Domestic Animal Endocrinology
Volume 31, Issue 2 , Pages 154-172, August 2006

Endocrine and cellular characteristics of corpora lutea from cows with a delayed post-ovulatory progesterone rise

  • R.S. Robinson

      Affiliations

    • Division of Animal Physiology, University of Nottingham, Sutton Bonington Campus, Loughborough, Leics LE12 5RD, UK
    • Corresponding Author InformationCorresponding author. Tel.: +44 115 9516342; fax: +44 115 9516302.
  • ,
  • A.J. Hammond

      Affiliations

    • Division of Animal Physiology, University of Nottingham, Sutton Bonington Campus, Loughborough, Leics LE12 5RD, UK
  • ,
  • L.T. Nicklin

      Affiliations

    • Division of Animal Physiology, University of Nottingham, Sutton Bonington Campus, Loughborough, Leics LE12 5RD, UK
  • ,
  • D. Schams

      Affiliations

    • Department of Physiology, Technical University Munich-Weihenstephan, Weihenstephaner Berg 3, D-85350 Freising, Germany
  • ,
  • G.E. Mann

      Affiliations

    • Division of Animal Physiology, University of Nottingham, Sutton Bonington Campus, Loughborough, Leics LE12 5RD, UK
  • ,
  • M.G. Hunter

      Affiliations

    • Division of Animal Physiology, University of Nottingham, Sutton Bonington Campus, Loughborough, Leics LE12 5RD, UK

Received 11 July 2005; received in revised form 26 September 2005; accepted 5 October 2005. published online 14 November 2005.

Abstract 

The timing of the post-ovulatory progesterone rise is critical to the embryonic development and survival. The aim of this study was to determine the underlying causes of delayed post-ovulatory progesterone rises. Two groups of non-lactating dairy cows with early (n=11) or late (n=9) post-ovulatory progesterone rises were created by inducing luteolysis in the presence of either a large (>10mm) or small (<10mm) follicle, respectively. LH pulses were measured on days 4 (all cows) and 7 (n=7, early; n=5, late) (day 1=ovulation). The cows were slaughtered on day 5 (n=4 each group) or 8 (n=7, early; n=5, late). Immunohistochemical analysis for endothelial cells (von Willebrand Factor, VWF), steroidogenic cells (3β-HSD) and proliferation marker (Ki67) were performed. The basal progesterone production and LH responsiveness (0.001–100ng/ml) of dispersed luteal cells was investigated. The luteal concentrations of FGF-2 and VEGF were measured by ELISA and RIA, respectively. There were no differences in LH pulse characteristics, area of VWF staining, proliferation index, steroidogenic cell characteristics, basal or LH-stimulated progesterone production by luteal cells between cows with an early or late progesterone rise (P>0.10). However, the area of VWF staining increased from days 5 to 8, while the proliferation index decreased (P<0.05). Furthermore, the luteal cells were more responsive to LH on day 8 (P<0.01). Luteal concentrations of FGF-2 were higher on day 5 (P=0.05), while VEGF was greater on day 8 (P<0.01). In conclusion, we have clearly shown that LH support, degree of vascularization or luteal cell steroidogenic capacity were not the major factors responsible for inadequate secretion of progesterone by the developing bovine CL.

Keywords: Progesterone, Corpus luteum, LH, Angiogenesis, Cow

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PII: S0739-7240(05)00214-6

doi:10.1016/j.domaniend.2005.10.003

Domestic Animal Endocrinology
Volume 31, Issue 2 , Pages 154-172, August 2006