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. 2021 Jul 14;226(7):2387–2399. doi: 10.1007/s00429-021-02339-z

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© The Author(s) 2021

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 4 — Illustration of the brain areas containing Cre expressing KP neurons (A and B), which underwent a virus-based identification in the preoptic (C), arcuate (D), and medial amygdala (E) regions, respectively. The expressed YFP has been immunohistochemically amplified to show membranes of KP neurons. Modifications of the atlas images from the mouse brain atlas of Paxinos and Franklin’s (2012). Scale bar 200 µm. Arc arcuate nucleus, AVPe anteroventral periventricular nucleus, ME median eminence, MePD posterodorsal subdivision of medial amygdala, och optic chiasm, opt optic tract, Pe periventricular hypothalamic nucleus, st stria terminalis, VMH ventromedial hypothalamic nucleus