Mapping of Kisspeptin Receptor mRNA in the Whole Rat Brain and its Co-Localisation with Oxytocin in the Paraventricular Nucleus

S. Higo
S. Honda
N. Iijima
H. Ozawa

The neuropeptide kisspeptin and its receptor play an essential role in reproduction as a potent modulator of the gonadotrophin-releasing hormone (GnRH) neurone. In addition to its reproductive function
 kisspeptin signalling is also involved in extra-hypothalamic-pituitary-gonadal (HPG) axis systems
 including oxytocin and arginine vasopressin (AVP) secretion. By contrast to the accumulating information for kisspeptin neurones and kisspeptin fibres
 the histological distribution and function of the kisspeptin receptor in the rat brain remain poorly characterised. Using in situ hybridisation combined with immunofluorescence
 the present study aimed to determine the whole brain map of Kiss1r mRNA (encoding the kisspeptin receptor)
 and to examine whether oxytocin or AVP neurones express Kiss1r. Neurones with strong Kiss1r expression were observed in several rostral brain areas
 including the olfactory bulb
 medial septum
 diagonal band of Broca and throughout the preoptic area
 with the most concentrated population being around 0.5 mm rostral to the bregma. Co-immunofluorescence staining revealed that
 in these rostral brain areas
 the vast majority of the Kiss1r-expressing neurones co-expressed GnRH. Moderate levels of Kiss1r mRNA were also noted in the rostral periventricular area
 paraventricular nucleus (PVN)
 and throughout the arcuate nucleus. Relatively weak Kiss1r expression was observed in the supraoptic nucleus and supramammillary nuclei. Moderate to weak expression of Kiss1r was also observed in several regions in the midbrain
 including the periaqueductal gray and dorsal raphe nucleus. We also examined whether oxytocin and AVP neurones in the PVN co-express Kiss1r. Immunofluorescence revealed the co-expression of Kiss1r in a subset of the oxytocin neurones but not in the AVP neurones in the PVN. The present study provides a fundamental anatomical basis for further examination of the kisspeptin signalling system in the extra-HPG axis
 as well as in reproductive function.

Journal of Neuroendocrinology

Blackwell Publishing Ltd

28

4

10.1111/jne.12356

https://doi.org/10.1111/jne.12356
https://www.ncbi.nlm.nih.gov/pubmed/26709462