Abstract

Metabolic interaction via lactate between glial cells and neurons has been proposed as one of the mechanisms involved in hypothalamic glucosensing. We have postulated that hypothalamic glial cells, also known as tanycytes, produce lactate by glycolytic metabolism of glucose. Transfer of lactate to neighboring neurons stimulates ATP synthesis and thus contributes to their activation. Because destruction of third ventricle (III-V) tanycytes is sufficient to alter blood glucose levels and food intake in rats, it is hypothesized that tanycytes are involved in the hypothalamic glucose sensing mechanism. Here, we demonstrate the presence and function of monocarboxylate transporters (MCTs) in tanycytes. Specifically, MCT1 and MCT4 expression as well as their distribution were analyzed in Sprague Dawley rat brain, and we demonstrate that both transporters are expressed in tanycytes. Using primary tanycyte cultures, kinetic analyses and sensitivity to inhibitors were undertaken to confirm that MCT1 and MCT4 were functional for lactate influx. Additionally, physiological concentrations of glucose induced lactate efflux in cultured tanycytes, which was inhibited by classical MCT inhibitors. Because the expression of both MCT1 and MCT4 has been linked to lactate efflux, we propose that tanycytes participate in glucose sensing based on a metabolic interaction with neurons of the arcuate nucleus, which are stimulated by lactate released from MCT1 and MCT4-expressing tanycytes.

Highlights

  • The ventromedial hypothalamus (VMH) is involved in the regulation of satiety and feeding behavior through its capacity to detect changes in glucose concentrations [1]

  • monocarboxylate transporters (MCTs) expression in rat hypothalamus was initially analyzed using RT-PCR with primers specific for MCT1 and MCT4 mRNAs

  • MCT1 expression was demonstrated using Western blot analysis of proteins isolated from rat kidney and hypothalamus (Fig. 1C, lanes 1–2)

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Summary

Introduction

The ventromedial hypothalamus (VMH) is involved in the regulation of satiety and feeding behavior through its capacity to detect changes in glucose concentrations [1]. Different in vitro studies have shown that lactate can influence the behavior of GE neurons from the VMH [4,6], suggesting that this monocarboxylate is required for glucose sensing in the brain. In this context, it has been proposed that glycolytic metabolism of glucose to lactate by hypothalamic glial cells and the subsequent release to neighboring neurons using monocarboxylate transporters (MCTs) may lead to enhanced ATP synthesis, closure of KATP channels, and neuronal depolarization [9]

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