J. L., Ying G. G. Steroid bioaccumulation profiles in typical freshwater aquaculture environments of South China and their human health risks via fish consumption // Environ. Pollut. 2017. Vol. 228. P. 72–81. doi: 10.1016/j.envpol.2017.05.031

Löhr H., Hammerschmidt M. Zebrafish in endocrine systems: recent advances and implications for human disease // Annu. Rev. Physiol. 2011. Vol. 73. P. 183–211. doi: 10.1146/annurev-physiol-012110-142320

Lokman P. M., Harris B., Kusakabe M., Kime D. E., Schulz R. W., Adachi S., Young G. 11-Oxygenated androgens in female teleosts: prevalence, abundance, and life history implications // Gen. Comp. Endocrinol. 2002. Vol. 129. no. 1. P. 1–12. doi: 10.1016/S0016-6480(02)00562-2

Luu-The V. Assessment of steroidogenesis and steroidogenic enzyme functions // J. Steroid Biochem. Mol. Biol. 2013. Vol. 137. P. 176–182. doi: 10.1016/j.jsbmb.2013.05.017

Luu-The V., Labrie F. The intracrine sex steroid biosynthesis pathways // Neuroendocrinology: The Normal Neuroendocrine System / Eds. L. Martini, G. Chrousos, F. Labrie, K. Pacak, D. W. Pfaff. Amsterdam: Elsevier, 2010. P. 177–192. doi: 10.1016/S0079-6123(08)81010-2

Madsen S. S., Kiilerich P., Tipsmark C. K. Multiplicity of expression of Na+,K+-ATPase -subunit isoforms in the gill of Atlantic salmon (Salmo salar): cellular localisation and absolute quantification in response to salinity change // J. Exp. Biol. 2009. Vol. 212. no. 1. P. 78–88. doi: 10.1242/jeb.024612

Maglich J. M. The first completed genome sequence from a teleost fish (Fugu rubripes) adds significant diversity to the nuclear receptor superfamily // Nucleic Acids Res. 2003. Vol. 31. no. 14. P. 4051–4058. doi: 10.1093/nar/gkg444

Margiotta-Casaluci L., Courant F., Antignac J. P., Le Bizec B., Sumpter J. P. Identification and quantification of 5α-dihydrotestosterone in the teleost fathead minnow (Pimephales promelas) by gas chromatography–tandem mass spectrometry // Gen. Comp. Endocrinol. 2013. Vol. 191. P. 202–209. doi: 10.1016/j.ygcen.2013.06.017

Margiotta-Casaluci L., Sumpter J. P. 5α-Dihydrotestosterone is a potent androgen in the fathead minnow (Pimephales promelas) // Gen. Comp. Endocrinol. 2011. Vol. 171. no. 3. P. 309–318. doi: 10.1016/j.ygcen.2011.02.012

Martyniuk C. J., Bissegger S., Langlois V. S. Current perspectives on the androgen 5 alpha-dihydrotestosterone (DHT) and 5 alpha-reductases in teleost fishes and amphibians // Gen. Comp. Endocrinol. 2013. Vol. 194. P. 264–274. doi: 10.1016/j.ygcen.2013.09.019

Marx C. E., Bradford D. W., Hamer R. M., Naylor J. C., Allen T. B., Lieberman J. A., Strauss J. L., Kilts J. D. Pregnenolone as a novel therapeutic candidate in schizophrenia: emerging preclinical and clinical evidence // Neuroscience. 2011. Vol. 191. P. 78–90. doi: 10.1016/j.neuroscience.2011.06.076

McCormick S. D. Endocrine control of osmoregulation in teleost fish // Am. Zool. 2001. Vol. 41. no. 4. P. 781–794. doi: 10.1668/0003-1569(2001)041[0781:ECOOIT]2.0.CO;2

McCormick S. D., Regish A., O'Dea M. F., Shrimpton J. M. Are we missing a mineralocorticoid in teleost fish? Effects of cortisol, deoxycorticosterone and aldosterone on osmoregulation, gill Na+,K+-ATPase activity and isoform mRNA levels in Atlantic salmon // Gen. Comp. Endocrinol. 2008. Vol. 157. no. 1. P. 35–40. doi: 10.1016/j.ygcen.2008.03.024

Mensah-Nyagan A. G., Saredi S., Schaeffer V., Kibaly C., Meyer L., Melcangi R. C., Patte-Mensah C. Assessment of neuroactive steroid formation in diabetic rat spinal cord using high-performance liquid chromatography and continuous flow scintillation detection // Neurochem. Int. 2008. Vol. 52. no. 4–5. P. 554–559. doi: 10.1016/j.neuint.2007.06.010

Meyer A., Van de Peer Y. From 2R to 3R: evidence for a fish-specific genome duplication (FSGD) // BioEssays. 2005. Vol. 27. no. 9. P. 937–945. doi: 10.1002/bies.20293

Miller W. L. Steroid hormone synthesis in mitochondria // Mol. Cell. Endocrinol. 2013. Vol. 379. no. 1–2. P. 62–73. doi: 10.1016/j.mce.2013.04.014

Miller W. L., Auchus R. J. The molecular biology, biochemistry, and physiology of human steroidogenesis and its disorders // Endocr. Rev. 2011. Vol. 32. no. 1. P. 81–151. doi: 10.1210/er.2010-0013

Miller W. L., Bose H. S. Early steps in steroidogenesis: intracellular cholesterol trafficking: Thematic Review Series: Genetics of Human Lipid Diseases // J. Lipid Res. 2011. Vol. 52. no. 12. P. 2111–2135. doi: 10.1194/jlr.R016675

Mindnich R., Haller F., Halbach F., Moeller G., Hrabé de Angelis M., Adamski J. Androgen metabolism via 17 -hydroxysteroid dehydrogenase type 3 in mammalian and non-mammalian vertebrates: comparison of the human and the zebrafish enzyme // J. Mol. Endocrinol. 2005. Vol. 35. no. 2. P. 305–316. doi: 10.1677/jme.1.01853

Moeller G., Adamski J. Integrated view on 17beta-hydroxysteroid dehydrogenases // Mol. Cell. Endocrinol. 2009. Vol. 301. no. 1–2. P. 7–19. doi: 10.1016/j.mce.2008.10.040

Mommsen T. P., Vijayan M. M., Moon T. W. Cortisol in teleosts: dynamics, mechanisms of action, and metabolic regulation // Rev. Fish Biol. Fish. 1999. Vol. 9. no. 3. P. 211–268.

Mooradian A. D., Morley J. E., Korenman S. G. Biological Actions of Androgens // Endocr. Rev. 1987. Vol. 8. no. 1. P. 1–28. doi: 10.1023/A:1008924418720

Moyes C. D., Schulte P. Ion and Water Balance // Principles of Animal Physiology. Edinburgh Gate: Pearson Education Limited, 2014. Second Edition. P. 500–555.

Müller J. Aldosterone: the minority hormone of the adrenal cortex // Steroids. 1995. Vol. 60. no. 1. P. 2–9. doi: 10.1016/0039-128X(94)00021-4

Nagahama Y. Endocrine regulation of gametogenesis in fish // Int. J. Dev. Biol. 1994. Vol. 38. no. 2. P. 217–229.

Nagahama Y., Yamashita M. Regulation of oocyte maturation in fish // Dev. Growth Differ. 2008. Vol. 50 Suppl 1. P. S195-S219. doi: 10.1111/j.1440-169X.2008.01019.x

Nematollahi M. A., van Pelt-Heerschap H., Atsma W., Komen J. High levels of corticosterone, and gene expression of star, cyp17a2, hsd3b, cyp21, hsd11b2 during acute stress in common carp with interrenal hyperplasia // Gen. Comp. Endocrinol. 2012. Vol. 176. no. 2. P. 252–258. doi: 10.1016/j.ygcen.2012.01.023

Norman A. W., Mizwicki M. T., Norman D. P. G. Steroid-hormone rapid actions, membrane receptors and a conformational ensemble model // Nat. Rev. Drug Discov. 2004. Vol. 3. no. 1. P. 27–41. doi: 10.1038/nrd1283

Olsen R. W., Sapp D. W. Neuroactive steroid modulation of GABAA receptors // Adv. Biochem. Psychopharmacol. 1995. Vol. 48. P. 57–74.

Olsson P.-E., Berg A. H., von Hofsten J., Grahn B., Hellqvist A., Larsson A., Karlsson J., Modig C., Borg B., Thomas P. Molecular cloning and characterization of a nuclear androgen receptor activated by 11-ketotestosterone // Reprod. Biol. Endocrinol. 2005. Vol. 3. P. 37. doi: 10.1186/1477-7827-3-37

Oren I., Fleishman S. J., Kessel A., Ben-Tal N. Free diffusion of steroid hormones across biomembranes: a simplex search with implicit solvent model calculations // Biophys. J. 2004. Vol. 87. no. 2. P. 768–779. doi: 10.1529/biophysj.103.035527

Páll M. K., Mayer I., Borg B. Androgen and behavior in the male three-spined stickleback, Gasterosteus aculeatus I.—Changes in 11-ketotestosterone levels during the nesting cycle // Horm. Behav. 2002. Vol. 41. no. 4. P. 377–383. doi: 10.1006/hbeh.2002.1777

Pankhurst N. W., Hilder P. I., Pankhurst P. M. Reproductive condition and behavior in relation to plasma levels of gonadal steroids in the spiny damselfish Acanthochromis polyacanthus // Gen. Comp. Endocrinol. 1999. Vol. 115. no. 1. P. 53–69. doi: 10.1006/gcen.1999.7285

Paul S. M., Purdy R. H. Neuroactive steroids // FASEB J. 1992. Vol. 6. no. 6. P. 2311–22. doi: 10.1096/fasebj.6.6.1347506

Petersen L. H., Hala D., Carty D., Cantu M., Martinović D., Huggett D. B. Effects of progesterone and norethindrone on female fathead minnow (Pimephales promelas) steroidogenesis // Environ. Toxicol. Chem. 2015. Vol. 34. no. 2. P. 379–390. doi: 10.1002/etc.2816

Pickford G. E., Pang P. K. T., Weinstein E., Torretti J., Hendler E., Epstein F. H. The response of the hypophysectomized cyprinodont, Fundulus heteroclitus, to replacement therapy with cortisol: Effects on blood serum and sodium-potassium activated adenosine triphosphatase in the gills, kidney, and intestinal mucosa // Gen. Comp. Endocrinol. 1970. Vol. 14. no. 3. P. 524–534. doi: 10.1016/0016-6480(70)90036-5

Pippal J. B., Cheung C. M., Yao Y. Z., Brennan F. E., Fuller P. J. Characterization of the zebrafish (Danio rerio) mineralocorticoid receptor // Mol. Cell. Endocrinol. 2011. Vol. 332. no. 1–2. P. 58–66. doi: 10.1016/j.mce.2010.09.014

Pittman K., Yúfera M., Pavlidis M., Geffen A. J., Koven W., Ribeiro L., Zambonino-Infante J. L., Tandler A. Fantastically plastic: fish larvae equipped for a new world // Rev. Aquac. 2013. Vol. 5. P. S224–S267. doi: 10.1111/raq.12034

Prunet P., Sturm A., Milla S. Multiple corticosteroid receptors in fish: From old ideas to new concepts // Gen. Comp. Endocrinol. 2006. Vol. 147. no. 1. P. 17–23. doi: 10.1016/j.ygcen.2006.01.015

Raisman G. An urge to explain the incomprehensible: Geoffrey Harris and the discovery of the neural control of the pituitary gland // Annu. Rev. Neurosci. 1997. Vol. 20. no. 1. P. 533–566. doi: 10.1146/annurev.neuro.20.1.533

De Renzis G., Bornancin M. Ion transport and gill ATPases // Gills: Ion and Water Transfer / Eds. W.S. Hoar, D.J. Randall. Orlando: Academic Press, Inc. 1984. P. 65–104. doi: 10.1016/S1546-5098(08)60182-X

Reul J. M. H. M., Gesing A., Droste S., Stec I. S. M., Weber A., Bachmann C., Bilang-Bleuel A., Holsboer F., Linthorst A. C. E. The brain mineralocorticoid receptor: greedy for ligand, mysterious in function // Eur. J. Pharmacol. 2000. Vol. 405. no. 1–3. P. 235–249. doi: 10.1016/S0014-2999(00)00677-4

Richards J. G. Na+/K+-ATPase -isoform switching in gills of rainbow trout (Oncorhynchus mykiss) during salinity transfer // J. Exp. Biol. 2003. Vol. 206. no. 24. P. 4475–4486. doi: 10.1242/jeb.00701

Rosner W. Sex steroids and the free hormone hypothesis. // Cell. 2006. Vol. 124. no. 3. P. 455-456. doi: 10.1016/j.cell.2006.01.026

Rossier B. C., Baker M. E., Studer R. A. Epithelial sodium transport and its control by aldosterone: the story of our internal environment revisited // Physiol. Rev. 2015. Vol. 95. no. 1. P. 297–340. doi: 10.1152/physrev.00011.2014

Rossier N. M., Chew G., Zhang K., Riva F., Fent K. Activity of binary mixtures of drospirenone with progesterone and 17α-ethinylestradiol in vitro and in vivo // Aquat. Toxicol. 2016. Vol. 174. P. 109–122. doi: 10.1016/j.aquatox.2016.02.005

Rove K. O., Crawford E. D., Perachino M., Morote J., Klotz L., Lange P. H., Andriole G. L., Matsumoto A. M., Taneja S. S., Eisenberger M. A., Reis L. O. Maximal testosterone suppression in prostate cancer–free vs total testosterone // Urology. 2014. Vol. 83. no. 6. P. 1217–1222. doi: 10.1016/j.urology.2014.02.001

Schally A. V. Arimura A., Kastin A. J., Matsuo H., Baba Y., Redding T. W., Nair R. M. G., Debeljuk L., White W. F. Gonadotropin-releasing hormone: one polypeptide regulates secretion of luteinizing and follicle-stimulating hormones // Science. 1971. Vol. 173. no. 4001. P. 1036–1038. doi: 10.1126/science.173.4001.1036

Schiffer L., Anderko S., Hannemann F., Eiden-Plach A., Bernhardt R. The CYP11B subfamily // J. Steroid Biochem. Mol. Biol. 2015. Vol. 151. P. 38–51. doi: 10.1016/j.jsbmb.2014.10.011

Schiller C. E., Schmidt P. J., Rubinow D. R. Allopregnanolone as a mediator of affective switching in reproductive mood disorders // Psychopharmacology (Berl). 2014. Vol. 231. no. 17. P. 3557–3567. doi: 10.1007/s00213-014-3599-x

Scholz S., Mayer I. Molecular biomarkers of endocrine disruption in small model fish // Mol. Cell. Endocrinol. 2008. Vol. 293. no. 1–2. P. 57–70. doi: 10.1016/j.mce.2008.06.008

Shen W.-J., Azhar S., Kraemer F. B. Lipid droplets and steroidogenic cells // Exp. Cell Res. 2016. Vol. 340. no. 2. P. 209–214. doi: 10.1016/j.yexcr.2015.11.024

Stein L. R., Trapp R. M., Bell A. M. Do reproduction and parenting influence personality traits? Insights from threespine stickleback // Anim. Behav. 2016. Vol. 112. P. 247–254. doi: 10.1016/j.anbehav.2015.12.002

Stoffel-Wagner B. Neurosteroid metabolism in the human brain // Eur. J. Endocrinol. 2001. Vol. 145. no. 6. P. 669–679. doi: 10.1530/eje.0.1450669

Stolte E. H., de Mazon A. F., Leon-Koosterziel K. M., Jesiak M., Bury N. R., Sturm A., Savelkoul H. F., Verburg van Kemenade B. M. L., Flik G. Corticosteroid receptors involved in stress regulation in common carp, Cyprinus carpio // J. Endocrinol. 2008. Vol. 198. no. 2. P. 403–417. doi: 10.1677/JOE-08-0100

Strous R. D., Maayan R., Weizman A. The relevance of neurosteroids to clinical psychiatry: from the laboratory to the bedside // Eur. Neuropsychopharmacol. 2006. Vol. 16. no. 3. P. 155–169. doi: 10.1016/j.euroneuro.2005.09.005

Sturm A., Bury N., Dengreville L., Fagart J., Flouriot G., Rafestin-Oblin M. E., Prunet P. 11-Deoxycorticosterone is a potent agonist of the rainbow trout (Oncorhynchus mykiss) mineralocorticoid receptor // Endocrinology. 2005. Vol. 146. no. 1. P. 47–55. doi: 10.1210/en.2004-0128

Takahashi H., Sakamoto T. The role of ‘mineralocorticoids’ in teleost fish: Relative importance of glucocorticoid signaling in the osmoregulation and ‘central’ actions of mineralocorticoid receptor // Gen. Comp. Endocrinol. 2013. Vol. 181. P. 223–228. doi: 10.1016/j.ygcen.2012.11.016

Tarkowská D., Strnad M. Plant ecdysteroids: plant sterols with intriguing distributions, biological effects and relations to plant hormones // Planta. 2016. Vol. 244. no. 3. P. 545–555. doi: 10.1007/s00425-016-2561-z

Taylor J. S., Braasch I., Frickey T., Meyer A., Van de Peer Y. Genome duplication, a trait shared by 22000 species of ray-finned fish // Genome Res. 2003. Vol. 13. no. 3. P. 382–390. doi: 10.1101/gr.640303

Thomas P. Rapid steroid hormone actions initiated at the cell surface and the receptors that mediate them with an emphasis on recent progress in fish models // Gen. Comp. Endocrinol. 2012. Vol. 175. no. 3. P. 367–383. doi: 10.1016/j.ygcen.2011.11.032

Tipsmark C. K., Breves J. P., Seale A. P., Lerner D. T., Hirano T., Grau E. G. Switching of Na+, K+-ATPase isoforms by salinity and prolactin in the gill of a cichlid fish // J. Endocrinol. 2011. Vol. 209. no. 2. P. 237–244. doi: 10.1530/JOE-10-0495

Tokarz J., Norton W., Möller G., Hrabé de Angelis M., Adamski J. Zebrafish 20β-hydroxysteroid dehydrogenase type 2 is important for glucocorticoid catabolism in stress response // PLoS One. 2013a. Vol. 8. no. 1. P. e54851. doi: 10.1371/journal.pone.0054851

Tokarz J., Möller G., Hrabé de Angelis M., Adamski J. Zebrafish and steroids: what do we know and what do we need to know? // J. Steroid Biochem. Mol. Biol. 2013b. Vol. 137. P. 165–173. doi: 10.1016/j.jsbmb.2013.01.003

Tokarz J., Möller G., Hrabě de Angelis M., Adamski J. Steroids in teleost fishes: A functional point of view // Steroids. 2015. Vol. 103. P. 123–144. doi: 10.1016/j.steroids.2015.06.011

Ubuka T., Parhar I. Dual actions of mammalian and piscine gonadotropin-inhibitory hormones, RFamide-related peptides and LPXRFamide peptides, in the hypothalamic-pituitary–gonadal axis // Front. Endocrinol. (Lausanne). 2018. Vol. 8. P. 377. doi: 10.3389/fendo.2017.00377

Veillette P. A., Sundell K., Specker J. L. Cortisol mediates the increase in intestinal fluid absorption in Atlantic salmon during parr-smolt transformation // Gen. Comp. Endocrinol. 1995. Vol. 97. no. 2. P. 250–258. doi: 10.1006/gcen.1995.1024

Viero C., Dayanithi G. Neurosteroids are excitatory in supraoptic neurons but inhibitory in the peripheral nervous system: it is all about oxytocin and progesterone receptors // Prog. Brain Res. 2008. Vol. 170. P. 177–192. doi: 10.1016/S0079-6123(08)00416-0

Vos J. G., Dybing E., Greim H. A., Ladefoged O., Lambré C., Tarazona J. V., Brandt I., Vethaak A. D. Health effects of endocrine-disrupting chemicals on wildlife, with special reference to the European situation // Crit. Rev. Toxicol. 2000. Vol. 30. no. 1. P. 71–133. doi: 10.1080/10408440091159176

de Waal P. P., Wang D. S., Nijenhuis W. A., Schulz R. W., Bogerd J. Functional characterization and expression analysis of the androgen receptor in zebrafish (Danio rerio) testis // Reproduction. 2008. Vol. 136. no. 2. P. 225–234. doi: 10.1530/REP-08-0055

Wehling M. Looking beyond the dogma of genomic steroid action: insights and facts of the 1990s // J. Mol. Med. (Berl). 1995. Vol. 73. no. 9. P. 439–447. doi: 10.1007/BF00202262

Willnow T. E., Nykjaer A. Response: Cellular Uptake of Sex Steroid Hormones // Cell. 2006. Vol. 124. no. 3. P. 456–457. doi: 10.1016/j.cell.2006.01.027

Wood C. M., Marshall W. S. Ion balance, acid-base regulation, and chloride cell function in the common killifish, Fundulus heteroclitus—a euryhaline estuarine teleost // Estuaries. 1994. Vol. 17. no. 1. P. 34-52. doi: 10.2307/1352333

Woolston C. ‘Living fossil’ genome unlocked // Nature. 2013. Vol. 496. no. 7445. P. 283–283. doi: 10.1038/496283a

Yu X., Wu L., Xie L., Yang S., Charkraborty T., Shi H., Wang D., Zhou L. Characterization of two paralogous StAR genes in a teleost, Nile tilapia (Oreochromis niloticus) // Mol. Cell. Endocrinol. 2014. Vol. 392. no. 1–2. P. 152–162. doi: 10.1016/j.mce.2014.05.013

Zhang Y., Zhang




DOI: http://dx.doi.org/10.17076/eb777

Ссылки

  • На текущий момент ссылки отсутствуют.


© Труды КарНЦ РАН, 2014-2019