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Reproduction in Domestic Animals - Facultad de Ciencias Veterinarias

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16 t h International Congress on Animal <strong>Reproduction</strong><br />

118 Poster Abstracts<br />

P273<br />

Modifications of prostagland<strong>in</strong> synthesis enzymes gene<br />

expression <strong>in</strong> the porc<strong>in</strong>e oviduct after <strong>in</strong>trauter<strong>in</strong>e<br />

<strong>in</strong>fusion of sem<strong>in</strong>al plasma<br />

Kaczmarek, MM*; Krawczynski, K; Kiewisz, J; Ziecik, AJ<br />

Department of Hormonal Action Mechanisms, Division of Reproductive<br />

Endocr<strong>in</strong>ology and Pathophysiology, Institute of Animal <strong>Reproduction</strong> and<br />

Food Research, Polish Aca<strong>de</strong>my of Sciences, Olsztyn, Poland<br />

Introduction Recent studies have <strong>in</strong>dicated that <strong>in</strong>troduction of<br />

semen/sem<strong>in</strong>al plasma (SP) <strong>in</strong>to the female reproductive tract<br />

orchestrates strik<strong>in</strong>g molecular and cellular changes that facilitate<br />

embryo <strong>de</strong>velopment, conception and pregnancy. These changes were<br />

also observed <strong>in</strong> the expression of enzymes of prostagland<strong>in</strong> (PG)<br />

synthesis pathway, however until now only sem<strong>in</strong>al-<strong>in</strong>duced<br />

expression of PGHS-2 (prostagland<strong>in</strong>-endoperoxi<strong>de</strong> synthase 2)<br />

mRNA <strong>in</strong> the porc<strong>in</strong>e endometrium has been showed. S<strong>in</strong>ce the<br />

oviduct plays a <strong>de</strong>cisive role <strong>in</strong> reproduction provid<strong>in</strong>g a beneficial<br />

environment for gamete maturation, fertilization and the early<br />

embryonic <strong>de</strong>velopment we have <strong>in</strong>vestigated whether <strong>in</strong>trauter<strong>in</strong>e<br />

<strong>in</strong>fusion of SP can modulate PG synthesis <strong>in</strong> the porc<strong>in</strong>e oviduct<br />

through regulation of prostagland<strong>in</strong> synthesis enzymes gene<br />

expression.<br />

Methods Fifty six synchronized crossbred gilts received 100 ml<br />

<strong>in</strong>trauter<strong>in</strong>e <strong>in</strong>fusion of either SP or phosphate buffered sal<strong>in</strong>e (PBS;<br />

control). Oviducts were collected 1, 3, 5 and 10 Day(s) after SP or<br />

PBS-treatment. Expression of PGHS-2, PGF synthase (PGFS), PGE<br />

synthase (mPGES-1), PG 9-ketoreductase (9-KR) and PGI synthase<br />

(PGIS) mRNA <strong>in</strong> oviducts was assessed by the real time PCR.<br />

Results Among tested enzymes only PGFS and 9-KR mRNA were<br />

significantly lower (4.6- and 2.1-fold, respectively) <strong>in</strong> oviducts 24 h<br />

after SP <strong>in</strong>fusion <strong>in</strong>to the uter<strong>in</strong>e horns, when compared to PBStreated<br />

animals (P

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