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Reproduction, Fertility and Development Reproduction, Fertility and Development Society
Vertebrate reproductive science and technology
RESEARCH ARTICLE

Radioimmunoassay of bovine placental lactogen using recombinant and native preparations: determination of fetal concentrations across gestation

A. V. Alvarez-Oxiley A , N. M. Sousa A , J. L. Hornick E , K. Touati B , G. C. van der Weijden C , M. A. M. Taverne C , O. Szenci D , J. Sulon A , P. Debliquy A and J. F. Beckers A F
+ Author Affiliations
- Author Affiliations

A Laboratory of Animal Endocrinology and Reproduction, Faculty of Veterinary Medicine, University of Liege, Liege, Belgium.

B Surgery for Large Animals, Faculty of Veterinary Medicine, University of Liege, Liege, Belgium.

C Department of Farm Animal Health, Faculty of Veterinary Medicine, Utrecht, the Netherlands.

D Clinic for Large Animals, Faculty of Veterinary Science, Szent Istvan University, Budapest, Hungary.

E Nutrition of Large Animals, Faculty of Veterinary Medicine, University of Liege, Liege, Belgium.

F Corresponding author. Email: jfbeckers@ulg.ac.be

Reproduction, Fertility and Development 19(7) 877-885 https://doi.org/10.1071/RD06173
Submitted: 22 December 2006  Accepted: 20 July 2007   Published: 6 September 2007

Abstract

Concentrations of bovine placental lactogen (bPL) were determined in fetal plasma samples by twelve double-antibody competitive radioimmunoassay systems (RIA I–XII) based on either recombinant bPL (non-glycosylated) or native bPL (glycosylated). Both preparations were used as standard and tracer, and for primary antisera production. The minimum detection limit measured by these RIA varied from 0.02 to 0.6 ng bPL mL–1. The coefficients of correlation of different bPL RIA systems were up to 90% (P < 0.0001) when each RIA was tested against the average values of all twelve RIA systems. All developed RIA were used to investigate the incidence of different bPL isoforms in bovine fetal serum samples (n = 71). Fetal concentrations ranged from 11.8 to 35.7 ng mL–1 at the third month and from 1.1 to 13.5 ng mL–1 at the ninth month of gestation. They tended to decrease with advancing gestation. In general, those RIA systems that used recombinant bPL as the standard measured higher values than those using the native bPL preparation. These differences decreased toward the end of gestation (P < 0.05), suggesting a lower rate of glycosylation. Our results provide evidence of different glycosylated isoforms of bPL in fetal serum at different gestation periods.

Additional keywords: fetal serum, glycosylated form.


Acknowledgements

We thank Dr B. El Amiri, Dr D. Idrissa-Sidikou and M. Machado (Agric. Tech.) for their collaboration during this study. We are grateful to Mrs R. Fares-Noucairi for her secretarial assistance. The first author also acknowledges her initial advisers: Drs Raquel Perez-Clariget, Laura Astigarraga and Alvaro Bermudez from the University of the Republic (Uruguay). This research was supported by grants from the Belgian Ministry of Agriculture and Ministry of the Wallonne Region-DGA, grant no. S6069.


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