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Recent advances in ovulation synchronization and superovulation in ...

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Abstracts. II International Symposium on Animal Biology of Reproduction, Nov. 19-22, 2008, São Paulo, SP, Brazil.<br />

Evaluation of luteolytic effects of Sodic cloprostenol (S<strong>in</strong>crocio®) <strong>in</strong> Mangalarga (Equus<br />

cabalus) mares treated <strong>in</strong> different days of estrous cycle<br />

E.D.F. Souza 1 , S.S. Carreiro 1 , J.R.G. Maio 1 , P.D.C. Fleury 2 , T.F.R. Ometto 2 , A.A. Teixeira 3 ,<br />

J.N.S. Sales 3 , G.A. Crepaldi 3 , P.S. Baruselli 3<br />

1 Ouro F<strong>in</strong>o Saúde Animal, Ribeirão Preto-SP. 2 Central Fleury de Reprodução Eqü<strong>in</strong>a, São José Rio Pardo-SP; 3 Animal<br />

Reproduction Department, FMVZ/USP, Brazil.<br />

Introduction<br />

The <strong>in</strong>duction of <strong>ovulation</strong> <strong>in</strong> mares is a practice to optimize the reproductive management <strong>and</strong> improve the use of<br />

stallions. Thus, the objective of the present study was to evaluate the luteolytic effect of Sodic cloprostenol<br />

(S<strong>in</strong>crocio®) adm<strong>in</strong>istered <strong>in</strong> different days of estrous cycle to <strong>in</strong>duce the heat <strong>in</strong> cyclic mares.<br />

Material <strong>and</strong> Methods<br />

In the present study, it was used 53 cyclic mares show<strong>in</strong>g good body condition. The animals that presented follicles<br />

>35mm were treated with 2500IU of hCG (Chorulon®, Intervet, Netherl<strong>and</strong>s) to <strong>in</strong>duce <strong>ovulation</strong>. Only the mares<br />

that ovulated <strong>in</strong> the same day (Day 0; n = 29) were used at this study. The animals were allocated <strong>in</strong> one of three<br />

experimental groups [Day 3 (n=9), Day 7 (n=10) <strong>and</strong> Day 12 (n=10)]. Animals from each group received 250 µg of<br />

Cloprostenol (PGF) i.m. <strong>in</strong> different days of the estrous cycle (Day 3, Day 7 <strong>and</strong> Day 12. Blood samples were<br />

collected immediately before <strong>and</strong> after the PGF adm<strong>in</strong>istration (0, 12, 24, 36 <strong>and</strong> 48 h). The samples were cooled,<br />

centrifuged (3000xg/5m<strong>in</strong>utes) <strong>and</strong> then frozen to measure plasma progesterone concentrations by<br />

radioimmunoassay (Coat-A-Count Progesterone® (Diagnostic Products Corporation, Los Angeles, EUA).<br />

Results <strong>and</strong> Discussion<br />

The plasma progesterone concentration was significantly different before the adm<strong>in</strong>istration of PGF on Day 3<br />

compared to Day 7 <strong>and</strong> Day 12. The P4 concentration did not differ between treatment performed on Day 7 <strong>and</strong> Day<br />

12 <strong>in</strong> any moment of the blood collection <strong>and</strong> decreased until 48 h after the adm<strong>in</strong>istration. The P4 concentration<br />

was similar between all groups only <strong>in</strong> 12 <strong>and</strong> 24 h after the treatment. The P4 concentration of Group Day 3<br />

decreased lesser (36 <strong>and</strong> 48 h) than Day 7 <strong>and</strong> Day 12 groups. Accord<strong>in</strong>g to these results, we can conclude that 250<br />

µg of Sodic cloprostenol (S<strong>in</strong>crocio®) was efficient to <strong>in</strong>duce luteolysis when the treatment was performed on Day<br />

7 <strong>and</strong> Day 12 after <strong>ovulation</strong>.<br />

Progesterone (ng/mL)<br />

10<br />

Figure 1. Plasma progesterone concentration immediately before <strong>and</strong> after (0, 12, 24, 36 <strong>and</strong> 48 h) the PGF<br />

adm<strong>in</strong>istration 3, 7 <strong>and</strong> 12 days after <strong>ovulation</strong> (* Day 3≠Day 7 e Day 12, P

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