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Journal of Endocrinology (2006) 188, 205-213    DOI: 10.1677/joe.1.06526
© 2006 Society for Endocrinology

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Region-specific expression of nitric oxide synthases in the bovine oviduct during the oestrous cycle and in vitro

S E Ulbrich, S Rehfeld2, S Bauersachs2, E Wolf2, R Rottmayer2, S Hiendleder2, M Vermehren3, F Sinowatz3, H H D Meyer and R Einspanier1

Physiology-Weihenstephan, Technical University of Munich, Alles Hörsaalgebäude, 85350 Freising, Germany
1 Institute of Veterinary Biochemistry, Free University of Berlin, Oertzenweg 19b, D-14163 Berlin, Germany
2 Institute of Molecular Animal Breeding and Biotechnology, Gene Centre of the Ludwig-Maximilians-University Munich, Munich, Germany
3 Institute of Veterinary Anatomy, Histology and Embryology, Ludwig-Maximilians-University Munich, Veterinaerstr. 13, 80539 Munich, Germany

(Requests for offprints should be addressed to R Einspanier; Email: einspani{at}zedat.fu-berlin.de)

Nitric oxide synthases (NOS) account for the endogenous production of nitric oxide (NO), a small and permeable bioreactive molecule. NO is known to act as a paracrine mediator during various processes associated with female reproduction. In the present study, the mRNA expression of the endothelial (eNOS) and inducible (iNOS) NO synthases were examined in bovine oviduct epithelial cells (BOEC) during the oestrous cycle. In addition, eNOS and iNOS mRNA and protein were localised by in situ hybridisation and immunocytochemistry respectively. Furthermore, the effects of exogenously applied oestradiol-17ß and progesterone on NOS mRNA regulation were studied in a suspension culture of BOEC. The eNOS mRNA abundance was low around ovulation (day 0) and increased significantly until pro-oestrus (day 18) in the ampulla. Immunoreactive protein of eNOS was detected predominantly in endothelial cells as well as in secretory oviduct epithelial cells at pro-oestrus. The iNOS mRNA concentration was significantly reduced in the isthmus at pro-oestrus (day 18) and oestrus (day 0) compared with persistently high levels in the ampulla. By in situ hybridisation, specific iNOS transcripts were additionally demonstrated in the oviduct epithelium. Immunoreactive iNOS protein was localised in secretory epithelial cells as well as in the lamina muscularis. The in vitro stimulation showed that both NOS were stimulated by progesterone, but not by oestradiol-17ß. The region-specific modulated expression of eNOS and iNOS provides evidence for an involvement of endogenously produced NO in the regulation of oviductal functions.







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