Literature DB >> 2357725

Cellular composition and steroidogenic capacity of the ovary of Macrotus californicus (Chiroptera: Phyllostomatidae) during and after delayed embryonic development.

E G Crichton1, P B Hoyer, P H Krutzsch.   

Abstract

In the leaf-nosed bat, Macrotus californicus, a 4.5-month period of delayed early embryogenesis (October-March) precedes a 3.5-month period of normal embryogenesis (March-June). This prolonged gestation provides a unique opportunity to correlate ovarian changes with the events following implantation. The present study investigated luteal cell development and follicular biology during gestation. Circulating progesterone (P) levels following implantation were unchanged before transition to normal development, and were maximal at the start of active gestation. Luteal cell diameters increased during this period. Serum P levels declined prior to parturition, when cells staining positive for 3 beta-hydroxy-5-steroid dehydrogenase-5,4-isomerase (3 beta-HSD) activity were reduced in number and diameter, and enzyme staining was less intense in tissue slices. Subcellular steroidogenic organelles were present during delayed development, but smooth endoplasmic reticulum (SER) was markedly increased after the resumption of normal development at which time also luteal cells reacted positively to staining for 17 beta-HSD. Before parturition, lipid droplet accumulation and reduced SER suggested a reduction in steroid secretion. Large multilaminar follicles stained positive for 3 beta-HSD activity throughout gestation and for 17 beta-HSD except in late delayed development. Thus, the delay in embryogenesis may be due to an inadequately developed corpus luteum or to the steroidogenic activity of the multilaminar follicles.

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Year:  1990        PMID: 2357725     DOI: 10.1007/bf00318638

Source DB:  PubMed          Journal:  Cell Tissue Res        ISSN: 0302-766X            Impact factor:   5.249


  44 in total

1.  Granulosa cell maturation in the rat: increased binding of human chorionic gonadotropin following treatment with follicle-stimulating hormone in vivo.

Authors:  A J Zeleznik; A R Midgley; L E Reichert
Journal:  Endocrinology       Date:  1974-09       Impact factor: 4.736

2.  The small luteal cell of the sheep.

Authors:  J D O'Shea; D G Cran; M F Hay
Journal:  J Anat       Date:  1979-03       Impact factor: 2.610

3.  The progesterone content of the fluid and the activity of the steroid-3beta-ol-dehydrogenase within the wall of the ovarian follicles.

Authors:  F Friedrich; G Breitenecker; H Salzer; J H Holzner
Journal:  Acta Endocrinol (Copenh)       Date:  1974-06

4.  Source of ovarian preovulatory progesterone.

Authors:  W W Leavitt; C G Bosley; G C Blaha
Journal:  Nat New Biol       Date:  1971-12-29

5.  3 Alpha-hydroxysteroid dehydrogenase and 3 beta-hydroxysteroid dehydrogenase in the ovary of young Mongolian gerbils.

Authors:  G M Rune; A Bahemann
Journal:  Histochemistry       Date:  1984

6.  Ovulation following unilateral ovariectomy in the California leaf-nosed bat (Macrotus californicus).

Authors:  W J Bleier; M Ehteshami
Journal:  J Reprod Fertil       Date:  1981-09

7.  Ultrastructural observations of delayed implantation in the Japanese long-fingered bat, Miniopterus schreibersii fuliginosus.

Authors:  K Kimura; T A Uchida
Journal:  J Reprod Fertil       Date:  1983-09

8.  Size distribution and hormonal responsiveness of dispersed rabbit luteal cells during pseudopregnancy.

Authors:  P B Hoyer; P L Keyes; G D Niswender
Journal:  Biol Reprod       Date:  1986-06       Impact factor: 4.285

9.  Varying response to luteinizing hormone of two luteal cell types isolated from bovine corpus luteum.

Authors:  J Ursely; P Leymarie
Journal:  J Endocrinol       Date:  1979-12       Impact factor: 4.286

10.  Steroidogenic capacity and ultrastructural morphology of cultured ovine luteal cells.

Authors:  P B Hoyer; W Kong; E G Crichton; L Bevan; P H Krutzsch
Journal:  Biol Reprod       Date:  1988-05       Impact factor: 4.285

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