7 research outputs found
Homeostasis Meets Motivation in the Battle to Control Food Intake.
Signals of energy homeostasis interact closely with neural circuits of motivation to control food intake. An emerging hypothesis is that the transition to maladaptive feeding behavior seen in eating disorders or obesity may arise from dysregulation of these interactions. Focusing on key brain regions involved in the control of food intake (ventral tegmental area, striatum, hypothalamus, and thalamus), we describe how activity of specific cell types embedded within these regions can influence distinct components of motivated feeding behavior. We review how signals of energy homeostasis interact with these regions to influence motivated behavioral output and present evidence that experience-dependent neural adaptations in key feeding circuits may represent cellular correlates of impaired food intake control. Future research into mechanisms that restore the balance of control between signals of homeostasis and motivated feeding behavior may inspire new treatment options for eating disorders and obesity
Serotonergic neurons are involved in the counter-regulatory response to hypoglycemia
Abstract
Objectives. Intensive insulin therapy provides optimal glycemic control in patients with
diabetes. However, intensive insulin therapy causes so-called iatrogenic hypoglycemia as a
major adverse effect. The ventromedial hypothalamus (VMH) has been described as the
primary brain area initiating the counter-regulatory response (CRR). Nevertheless, the VMH
receives projections from other brain areas which could participate in the regulation of the
CRR. In particular, studies suggest a potential role of the serotonin (5-HT) network. Thus, the
objective of this work is to determine the contribution of 5-HT neurons in CRR control.
Methods. Complementary approaches have been used to test this hypothesis in quantifying the level of 5-HT in several brain areas by HPLC in response to insulin-induced hypoglycemia, measuring the electrical activity of dorsal Raphe (DR) 5-HT neurons in response to insulin or decreased glucose level by patch-clamp electrophysiology; and measuring the CRR hormone glucagon as an index of the counterregulatory responseCRR to the modulation of the activity of 5-HT neurons using pharmacological or pharmacogenetic approaches.
Results. HPLC measurements show that the 5HIAA/5HT ratio is increased in several brain
regions including the VMH in response to insulin-induced hypoglycemia. Patch-clamp
electrophysiological recordings show that insulin, but not decreased glucose level, increases
the firing frequency of DR 5-HT neurons in the DR. In vivo, both the pharmacological inhibition of 5-HT neurons by intraperitoneal injection of the 5-HT1A receptor agonist 8-OH-DPAT or the chemogenetic inhibition of these neurons reduces glucagon secretion, suggesting an impaired CRR.
Conclusion. Taken together, these data highlight a new neuronal network involved in the
regulation of the CRR. In particular, this study shows that DR 5-HT neurons detect iatrogenic
hypoglycemia in response to the increased insulin level and may play an important role in the regulation of CRR