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dc.creatorMucio-Ramírez, Samueles_ES
dc.creatorSánchez-Islas, Eduardoes_ES
dc.creatorSánchez-Jaramillo, Edithes_ES
dc.creatorCurrás-Collazo, Margaritaes_ES
dc.creatorJuárez-González, Victor R.es_ES
dc.creatorÁlvarez-González, Mhar Y.es_ES
dc.creatorOrser, L.E.es_ES
dc.creatorHou, Borines_ES
dc.creatorPellicer, Franciscoes_ES
dc.creatorKodavanti, Prasada Rao S.es_ES
dc.creatorLeón-Olvera, Martha
dc.date2017
dc.date.accessioned2023-10-31T20:14:20Z
dc.date.available2023-10-31T20:14:20Z
dc.date.issued2017
dc.identifier.issn0041-008X
dc.identifier.urihttp://repositorio.inprf.gob.mx/handle/123456789/7801
dc.identifier.urihttp://dx.doi.org/10.1016/j.taap.2017.05.039
dc.descriptionPolychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs) are environmental pollutants that produce neurotoxicity and neuroendocrine disruption. They affect the vasopressinergic system but their disruptive mechanisms are not well understood. Our group reported that rats perinatally exposed to Aroclor-1254 (A1254) and DE-71 (commercial mixtures of PCBs and PBDEs) decrease somatodendritic vasopressin (AVP) release while increasing plasma AVP responses to osmotic activation, potentially emptying AVP reserves required for body-water balance. The aim of this research was to evaluate the effects of perinatal exposure to A1254 or DE-71 (30 mg kg/day) on AVP transcription and protein content in the paraventricular and supraoptic hypothalamic nuclei, of male and female rats, by in situ hybridization and immunohistochemistry. cFOS mRNA expression was evaluated in order to determine neuroendocrine cells activation due to osmotic stimulation. Animal groups were: vehicle (control); exposed to either A1254 or DE-71; both, control and exposed, subjected to osmotic challenge. The results confirmed a physiological increase in AVP-immunoreactivity (AVP-IR) and gene expression in response to osmotic challenge as reported elsewhere. In contrast, the exposed groups did not show this response to osmotic activation, they showed significant reduction in AVP-IR neurons, and AVP mRNA expression as compared to the hyperosmotic controls. cFOS mRNA expression increased in A1254 dehydrated groups, suggesting that the AVP-IR decrease was not due to a lack of the response to the osmotic activation. Therefore, A1254 may interfere with the activation of AVP mRNA transcript levels and protein, causing a central dysfunction of vasopressinergic system.
dc.formatPDF
dc.language.isoeng
dc.publisherElsevier
dc.relation2017:329()173-189
dc.rightsAcceso Cerrado
dc.titlePerinatal exposure to organohalogen pollutants decreases vasopressin content and its mRNA expression in magnocellular neuroendocrine cells activated by osmotic stress in adult ratses_ES
dc.typeArtículo
dc.contributor.affiliationDepartamento de Neuromorfología Funcional, Dirección de Investigaciones en Neurociencias, Instituto Nacional de Psiquiatría Ramón de la Fuente Muñiz, Calz. México Xochimilco No. 101, Col. San Lorenzo Huipulco, México D.F. C.P. 14370, México
dc.contributor.emailmucios@imp.edu.mx (S. Mucio-Ramírez)
dc.contributor.emailedaxy@imp.edu.mx (E. Sánchez-Islas)
dc.contributor.emailesanchez@imp.edu.mx (E. Sánchez-Jaramillo)
dc.contributor.emailmargarita.curras@ucr.edu (M. Currás-Collazo)
dc.contributor.emailrivelino@ibt.unam.mx (V.R. Juárez-González)
dc.contributor.emailmhar123@hotmail.com (M.Y. Álvarez-González)
dc.contributor.emailpellicer@imp.edu.mx (F. Pellicer)
dc.contributor.emailKodavanti.Prasada@epa.gov (P.R.S. Kodavanti)
dc.contributor.emailmarthalo@imp.edu.mx (M. León-Olea)
dc.relation.jnabreviadoTOXICOL APPL PHARMACOL
dc.relation.journalToxicology and Applied Pharmacology
dc.identifier.placeUnited States
dc.date.published2017
dc.identifier.organizacionInstituto Nacional de Psiquiatría Ramón de la Fuente Muñiz
dc.identifier.eissn1096-0333
dc.identifier.doi10.1016/j.taap.2017.05.039
dc.subject.kwVasopressin
dc.subject.kwNeuroendocrine disruption
dc.subject.kwPCBs
dc.subject.kwPBDEs
dc.subject.kwSalt loading
dc.subject.kwcFOS


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