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Reproduction (2004) 127 229-238
DOI: 10.1530/rep.1.00083
Copyright © 2004 Society for Reproduction and Fertility
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RESEARCH

Expression patterns of cytokines, p53 and nitric oxide synthase isoenzymes in corpora lutea of pseudopregnant rabbits during spontaneous luteolysis

Cristiano Boiti, Gabriella Guelfi, Massimo Zerani1, Danilo Zampini, Gabriele Brecchia and Anna Gobbetti1

Dipartimento di Scienze Biopatologiche Veterinarie, Università di Perugia, S. Costanzo 4, 06126 Perugia, Italy and 1 Dipartimento di Biologia Molecolare, Cellulare e Animale, Università di Camerino, Camerino, Italy

Correspondence should be addressed to C Boiti; Email: cristiano.boiti{at}unipg.it

The gene expressions for macrophage chemoattractant protein-1 (MCP-1), interleukin (IL)-1ß, IL-2 and p53 were examined by semi-quantitative RT-PCR in corpora lutea (CL) of rabbits during spontaneous luteolysis at days 13, 15, 18 and 22 of pseudopregnancy. In the same luteal tissue, total activity of nitric oxide (NO) synthase (NOS) and genes for both endothelial (eNOS) and inducible (iNOS) isoforms were also analysed. From day 13 to 15, MCP-1 and IL-1ßmRNA levels rose (P <= 0.01) almost 2-fold, and the transcript for p53 almost 8-fold, but then all dropped (P <= 0.05) from day 18 onward. IL-2 mRNA abundance was higher (P <= 0.01) on day 13 and then gradually declined. During luteolysis, eNOS mRNA decreased 40% (P <= 0.05) by day 15, but thereafter remained unchanged, while iNOS mRNA was barely detectable and did not show any clear age-related pattern throughout the late luteal stages. Total NOS activity progressively increased (P <= 0.01) from day 13 to 18 of pseudopregnancy and then dropped to the lowest (P <= 0.01) levels on day 22. Luteal progesterone content also declined during CL regression from 411 to 17 pg/mg found on days 13 and 22 respectively, in parallel with the decrease in blood progesterone concentrations. These data further support a physiological role of NO as modulator of luteal demise in rabbits. Locally, luteal cytokines may be involved in the up-regulation of NOS activity, while downstream NO may inhibit steroroidogenesis and induce expression of p53 gene after removal of the protective action of progesterone.




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