2017
DOI: 10.1111/joa.12603
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Kisspeptin innervation of the hypothalamic paraventricular nucleus: sexual dimorphism and effect of estrous cycle in female mice

Abstract: The hypothalamic paraventricular nucleus (PVN) is the major autonomic output area of the hypothalamus and a critical regulatory center for energy homeostasis. The organism's energetic balance is very important for both the regular onset of puberty and regulation of fertility. Several studies have suggested a relationship among neural circuits controlling food intake, energy homeostasis and the kisspeptin peptide. The kisspeptin system is clustered in two main groups of cell bodies [the anterior ventral periven… Show more

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Cited by 30 publications
(29 citation statements)
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References 83 publications
(159 reference statements)
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“…3b). However as demonstrated in our previous study, the distribution of PVN kiss-ir fibers is not homogeneous in PVN comparing the medial with the lateral part of the nucleus (Marraudino et al, 2017).…”
Section: Resultsmentioning
confidence: 45%
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“…3b). However as demonstrated in our previous study, the distribution of PVN kiss-ir fibers is not homogeneous in PVN comparing the medial with the lateral part of the nucleus (Marraudino et al, 2017).…”
Section: Resultsmentioning
confidence: 45%
“…Therefore, sex steroids indirectly regulate GnRH neurons and the mediator is Kisspeptin, whose neurons express estrogen receptor alpha, ERα ( 90%; Franceschini et al, 2006;Smith et al, 2005), AR ( 65%; Smith et al, 2005), and the progesterone receptor ( 86%; Smith et al, 2007). In rodents, sex steroids differentially regulate Kisspeptin expression in hypothalamus, which increases in the RP3V region (Kauffman et al, 2007;Smith et al, 2005) and PVN (Marraudino et al, 2017), and decreases in the ARC (Smith et al, 2005).…”
Section: Resultsmentioning
confidence: 99%
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“…For frozen sections, the brains were gradually transferred into 15% and 30% sucrose. After the brains completely sank to the bottom in 30% sucrose, coronal sections (30 μm) through the AVPV (from bregma +0.62 to +0.02 mm) 28 and ARC (from bregma −1.22 to −2.80 mm) 34,35 were serially cut using a cryostat (Leica Microsystems, Wetzlar, Germany). All free‐floating sections through the AVPV and ARC were collected and incubated in 0.5% sodium metaperiodate for 20 minutes and then in 1% sodium borohydride for 20 minutes.…”
Section: Methodsmentioning
confidence: 99%