Abstract
The adipocyte‐derived hormone leptin plays a critical role in the control of reproduction via signalling in hypothalamic neurones. The drivers of the hypothalamic‐pituitary‐gonadal axis, the gonadotrophin‐releasing hormone (GnRH) neurones, do not have the receptors for leptin. Therefore, intermediate leptin responsive neurones must provide leptin‐to‐Gn RH signalling. We investigated the populations of leptin responsive neurones that provide input to the rostral preoptic area ( rPOA ) where Gn RH cell bodies reside. Fluorescent retrograde tracer beads (RetroBeads; Lumafluor Inc., Naples, FL, USA) were injected into the rPOA of transgenic leptin receptor enhanced green fluorescent protein ( Lepr ‐eGFP) reporter mice. Uptake of the RetroBeads by Lepr ‐ eGFP neurones was assessed throughout the hypothalamus. RetroBead uptake was most evident in the medial arcuate nucleus (ARC), the dorsomedial nucleus ( DMN ) and the ventral premammillary nucleus ( PMV ) of the hypothalamus. The uptake of RetroBeads specifically by Lepr ‐ eGFP neurones was highest in the medial ARC (18% of tracer‐labelled neurones Lepr ‐ eGFP ‐positive). Because neurones that are both leptin responsive and GABA ergic play a critical role in the regulation of fertility by leptin, we next focussed on the location of these populations. To address whether GABA ergic neurones in leptin‐responsive hypothalamic regions project to the rPOA , the experiment was repeated in GABA neurone reporter mice ( Vgat ‐tdTomato). Between 10% and 45% of RetroBead‐labelled neurones in the ARC were GABA ergic, whereas uptake of tracer by GABA ergic neurones in the DMN and PMV was very low (< 5%). These results show that both leptin responsive and GABA ergic neurones from the ARC project to the region of the Gn RH cell bodies. Our findings suggest that LEPR ‐expressing GABA neurones from the ARC may be mediators of leptin‐to‐Gn RH signalling.