ÉTUDE COMPARÉE DE L'ACTION DES HORMONES HYPOPHYSAIRES ET STÉROÏDES SUR LA MATURATION IN VITRO DES OVOCYTES DE LA TRUITE ET DU CARASSIN (POISSONS TÉLÉOSTÉENS)
Ann. Biol. anim. Bioch. Biophys., 13 Hors-série (1973) 59-73
Articles citing this article
The Citing articles tool gives a list of articles citing the current article.
The citing articles come from EDP Sciences database, as well as other publishers participating in CrossRef Cited-by Linking Program. You can set up your personal account to receive an email alert each time this article is cited by a new article (see the menu on the right-hand side of the abstract page).
Cited article:
This article has been cited by the following article(s):
Special features of neuroendocrine interactions between stress and reproduction in teleosts
Karine Rousseau, Patrick Prunet and Sylvie DufourGeneral and Comparative Endocrinology 300 113634 (2021)
https://doi.org/10.1016/j.ygcen.2020.113634
Transfection of isolated rainbow trout, Oncorhynchus mykiss, granulosa cells through chemical transfection and electroporation at 12 °C
E. Marivin, B. Mourot, P. Loyer, et al.General and Comparative Endocrinology 221 165 (2015)
https://doi.org/10.1016/j.ygcen.2015.03.012
Out‐of‐season production of 17,20β‐dihydroxypregn‐4‐en‐3‐one in the roach Rutilus rutilus
A. P. Scott, T. Hill, N. Beresford, T. J. Runnalls, J. P. Sumpter and T. EllisJournal of Fish Biology 83 (2) 233 (2013)
https://doi.org/10.1111/jfb.12150
Determination of hormones inducing oocyte maturation in Chalcalburnus tarichi (Pallas, 1811)
G. Ünal, E. Erdoğan, A. R. Oğuz, et al.Fish Physiology and Biochemistry 34 (4) 447 (2008)
https://doi.org/10.1007/s10695-008-9203-8
Targeted Gene Expression Profiling in the Rainbow Trout (Oncorhynchus mykiss) Ovary During Maturational Competence Acquisition and Oocyte Maturation
Julien Bobe, Thaovi Nguyen and Bernard JalabertBiology of Reproduction 71 (1) 73 (2004)
https://doi.org/10.1095/biolreprod.103.025205
In vivo and in vitro effects of 17α,20β-dihydroxy-4-pregnene-3-one on testicular androgens in atlantic salmon,Salmo salar, mature parr
Efthimia Antonopoulou, Staffan Jakobsson, Ian Mayer, Penny Swanson and Bertil BorgThe Journal of Experimental Zoology 277 (1) 66 (1997)
https://doi.org/10.1002/(SICI)1097-010X(19970101)277:1<66::AID-JEZ7>3.0.CO;2-9
Effects of Incubation Media on Maturation of Isolated Ovarian Follicles of Siberian Sturgeon (Acipenser baeri Brandt) Induced by Sturgeon Gonadotropic Preparation or 17α,20β-Dihydroxyprogesterone
P. WilliotComparative Biochemistry and Physiology Part C: Pharmacology, Toxicology and Endocrinology 118 (3) 285 (1997)
https://doi.org/10.1016/S0742-8413(97)00178-3
Principles of Salmonid Culture
Roland Billard and Jørgen (JOHN) O.T. JensenDevelopments in Aquaculture and Fisheries Science, Principles of Salmonid Culture 29 291 (1996)
https://doi.org/10.1016/S0167-9309(96)80008-1
Impact of γ-hexachlorocyclohexane on the in vitro production of steroids from endogenous and exogenous precursors in the spermiating roach, Rutilus rutilus
Pratap B. Singh and David E. KimeAquatic Toxicology 31 (3) 231 (1995)
https://doi.org/10.1016/0166-445X(94)00068-2
Impact of γ‐hexachlorocyclohexane exposure on plasma gonadotropin levels and in vitro stimulation of gonadal steroid production by carp hypophyseal homogenate in Carassius auratus
P. B. Singh, D. E. Kime, P. Epler and J. ChybJournal of Fish Biology 44 (2) 195 (1994)
https://doi.org/10.1111/j.1095-8649.1994.tb01198.x
Substrate concentration affects the in vitro metabolism of 17-hydroxyprogesterone by ovaries of the carp, Cyprinus carpio
David E. Kime, Mohammad A. S. Abdullah, Miroslawa Sokolowska-Mikolajczyk and Piotr EplerFish Physiology and Biochemistry 13 (4) 317 (1994)
https://doi.org/10.1007/BF00003436
Effect of Dietary Keto Acids on Intermediary Metabolism of Nutrients in Atlantic Salmon (Salmo salar) during 17-β-Estradiol-Induced Vitellogenin Synthesis
Thomas Olin, Eva Bergström, Hans Jungvid and Alexandra von der DeckenActa Agriculturae Scandinavica, Section A - Animal Science 42 (4) 246 (1992)
https://doi.org/10.1080/09064709209410136
Progestogen metabolism by ovaries of the roach (Rutilus rutilus L.) and the rudd (Scardinius erythrophthalmus L.)
David E. KimeFish Physiology and Biochemistry 9 (5-6) 497 (1992)
https://doi.org/10.1007/BF02274230
A comparison of tritiated vitellogenins prepared by in vivo and in vitro techniques for studies of ovarian uptake in fish
James J. Nagler, David R. Idler and Ying P. SoJournal of Experimental Zoology 264 (1) 107 (1992)
https://doi.org/10.1002/jez.1402640116
Effect of salmon gonadotropic hormone on sex steroids in male rainbow trout: plasma levels and testicular secretion in vitro
R. W. Schulz, M. Andriske, P. J. Lembke and V. Bl�mJournal of Comparative Physiology B 162 (3) 224 (1992)
https://doi.org/10.1007/BF00357528
Animal Species for Developmental Studies
G. M. IgnatievaAnimal Species for Developmental Studies 89 (1991)
https://doi.org/10.1007/978-1-4615-3654-3_4
Extragonadal 17β-hydroxysteroid dehydrogenase activity in rainbow trout
Rüdiger Schulz and Volker BlümGeneral and Comparative Endocrinology 82 (2) 197 (1991)
https://doi.org/10.1016/0016-6480(91)90184-8
The insemination of goldfish (Carassium auratus) oocyte maturedin vitro
Wang Renxue, Wu Xianhan, Zhou Jing, et al.Chinese Journal of Oceanology and Limnology 9 (1) 88 (1991)
https://doi.org/10.1007/BF02849794
Stimulation of in vitro ovarian estradiol-17β synthesis in the rainbow trout by the carbohydrate-poor protein fraction from sockeye salmon pituitary glands
James J. Nagler and David R. IdlerThe Journal of Steroid Biochemistry and Molecular Biology 39 (4) 513 (1991)
https://doi.org/10.1016/0960-0760(91)90245-Z
Conversion of 11-ketoandrostenedione to 11-ketotestosterone by blood cells of six fish species
Ian Maye, Bertil Borg and Rüdiger SchulzGeneral and Comparative Endocrinology 77 (1) 70 (1990)
https://doi.org/10.1016/0016-6480(90)90207-3
Steroid secretion of rainbow trout testis in vitro: Variation during the reproductive cycle
Rüdiger Schulz and Volker BlümGeneral and Comparative Endocrinology 80 (2) 189 (1990)
https://doi.org/10.1016/0016-6480(90)90164-H
Evidence for an androgen binding protein in the testis of a teleost fish (Salmo gairdneri R.): A potential marker of sertoli cell function
Jean-Luc Foucher and Florence Le GacJournal of Steroid Biochemistry 32 (4) 545 (1989)
https://doi.org/10.1016/0022-4731(89)90388-9
Structure-activity relationships of C21 steroids in an in vitro oocyte maturation bioassay in rainbow trout, Salmo gairdneri
A.V.M. Canario and A.P. ScottGeneral and Comparative Endocrinology 71 (2) 338 (1988)
https://doi.org/10.1016/0016-6480(88)90262-6
Salmon gonadotropin (sGTH) immunoreactivity and 11-oxotestosterone secretion of mature rainbow trout (Salmo gairdneri) testes in vitro: an alternative to radio-receptor assay for sGTH-binding studies
R�diger Schulz, HenkJ.Th. Goos and Volker Bl�mCell and Tissue Research 251 (3) 665 (1988)
https://doi.org/10.1007/BF00214015
Recent trends in research on induced spawning of fish in aquaculture
M. AbrahamJournal of Applied Ichthyology 4 (2) 49 (1988)
https://doi.org/10.1111/j.1439-0426.1988.tb00468.x
Oocyte Growth and Maturation
T. A. DettlaffOocyte Growth and Maturation 165 (1988)
https://doi.org/10.1007/978-1-4684-0682-5_3
Gonadotropin stimulated androgen secretion of rainbow trout (Salmo gairdneri richardson) testis In vitro
Rüdiger Schulz and Volker BlümComparative Biochemistry and Physiology Part A: Physiology 88 (1) 49 (1987)
https://doi.org/10.1016/0300-9629(87)90097-1
The effect of pimozide/LHRHa and 17α-hydroxyprogesterone on plasma steroid levels and ovulation in the African catfish, Clarias gariepinus
C.J.J. Richter, E.H. Eding, H.J.Th. Goos, et al.Aquaculture 63 (1-4) 157 (1987)
https://doi.org/10.1016/0044-8486(87)90068-8
Effects of carp hypophyseal homogenate doses, incubation times, and temperatures on carp oocyte maturation and steroidogenesis in vitro
P. Epler, D.E. Kime, Nguyen Kiem Son and K. BieniarzGeneral and Comparative Endocrinology 66 (3) 343 (1987)
https://doi.org/10.1016/0016-6480(87)90243-7
Gonadotropin-induced changes in steroid production by ovaries of the common careCyprinus carnio L. around the time of ovulation
David E. Kime and Krzysztof BieniarzFish Physiology and Biochemistry 3 (1) 49 (1987)
https://doi.org/10.1007/BF02183993
Autoradiographic localization of gonadotrophin receptors in ovaries of the common carp, Cyprinus carpio L
Krzysztof Bieniarz and David E. KimeGeneral and Comparative Endocrinology 64 (1) 151 (1986)
https://doi.org/10.1016/0016-6480(86)90041-9
Immunocytochemical demonstration of steroid hormones in the granulosa cells of the medaka, Oryzias latipes
Kazuo Onitake and Takashi IwamatsuJournal of Experimental Zoology 239 (1) 97 (1986)
https://doi.org/10.1002/jez.1402390112
Short-term profiles of plasma gonadotropin and 17α-hydroxy, 20β-dihydroprogesterone levels in the female rainbow trout at the periovulatory period
Y. Zohar, B. Breton and A. FostierGeneral and Comparative Endocrinology 64 (2) 189 (1986)
https://doi.org/10.1016/0016-6480(86)90003-1
In vitro metabolism of steroid hormones in the liver and in blood cells of male rainbow trout (Salmo gairdneri Richardson)
Rüdiger SchulzGeneral and Comparative Endocrinology 64 (2) 312 (1986)
https://doi.org/10.1016/0016-6480(86)90019-5
In vitro induction of Xenopus oocyte maturation by 4-pregnene-17α,20β-diol-3-one
Amrut K. Deshpande and S.S. KoideGeneral and Comparative Endocrinology 57 (1) 130 (1985)
https://doi.org/10.1016/0016-6480(85)90209-6
Comparative aspects of the assay of carp gonadotropin
D.R Idler, H.C.H Komourdjian and M.D WiegandComparative Biochemistry and Physiology Part A: Physiology 79 (3) 441 (1984)
https://doi.org/10.1016/0300-9629(84)90542-5
Relative in vitro effectiveness of 17α,20β-dihydroxy-4-pregnen-3-one and other pregnene derivatives on germinal vesicle breakdown in oocytes of ayu (Plecoglossus altivelis), amago salmon (Oncorhynchus rhodurus), rainbow trout (Salmo gairdneri), and goldfish (Carassius autatus)
Yoshitaka Nagahama, Keiji Hirose, Graham Young, Shinji Adachi, Keiko Suzuki and Bun-ichi TamaokiGeneral and Comparative Endocrinology 51 (1) 15 (1983)
https://doi.org/10.1016/0016-6480(83)90092-8
Impairment of early ovarian growth in landlocked Atlantic salmon by an antibody to carbohydrate-rich gonadotropin
Murray D. Wiegand and David R. IdlerGeneral and Comparative Endocrinology 49 (2) 210 (1983)
https://doi.org/10.1016/0016-6480(83)90137-5
Reproduction - Behavior and Fertility Control
Frederick W. GoetzFish Physiology, Reproduction - Behavior and Fertility Control 9 117 (1983)
https://doi.org/10.1016/S1546-5098(08)60303-9
Estradiol-17β production in isolated amago salmon (Oncorhynchus rhodurus) ovarian follicles and its stimulation by gonadotropins
Hirohiko Kagawa, Graham Young and Yoshitaka NagahamaGeneral and Comparative Endocrinology 47 (3) 361 (1982)
https://doi.org/10.1016/0016-6480(82)90245-3
Oocyte maturation in the amago salmon (Oncorhynchus rhodurus): In vitro effects of salmon gonadotropin, steroids, and cyanoketone (an inhibitor of 3β‐hydroxy‐Δ5‐steroid dehydrogenase)
Graham Young, Hirohiko Kagawa and Yoshitaka NagahamaJournal of Experimental Zoology 224 (2) 265 (1982)
https://doi.org/10.1002/jez.1402240217
Inhibitory effect of cyanoketone on salmon gonadotropin-induced estradiol-17β production by ovarian follicles of the amago salmon (Oncorhynchus rhodurus) in vitro
Graham Young, Hirohiko Kagawa and Yoshitaka NagahamaGeneral and Comparative Endocrinology 47 (3) 357 (1982)
https://doi.org/10.1016/0016-6480(82)90244-1
The in vitro effects of 17α-hydroxy-20β-dihydroprogesterone on germinal vesicle breakdown in brook trout (Salvelinus fontinalis) oocytes
Richard J. Duffey and Frederick W. GoetzGeneral and Comparative Endocrinology 41 (4) 563 (1980)
https://doi.org/10.1016/0016-6480(80)90062-3
The metabolism of gonadotropin in goldfish, Carassius auratus: Tissue uptake and distribution during the reproductive cycle
Alan Frank Cook and R.E. PeterGeneral and Comparative Endocrinology 42 (1) 91 (1980)
https://doi.org/10.1016/0016-6480(80)90260-9
Differential sensitivity of cells of follicular epithelium and oocytes in the stellate sturgeon to unfavorable conditions, and correlating influence of triiodothyronine
T.A. Dettlaff and S.I. DavydovaGeneral and Comparative Endocrinology 39 (2) 236 (1979)
https://doi.org/10.1016/0016-6480(79)90228-4
In vitro stimulation of germinal vesicle breakdown and ovulation of yellow perch (Perca flavescens) oocytes. Effects of 17α-hydroxy-20β-dihydroprogesterone and prostaglandins
Frederick Wm. Goetz and Georgia TheofanGeneral and Comparative Endocrinology 37 (3) 273 (1979)
https://doi.org/10.1016/0016-6480(79)90001-7
Some aspects of oocyte maturation in catfish
Bangalore I. Sundararaj, Shashi V. Goswami and Virenderjeet LambaJournal of Steroid Biochemistry 11 (1) 701 (1979)
https://doi.org/10.1016/0022-4731(79)90003-7
Hormonal Steroids
BANGLORE I. SUNDARARAJ, SHASHI V. GOSWAMI and VIRENDERJEET LAMBAHormonal Steroids 701 (1979)
https://doi.org/10.1016/B978-0-08-023796-1.50103-1
Effect of teleost pituitary gonadotropins on the in vitro maturation of carp oocytes
Piotr Epler, Ewa Marosz and Krzysztof BieniarzAquaculture 18 (4) 379 (1979)
https://doi.org/10.1016/0044-8486(79)90041-3
Studies on oocyte maturation of the medaka, Oryzias latipes V. On the structure of steroids that induce maturation in vitro
Takashi IwamatsuJournal of Experimental Zoology 204 (3) 401 (1978)
https://doi.org/10.1002/jez.1402040311
The histological picture of the hypothalamus (the nucleus preopticus) and hypophysis in male Anguilla anguilla L. treated with hormones
M. Sokolowska, P. Epler and K. BieniarzJournal of Fish Biology 12 (1) 1 (1978)
https://doi.org/10.1111/j.1095-8649.1978.tb04143.x
A new tool for induced spawning: The use of 17α-hydroxy-20β-dihydroprogesterone to spawn carp at low temperature
B. Jalabert, B. Breton, E. Brzuska, A. Fostier and J. WieniawskiAquaculture 10 (4) 353 (1977)
https://doi.org/10.1016/0044-8486(77)90126-0
Hormonal regulation of in vivo and in vitro oocyte maturation in the catfish, Heteropneustes fossilis (bloch)
Bangalore I. Sundararaj and Shashi V. GoswamiGeneral and Comparative Endocrinology 32 (1) 17 (1977)
https://doi.org/10.1016/0016-6480(77)90079-X
Steroids in the plasma of the winter flounder (Pseudopleuronectes americanus walbaum). A seasonal study and investigation of steroid involvement in oocyte maturation
C.M. Campbell, J.M. Walsh and D.R. IdlerGeneral and Comparative Endocrinology 29 (1) 14 (1976)
https://doi.org/10.1016/0016-6480(76)90002-2
In vitro ovulation of trout oocytes : Effect of prostaglandins on smooth muscle-like cells of the theca
Bernard Jalabert and Daniel SzöllösiProstaglandins 9 (5) 765 (1975)
https://doi.org/10.1016/0090-6980(75)90113-6
Effects of ovine luteinizing hormone and porcine adrenocorticotropin on maturation of oocytes of the catfish, Heteropneustes fossilis (Bloch), in ovary-interrenal coculture
Bangalore I. Sundararaj and Shashi V. GoswamiGeneral and Comparative Endocrinology 23 (3) 276 (1974)
https://doi.org/10.1016/0016-6480(74)90070-7