Hostname: page-component-586b7cd67f-2brh9 Total loading time: 0 Render date: 2024-11-26T15:09:07.276Z Has data issue: false hasContentIssue false
  • English
  • Français

Gonadotropic Mitogenic Activity of the Optic Gland of the Cuttlefish, Sepia Officinalis, During Sexual Maturation

Published online by Cambridge University Press:  11 May 2009

N. Koueta ,
E. Camou-Boucaud  and
A.M. Renou
N. Koueta
Affiliation:
Laboratoire de Biologie et Biotechnologies Marines, Université de Caen, 14032 Caen Cedex, France
E. Camou-Boucaud
Affiliation:
Laboratoire de Biologie et Biotechnologies Marines, Université de Caen, 14032 Caen Cedex, France
A.M. Renou
Affiliation:
Laboratoire de Biologie et Biotechnologies Marines, Université de Caen, 14032 Caen Cedex, France
Get access Rights & Permissions [Opens in a new window]

Extract

A cytological study was carried out on the main cells of the optic gland of male and female Sepia officinalis L. during sexual maturation (animals collected in the field). The results were correlated with experimental data on the mitogenic action of optic gland extracts collected during a period of secretory activity.

The main cells of the optic gland show some of the features of protein-secreting cells, although they are not very pronounced. The secretory activity of the cell was found to be correlated with a peak of mitogenic activity occurring in September/October in the case of the males and in November in that of the females. The secretion of gonadotropic mitogenic factor varies throughout the sexual cycle of Sepia officinalis. This activity is correlated with a rapid multiplication of spermatocytes and spermatogonia in the males, whereas in the females it corresponds to previtellogenesis.

Type
Research Article
Information
Journal of the Marine Biological Association of the United Kingdom , Volume 75 , Issue 2 , May 1995 , pp. 391 - 404
Copyright
Copyright © Marine Biological Association of the United Kingdom 1995

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Bottke, W., 1974. The fine structure of the ovarian follicle of Alloteuthis subulata Lam. (Mollusca, Cephalopoda). Cell and Tissue Research, 150, 463–479.CrossRefGoogle ScholarPubMed
Boucaud-Camou, E., Koueta, N., Boismery, J. & Medhioub, A., 1991. The sexual cycle of Sepia officinalis L. from the Bay of Seine. In The cuttlefish. Ada 1st international symposium on the cuttlefish Sepia (ed. E., Boucaud-Camou), pp. 141–151. Université de Caen: Centre de Publications.Google Scholar
Boucaud-Camou, E., Medhioub, A. & Catania, R., 1988. Développement du follicule ovarien chez la seiche Sepia officinalis L. Bulletin de la Société Zoologique de France, 113, 257–262.Google Scholar
Bresnick, E. & Mosse, H., 1966. Aspartate carbamoyltransferase from rat liver. Biochemical Journal, 101, 63–69.CrossRefGoogle ScholarPubMed
Cosquer, L. & Boucaud-Camou, E., 1991. Isolation, separation and culture of cells from the gonads of Sepia officinalis L. (Mollusca: Cephalopoda): preliminary results. In The cuttlefish. Ada 1st international symposium on the cuttlefish Sepia (ed. E., Boucaud-Camou), pp. 263–270. Université de Caen: Centre de Publications.Google Scholar
Durchon, M. & Richard, A., 1967. Étude en culture organotypique, du rôle endocrine de la glande optique dans la maturation ovarienne chez Sepia officinalis L. (Mollusque: Céphalopode). Comptes Rendus de l'Académie des Sciences. Paris, 265D, 1497–1500.Google Scholar
Froesch, D., 1979. Antigen-induced secretion in the optic gland of Octopus vulgaris. Proceedings of the Royal Society B, 205, 379–384.Google ScholarPubMed
Koueta, N. & Boucaud-Camou, E., 1986. Study of the secretion of the posterior salivary gland of decapod cephalopods:Sepia officinalis L. Cellular and Molecular Biology, 32, 333–341.Google ScholarPubMed
Koueta, N. & Boucaud-Camou, E., 1991. Aspartate transcarbamylase activity: a bioassay for a gonial-mitosis stimulating factor from the optic gland of Sepia officinalis L. In The cuttlefish. Acta 1st international symposium on the cuttlefish Sepia (ed. E., Boucaud-Camou), pp. 271–279. Universite de Caen: Centre de Publications.Google Scholar
Koueta, N. & Boucaud-Camou, E., 1992. Changes of aspartate transcarbamylase activity in the gonad of Sepia officinalis L. during the sexual cycle. Comparative Biochemistry and Physiology, 102B, 413–418.Google Scholar
Koueta, N., Boucaud-Camou, E. & Renou, A.M., 1993. Etude cytologique des gonades au cours de la maturation sexuelle des Seiches Sepia officinalis L. de la Baie de Seine: intérêt pour une étude expérimentale. Cahiers de Biologie Marine, 34, 461–476.Google Scholar
Koueta, N., Mathieu, M. & Boucaud-Camou, E., 1987. Aspartate transcarbamylase activity in Sepia officinalis L. (Mollusca: Cephalopoda). Comparative Biochemistry and Physiology, 87B, 351–356.Google Scholar
Koueta, N., Robbins, I. & Boucaud-Camou, E., 1992. Partial characterization of a gonadotropic mitogenic factor from the optic gland and hemolymph of the cuttlefish Sepia officinalis L. Comparative Biochemistry and Physiology, 102A, 229–234.CrossRefGoogle Scholar
Lenoir, F. & Mathieu, M., 1986. Utilisation de cultures de cellules dissociees dans l'étude des contrôles exercés sur la gamétogénèse chez la moule Mytilus edulis L. Comptes Rendus de l'Académie des Sciences. Paris, 303, 523–528.Google Scholar
Mangold, K., 1983. Food, feeding and growth in cephalopods. Memoirs of the Natural Museum Victoria, 44, 81–93.CrossRefGoogle Scholar
Mangold, K., 1987. Reproduction. In Cephalopod life cycles. Vol. II. Comparative reviews (ed. P.R., Boyle), pp. 157–200, London: Academic Press.Google Scholar
Mangold, K., 1989. Anatomie, systématique et biologie des Céphalopodes. Traitedé Zoologie, tome V, fascicule 4, Paris: Masson et Cie.Google Scholar
Mangold, K. & Froesch, D., 1977. A reconsideration of factors associated with sexual maturation. Symposia of the Zoological Society of London, 38, 541–555.Google Scholar
Mathieu, M., Bergeron, J.P. & Alayse-Danet, A.M., 1982. L'aspartate transcarbamylase, indice d'activité gamétogénétique chez la moule Mytilus edulis. International journal of Invertebrate Reproduction. Amsterdam, 5, 337–343.CrossRefGoogle Scholar
Medhioub, A. & Boucaud-Camou, E., 1989. Etude de la maturation gonadique de la seiche, Sepia officinalis L. des cotes Normandes. Haliotis, 19, 183–188.Google Scholar
Phillips, H.J., 1973. Dye exclusion test for cell viability. In Tissue culture methods and applications (ed. P.P., Kruse Jr and M.K., Patterson), pp. 406–408. New York: Academic Press.CrossRefGoogle Scholar
Porter, R.W., Modebe, M.O. & Stark, G.R., 1969. Aspartate transcarbamylase kinetic studies of the catalytic subunit. Journal of Biological Chemistry, 244, 1846–1859.CrossRefGoogle ScholarPubMed
Reynolds, E.S., 1963. The use of lead citrate of high pH as an electron opaque stain in electron microscopy. Journal of Cell Biology, 17, 208–213.CrossRefGoogle ScholarPubMed
Richard, A., 1971. Contribution à l'étude expérimental de la croissance et de la maturation sexuelle de Sepia officinalis L. (Mollusque: Céphalopode). Thèse Doctorat des Sciences Naturelles, Université de Lille.Google Scholar
Roth, T.F. & Porter, K.R., 1964. Yolk protein uptake in the oocyte of the mosquito Aedes aegypti L. Journal of Cell Biology, 20, 313–322.CrossRefGoogle ScholarPubMed
Tait, R.W., 1986. Aspects physiologiques de la sénescence post reproductive chez Octopus vulgaris. Thèse Doctorat d'Université de Paris VI.Google Scholar
Tresgots, A., 1982. Etude en cultures organotypiques de la glande digestive de Sepia officinalis L. Essais d'association avec la glande optique. Thése Doctorat 3éme cycle, Université de Caen.Google Scholar
Wells, M.J. & Wells, J., 1959. Hormonal control of sexual maturity in Octopus. Journal of Experimental Biology, 36, 1–33.CrossRefGoogle Scholar
Wells, M.J. & Wells, J., 1977. Optic glands and the endocrinology of reproduction. Symposia of the Zoological Society of London, 38, 525–540.Google Scholar
Wodinsky, J., 1977. Hormonal inhibition of feeding and death in Octopus: control by optic gland secretion. Science, New York, 198, 948–951.CrossRefGoogle ScholarPubMed