Skip to main content
Log in

Sexual maturation in the black seabream Mylio macrocephalus Teleostei, Sparidae: changes in pituitary gonadotropes, hepatocytes and related biochemical constituents in liver and serum

  • Published:
Cell and Tissue Research Aims and scope Submit manuscript

Summary

The black seabream, Mylio macrocephalus, exhibits the phenomenon of sex segregation. Immature fish are developing hermaphrodites, and show a considerable overlap with mature males in their body weights. Mature females tend to be the heaviest group. Fish can be classified into immature, developing and mature groups, with a further division into definitive males or females in the two latter groups. The developing groups still have bisexual gonads, whereas mature males have testes with only a comparatively inconspicuous portion of ovarian tissue, and mature females possess ovaries with vitellogenic oocytes and a greatly regressed testicular component. In the present study, monthly samples were collected over a 3-year period, and changes in pituitary gonadotropes and liver tissue studied by light, and electron microscopy. Seasonal changes in serum constituents were also studied by biochemical techniques.

Gonadotropes increased in number and became hypertrophied during sexual maturation, showing an enhanced cytoplasmic vacuolation and degranulation of alcian blue- and periodic acid-Schiff-positive material. The levels of various biochemical constituents in the liver and serum of developing fish tended to be intermediate between those recorded in the immature and mature groups. In mature fish, the serum levels of glucose, sodium and calcium were elevated, but hepatic glycogen content was less than the developing group, and hepatocytes contained activated mitochondria. The seasonal changes in pituitary cytology, hepatic ultrastructure and serum constituents, could be correlated with the metabolic adaptations to sexual maturation.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Aida K, Hirose H, Yokote M (1973) Physiological studies on gonadal maturation of fishes II. Histological changes in the liver cells of ayu following gonadal maturation and estrogen administration. Bull Jpn Soc Sci Fish 39:1107–1115

    Google Scholar 

  • D'Anconna U (1949) II differenziamento delia gonade e l'inversione sessuale degli sparidi. Arch Oceanigr Limnol 6:97–163

    Google Scholar 

  • Ball JN, Baker BI (1969) The pituitary gland: anatomy and histophysiology. In: Hoar WS, Randall DJ (eds) Fish physiology, Vol II The endocrine system. Academic Press, New York London, pp 1–111

    Google Scholar 

  • Chan STH, O WS, Tang F, Lofts B (1972) Biopsy studies on the natural sex reversal in Monopterus albus (Pisces:Teleostei). J Zool 167:415–421

    Google Scholar 

  • Dasmahapatra AK, Medda AK (1982) Effect of estradiol dipropionate and testosterone propionate on the glycogen, lipid and water contents of liver, muscle and gonad of male and female (vitellogenic and previtellogenic) Singi fish (Heteropneustes fossilis Bloch). Gen Comp Endocrinol 48:476–484

    Google Scholar 

  • Elliot JAK, Bromage MR, Whitehead C (1979) Effects of estradiol-17 on serum calcium and vitellogenin levels in rainbow trout. J Endocrinol 83:549–559

    Google Scholar 

  • Fletcher DJ (1984) Plasma glucose and plasma fatty acid levels of Limanda limanda (L.) in relation to season, stress, glucose loads and nutritional state. J Fish Biol 25:629–648

    Google Scholar 

  • Gopakumar K (1965) Seasonal variation in lipid composition of oil sardine Sardinella longiceps. Ind J Fish 12:1–5

    Google Scholar 

  • Hardig J, Hogland LB (1984) Seasonal variation in blood components of reared Baltic salmon Salmo salar. J Fish Biol 24:565–580

    Google Scholar 

  • Hartree EF (1972) Determination of protein: a modification of the Lowry method that gives a linear photometric response. Anal Biochem 48:422–427

    CAS  PubMed  Google Scholar 

  • Hoffmann R, Wonderak T, Groth W (1980) Seasonal and anatomical variation in the testis of European pike Esox lucius. J Fish Biol 16:475–482

    Google Scholar 

  • Hori SH, Kodama T, Tananakashi K (1979) Induction of vitellogenin synthesis in goldfish by massive doses of androgens. Gen Comp Endocrinol 37:306–320

    Google Scholar 

  • Jafri AK, Khawaja DK (1968) Seasonal changes in the biochemical composition of the freshwater murrel Ophiocephalus punctatus. Hydrobiologia 32:206–218

    Google Scholar 

  • Jafri AK, Khawaja DK (1970) Seasonal variation in the fat-water ratio of the liver of common pond murrel Ophiocephalus punctatus. Bioteria 34:135–142

    Google Scholar 

  • Khanna SS, Singh T (1971) Studies on the blood glucose level in Channa punctatus. Acta Zool 52:97–101

    Google Scholar 

  • Lam TJ (1983) Environmental influences on gonadal activity. In: Hoar WS, Randall DJ, Donaldson EM (eds) Fish Physiology, Vol 9, Part B, Academic Press, New York London, pp 65–116

    Google Scholar 

  • Mahajan CL, Dheer JS (1979) Seasonal variation in blood constituents of an airbreathing fish Channa punctatus. J Fish Biol 14:413–418

    Google Scholar 

  • Matthews DM, Muir GG, Baron DN (1964) Estimation of alpha-amino nitrogen in plasma and urine by the colorimetric ninhydrin reaction. J Clin Pathol 17:150–153

    Google Scholar 

  • Medda A, Dasmahapatra AK, Ray AK (1980) Effects of estrogen and testosterone on the protein and nucleic acid content of the male and female (vitellogenic and nonvitellogenic) Singi fish, Heteropneustes fossilis Bloch. Gen Comp Endocrinol 42:427–436

    Google Scholar 

  • Murat JC, Serfarty A (1974) Simple enzymatic determination of polysaccharide (glycogen) content of animal tissues. Clin Chem 20:1276–1577

    Google Scholar 

  • Ng TB, Idler TB (1983) Yolk formation and differentiation in teleost fishes. In: Hoar WS, Randall DJ, Donaldson EM (ed.) Fish Physiology, Vol 9, Part B, Academic Press, New York London, pp 373–404

    Google Scholar 

  • Ng TB, Woo NYS, Tarn PPL, Au CYW (1984) Changes in metabolism and hepatic ultrastructure induced by estradiol and testosterone in immature female Epinephelus akaara (Teleostei, Serranidae). Cell Tissue Res 236:651–659

    Google Scholar 

  • Okada YK (1965) Bisexuality in sparid fishes II. Sex segregation in Mylio macrocephalus. Proc Jpn Acad 41:300–304

    Google Scholar 

  • Olivereau M, Olivereau J (1979) Effect of estradiol-17β on the cytology of the liver, gonad and pituitary, and on the plasma electrolytes in the female freshwater eel. Cell Tissue Res 199:431–454

    Google Scholar 

  • Petersen IM, Emmersen BK (1977) Changes in serum glucose and lipids, and liver glycogen and phosphorylase during vitellogenesis in nature in the flounder (Platichtys flesus, L.). Comp Biochem Physiol 588:167–171

    Google Scholar 

  • Peute J, Van der Gang MA, Lambert JGD (1978) Ultrastructure and lipid content of the liver of the zebrafish, Brachydanio rerio, related to vitellogenin synthesis. Cell Tissue Res 186:297–308

    Google Scholar 

  • Reinboth R (1962) Morphologische und funktioneile Zweigeschlechtlichkeit bei marinen Teleostiern (Serranidae, Sparidae, Centracanthidae, Labridae). Zool Jb (Physiol) 69:405–480

    Google Scholar 

  • Tarn PPL, Ng TB, Woo NYS (1983) Effects of oestradiol-17β and testosterone on the histology of pituitary, liver, ovary and skin of previtellogenic Epinephelus akaara (Teleostei, Serranidae). Cell Tissue Res 231:579–592

    Google Scholar 

  • Woodman DD, Price CP (1972) Estimation of serum total lipids. Clin Chim Acta 38:39–43

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ng, T.B., Tam, P.P.L. & Woo, N.Y.S. Sexual maturation in the black seabream Mylio macrocephalus Teleostei, Sparidae: changes in pituitary gonadotropes, hepatocytes and related biochemical constituents in liver and serum. Cell Tissue Res. 245, 207–213 (1986). https://doi.org/10.1007/BF00218102

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00218102

Key words

Navigation