4.5 Article

Repeated Activation of Noradrenergic Receptors in the Ventromedial Hypothalamus Suppresses the Response to Hypoglycemia

期刊

ENDOCRINOLOGY
卷 162, 期 3, 页码 -

出版社

ENDOCRINE SOC
DOI: 10.1210/endocr/bqaa241

关键词

hypoglycemia; ventromedial hypothalamus (VMH); norepinephrine; lactate; counterregulatory response

资金

  1. Juvenile Diabetes Research Foundation [3-SRA-2017-487-S-B]
  2. National Institutes of Health [R01 DK099315]

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Repeated activation of noradrenergic receptors in the ventromedial hypothalamus increases local lactate levels, leading to a blunted counterregulatory hormone response to hypoglycemia.
Activation of the adrenergic system in response to hypoglycemia is important for proper recovery from low glucose levels. However, it has been suggested that repeated adrenergic stimulation may also contribute to counterregulatory failure, but the underlying mechanisms are not known.The aim of this study was to establish whether repeated activation of noradrenergic receptors in the ventromedial hypothalamus (VMH) contributes to blunting of the counterregulatory response by enhancing local lactate production.The VMH of nondiabetic rats were infused with either artificial extracellular fluid, norepinephrine (NE), or salbutamol for 3 hours/day for 3 consecutive days before they underwent a hypoglycemic clamp with microdialysis to monitor changes in VMH lactate levels. Repeated exposure to NE or salbutamol suppressed both the glucagon and epinephrine responses to hypoglycemia compared to controls. Furthermore, antecedent NE and salbutamol treatments raised extracellular lactate levels in the VMH. To determine whether the elevated lactate levels were responsible for impairing the hormone response, we pharmacologically inhibited neuronal lactate transport in a subgroup of NE-treated rats during the clamp. Blocking neuronal lactate utilization improved the counterregulatory hormone responses in NE-treated animals, suggesting that repeated activation of VMH beta 2-adrenergic receptors increases local lactate levels which in turn, suppresses the counterregulatory hormone response to hypoglycemia.

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