Inositol triphosphate participates in an oestradiol nongenomic signalling pathway involved in accelerated oviductal transport in cycling rats

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dc.contributor.authorOrihuela, PA
dc.contributor.authorParada-Bustamante, A
dc.contributor.authorZuñiga, LM
dc.contributor.authorCroxatto, HB
dc.date.accessioned2025-01-21T01:06:20Z
dc.date.available2025-01-21T01:06:20Z
dc.date.issued2006
dc.description.abstractOestradiol (E,) accelerates oviductal transport of oocytes in cycling rats through a nongenomic pathway that involves the cAMP-PKA signalling cascade. Here we examined the role of the inositol triphosphate (IP3) and mitogen-activated protein kinase (MAPK) signalling cascades in this nongenomic pathway. Oestrous rats were injected with E-2 s.c. and intrabursally (i.b) with the selective inhibitors of phospholipase C (PLC) ET-18OCH(3) or MAPK PD98059. The number of eggs in the oviduct assessed 24 h later showed that ET-18-OCH3 blocked E-2-induced egg transport acceleration, whereas PD980559 had no effect. Other oestrous rats were treated with E-2 s.c. and 1, 3 or 6 h later oviducts were excised and the levels of IP3 and phosphorylated MAPK p44/42 (activated) were determined by radioreceptor assay and Western blot, respectively. Oestradiol administration increased IP3 level at 1 and 6 h after treatment, whereas activated MAPK p44/42 level was unchanged. Finally, e 0 1 we explored whether cAMP-PKA and PLC-IP3 signalling cascades are coupled. Inhibition of adenylyl cyclase by i.b. injection of SQ 22536 blocked the increase of IP3 levels induced by E, while inhibition of PLC by ET-18OCH(3) had no effect on E(2-)induced PKA activity. Furthermore, activation of adenylyl cylase by Forskolin increased oviducral IP3 levels. Thus, activation of PLC-IP3 by E, requires previous stimulation of cAMP-PKA. We conclude that the nongenomic pathway utilised by E, to accelerate oviductal transport of oocytes in cycling rats involves Successive activation of the cAMP-PKA and PLC-IP3 signalling cascades and does not require activation of MAPK. These findings clearly illustrate a non-genomic pathway triggered by E-2 that regulates a complex physiologic process accomplished by in entire organ.
dc.fuente.origenWOS
dc.identifier.doi10.1677/joe.1.06448
dc.identifier.eissn1479-6805
dc.identifier.issn0022-0795
dc.identifier.urihttps://doi.org/10.1677/joe.1.06448
dc.identifier.urihttps://repositorio.uc.cl/handle/11534/96137
dc.identifier.wosidWOS:000236107700020
dc.issue.numero3
dc.language.isoen
dc.pagina.final588
dc.pagina.inicio579
dc.revistaJournal of endocrinology
dc.rightsacceso restringido
dc.subject.ods03 Good Health and Well-being
dc.subject.odspa03 Salud y bienestar
dc.titleInositol triphosphate participates in an oestradiol nongenomic signalling pathway involved in accelerated oviductal transport in cycling rats
dc.typeartículo
dc.volumen188
sipa.indexWOS
sipa.trazabilidadWOS;2025-01-12
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