Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/123502
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dc.contributor.authorSuárez Trujillo, Aridanyen_US
dc.contributor.authorRivero Santana, Miguel Antonioen_US
dc.contributor.authorArgüello Henríquez, Anastasioen_US
dc.contributor.authorCapote Álvarez, Juan Franciscoen_US
dc.contributor.authorCastro Navarro, Noemíen_US
dc.date.accessioned2023-06-14T07:49:01Z-
dc.date.available2023-06-14T07:49:01Z-
dc.date.issued2016en_US
dc.identifier.urihttp://hdl.handle.net/10553/123502-
dc.description.abstractMammary gland function and structure is modulated by local (produced by mammary epithelial cells) or systemic (produced outside the mammary gland) serotonin. It acts through serotonin receptors (5-HTR), transmembrane proteins. The presence of different serotonin receptors subtypes has been described in cow, mouse, rat and human mammary tissue. In goats, 5-HTR presence in mammary gland tissue has not been described yet. The objectives of this study are to elucidate if goat lactating mammary tissue presents any of the serotonin receptors subtypes (5-HTR 1A, 1B, 1D, 1E, 1F, 2A, 2B, 2C, 3A, 4, 5a, 6 and 7) using qPCR analysis; and then, to describe by immunohistochemistry (IHC), the arrangement of some of those qPCRpositive receptors, in the mammary tissue of lactating and dry off goats. Tissue samples for qPCR were taken from three lactating Majorera goats at the slaughterhouse. Hypothalamic tissue was also collected as positive control. RNA extraction and cDNA synthesis were performed. Specific primers for each receptor subtype were developed in goat tissue, and used for qPCR analysis. Hypoxanthine phosphosibosyltransferase I, Ribosomal Protein, β-Actin and Glyceraldehyde 3-Phosphate Dehydrogenase genes were utilized as internal control. IHC for 5-HTR 1B, 1E, 2A, 2B, 5 and 7 was performed in paraffin-embedded tissue from three lactating and three dry off Majorera goats. 5μm sections were immunostained using rabbit primary antibodies against each 5-HTR subtypes. Anti-rabbit secondary antibody was conjugated with streptavidin peroxidase, and visualization of binding was realized using diaminobenzidine substrate. Hypothalamic tissue was also used as positive control. qPCR analysis showed that 5-HTR 1B, 1D, 1E, 2A, 2B, 4, 5a and 7 were presented in goat lactating tissue. In the IHC analysis, all six studied receptors were expressed in mammary epithelial cells. Furthermore, 5-HTR 1E was expressed in the myoepithelial cells. Blood vessels were positively stained for receptors 1B, 2A and 2B. In lactating animals, receptor disposition in the mammary epithelial cells was cytoplasmic. However, in mammary tissue from non-lactating animals, arrangement changed to the apical membrane in all receptor subtypes. In conclusion, 5-HTR 1B, 1D, 1E, 2A, 2B, 4, 5a and 7 are expressed in goat mammary tissue and receptors 1B, 1E, 2A, 2B, 2 and 7 were expressed in different cells of the mammary tissue. This is the first approach to describe the presence of serotoninergic components in the goat udder, and further studies need to be performed in order to elucidate the function of serotonin on this species.en_US
dc.languageengen_US
dc.publisherInternational Goat Associationen_US
dc.source12th International Conference on Goats (ICG 2016)en_US
dc.subject3104 Producción Animalen_US
dc.subject240101 Anatomía animalen_US
dc.titleSerotonin receptors description in goat mammary glanden_US
dc.typeinfo:eu-repo/semantics/lectureen_US
dc.typeLectureen_US
dc.relation.conference12th International Conference on Goats (ICG 2016)en_US
dc.description.lastpage153en_US
dc.description.firstpage153en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Ponenciaen_US
dc.description.numberofpages1en_US
dc.utils.revisionen_US
dc.date.coverdateSeptiembre 2016en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-VETen_US
item.grantfulltextopen-
item.fulltextCon texto completo-
crisitem.author.deptGIR IUSA-ONEHEALTH 3: Histología y Patología Veterinaria y Forense (Terrestre y Marina)-
crisitem.author.deptIU de Sanidad Animal y Seguridad Alimentaria-
crisitem.author.deptDepartamento de Morfología-
crisitem.author.deptGIR IUSA-ONEHEALTH 4. Producción y Biotecnología Animal-
crisitem.author.deptIU de Sanidad Animal y Seguridad Alimentaria-
crisitem.author.deptDepartamento de Patología Animal, Producción Animal, Bromatología y Tecnología de Los Alimentos-
crisitem.author.deptGIR IUSA-ONEHEALTH 4. Producción y Biotecnología Animal-
crisitem.author.deptIU de Sanidad Animal y Seguridad Alimentaria-
crisitem.author.deptDepartamento de Patología Animal, Producción Animal, Bromatología y Tecnología de Los Alimentos-
crisitem.author.orcid0000-0002-9343-5016-
crisitem.author.orcid0000-0003-3766-1569-
crisitem.author.orcid0000-0002-4426-0678-
crisitem.author.orcid0000-0002-3026-2031-
crisitem.author.parentorgIU de Sanidad Animal y Seguridad Alimentaria-
crisitem.author.parentorgIU de Sanidad Animal y Seguridad Alimentaria-
crisitem.author.parentorgIU de Sanidad Animal y Seguridad Alimentaria-
crisitem.author.fullNameSuárez Trujillo, Aridany-
crisitem.author.fullNameRivero Santana, Miguel Antonio-
crisitem.author.fullNameArgüello Henríquez, Anastasio-
crisitem.author.fullNameCapote Álvarez, Juan Francisco-
crisitem.author.fullNameCastro Navarro, Noemí-
crisitem.event.eventsstartdate25-09-2016-
crisitem.event.eventsenddate30-09-2016-
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