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Saliva crystallization in sheep subjected to estrus induction and synchronization protocols
Gonçalves, Andressa Silveira; Oberst, Eneder Rosana; Raimondo, Raquel Fraga e Silva.
Affiliation
  • Gonçalves, Andressa Silveira; Universidade Federal do Rio Grande do Sul. Faculdade de Veterinária. Núcleo RuminAção, Ensino, Pesquisa e Extensão em Ruminantes. Porto Alegre. BR
  • Oberst, Eneder Rosana; Universidade Federal do Rio Grande do Sul. Faculdade de Veterinária. Núcleo RuminAção, Ensino, Pesquisa e Extensão em Ruminantes. Porto Alegre. BR
  • Raimondo, Raquel Fraga e Silva; Universidade Federal do Rio Grande do Sul. Faculdade de Veterinária. Núcleo RuminAção, Ensino, Pesquisa e Extensão em Ruminantes. Porto Alegre. BR
Acta sci. vet. (Impr.) ; 48: Pub.1719-Jan. 30, 2020. ilus, graf
Article in En | VETINDEX | ID: biblio-1458241
Responsible library: BR68.1
Localization: BR68.1
ABSTRACT

Background:

The crystallization of bodily fluids, primarily saliva, has been the subject of study in many species and is asimple alternative to detect estrus because it demands neither a significant financial investment nor qualified professionalsto execute the examination. Fern pattern crystallization has been described in the cervical and nasal mucus, saliva andtear secretion, and in colostrum. Changes in salivary crystallization during the reproduction cycle are related to differenthormonal concentrations in this period. Thus, the present study has evaluated the patterns of saliva crystallization in sheepsubjected to estrus induction and synchronization protocols.Materials, Methods &

Results:

The sample consisted of 11 crossbreed Corriedale sheep, which were evaluated during twoexperimental periods (spring and autumn), and that underwent induction and synchronizing estrus protocols. In a randomphase of the estrus cycle (day 0), each sheep was implanted with an intravaginal device (Primer®), impregnated with 0.36g of progesterone for seven days. This device was inserted according to manufacturer’s instructions of the manufacturerand with the assistance of a specific applicator. On the day of device removal (day 7), the animals received 0.0375 mg ofD-Cloprostenol (Prolise®) and 10 mg of Folltropin® extracted from the swine pituitary (NIH-FSH-P1 of Folltropin-V) byintramuscular administration. The saliva was collected at six points during the experimental periods day 1 (3 days beforeplacement of the implant); day 4 (day of insertion of the implant); day 9 (5 days after the insertion of the implant); day11 (day of removal of the implant and application of hormones); day 12 (24 h after removal of the implant [presumableestrus]); and day 13 (48 h after removal of the implant). Smears containing 10 µL of saliva were observed under an opticallight microscope...
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Full text: 1 Database: VETINDEX Main subject: Saliva / Estrus / Sheep / Estrus Detection / Estrus Synchronization Limits: Animals Language: En Journal: Acta sci. vet. (Impr.) Year: 2020 Document type: Article

Full text: 1 Database: VETINDEX Main subject: Saliva / Estrus / Sheep / Estrus Detection / Estrus Synchronization Limits: Animals Language: En Journal: Acta sci. vet. (Impr.) Year: 2020 Document type: Article