The kisspeptin system is clustered in two main groups of cell bodies (the periventricular region, RP3V and the arcuate nucleus, ARC) that send fibers mainly to the GnRH neurons and in a few other locations, including the paraventricular nucleus, PVN. In physiological conditions, gonadal hormones modulate the kisspeptin system with expression changes according to different phases of the estrous cycle: the highest being in estrus phase in RP3V and PVN (positive feedback), and in ARC during the diestrus phase (negative feedback). In this work we wanted to study these hormonal fluctuations during the estrous cycle, investigating the role played by progesterone (P) or estradiol (E2), alone or together, on the kisspeptin system. Gonadectomized CD1 female mice were treated with P, E2 or both (E2+P), following a timing of administration that emulates the different phases of estrous cycle, for two cycles of 4 days. As expected, the two cell groups were differentially affected by E2; the RP3V group was positively influenced by E2 (alone or with the P), whereas in the ARC the administration of E2 did not affect the system. However P (alone) induced a rise in the kisspeptin immunoreactivity. All the treatments significantly affected the kisspeptin innervation of the PVN, with regional differences, suggesting that these fibers arrive from both RP3V and ARC nuclei.

Kisspeptin system in ovariectomized mice: estradiol and progesterone regulation

Marilena Marraudino;Mariangela Martini;Sara Trova;Alice Farinetti;Giovanna Ponti;Stefano Gotti;GianCarlo Panzica
2018-01-01

Abstract

The kisspeptin system is clustered in two main groups of cell bodies (the periventricular region, RP3V and the arcuate nucleus, ARC) that send fibers mainly to the GnRH neurons and in a few other locations, including the paraventricular nucleus, PVN. In physiological conditions, gonadal hormones modulate the kisspeptin system with expression changes according to different phases of the estrous cycle: the highest being in estrus phase in RP3V and PVN (positive feedback), and in ARC during the diestrus phase (negative feedback). In this work we wanted to study these hormonal fluctuations during the estrous cycle, investigating the role played by progesterone (P) or estradiol (E2), alone or together, on the kisspeptin system. Gonadectomized CD1 female mice were treated with P, E2 or both (E2+P), following a timing of administration that emulates the different phases of estrous cycle, for two cycles of 4 days. As expected, the two cell groups were differentially affected by E2; the RP3V group was positively influenced by E2 (alone or with the P), whereas in the ARC the administration of E2 did not affect the system. However P (alone) induced a rise in the kisspeptin immunoreactivity. All the treatments significantly affected the kisspeptin innervation of the PVN, with regional differences, suggesting that these fibers arrive from both RP3V and ARC nuclei.
2018
1688
8
14
https://www.sciencedirect.com/science/article/pii/S0006899318301495
kisspeptin, estrogen, progesterone, periventricular region, arcuate nucleus, paraventricular nucleus.
Marilena Marraudino, Mariangela Martini, Sara Trova, Alice Farinetti, Giovanna Ponti, Stefano Gotti, GianCarlo Panzica
File in questo prodotto:
File Dimensione Formato  
2018MarraudinoBR-MS.pdf

Open Access dal 02/04/2019

Descrizione: 2018 Marraudino Brain Res PostPrint
Tipo di file: POSTPRINT (VERSIONE FINALE DELL’AUTORE)
Dimensione 7.43 MB
Formato Adobe PDF
7.43 MB Adobe PDF Visualizza/Apri
2018MarraudinoBR.pdf

Accesso riservato

Descrizione: 2018 Marraudino Brain Res
Tipo di file: PDF EDITORIALE
Dimensione 2.05 MB
Formato Adobe PDF
2.05 MB Adobe PDF   Visualizza/Apri   Richiedi una copia
2018Marraudino.pdf

Accesso riservato

Tipo di file: PDF EDITORIALE
Dimensione 2.05 MB
Formato Adobe PDF
2.05 MB Adobe PDF   Visualizza/Apri   Richiedi una copia

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1662242
Citazioni
  • ???jsp.display-item.citation.pmc??? 10
  • Scopus 15
  • ???jsp.display-item.citation.isi??? 13
social impact