Literature DB >> 24197495

The effects of gonadal development and sex steroids on growth hormone secretion in the male tilapia hybrid (Oreochromis niloticus × O. aureus).

P Melamed1, N Eliahu, M Ofir, B Levavi-Sivan, J Smal, F Rentier-Delrue, Z Yaron.   

Abstract

Profiles of plasma growth hormone (GH) in male tilapia hybrid (Oreochromis niloticus x O. aureus) were measured and compared at different times of the year. The profiles did not appear to be repetitive, however, differences in their nature were observed at the different seasons; the most erratic profiles were seen in the height of the reproductive season (July), while the peaks were more subdued in the spring and disappeared in the autumn. Peaks in male fish were more prominent than in the females when measured in July. Perifused pituitary fragments from fish with a high GSI responded to salmon gonadotropin-releasing hormone (sGnRH) analog (10 nM-1 μM), while those from fish with a low GSI barely responded to even the highest dose. Exposure of perifused pituitary fragments from sexually-regressed fish to carp growth hormone-releasing hormone (cGHRH; 0.1 μM) or sGnRH (I μM) stimulated GH release only after injection of the fish with methyl testosterone (MT; 3 injections of 0.4 mg kg (1)). The same MT pretreatment did not alter the response to dopamine (DA; 1 or 10 μM). GH pituitary content in MT-treated fish was lower than in control fish, which may be explained by the higher circulating GH levels in these fish, but does not account for the increased response to the releasing hormones. Castration abolished the response of cultured pituitary cells to sGnRH (I fM-100 nM) without altering either their basal rate of secretion or circulating GH levels. Addition of steroids to the culture medium (MT or estradiol at 10 nM for 2 days) enabled a GH response to sGnRH stimulation in cells from sexually regressed fish. Pituitary cells which had not been exposed to steroids failed to respond to sGnRH, although their response to forskolin or TPA was similar to that of steroid-exposed cells. It would appear, therefore, that at least one of the effects of the sex steroids on the response to GnRH is exerted proximally to the formation of cAMP, or PKC, presumably at the level of the receptor. An increase in the number of receptors to the GH-releasing hormones, following steroid exposure, would explain also the changing nature of the GH secretory profile in different stages of the reproductive season.

Entities:  

Year:  1995        PMID: 24197495     DOI: 10.1007/BF00004065

Source DB:  PubMed          Journal:  Fish Physiol Biochem        ISSN: 0920-1742            Impact factor:   2.794


  41 in total

1.  Pituitary gonadotropin-releasing hormone (GnRH) receptor activity in goldfish and catfish: seasonal and gonadal effects.

Authors:  H R Habibi; R De Leeuw; C S Nahorniak; H J Goos; R E Peter
Journal:  Fish Physiol Biochem       Date:  1989-06       Impact factor: 2.794

2.  Does the time of feeding affect the diurnal rhythms of plasma hormone and glucose concentration and hepatic glycogen content of rainbow trout?

Authors:  P K Reddy; J F Leatherland
Journal:  Fish Physiol Biochem       Date:  1994-06       Impact factor: 2.794

3.  Effects of ovariectomy and oestrogen treatment on the ultrastructure of the adenohypophysis in the teleost Poecilia latipinna [proceedings].

Authors:  G Young; J N Ball
Journal:  J Endocrinol       Date:  1979-10       Impact factor: 4.286

4.  Differential effects of neonatal and adult androgen exposure on the growth hormone secretory pattern in male rats.

Authors:  J O Jansson; L A Frohman
Journal:  Endocrinology       Date:  1987-04       Impact factor: 4.736

5.  Circadian pattern of hepatosomatic index, liver glycogen and lipid content, plasma non-esterified fatty acid, glucose, T3, T 4, growth hormone and cortisol concentrations in Oncorhynchus mykiss held under different photoperiod regimes and fed using demand-feeders.

Authors:  T Boujard; J F Leatherland
Journal:  Fish Physiol Biochem       Date:  1992-08       Impact factor: 2.794

6.  Hypothalamic and thyroidal regulation of growth hormone in tilapia.

Authors:  P Melamed; N Eliahu; B Levavi-Sivan; M Ofir; O Farchi-Pisanty; F Rentier-Delrue; J Smal; Z Yaron; Z Naor
Journal:  Gen Comp Endocrinol       Date:  1995-01       Impact factor: 2.822

7.  Development and validation of a highly sensitive radioimmunoassay for chinook salmon (Oncorhynchus tshawytscha) growth hormone.

Authors:  P Y Le Bail; J P Sumpter; J F Carragher; B Mourot; P D Niu; C Weil
Journal:  Gen Comp Endocrinol       Date:  1991-07       Impact factor: 2.822

8.  The effect of feeding methyltestosterone on the growth and body composition of common carp (Cyprinus carpio L.).

Authors:  K P Lone; A J Matty
Journal:  Gen Comp Endocrinol       Date:  1980-04       Impact factor: 2.822

9.  Ultrastructural changes in the adenohypophysis during the ovarian cycle of the viviparous teleost Poecilia latipinna. III. The growth hormone, adrenocorticotrophic, and prolactin cells and the pars intermedia.

Authors:  G Young; J N Ball
Journal:  Gen Comp Endocrinol       Date:  1983-10       Impact factor: 2.822

10.  Interactions of somatostatin, gonadotropin-releasing hormone, and the gonads on dopamine-stimulated growth hormone release in the goldfish.

Authors:  A O Wong; J P Chang; R E Peter
Journal:  Gen Comp Endocrinol       Date:  1993-12       Impact factor: 2.822

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  2 in total

1.  Expression and ontogeny of growth hormone (Gh) in the protogynous hermaphroditic ricefield eel (Monopterus albus).

Authors:  Dong Chen; Jiang Liu; Wanping Chen; Shuxia Shi; Weimin Zhang; Lihong Zhang
Journal:  Fish Physiol Biochem       Date:  2015-07-23       Impact factor: 2.794

2.  Comparing Transcriptomes Reveals Key Metabolic Mechanisms in Superior Growth Performance Nile Tilapia (Oreochromis niloticus).

Authors:  Binglin Chen; Wei Xiao; Zhiying Zou; Jinglin Zhu; Dayu Li; Jie Yu; Hong Yang
Journal:  Front Genet       Date:  2022-07-12       Impact factor: 4.772

  2 in total

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