Literature DB >> 19318108

Broodstock management and hormonal manipulations of fish reproduction.

Constantinos C Mylonas1, Alexis Fostier, Silvia Zanuy.   

Abstract

Control of reproductive function in captivity is essential for the sustainability of commercial aquaculture production, and in many fishes it can be achieved by manipulating photoperiod, water temperature or spawning substrate. The fish reproductive cycle is separated in the growth (gametogenesis) and maturation phase (oocyte maturation and spermiation), both controlled by the reproductive hormones of the brain, pituitary and gonad. Although the growth phase of reproductive development is concluded in captivity in most fishes-the major exemption being the freshwater eel (Anguilla spp.), oocyte maturation (OM) and ovulation in females, and spermiation in males may require exogenous hormonal therapies. In some fishes, these hormonal manipulations are used only as a management tool to enhance the efficiency of egg production and facilitate hatchery operations, but in others exogenous hormones are the only way to produce fertilized eggs reliably. Hormonal manipulations of reproductive function in cultured fishes have focused on the use of either exogenous luteinizing hormone (LH) preparations that act directly at the level of the gonad, or synthetic agonists of gonadotropin-releasing hormone (GnRHa) that act at the level of the pituitary to induce release of the endogenous LH stores, which, in turn act at the level of the gonad to induce steroidogenesis and the process of OM and spermiation. After hormonal induction of maturation, broodstock should spawn spontaneously in their rearing enclosures, however, the natural breeding behavior followed by spontaneous spawning may be lost in aquaculture conditions. Therefore, for many species it is also necessary to employ artificial gamete collection and fertilization. Finally, a common question in regards to hormonal therapies is their effect on gamete quality, compared to naturally maturing or spawning broodfish. The main factors that may have significant consequences on gamete quality-mainly on eggs-and should be considered when choosing a spawning induction procedure include (a) the developmental stage of the gonads at the time the hormonal therapy is applied, (b) the type of hormonal therapy, (c) the possible stress induced by the manipulation necessary for the hormone administration and (d) in the case of artificial insemination, the latency period between hormonal stimulation and stripping for in vitro fertilization. Copyright 2009 Elsevier Inc. All rights reserved.

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Year:  2009        PMID: 19318108     DOI: 10.1016/j.ygcen.2009.03.007

Source DB:  PubMed          Journal:  Gen Comp Endocrinol        ISSN: 0016-6480            Impact factor:   2.822


  36 in total

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2.  Studies in zebrafish reveal unusual cellular expression patterns of gonadotropin receptor messenger ribonucleic acids in the testis and unexpected functional differentiation of the gonadotropins.

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3.  Relation of gilthead seabream (Sparus aurata) seasonal reproductive activity to hematology, serum biochemistry, histopathology, and Brdt gene expression.

Authors:  Salah M Aly; Safaa M Sharaf; Abeer A I Hassanin; Alaa Sh Griesh
Journal:  Fish Physiol Biochem       Date:  2021-05-10       Impact factor: 2.794

4.  Effect of oral administration of GnRHa+nanoparticles of chitosan in oogenesis acceleration of goldfish Carassius auratus.

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5.  The involvement of gonadotropins and gonadal steroids in the ovulatory dysfunction of the potamodromous Salminus hilarii (Teleostei: Characidae) in captivity.

Authors:  Renata Guimarães Moreira; Renato Massaaki Honji; Renato Garcia Melo; Amanda de Moraes Narcizo; Juliane Suzuki Amaral; Ronaldo de Carvalho Araújo; Alexandre Wagner Silva Hilsdorf
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6.  Sperm quality of greater amberjack Seriola dumerili throughout the reproductive season and in response to GnRHa treatment with controlled release implants.

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Journal:  Fish Physiol Biochem       Date:  2021-01-06       Impact factor: 2.794

7.  Influence of light intensity and spectral composition of artificial light at night on melatonin rhythm and mRNA expression of gonadotropins in roach Rutilus rutilus.

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8.  Induction of Gonadal Development in Protogynous Grouper with Orally Delivered FSH DNA.

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9.  Effects of luteinizing hormone-releasing hormone and arginine-vasotocin on the sperm-release response of Günther's Toadlet, Pseudophryne guentheri.

Authors:  Aimee J Silla
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10.  Isolation of the pituitary gonadotrophic α-subunit hormone of the giant amazonian fish: pirarucu (Arapaima gigas).

Authors:  M T Faria; R F Carvalho; T C A Sevilhano; N A J Oliveira; C F P Silva; J E Oliveira; C R J Soares; R Garcez; P R E Santo; P Bartolini
Journal:  Fish Physiol Biochem       Date:  2012-10-17       Impact factor: 2.794

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