Author | dc.contributor.author | Reyes Solovera, Mónica de los | es_CL |
Author | dc.contributor.author | Carrion, R. | |
Author | dc.contributor.author | Barros, Claudio | es_CL |
Admission date | dc.date.accessioned | 2012-10-23T15:00:35Z | |
Available date | dc.date.available | 2012-10-23T15:00:35Z | |
Publication date | dc.date.issued | 2006-10 | |
Cita de ítem | dc.identifier.citation | THERIOGENOLOGY Volume: 66 Issue: 6-7 Special Issue: SI Pages: 1682-1684 | es_CL |
Identifier | dc.identifier.issn | 0093-691X | |
Identifier | dc.identifier.other | DOI: 10.1016/j.theriogenology.2006.02.002 | |
Identifier | dc.identifier.uri | https://repositorio.uchile.cl/handle/2250/122448 | |
General note | dc.description | Artículo de Publicación ISI | es_CL |
Abstract | dc.description.abstract | Experiments were conducted to evaluate in vitro fertilization (IVF) of in vitro matured (IVM) bitch oocytes using dog spermatozoa frozen in three different extenders. Sperm-rich fraction from eight ejaculates of five dogs was frozen in each one of three egg yolk Tris extenders with additional: (A) 1.4 g citric acid and 0.8 g glucose; (B) 0.7 g citric acid and 3.5 g glucose; or (C) 1.4 g citric acid and 0.8 g fructose (all with 5% glycerol in 100 mL milliQ water). Thawed sperm were co-incubated with IVM bitch oocytes for 6 It. Oocytes were fixed and evaluated under an epifluorescence microscope; penetrated oocytes were defined as those having sperm heads in the perivitelline space or in the oocyte cytoplasm. Higher penetration rates (P < 0.05) were obtained in oocytes cultured with spermatozoa frozen in extenders B and C than those frozen in extender A (33.1, 34.2 and 26.4%, respectively). | es_CL |
Lenguage | dc.language.iso | en | es_CL |
Publisher | dc.publisher | ELSEVIER SCIENCE INC | es_CL |
Keywords | dc.subject | spermatozoa | es_CL |
Título | dc.title | In vitro fertilization of in vitro matured canine oocytes using frozen-thawed dog semen | es_CL |
Document type | dc.type | Artículo de revista | |