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Neuroanatomical connections between kisspeptin neurones and somatostatin neurones in the female and male rat hypothalamus: A possible involvement of SSTR 1 in kisspeptin release
Author(s) -
Dufourny L.,
Delmas O.,
TeixeiraGomes A.P.,
Decourt C.,
Sliwowska J. H.
Publication year - 2018
Publication title -
journal of neuroendocrinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.062
H-Index - 116
eISSN - 1365-2826
pISSN - 0953-8194
DOI - 10.1111/jne.12593
Subject(s) - endocrinology , medicine , kisspeptin , hypothalamus , biology , somatostatin , arc (geometry) , gonadotropin releasing hormone , periventricular nucleus , arcuate nucleus , neuropeptide , immunocytochemistry , photostimulation , receptor , neuroscience , hormone , luteinizing hormone , geometry , mathematics
Somatostatin ( SST ), a neuropeptide involved in the central modulation of several physiological functions, is co‐distributed in the same hypothalamic areas as kisspeptin ( KP ), the most potent secretagogue of the gonadotrophin‐releasing hormone (Gn RH ) secretion known to date. Because SST infused i.c.v. evoked a potent inhibition of Gn RH release, we explored the neuroanatomical relationships between KP and SST populations in male and female rats. Accordingly, intact males and ovariectomised oestradiol‐replaced females were killed and their brains processed aiming to simultaneously detect KP , SST and synapsin, a marker for synapses. We observed numerous appositions of KP on SST neurones both in the female and male arcuate nucleus ( ARC ) and ventromedial hypothalamus. A large association between SST terminals and KP neurones at the level of the pre‐optic area was also observed in female rats and in a more limited frame in males. Finally, most KP neurones from the ARC showed SST appositions in both sexes. To determine whether SST could affect KP cell activity, we assessed whether SST receptors ( SSTR ) were present on KP neurones in the ARC . We also looked for the presence of SSTR 1 and SSTR 2A in the brain of male rats. Brains were processed using a sequential double immunocytochemistry aiming to detect KP and SSTR 1 or KP and SSTR 2A. We observed overlapping distributions of immunoreactive neurones for SSTR 1 and KP and counted approximately one‐third of KP neurones with SSTR 1. By contrast, neurones labelled for SSTR 2A or KP were often juxtaposed in the ARC and the occurrence of double‐labelled neurones was sporadic (< 5%). These results suggest that the action of SST on KP neurones would pass mainly through SSTR 1 at the level of the ARC .