Bakker, J., Pierman, S., González-Martínez, D., Effects of aromatase mutation (ArKO) on the sexual differentiation of kisspeptin neuronal numbers and their activation by same versus opposite sex urinary pheromones. Horm. Behav. 57 (2010), 390–395, 10.1016/j.yhbeh.2009.11.005.
Boehm, U., Zou, Z., Buck, L.B., Feedback loops link odor and pheromone signaling with reproduction. Cell 123 (2005), 683–695, 10.1016/j.cell.2005.09.027.
Castellano, J.M., Roa, J., Luque, R.M., Dieguez, C., Aguilar, E., Pinilla, L., Tena-Sempere, M., KiSS-1/kisspeptins and the metabolic control of reproduction: physiologic roles and putative physiopathological implications. Peptides, Kisspeptins 30 (2009), 139–145, 10.1016/j.peptides.2008.06.007.
Chachlaki, K., Malone, S.A., Qualls-Creekmore, E., Hrabovszky, E., Münzberg, H., Giacobini, P., Ango, F., Prevot, V., Phenotyping of nNOS neurons in the postnatal and adult female mouse hypothalamus. J. Comp. Neurol. 525 (2017), 3177–3189, 10.1002/cne.24257.
Clarkson, J., Han, S.-K., Liu, X., Lee, K., Herbison, A.E., Neurobiological mechanisms underlying kisspeptin activation of gonadotropin-releasing hormone (GnRH) neurons at puberty. Mol. Cell. Endocrinol., Special Issue: Neuroendocrinology of Puberty 324 (2010), 45–50, 10.1016/j.mce.2010.01.026.
Clarkson, J., Herbison, A.E., Postnatal development of kisspeptin neurons in mouse hypothalamus; sexual dimorphism and projections to gonadotropin-releasing hormone neurons. Endocrinology 147 (2006), 5817–5825, 10.1210/en.2006-0787.
de Roux, N., Genin, E., Carel, J.-C., Matsuda, F., Chaussain, J.-L., Milgrom, E., Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54. Proc. Natl. Acad. Sci. U.S.A. 100 (2003), 10972–10976, 10.1073/pnas.1834399100.
Dudley, C.A., Moss, R.L., Facilitation of lordosis in female rats by CNS-site specific infusions of an LH-RH fragment, Ac-LH-RH-(5-10). Brain Res. 441 (1988), 161–167, 10.1016/0006-8993(88)91394-7.
Foreman, M.M., Moss, R.L., Effects of subcutaneous injection and intrahypothalamic infusion of releasing hormones upon lordotic response to repetitive coital stimulation. Horm. Behav. 8 (1977), 219–234, 10.1016/0018-506X(77)90039-3.
Hanchate, N.K., Parkash, J., Bellefontaine, N., Mazur, D., Colledge, W.H., d'Anglemont de Tassigny, X., Prevot, V., Kisspeptin-GPR54 signaling in mouse NO-synthesizing neurons participates in the hypothalamic control of ovulation. J. Neurosci. 32 (2012), 932–945, 10.1523/JNEUROSCI.4765-11.2012.
Hellier, V., Brock, O., Bakker, J., The role of kisspeptin in sexual behavior. Semin. Reprod. Med., 37, 2019, 10.1055/s-0039-3400992 084–092.
Hellier, V., Brock, O., Candlish, M., Desroziers, E., Aoki, M., Mayer, C., Piet, R., Herbison, A., Colledge, W.H., Prévot, V., Boehm, U., Bakker, J., Female sexual behavior in mice is controlled by kisspeptin neurons. Nat. Commun., 9, 2018, 400, 10.1038/s41467-017-02797-2.
Higo, S., Honda, S., Iijima, N., Ozawa, H., Mapping of kisspeptin receptor mRNA in the whole rat brain and its Co-localisation with oxytocin in the paraventricular nucleus. J. Neuroendocrinol., 28, 2016, 10.1111/jne.12356.
Inoue, S., Yang, R., Tantry, A., Davis, C., Yang, T., Knoedler, J.R., Wei, Y., Adams, E.L., Thombare, S., Golf, S.R., Neve, R.L., Tessier-Lavigne, M., Ding, J.B., Shah, N.M., Periodic remodeling in a neural circuit governs timing of female sexual behavior. Cell 179 (2019), 1393–1408, 10.1016/j.cell.2019.10.025 e16.
Kauffman, A.S., Park, J.H., McPhie-Lalmansingh, A.A., Gottsch, M.L., Bodo, C., Hohmann, J.G., Pavlova, M.N., Rohde, A.D., Clifton, D.K., Steiner, R.A., Rissman, E.F., The kisspeptin receptor GPR54 is required for sexual differentiation of the brain and behavior. J. Neurosci. 27 (2007), 8826–8835, 10.1523/JNEUROSCI.2099-07.2007.
Kumar, D., Candlish, M., Periasamy, V., Avcu, N., Mayer, C., Boehm, U., Specialized subpopulations of kisspeptin neurons communicate with GnRH neurons in female mice. Endocrinology 156 (2015), 32–38, 10.1210/en.2014-1671.
Liu, X., Herbison, A., Kisspeptin regulation of arcuate neuron excitability in kisspeptin receptor knockout mice. Endocrinology 156 (2015), 1815–1827, 10.1210/en.2014–1845.
Lolait, S.J., Stewart, L.Q., Jessop, D.S., Young, W.S. 3rd, O'Carroll, A.-M., The hypothalamic-pituitary-adrenal Axis response to stress in mice lacking functional vasopressin V1b receptors. Endocrinology 148 (2007), 849–856, 10.1210/en.2006-1309.
Marraudino, M., Miceli, D., Farinetti, A., Ponti, G., Panzica, G., Gotti, S., Kisspeptin innervation of the hypothalamic paraventricular nucleus: sexual dimorphism and effect of estrous cycle in female mice. J. Anat. 230 (2017), 775–786, 10.1111/joa.12603.
Mayer, C., Boehm, U., Female reproductive maturation in the absence of kisspeptin/GPR54 signaling. Nat. Neurosci. 14 (2011), 704–710, 10.1038/nn.2818.
McCarthy, E.A., Naik, A.S., Coyne, A.F., Cherry, J.A., Baum, M.J., Effect of ovarian hormones and mating experience on the preference of female mice to investigate male urinary pheromones. Chem. Senses 43 (2018), 97–104, 10.1093/chemse/bjx073.
Moss, R.L., McCann, S.M., Induction of mating behavior in rats by luteinizing hormone-releasing factor. Science 181 (1973), 177–179, 10.1126/science.181.4095.177.
Neumann, I.D., Chapter 12 Involvement of the brain oxytocin system in stress coping: interactions with the hypothalamo-pituitary-adrenal axis. Progress in Brain Research, Vasopressin and Oxytocin: from Genes to Clinical Applications, 2002, Elsevier, 147–162, 10.1016/S0079-6123(02)39014-9.
Oishi, S., Misu, R., Tomita, K., Setsuda, S., Masuda, R., Ohno, H., Naniwa, Y., Ieda, N., Inoue, N., Ohkura, S., Uenoyama, Y., Tsukamura, H., Maeda, K., Hirasawa, A., Tsujimoto, G., Fujii, N., Activation of neuropeptide FF receptors by kisspeptin receptor ligands. ACS Med. Chem. Lett. 2 (2010), 53–57, 10.1021/ml1002053.
Pfaff, D.W., Estrogens and Brain Function: Neural Analysis of a Hormone-Controlled Mammalian Reproductive Behavior. 1980, Springer-Verlag, New York, 10.1007/978-1-4613-8084-9.
Rao, Y.S., Mott, N.N., Pak, T.R., Effects of kisspeptin on parameters of the HPA axis. Endocrine 39 (2011), 220–228, 10.1007/s12020-011-9439-4.
Sirinathsinghji, D.J.S., GnRH in the spinal subarachnoid space potentiates lordosis behavior in the female rat. Physiol. Behav. 31 (1983), 717–723, 10.1016/S0031-9384(83)80009-2.
Stowers, L., Kuo, T.-H., Mammalian pheromones: emerging properties and mechanisms of detection. Curr. Opin. Neurobiol. 34 (2015), 103–109, 10.1016/j.conb.2015.02.005.
Taziaux, M., Bakker, J., Absence of female-typical pheromone-induced hypothalamic neural responses and kisspeptin neuronal activity in α-fetoprotein knockout female mice. Endocrinology 156 (2015), 2595–2607, 10.1210/en.2015-1062.
Ward, B.J., Charlton, H.M., Female sexual behaviour in the GnRH deficient, hypogonadal (hpg) mouse. Physiol. Behav. 27 (1981), 1107–1109, 10.1016/0031-9384(81)90378-4.
Warembourg, M., Leroy, D., Jolivet, A., Nitric oxide synthase in the Guinea pig preoptic area and hypothalamus: distribution, effect of estrogen, and colocalization with progesterone receptor. J. Comp. Neurol. 407 (1999), 207–227, 10.1002/(sici)1096-9861(19990503)407:2<207::aid-cne5>3.0.co;2-a.
Wen, S., Götze, I.N., Mai, O., Schauer, C., Leinders-Zufall, T., Boehm, U., Genetic identification of GnRH receptor neurons: a new model for studying neural circuits underlying reproductive physiology in the mouse brain. Endocrinology 152 (2011), 1515–1526, 10.1210/en.2010-1208.
Yang, C.F., Chiang, M.C., Gray, D.C., Prabhakaran, M., Alvarado, M., Juntti, S.A., Unger, E.K., Wells, J.A., Shah, N.M., Sexually dimorphic neurons in the ventromedial hypothalamus govern mating in both sexes and aggression in males. Cell 153 (2013), 896–909, 10.1016/j.cell.2013.04.017.
Yeo, S.-H., Kyle, V., Morris, P.G., Jackman, S., Sinnett-Smith, L.C., Schacker, M., Chen, C., Colledge, W.H., Visualisation of Kiss1 neurone distribution using a kiss1-CRE transgenic mouse. J. Neuroendocrinol., 28, 2016, 10.1111/jne.12435.
Yip, S.H., Boehm, U., Herbison, A.E., Campbell, R.E., Conditional viral tract tracing delineates the projections of the distinct kisspeptin neuron populations to gonadotropin-releasing hormone (GnRH) neurons in the mouse. Endocrinology 156 (2015), 2582–2594, 10.1210/en.2015-1131.
Zinck, L., Lima, S.Q., Mate choice in Mus musculus is relative and dependent on the estrous state. PloS One, 8, 2013, e66064, 10.1371/journal.pone.0066064.
