THE EFFECTS OF GONADAL DEVELOPMENT AND SEX STEROIDS ON GROWTH-HORMONE SECRETION IN THE MALE TILAPIA HYBRID (OREOCHROMIS-NILOTICUS X OREOCHROMIS-AUREUS)

被引:39
作者
MELAMED, P
ELIAHU, N
OFIR, M
LEVAVISIVAN, B
SMAL, J
RENTIERDELRUE, F
YARON, Z
机构
[1] EUROGENTEC SA,B-4102 SERAING,BELGIUM
[2] UNIV LIEGE,BIOL MOLEC & GENIE GENET LAB,B-4000 LIEGE,BELGIUM
关键词
TILAPIA; OREOCHROMIS NILOTICUS X OREOCHROMIS-AUREUS; PITUITARY; GONADS; GROWTH HORMONE; GNRH; GHRH; DOPAMINE; METHYL TESTOSTERONE; ESTRADIOL; CASTRATION;
D O I
10.1007/BF00004065
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 mu M), 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 mu M) or sGnRH (1 mu M) stimulated GH release only after injection of the fish with methyl testosterone (MT; 3 injections of 0.4 mg kg-l). The same MT pretreatment did not alter the response to dopamine (DA; 1 or 10 mu M). 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 (1 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.
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页码:267 / 277
页数:11
相关论文
共 45 条
[1]  
Bates D.J., Barrett B.A., McKeown B.A., Daily variation in plasma growth hormone of juvenile coho salmon, Oncorhynchus kisutch, Canadian Journal of Zoology, 67, pp. 1246-1248, (1989)
[2]  
Berglund I., Mayer I., Borg B., Effects of sexual maturation, castration, and androgen implants on growth in one and two year old parr in a Baltic Atlantic salmon (Salmo salar L.) stock, J. Fish Biol., 40, pp. 281-292, (1992)
[3]  
Boujard T., Leatherland J.F., Circadian pattern of hepatosomatic index, liver glycogen and lipid content, plasma non-esterifled fatty acid, glucose, T<sub>3</sub>, T<sub>4</sub>, growth hormone and cortisol concentrations in Oncorhynchus mykiss held under different photoperiod regimes and fed using demand-feeders, Fish Physiology and Biochemistry, 10, pp. 111-122, (1992)
[4]  
Brooks J., Taylor P.L., Saunders P.T.K., Eidne K.A., Struthers W.J., McNeilly A.S., Cloning and sequencing of the sheep pituitary gonadotropin-releasing hormone receptor and changes in expression of its mRNA during the estrous cycle, Mol. Cell. Endocrinol., 94, pp. R23-R27, (1993)
[5]  
Chang J.P., Yu K., Wong A.O.L., Peter R.E., Differential actions of dopamine receptor subtypes on gonadotropin and growth hormone release in vitro in goldfish, Neuroendocrinology, 51, pp. 664-674, (1990)
[6]  
Chang J.P., Jobin R.M., Wong A.O.L., Intracellular mechanisms mediating gonadotropin and growth hormone release in the goldfish, Carassius auratus, Fish Physiol. Biochem., 11, pp. 25-33, (1993)
[7]  
Cook H., Berkenbosch J.W., Fernhout M.J., Yu K.-L., Peter R.E., Chang J.P., Rivier J.E., Demonstration of gonadotropin releasing-hormone receptors on gonadotrophs and somatotrophs of the goldfish: an electron microscope study, Reg. Peptides, 36, pp. 369-378, (1991)
[8]  
Cronin M.J., Rogol A.D., Sex differences in the cyclic adenosine 3′:5′-monophosphate and growth hormone response to growth hormone-releasing factor in vitro, Biol. Reprod., 31, pp. 984-988, (1984)
[9]  
Devesa J., Lois N., Arce V., Diaz M.J., Lima L., Tresguerres J.A.F., The role of sexual steroids in the modulation of growth hormone secretion in humans, J. Steroid Biochem. Molec. Biol., 40, pp. 165-173, (1991)
[10]  
Frohman L., Downs T.R., Chomczynski P., Regulation of growth hormone secretion, Frontiers in Neuroendocrinol., 13, pp. 344-405, (1992)