Abstract

Background: Glucose-sensing neurons are located in several parts of the brain, but are concentrated in the ventromedial nucleus of the hypothalamus (VMH). The importance of these VMH neurons in glucose homeostasis is well-established, however, little is known about their individual identity. In the present study, we identified a distinct glucose-sensing population in the VMH and explored its place in the glucose-regulatory network.Methods: Using patch-clamp electrophysiology on Pacap-cre::EYFP cells, we explored the glucose-sensing ability of the pituitary adenylate cyclase-activating peptide (PACAP) neurons both inside and outside the VMH. We also mapped the efferent projections of these neurons using anterograde and retrograde tracing techniques. Finally, to test the functionality of PACAPVMH in vivo, we used DREADD technology and measured systemic responses.Results: We demonstrate that PACAP neurons inside (PACAPVMH), but not outside the VMH are intrinsically glucose inhibited (GI). Anatomical tracing techniques show that PACAPVMH neurons project to several areas that can influence autonomic output. In vivo, chemogenetic stimulation of these neurons inhibits insulin secretion leading to reduced glucose tolerance, implicating their role in systemic glucose regulation.Conclusion: These findings are important as they identify, for the first time, a specific VMH neuronal population involved in glucose homeostasis. Identifying the different glucose-sensing populations in the VMH will help piece together the different arms of glucose regulation providing vital information regarding central responses to glucose metabolic disorders including hypoglycaemia.

Highlights

  • Glucose is the primary source of energy for the brain, so it is not surprising that several redundant neural pathways are involved in the detection and tight regulation of this nutrient

  • The densest concentration of glucose-sensing neurons is found in the Glucose-Sensing ventromedial nucleus of the hypothalamus (VMH) pituitary adenylate cyclaseactivating peptide (PACAP) Neurons ventromedial hypothalamus and, in the ventromedial nucleus (VMH), though little is known about their identity

  • Using dual-label immunohistochemistry, we observed that PACAP-EYFP is expressed in 15% of neurons staining for neuronal nitric oxide synthase 1 within the VMH (Figure 1B)

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Summary

Introduction

Glucose is the primary source of energy for the brain, so it is not surprising that several redundant neural pathways are involved in the detection and tight regulation of this nutrient. 14% of rat VMH neurons are inherently sensitive to increased glucose and respond with an increase in electrical activity These are termed glucose excited (GE) and are thought to depend on glucose metabolism and inhibition of an ATP-sensitive potassium channel for their intrinsic sensing ability [8, 9]. 14% of VMH neurons are depolarized by reduced glucose, but this is dependent on synaptic transmission These have been termed presynaptically excited by decreased glucose (PED), but it is not clear whether their synaptic drive comes from within or from outside the VMH (or perhaps both). Glucose-sensing neurons are located in several parts of the brain, but are concentrated in the ventromedial nucleus of the hypothalamus (VMH) The importance of these VMH neurons in glucose homeostasis is well-established, little is known about their individual identity. We identified a distinct glucose-sensing population in the VMH and explored its place in the glucose-regulatory network

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