Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/51556
Título: A comparison of diagnosis of pregnancy in the goat via transrectal ultrasound scanning, progesterone, and pregnancy-associated glycoprotein assays
Autores/as: González, Fernando
Cabrera, Fernando 
Batista, Miguel 
Rodríguez, Noemí
Álamo, Desiré
Sulon, Jose
Beckers, Jean François
Gracia, Anselmo 
Palabras clave: Sheep
Ultrasonography
Samples
Serum
Milk
Fecha de publicación: 2004
Editor/a: 0093-691X
Publicación seriada: Theriogenology 
Resumen: Real-time ultrasound scanning (US) via the transrectal route, progesterone (P4) assay, and pregnancy-associated glycoprotein (PAG) detection can be used to diagnose pregnancy at around 3 weeks after breeding. Although several studies have been carried out to evaluate each of these different methods individually, it is difficult to establish adequate comparisons due to differences, such as the breed of goat, age, and farming conditions, among others. The aim of the present paper is to compare the accuracy of diagnosis of pregnancy using transrectal US, P4 assay and PAG detection at the same time and on the same animals. Canary dairy goats (n = 143) were synchronized with an 11-day fluorogestone acetate (FGA) intravaginal sponge followed by PGF(2 alpha), and eCG 2 days before the FGA withdrawal. Blood samples were collected on Days 20, 22, 24, and 26 after mating to determine P4 and PAG concentrations. Transrectal US examinations were performed at the same time. There were 79 pregnant goats and another 64 non-pregnant. The US via the transrectal method and the determination of PAG concentrations provide very accurate pregnancy diagnosis at 24-26 days after breeding; on the contrary, P4 assay on plasma samples performed on Day 22 after breeding was accurate, in this case, in detecting pregnant animals but did not always detect the non-pregnant does. (c) 2004 Elsevier Inc. All rights reserved.
URI: http://hdl.handle.net/10553/51556
ISSN: 0093-691X
DOI: 10.1016/j.theriogenology.2003.12.009
Fuente: Theriogenology[ISSN 0093-691X],v. 62, p. 1108-1115
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