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Neuronal control of peripheral insulin sensitivity and glucose metabolism

Nature Communications volume 8, Article number: 15259 (2017) | Download Citation

The central nervous system (CNS) has an important role in the regulation of peripheral insulin sensitivity and glucose homeostasis. Research in this dynamically developing field has progressed rapidly due to techniques allowing targeted transgenesis and neurocircuitry mapping, which have defined the primary responsive neurons, associated molecular mechanisms and downstream neurocircuitries and processes involved. Here we review the brain regions, neurons and molecular mechanisms by which the CNS controls peripheral glucose metabolism, particularly via regulation of liver, brown adipose tissue and pancreatic function, and highlight the potential implications of these regulatory pathways in type 2 diabetes and obesity.

More than one third of the adult population is obese in many countries, including newly industrialized states, making obesity a global human health problem1. Obesity is often accompanied by insulin resistance (the condition when cells fail to respond to insulin) and glucose intolerance (the inability of cells to clear glucose from the blood stream after a glucose load), the prevalence of which are estimated to advance as the number of obese individuals continues to increase2. Obesity constitutes an important risk factor not only for the development of type 2 diabetes (T2D), but also for cardiovascular disease and even certain types of cancer, all of which ultimately reduce life expectancy3,4.

Insulin resistance and glucose intolerance result in a disturbed glucose homeostasis, a state that describes the inability to maintain stable glucose levels (euglycemia). Maintenance of euglycemia is controlled via the tightly balanced action of hormones, such as cortisol and glucagon, which increase blood glucose concentrations; insulin, on the other hand, is the only hormone identified that is capable of clearing glucose from the blood. Insulin acts on the insulin receptor (IR), a membrane bound tyrosine kinase5, which lowers blood glucose concentrations by promoting glucose uptake, while also suppressing hepatic glucose production (HGP) (Fig. 1).

Figure 1: Glucoregulatory roles of the pancreatic-derived hormones insulin and glucagon.
Figure 1

The pancreatic islets of Langherhans, containing alpha cells and beta cells, secrete glucagon and insulin respectively. Insulin and glucagon exert antagonistic effects on peripheral organs to control blood glucose levels. Insulin exerts its glucose lowering effects by stimulating glucose uptake in skeletal muscle, through inhibiting hepatic glucose production and by blunting lipolysis. By contrast, glucagon raises circulating glucose levels by increasing gluconeogenesis and lipolysis.

Over the past 20 years, novel molecular mechanisms linking obesity and the development of insulin resistance have been deciphered, including obesity-associated inflammation, deregulated endoplasmic reticulum-stress regulation, mitochondrial dysfunction and lipotoxicity. Whereas the field has largely focused on direct effects of obesity-associated alterations in peripheral tissues such as liver, skeletal muscle and adipose tissue (Fig. 1), the role of the central nervous system (CNS) as a regulator of energy fluxes across different organs and with effects on glucose homeostasis has not received the same attention. Recently, an important role for the CNS in the regulation of peripheral insulin sensitivity and glucose homeostasis has been unravelled. We review the progress made in this research field and place particular emphasis on the central control of liver and brown adipose tissue (BAT) as well as pancreatic islet function in control of glucose metabolism. We provide an update on the key brain regions, neurons and molecular mechanisms in these neurons and the downstream neurocircuitries identified, as well as outline relevant peripheral mediators that act on the these brain circuits in the control of glucose homeostasis. We also review recent literature on how obesity perturbs CNS-dependent control of glucose metabolism, and highlight the potential clinical relevance of these regulatory CNS pathways in T2D.

Key CNS sites in control of glucose metabolism

Solid evidence for a role of CNS circuits in regulating systemic glucose homeostasis dates back to the 1850s (Box 1). Today, a large literature substantiates energy-regulatory capabilities of a plethora of areas in the rodent brain (Fig. 2). Among those, several nuclei residing in the hypothalamus stand out, of which the arcuate nucleus (ARH), the ventromedial nucleus (VMH) and lateral hypothalamic area (LHA) have received most attention. We now recognize a neuroregulatory network governing control over feeding, peripheral insulin sensitivity and glucose metabolism extending beyond the ARH, VMH and LHA (Table 1). These regulatory centres also include a number of extra-hypothalamic nuclei, such as sensory and integrative clusters in the hindbrain6,7, as well as autonomic, parasympathetic and sympathetic preganglionic brainstem neurons8,9. Owing to the application of cell-specific chemogenetic and optogenetic techniques10,11, several of these nuclei were initially documented to orchestrate the behavioural and autonomic repertoire that controls feeding (Table 2) and some of these neurons have more recently been assigned gluco-regulatory properties beyond and even independent of their food intake-regulatory function.

Box 1: Claude Bernard revisited.

In the 1850s, physiologist Claude Bernard observed that manipulation to the floor of the fourth ventricle in the hindbrain of experimental animals caused blood glucose levels to rise above normal, and that the excess sugar was excreted in the urine99. Befittingly, Bernard is associated with articulating the concept of homeostasis (milieu intérieur; French for ‘the environment within’). Walter Bradford Cannon later conceptualized and developed it further. Although these observations and Bernard’s finding that the liver contains glycogen (indicating that the liver stores an energy source that can be converted into glucose) were epoch-making, the extraordinary important discovery of insulin in the 1920s by Banting and fellow workers made scientists to shift their focus and research activities. With diminished enthusiasm for the brain as an interesting target for intervention, research was now devoted to deciphering insulin action in peripheral organs and defects in pancreatic insulin secretion. In hindsight, however, and considering that the brain governs control of most homeostatic networks, it seems improbable that glucose metabolism would be controlled by mechanisms independent of the CNS.

Figure 2: Key brain nuclei and areas involved in CNS control of glucose homeostasis.
Figure 2

Schematic representing a sagittal section of a mouse brain in which critical brain regions controlling glucose homeostasis and peripheral insulin sensitivity as well as brown fact activity are depicted. Three main regions are highlighted: the bed nucleus of the stria terminalis (BNST), the hypothalamus and the medulla. The hypothalamus contains the preoptic area, the paraventricular nucleus (PVH), the lateral hypothalamic area (LHA), the ventromedial nucleus of the hypothalamus (VMH, where SF-1-expressing neurons reside), the dorsomedial nucleus of the hypothalamus (DMH) and the arcuate nucleus of the hypothalamus (ARH) where AgRP/NPY and POMC neurons are located. In the caudal part the brain, the medulla contains key areas such as the dorsal vagal complex (DVC) and the raphe pallidus nucleus (RPA). 3V, third ventricle; 4V, fourth ventricle; fx, fornix; LV, lateral ventricle; me, median eminence.

Table 1: Cell type- and neurocircuit-specific manipulations reported to modulate peripheral insulin sensitivity and/or glucose homeostasis acutely or chronically.
Table 2: Cell type-specific manipulations reported to alter food intake.

The arcuate nucleus of the hypothalamus

The ARH is located at the floor of the third ventricle, leveling with the base of the pituitary stalk (a funnel of nerves connecting the brain with the pituitary gland) and bridges with the median eminence. ARH neurons sense peripheral substances that signal the energy state of the organism. Accordingly, pro-opiomelanocortin (POMC), and agouti-related peptide (AgRP)/neuropeptide Y (NPY), expressed in two anatomically neighbouring and molecularly defined neuronal populations in the ARH (Fig. 2) are vital for the control of energy homeostasis in that they have profound effects on appetite and feeding behaviour (Box 2). In line with their ability to integrate peripheral signals and adapt their electrical activity according to energy availability, chronic manipulations of hormonal and nutrient signalling in POMC and AgRP neurons affect glucose metabolism in peripheral tissues12,13. However, whether POMC or AgRP neuron firing acutely controls glucose metabolism was not established until recently. Using cell-specific excitatory techniques, acute activation of AgRP neurons was found to impair systemic insulin sensitivity and glucose tolerance after acutely raising insulin or glucose in the bloodstream14. Specifically, AgRP-neuron activation halved insulin-stimulated glucose uptake selectively into BAT, likely through re-programming the gene expression profile towards a myogenic signature14. The most strongly upregulated gene in BAT was myostatin, a molecule previously linked to abnormal glucose metabolism15. Indeed, acute induction of myostatin partially explained the insulin resistance downstream of AgRP-neuron stimulation14.

Box 2: AgRP and POMC ARH neurons are key regulators of food intake.

The activity of POMC and AgRP neurons bi-modally and rapidly controls appetitive behavior even upon mere sensory perception of food100. Activation of POMCARH neurons selectively suppresses appetite19,98 (Table 2), and mutations in the POMC gene are associated with obesity in a range of species including humans, mice and dogs101. Best known for signaling satiety, recent intriguing data reveal a previously unprecedented function of a subset of POMC neurons to promote feeding behavior through cannabinoid-receptor mediated release of β-endorphin, an endogenous opioid neuropeptide originating from the POMC precursor molecule102. By contrast, AgRP neurons are hunger sensitive and signal energy deficits: their activation rapidly evokes eating and their ablation in the adult animal causes rapid weight loss due to cessation of feeding16,19,103,104. Mechanistically, the neuropeptide AgRP competes with α-melanocyte-stimulating hormone (α-MSH) released from POMC neurons for binding sites on the melanocortin 4-receptor (MC4R), blocks the coupling to a Gαs signaling pathway, and promotes feeding when AgRP has the upper hand. Besides the canonical view of neuronal MC4R signaling, new fascinating data however suggest that AgRP can act independently of Gαs and through regulating the pore state of an inwardly rectifying potassium channel, Kir7.1. According to these results, binding of AgRP onto MC4R opens Kir7.1 and hyperpolarizes the downstream target second order neuron without its inhibition of α-MSH binding, some of which are located in the paraventricular hypothalamus, a nucleus crucial to the control of hunger (Fig. 2)97,105.

Previous studies showed that acute activation of AgRP neurons reduces energy expenditure16, whereas mice genetically modified to lack AgRP neurons burn slightly more calories17, indicating a relationship between AgRP neurons and brown fat function. Consistent with these observations, acute activation of AgRP neurons decreased the activity in sympathetic nerves supplying BAT, and a lower β-adrenergic tone contributed to the development of systemic insulin resistance upon AgRP-neuron activation14. Pursuing the neurocircuitry downstream of AgRP-neuron driven insulin resistance using optogenetic circuit mapping, impaired insulin sensitivity and induced myostatin expression in BAT ensued when acutely stimulating fibres comprising AgRPARH→BNST projections, involving the ventrolateral subnucleus of the anterior BNST (AgRPARH→vlBNST). Activating this projection in the vlBNST did not induce a feeding response however14. With respect to appetite control, activation of long- and short-range outputs from distinct subpopulations of AgRP neurons to several downstream sites is sufficient to evoke feeding alone. These observations point to a parallel and redundant organization of AgRP neuronal circuits that controls feeding behaviour18. As far as glucose homeostasis is concerned, one projection from AgRP neurons to the dorsomedial subnucleus of the aBNST controls feeding but not insulin sensitivity14, whereas one AgRPARH→vlBNST pathway controlling insulin sensitivity also encodes induction of BAT myostatin but not feeding. Although all AgRP neuron projections sites potentially controlling systemic glucose metabolism have not yet been probed, the data available thus suggest that peripheral insulin sensitivity is controlled by less redundant AgRP neuron circuits compared to those in control of feeding behaviour.

By contrast, acute activation of POMC neurons had no effect on glucose metabolism in these studies14, suggesting that acute AgRP neuron activation controls peripheral insulin sensitivity without interfering with the melanocortin pathway. Experiments defining melanocortin-dependent feeding behaviour have shown that the hypophagia from stimulating POMC neurons is prevented in Ay mice, in which AgRP constitutively blocks melanocortin signalling. By contrast, the hyperphagia from activating AgRP neurons is intact in Ay mice19, and melanocortin receptor blockade cannot prevent the hypophagic response upon AgRP neuron ablation20. Taken together, AgRP neurons may similarly control glucose metabolism independently of melanocortin signalling. To this end, AgRP neurons also synthesize NPY and GABA, and whereas AgRP through its action on MC4Rs is sufficient to trigger sustained but delayed increase in food intake, both NPY and GABAergic signalling contribute to the rapid hyperphagia observed upon AgRP neuron excitation21,22. AgRP neurons may thus govern control over glucose metabolism through NPY, GABA receptor signalling, or a combination of both. Interestingly, induced NPY expression specifically from the ARH reduces energy expenditure and decreases BAT thermogenesis via NPY1-receptor signalling in key nuclear relay stations, including the locus coeruleus, solitary tract nucleus and ventrolateral medulla in the hindbrain, some of which modulate sympathetic outflow to BAT23. These observations indicate that NPY-receptor signalling downstream of AgRP neurons may explain some of the effects on brown fat physiology exerted by AgRP neurons, and possibly systemic insulin sensitivity. Thus, further studies will have to address if NPY and/or GABA signalling exert the rapid glucose regulatory function of AgRP neurons.

Finally, although acute activation of POMC neurons was ineffective in affecting glucose metabolism in these studies, it is noteworthy that a recent study reported that chemogenetic activation of POMCARH neurons markedly and rapidly (within minutes) increases BAT temperature by several degrees24, demonstrating that POMCARH neurons promote BAT thermogenesis. The reasons why POMC-positive ARH cells potently affect BAT temperature without clear effects on insulin sensitivity are currently unknown, and future studies will be needed to address the nature of this divergence.

The ventromedial nucleus of the hypothalamus

The brain launches an adaptive and protective counter-regulatory response when glucose levels fall out of range. The VMH (Fig. 2) is known to be particularly important for this counter-regulatory response25. Glucose-sensing mechanisms in VMH neurons, which are excited or inhibited by local changes in ambient glucose concentrations, and exert important roles in maintaining energy balance and glucose metabolism, have been carefully analysed, in particular in VMH neurons expressing steroidogenic factor-1 (SF-1)26 and/or the gene encoding glucokinase. In mice that are hypoglycemic owing to a high dose of insulin, the ability to normalize glycaemia fails when SF-1 neurons are optogenetically inhibited, as the anticipated rebound from hypoglycemia elicited by insulin is attenuated27. In turn, optogenetic activation of SF-1 neurons increases blood glucose, and causes profound hyperglycaemia when blood glucose levels are elevated either by stimulating HGP or by injecting glucose into mice27. The differential responses may stem from a failure of stimulating glucagon and corticosterone release (when SF-1 neurons are inhibited), or from the inability to balance glucagon and corticosterone secretion and control HGP (when SF-1 neurons are stimulated). It is conceivable that photostimulation of SF-1-expressing neurons mimics a state of glucodeprivation in the VMH since they stimulate the counter-regulatory response to hypoglycemia, including effects on pancreas and liver. Further expanding our understanding of the neural network for counterregulation, stimulating SF-1VMH→aBNST axonal projections was recently shown to result in increased plasma levels of glucagon and corticosterone and hyperglycaemia27. Thus, a defined circuit spanning from glucose-sensing VMH neurons to the aBNST specifically regulates expression of key genes for hepatic gluconeogenesis and influences the abundance of counter-regulatory hormones striving to restore glycaemia.

In another study, investigators used radiowaves to manipulate glucokinase-expressing VMH neurons engineered to respond to an electromagnetic field, and showed that activation of VMH neurons robustly elevates blood glucose and glucagon concentrations in the circulation as well as drives the expression of key hepatic gluconeogenic genes, whereas inhibition quells these responses28. These findings further substantiate a role for the VMH in the control of peripheral glucose metabolism, and the authors describe a novel technique, dubbed magnetogenetics, to affect neuronal activity through a genetically encoded fusion protein between the iron-binding protein ferritin and a thermo-sensitive ion channel protein. Although the paper describes a way to remotely manipulate the electrical activity of neurons in mice with a very clear outcome28 and whereas a string of recent articles report the successful use of magnetogenetics, the way the underlying operative mechanism biophysically works is unclear and has turned into a subject of debate29.

To ensure that the field strength was adequate to affect neuronal activity, while permitting assessments of its impact on glucose metabolism in vivo, the mice had to be anesthetized in those studies28. Although the findings obtained from manipulating VMH neurons were the expected, whether exactly the same outcome is present in awake mice could not be proven with the confines of the method, as narcosis might have intrinsic effects on neural activity and glucose homeostasis. Thus, refinements of the necessary equipment for electromagnetics is required for large-scale use and to set the stage for further exciting discoveries. Moreover, future studies are encouraged to define the precise mechanism of magnetogenetics.

Although recent research has provided a wealth of information, the functional organization of the neurocircuity influencing counter-regulatory mechanisms of glycemic control remains to be better understood, and electromagnetics is hoped to provide more answers on the neuroendocrine components and architecture contributing. While the aBNST has surfaced as a key integrative glucoregulatory node, the details about this system remain to be specified. Specifically, which descending neural network downstream of the aBNST, tethering it do BAT glucose utilization, insulin sensitivity and counter-regulatory responses, as well as the exact cellular phenotype of the crucial aBNST neurons are issues that clearly call for additional study.

The preoptic area and lateral hypothalamic area

Located along the midline of the anterior hypothalamus, the preoptic area (PoA) is situated closely below the anterior commissure (where nerve bundles pass between the two brain hemispheres) and above the optic chiasm (where optic nerve fibres from the retinas cross between the two hemispheres) (Fig. 2). The PoA regulates BAT heat production, a process that depends on the metabolism of significant amounts of glucose and triglycerides30,31,32. Nevertheless, the thermoregulatory function of this brain region has been primarily studied in the context of fever, which is driven by prostaglandin signalling in the median preoptic subnucleus33 and activates brown fat thermogenesis via a neural pathway including the rostral raphe pallidus (Fig. 2).

Surgical or electric manipulations of the LHA neurons over 50 years ago were shown to control food intake. We now know that a part of this effect is explained by an inhibitory synaptic innervation from the BNST to glutamatergic LHA neurons, eliciting voracious feeding in mice that are already satiated when optogenetically manipulated34. In food-deprived animals, inhibiting this input onto the LHA conversely suppresses feeding34. Furthermore, projections to the LHA from AgRP neurons impair systemic insulin sensitivity when activated14. Whether impairments in insulin sensitivity induced by the AgRPARH→LHA circuit also involve excitatory LHA neurons is currently unknown.

So far, recent observations point toward a critical role for MC4R signalling in the LHA in control of glucose homeostasis35. By reconstituting MC4R expression specifically in LHA neurons of obese mice carrying a null MC4R allele (MC4RLHA), Morgan et al. were able to improve glucose tolerance and glycaemia in both normal chow and high-fat diet (HFD)-fed mice independent of changes in body weight, adiposity or insulin concentrations35. Activation of the MC4R using an α-melanocyte stimulating hormone (α-MSH) analogue in mice with MC4Rs re-expressed in the LHA increased glucose uptake specifically into brown fat; this effect correlated with subtle increments in glucose transporter 4 (GLUT-4) gene expression and upregulation of a thermogenic gene expression programme in BAT35. Consistent with the idea that MC4RLHA signalling facilitates BAT glucose utilization via the sympathetic nervous system, nerves innervating BAT showed normal spiking responses to a MC4R agonist in mice carrying a reactivated MC4R gene in the LHA, in contrast to the nerves in obese whole-body MC4R knockouts that were insensitive, and surgically eliminating BAT from sympathetic input furthermore impaired the improved glucose tolerance obtained from MC4RLHA reactivation35. Thus, MC4RLHA signalling activates sympathetic outflow to BAT, and intact sympathetic control over BAT glucose uptake is required to rescue the glucose tolerance when the MC4R is gone in every cell but in LHA neurons, as judged from this comprehensive study in mice35.

Brown fat activity and humans

In humans, the quantity of BAT correlates inversely with BMI, BAT is highly responsive to cold and diet exposure, an adaptive response that is reduced in obese and overweight subjects, and insulin36,37,38,39,40. There is evidence that BAT is less active in diabetics41 and that BAT activation improves whole-body glucose homeostasis and insulin sensitivity42. Such observations have fostered the notion that strong actuators of BAT activity could be used to treat obesity and diabetes.

Brown fat function is often studied under cold conditions, a state that does not allow capturing whether BAT plays a role in glucose metabolism at euthermia. To measure whether metabolic activity in human BAT affects blood glucose levels over time and depending on feeding state and circadian rhythm, Lee and colleagues measured the temperature profile of the skin overlying supraclavicular BAT as a surrogate of conventional fluorodeoxyglucose positron emission tomography (FDG-PET) imaging43. At thermoneutrality, supraclavicular BAT temperature progressively rose during a glucose load, indicating that BAT utilizes glucose. The authors also observed a noteworthy rhythmicity in glucose uptake into human brown adipocytes, especially after insulin stimulation, together with oscillating trafficking of GLUT-4 to the plasma membrane, which mirrored the fluctuations in glucose uptake and generated heat43. In humans (normal weight, non-diabetic men in their mid-twenties) with larger than average active BAT depots, changes in BAT thermogenesis predicted subcutaneous blood glucose levels, whereas BAT thermogenic activity responded to systemic changes in glycaemia in individuals with comparatively small amounts of BAT43. Notably, men devoid of supraclavicular BAT exhibited the largest glycemic variability. Conceivably, human BAT glucose utilization is linked to thermogenesis, and BAT shows a glucose-responsive rhythm entrained by circadian oscillations in GLUT-4 in a similar manner as mechanisms coordinating body temperature rhythmicity and responses to cold44. In light of these findings, whether greater fluctuations in glucose levels as a consequence of the amount of functionally active BAT pre-dispose for diabetes warrant further investigations.

Hormonal signalling to the brain and effects on glucose metabolism

Afferent hormonal and nutritional cues provide feedback signals to the brain that are crucial for systemic glucose homeostasis. On the other hand, efferent signalling from the brain to peripheral tissues is promoted via the autonomic nervous system, for example to control HGP, BAT activity and pancreatic hormone secretion (Fig. 3). Although Claude Bernard’s (Box 1) work was an exciting starting-point, the idea that the brain controls peripheral glucose metabolism was largely ignored by the scientific community for a long time. However, several discoveries made in the past 20 years have reignited interest in this concept. Firstly, activation of the IR, which is widely expressed throughout the CNS, was shown to curb eating. Secondly, manipulation of key IR signalling components (such as PI3 kinases), activation of neuronal ATP sensitive potassium channels45, or depletion of functional IRs from the brain46, affect not only energy homeostasis but also systemic glucose metabolism. In humans, insulin quenches HGP via the same class of potassium channels (KATP) as it does in rodents47. Insulin activates KATP channels in a PI3 kinase-dependent manner resulting in hyperpolarization of neurons13,48. However, how various hypothalamic neurons respond electrically to insulin might differ, as exemplified by the recent findings that insulin can excite POMC neurons via activation of canonical transient receptor potential channels in a PI3 kinase-dependent manner49. Similarly, insulin promotes PI3 kinase signalling in melanin-concentrating hormone (MCH) neurons in the LHA and increases their excitability50. Physiologically, insulin-dependent activation of these neurons impairs locomotor activity and glucose homeostasis by controlling hepatic insulin sensitivity and HGP in mice fed a HFD. Given that the phenotypic alterations dependent on IR signalling in MCH neurons were observable in HFD-fed mice but not lean mice fed a normal mouse chow suggest that this mechanism is engaged only during conditions when insulin levels rise. Consistent with this, HFD feeding associated with hyperinsulinemia increases PI3-kinase activity in MCH neurons via the IR50.

Figure 3: Pathways involved in the control of glucose homeostasis.
Figure 3

The central nervous system contains high density of receptors for the white adipose tissue (WAT)-derived hormone leptin as well as receptors for the pancreatic hormone insulin. Leptin and insulin act on specific brain regions that will in turn modulate glucose utilization and production in peripheral tissue via the autonomic nervous system. Notably, the vagus nerve links brain insulin action and the liver in the control of hepatic gluconeogenesis. At the pancreatic level, the autonomic nervous system is involved in pancreatic hormone secretion. The brown adipose tissue (BAT) receives sympathetic innervation which activity directly control BAT glucose uptake. NA, noradrenaline.

The insulin-dependent effects on MCH-expressing cells supports the existence of selective hormone resistance, which describes the occurrence of insulin resistance in cell types within the CNS with simultaneous retained or even over-activated insulin action in other CNS cell types. Indeed, the manifestation of selective CNS resistance to insulin represents a rule rather than exception26. In fact, insulin activates PI3K signalling and reduces the firing rate of a proportion of SF-1VMH neurons through KATP channel activation26. Mice lacking the IR on these subsets of neurons are partially protected from diet-induced obesity upon HFD feeding, associated with reduced systemic insulin levels and improved glucose metabolism26. Thus, the hyperinsulinemia present under prolonged HFD feeding predictably silences the SF-1 neurons, and IR signalling via the PI3K pathway in SF-1VMH neurons mediates systemic insulin resistance and obesity in response to a HFD. Thus, the manifestation of selective insulin resistance clearly necessitates work on the underlying molecular mechanisms. Future studies should focus on region-specific mechanisms of selective hormone resistance, and, ultimately, to develop cell-specific insulin (de)sensitizers in the treatment of obesity-associated alterations such as uncontrolled HGP.

Central insulin action controls HGP

Chronically elevated HGP contributes significantly to the hyperglycaemia associated with T2D (ref. 51). Understanding how the liver fails to respond to insulin and to the efferent signals originating from the CNS in the regulation of this process is thus of great importance.

Pharmacological approaches were the first to document a role for central insulin signalling in the control of peripheral glucose homeostasis, as infusion of insulin into the cerebral ventricle adjacent to the hypothalamus suppresses HGP and lowers blood glucose52. Similarly, genetic inactivation of the IR in neurons and astroglia throughout the brain causes uncontrolled HGP53, although this approach did not clarify which specific neuronal population(s) or other cell types in the CNS are responsible for mediating insulin’s ability to inhibit HGP. A key observation in the search for the neuronal substrate explaining how brain IR signalling can inhibit HGP came from mice genetically modified to lack the IR specifically in AgRP neurons. Here, Könner et al. observed that failure to activate IR signalling in AgRP neurons substantially reduced the ability of peripherally applied insulin to suppress HGP under a euglycemic-hyperinsulinemic clamp. These findings thus demonstrated that the site for central insulin signalling to inhibit HGP is, indeed, AgRP neurons13. In agreement with these data, selective restoration of the IR specifically in AgRP neurons in addition to liver and pancreatic β-cells rescues the ability of insulin to curb HGP, whereas selective re-expression of the IR to POMC neurons in otherwise IR-deficient mice exacerbates insulin resistance and increases HGP54. Thus, these findings suggest a functional dichotomy in regulation of HGP originating from POMC and AgRP neurons, similar to their opposing effect on feeding and energy expenditure19 (Box 2).

In addition, hypothalamic insulin action reduces the breakdown of lipids (lipolysis) and promotes fatty acid and triglyceride synthesis (lipogenesis) in adipocytes through a reduction in the sympathetic tone to white adipose tissue55. Thus, in addition to insulin’s direct effect on adipocytes and insulin action in the ARH to inhibit HGP, suppression of lipolysis as a result of insulin signalling in the brain may represent an additional mechanism for central control of glucose metabolism, since inhibition of lipolysis limits the supply of glycerol and non-esterified fatty acids from white fat, which serve as substrates for HGP.

The vagus nerve (the tenth cranial nerve) innervates large parts of the viscera and has been suggested to create the critical interface between the brain and the liver (Fig. 3). The vagus nerve also links brain IR signalling to gluconeogenesis, as central insulin action requires intact hepatic vagal nerve branches to suppress HGP6,45. Insulin hyperpolarizes AgRP neurons and inhibits their firing frequency through opening of KATP channels13. The reduced activity of AgRP neurons, in turn, results in IL-6-mediated activation of STAT3 signalling in the liver, and downregulates the abundance of key gluconeogenic genes, including Pepck and G6Pase13,45,53,56,57. Inhibition of hypothalamic PI3 kinase attenuates insulin’s effect on blood glucose levels, whereas potentiating PI3K activity in the hypothalamus enhances the response to insulin in severely diabetic rats, suggesting that hypothalamic IR and PI3K signalling modulates the insulin response in diabetes58. Conversely, inhibition of IR signalling, for example owing to overactivation of p70S6/S6K1 kinase, in the ARH promotes hepatic insulin resistance in normal chow-fed mice, similar to what is observed in acutely HFD-fed mice59. These data suggest that diet-induced obesity blunts hypothalamic IR signalling and inhibits its control of HGP, substantiating a role for central insulin resistance in obese, diabetic animals. S6K1 signalling in POMC neurons is, however, also reported to suppress HGP in hyperinsulinemic clamps60. The disparate outcome from these experiments may not be mutually exclusive and differences in cells targeted because of varying methodology (adenoviral-based, acute pan-neuronal overexpression versus chronic POMC cell-specific gene inactivation) are likely one explanation to these seemingly discordant findings, especially considering neuronal heterogeneity, that is, existence or different subpopulations of functionally distinct POMC neurons.

Insulin is not the only hormone that affects systemic glucose homeostasis through CNS-mediated mechanisms. For example, glucagon-like peptide 1 (GLP-1) augments glucose-stimulated insulin secretion and reduces HGP, likely mediated by GLP-1 receptor signalling in the ARH61. The peptide hormone glucagon secreted from pancreatic alpha-cells (Fig. 1), which shares a common precursor peptide with GLP-1, has on the other hand lately been reported to suppress HGP. Hypothalamic glucagon receptor activation was found to inhibit HGP through a KATP channel-dependent mechanism, and the increase in HGP from raising peripheral glucagon concentrations could be abated by blocking glucagon action in the CNS62,63. These data led to the conclusion that, in contrast to its direct actions on the liver, hypothalamic glucagon signalling inhibits HGP62,63. This was surprising, because glucagon drives HGP by direct effects on hepatocytes (Fig. 1). That a peptide promotes HGP through its stimulatory effects on the liver, and on the other hand inhibits the very same process through effects on the brain may seem counter-intuitive, as these two forces are counteracting. The findings may however point to the existence of a self-regulatory feedback loop to fine-tune HGP, in which central glucagon signalling explains why the hepatic effect of high glucagon concentration on HGP is transient, tapering off within hours even during continuous glucagon infusion.

Experiments aimed at delineating the mechanisms by which glucagon inhibits HGP are necessary to provide further clarification of glucagon’s action in the brain, and could also pave the way to new treatment strategies. A monomeric peptide conjugate between glucagon, GLP-1 and GIP (glucose-dependent insulinotropic polypeptide) that acts as an agonist at each receptor vastly improves metabolic and glycemic control in obese and diabetic rodents64. As judged from its impact on whole-animal physiology (increased energy expenditure, reduced caloric intake and better glycemic control), it is reasonable to believe that the triple agonist exerts some of its key functions by acting on the brain. Whether the metabolic outcome of such triagonist treatment is attributed to signalling effects in the CNS, and whether activation of glucagon signalling in the hypothalamus by the polyagonist counteracts glucagon’s peripheral effects on HGP are issues that merit additional studies.

Finally, whether the data in rodents on central glucagon action, with the purpose of limiting its own effects on the liver, extend to humans is important to investigate.

Of mice and men: IR signalling in the human brain

Whether insulin action in the CNS is relevant for day-to-day or acute control of blood glucose in humans has been a matter of intense discussions65. While causally proving the existence of a CNS-dependent mechanism of insulin action to inhibit HGP in humans is inherently challenging, administering insulin through a spray formulation into the nose has shed some light on the physiological relevance of insulin signalling in the human brain. Intranasal application of insulin rapidly elevates levels of the hormone in the cerebrospinal fluid at concentrations that are too low to be detected in the blood, suggesting that insulin penetrated directly into the brain from the nose without increasing insulin levels in the systemic circulation66. Daily intranasal insulin administration over 8 weeks reduces body fat and weight in healthy men (but not woman) ranging between 0.5 and 2 kg, and acute intranasal insulin application enhances the metabolic rate to food intake by almost 20% (one treatment session; 160 IU insulin), suggesting that activation of brain IR signalling regulates peripheral fat mobilization and contributes to diet-induced thermogenesis67,68. Importantly, Heni et al.69 tested whether intranasal insulin delivery affects systemic glucose metabolism, and found evidence that reinforces a role for brain insulin action on insulin sensitivity. In their study, lean individuals required more glucose to maintain euglycemia after intranasal delivery of insulin in a clamp setting compared with placebo-treated individuals in the presence of similar venous insulin levels. These data indicated improvements in whole-body insulin sensitivity, and the amount of glucose infused interestingly correlated with increased hypothalamic activity and indices of increased parasympathetic descending vagal nerve activity69. Therefore, the authors concluded that short-term insulin action as a result of intranasal application of insulin improves systemic insulin sensitivity in humans, possibly via a hypothalamic-mediated vagal mechanism like in rodents6,45. However, these studies do not provide definitive evidence that endogenously produced insulin has a similar physiological role in the human brain. The responses to intranasal insulin therapy, and the cortical response to systemic hyperinsulinemia are weaker in obese humans, suggesting that obesity renders the brain less responsive to insulin69,70. This phenomenon also occurs in animals with reduced amounts of IR protein in the ARH, a situation that is accompanied by a failure to efficiently suppress HGP and whole-body insulin resistance71. Besides being a methodological bedrock for experiments aiming to elucidate the role of insulin signalling in the brain, the question is whether nasal insulin administration therefore represents an attractive alternative medical regimen to current therapies to treat obesity-associated diabetes.

Central leptin signalling and systemic glucose metabolism

The brain’s capacity to affect glucose homeostasis also involves mechanisms that are not exclusively dependent on insulin action. The development of T2D can be preceded by defects in not only insulin-dependent but also in insulin-independent glucose uptake more than a decade before the disease is diagnosed72. Thus, how efficiently glucose promotes its own disposal unrelated to insulin action predicts the future risk of developing glucose intolerance. Secreted from white adipose tissue in proportion to fat mass, leptin is intimately linked to CNS-dependent control of glucose homeostasis; as such leptin administration has been reported to rescue insulin-deficient diabetes73. The complete mechanism behind this observation is unclear, but leptin infusion directly into the cerebral ventricles, at a dose and route that is believed to act locally in the brain and not outside the CNS, attenuates hyperglycaemia in rats with profound diabetes due to severe insulin deficiency; this effect was independent from leptin’s effect on feeding and hepatic insulin sensitivity, but involved reduced HGP and increasing glucose uptake into brain, muscle and brown fat74. Thus, leptin receptor signalling in the brain appears to normalize diabetic hyperglycaemia across different tissues and mechanisms, giving rise to the idea that leptin compensates for the lack of insulin in animal models of diabetes where loss of islet β-cell function is prominent75. In addition, combined leptin and insulin signalling in POMC neurons is broadly accepted to regulate peripheral glucose metabolism. Supporting this notion, mice lacking both the insulin and leptin receptors on POMC neurons do not suppress HGP normally, an effect associated with systemic glucose intolerance and insulin resistance12. Reconstitution of leptin receptor signalling on the same neurons conversely normalizes blood glucose and increases hepatic insulin sensitivity76. Collectively, these data point to a key role for leptin action in the ARH. However, hypoinsulinaemia as a consequence of islet failure does not seem to increase compensatory leptin receptor signalling in the CNS with the purpose of rescuing euglycemia as the hyperglycaemia usually persists in conditions characterized by insulin deficiency. Whether leptin alone can replace or compensate for insulin deficiency can thus be debated.

Central control of pancreatic islet function

The islets of the pancreas are subject to regulation by insulin signalling in the brain, and their connection with the CNS and the efferent arm of the autonomic nervous system is remarkably vulnerable during a specific developmental time window of the hypothalamic neurocircuitry77. Work from Vogt et al. has shown that feeding mothers a HFD exclusively during the lactation period leads to abnormal formation of axons from POMC neurons to the posterior part of the paraventricular nucleus of the hypothalamus (PVH (Fig. 2)), as well as of parasympathetic nerve fibres innervating the pancreas in the offspring. Ultimately, these perturbations are associated with obesity, impaired glucose-stimulated insulin secretion as well as glucose intolerance in the offspring that received fat milk77. On the other hand, pups genetically modified to lack the IR in POMC neurons were protected from disturbances in glucose homeostasis in response to maternal HFD feeding during lactation77. Thus, hyperinsulinemia may predispose the progeny of an overnutritioned breast-feeding mother for future long-lived metabolic disease through hypothalamic IR signalling, whereas the inability to sense the abnormally high levels of insulin acting on POMC neurons during lactation prevents it. Given the escalating numbers of obese and diabetic pregnant or breast-feeding women, a better understanding of metabolic, developmental programming is thus urgently needed.

Recent results obtained by combining neural tracing experiments and functional interventions directed to different hypothalamic nuclei provided new insights into the innervation of the pancreas and its influence over glucose metabolism78. Backtracking the CNS sites innervating the pancreas provide the evidence that glucokinase-expressing neurons in the ARH send signals via multiple synapses to this tissue78. Functionally, inhibiting glucose sensing in the ARH reduced insulin secretion and led to glucose intolerance, demonstrating a causal relationship between the innervation and pancreatic secretory function78. As the intervention was not directed towards a specific sub-set of neurons in the ARH, the identity of the neurons regulating pancreatic function remains unknown. POMC and AgRP neurons are both known to change their excitability to fluctuations in extracellular glucose concentrations in electrophysiological studies. POMC neurons are glucose excited, driven by closing of KATP channels. When POMC neurons lost the ability to sense glucose, through genetically preventing ATP-mediated closure of KATP channels, or made defective via HFD feeding, glucose tolerance is impaired79. Whether the effect seen stems from a failure to correctly regulate insulin secretion, however, currently remains unclear.

Other than in the ARH, Pomc mRNA is only expressed in the nucleus of the solitary tract within the CNS, and thus shows a very restricted expression pattern. This is in contrast to the MC4R distribution, the receptor for POMC-derived α-MSH, which is broadly expressed in the brain, including in nuclear groups in the medulla oblongata. Deletion of the MC4R in the dorsal motor nucleus of the vagus nerve (DMV), part of the dorsal vagal complex (DVC (Fig. 2))—consisting of preganglionic, parasympathetic nerve cells controlling vagal outflow—results in hyperinsulinemia and modest insulin resistance in a weight-independent manner and without changes in glucose tolerance or blood glucose levels9. In agreement with these findings, in obese, glucose intolerant and hyperinsulinemic MC4R-null mice, selective restoration of MC4R expression to DMV neurons attenuated the hyperinsulinemia without affecting body weight8. Thus, DMV MC4R signalling has an essential role in regulating blood insulin levels. Given the dissociation between improvements in insulin levels and lack of body weight reduction, these data also support the existence of divergent melanocortin pathways in control of glucose metabolism and energy balance. Whether AgRP neurons and/or other nerve cells in the melanocortin circuitry operate to regulate insulin levels, and whether the source of the ligand to the MC4R comes from the nucleus of the solitary tract or ARH, or both, should be subject of future studies. Possibly linking hypothalamic neurons to regulation of insulin secretion are insulin-sensitive GLUT-4-expressing neurons of the hypothalamus (GLUT-4HYPO). Cre-dependent viral tracing experiments have provided evidence that GLUT-4HYPO neurons project to the DMV, and mice in which GLUT-4HYPO neurons have been ablated present with elevated plasma glucose and reduced insulin levels but normal pancreatic beta-cell morphometry80. Accordingly, mice devoid of GLUT-4HYPO neurons display impaired glucose tolerance. To that end, the authors suggested that the hyperglycaemia is a consequence of impaired insulin secretion involving a GLUT-4HYPO to DMV projection80. While the data clearly define a role for GLUT-4HYPO neurons in the control of energy and glucose metabolism, the experimental approach relied on the death of GLUT-4HYPO neurons, and did not permit an evaluation on the role of GLUT-4 neurons in discrete hypothalamic areas. Genetic cell ablation may not come without caveats, such as gliosis (see below) appearing following GLUT-4HYPO neuron ablation, and a vast array of neurons are GLUT-4-expressing, making the application of cell-specific excitatory or inhibitory control of viable GLUT-4HYPO neurons an attractive complement for further expansion of our knowledge on their role in energy metabolism and insulin signalling81.

Obesity perturbs CNS control of peripheral glucose metabolism

The reduced propensity of the CNS to respond to hormones during obesity has been extensively studied; the resistance to insulin and leptin within the melanocortin circuitry in the hypothalamus being best defined82,83,84. Moreover, in the CNS, activation of inflammatory processes is a key event in the manifestation of peripheral insulin resistance in obese animals85,86. Inflammatory insults to AgRP neurons have a dominant role in these processes87 as attenuation of the neuroinflammatory response by depriving AgRP neurons of the inhibitor of nuclear factor kappa-B kinase 2 (IKK-β) gene, an essential trigger of the immune response, protects against obesity and systemic glucose intolerance from HFD feeding88. Moreover, c-Jun N-terminal kinase 1- and IKK-β-dependent inflammatory signalling is sufficient to drive neuronal and systemic leptin or insulin resistance, respectively, even in the absence of HFD feeding when constitutively activated in AgRP neurons89. The onset of hypothalamic inflammation is rapid. Gliosis, the process of glial cells in the central nervous system reacting and proliferating to a trauma or injury (and a prominent feature of neurodegenerative diseases), surrounding AgRP neurons can be seen within three days and before fat accumulation is measurable in rodents confronted acutely to a HFD90. Such observations have fostered the hypothesis that neuroinflammation is an actuator of obesity development rather than a secondary consequence of weight gain. The acute HFD-induced gliosis gradually tapers off in rodents90,91, indicative of an induction of a neuroprotective mechanism, but that is eventually overridden as gliosis, leptin resistance and glucose intolerance persist upon chronic HFD feeding unless the unhealthy diet is discontinued83. Similar signs of inflammation have been reported in obese humans from neuroradiologic assessments of gliosis90, and gliosis has recently been found to associate with higher BMI, fasting insulin and HOMA-IR (Homeostatic Model Assessment, a model to assess beta-cell function and insulin resistance) in obese humans. Insulin levels and HOMA-IR did not correlate with BMI in these investigations, suggesting a link between gliosis, pancreatic responses and insulin resistance unrelated to the degree of adiposity92. Recent observations offer evidence in support of a neuroprotective mechanism clearly linked to inflammatory signalling, characterized by similar temporal dynamics and kinetics as the onset and disappearance of HFD-induced gliosis93. Here, perivascular macrophages are recruited to the blood–brain barrier of the cerebral blood vessels when the brain is challenged with a HFD to limit central inflammation. Via local vascular endothelial growth factor production and increased expression of glucose transporters (GLUT-1), these events are believed to warrant cerebral glucose homeostasis during consumption of energy-dense foods93.

Despite the existences of mechanisms offering acute protection of neuronal function, the extent of the exposure to fatty food is a denominator for the magnitude of hypothalamic inflammation, as prolonged HFD feeding causes leptin and insulin resistance and disturbances in peripheral glucose homeostasis. To this end, non-neuronal cells other than astrocytes and immune cells associated to the cerebral blood vessels as described above are also involved. Evidence suggests that saturated fat can be sensed predominantly by mediobasal hypothalamic, intraparenchymal microglia94. Activating an inflammatory M1 cytokine response to the buildup of saturated fatty acids in microglia may set the stage for hypothalamic neuronal stress and reduced leptin responsiveness, which in turn may reduce peripheral insulin sensitivity. Understanding the pathomechanisms behind diet-induced neuroinflammation is thus of high priority in the field of metabolism research, as it has implications for our understanding of obesity and insulin resistance as well as a better comprehension of the neurological complications such as neuropathies, cognitive dysfunction and stroke associated with diabetes.

Future directions

Significant advancements to our understanding of how the brain influences peripheral glucose homeostasis have been made owing to studies revealing key brain regions and the identities of the neurons involved, their connectivity and the molecular components causally associated, as well as the peripheral organs and cellular events targeted by the brain. Specifically, HGP, brown fat glucose utilization and control of insulin secretion are processes importantly regulated by the CNS. Although great progress in this area of research has been made, several issues nonetheless remain to be resolved. To this end, while the application of techniques with high spatial resolution in neuroscientific research, relying on the existence of a known cell-specific promoter, has moved us several steps forward towards better control over functional neurocircuits, unique marker genes for many CNS cell-types potentially involved are yet nonetheless still inconspicuous. Moreover, there is extensive heterogeneity in gene expression within single CNS nuclei, and better characterization of this molecular diversity would subsequently improve our comprehension of the neuronal mechanisms controlling peripheral insulin sensitivity and glucose metabolism. Furthermore, a remaining challenge is to directly test whether processes regulating BAT activity and HGP can be exploited for the development of better and safer viable therapeutics. In fact, the beneficial effects of current anti-diabetic therapies, such as insulin supplementation, drugs triggering insulin release, insulin-resistance reducing agents and insulin-sensitizing medications are explained by peripheral actions, and although they successfully reduce hyperglycaemia, they were developed under the assumption that the brain has little, if any, influence on these processes. The inherent adverse effects including hypoglycemia, weight gain and gastrointestinal problems accompanying some of these medications are also problematic. To this end, identifying strong, selective actuators of BAT activation and agents dampening HGP will be important. Indeed, work on defining the neuronal mechanisms controlling BAT and liver biology may not only reveal potential CNS targets, but also facilitate the identification of pathways in liver and BAT directly controlled by the CNS. The findings revealing a role for myostatin signalling to impede insulin action in brown adipocytes, and myostatin’s effects on reducing BAT glucose uptake in response to increased activity of AgRP neurons, is one example of such synergistic development. Key players of energy and glucose homeostasis, including AgRP neurons, myostatin and melanocortin’s, are found in both rodents and humans, and pharmacological myostatin inhibition improves insulin sensitivity14,95. Realistically, drug candidates in the myostatin signalling cascade, well-studied in the context of muscle growth, sarcopenia and cachexia, could rapidly be advanced into clinical trials assessing their therapeutic potential to moderate insulin resistance.

There is also a need to define novel regulators of key glucoregulatory neuronal populations, which may lead to innovative therapies. For instance, recent publications identified the purinergic-receptor 6 (P2Y6) as novel regulator of AgRP neuron activity and further revealed that selectively abrogating P2Y6 signalling in AgRP neurons alleviates obesity-associated insulin resistance96. Translational studies will be necessary to validate if P2Y6-antagonism represents a pharmaceutical way for diabetic treatment. Finally, as failure to suppress HGP or impaired insulin sensitivity and glucose intolerance may develop as consequences of central hormone resistance, especially upon central inflammation, continued efforts in defining the intracellular pathways that are altered in obesity are required, and whether normalization of their function rescues energy and glucose metabolism. Ideally, this knowledge will facilitate to the development of novel pharmaceutical interventions for the treatment of obesity and diabetes. Such discoveries are also expected to furnish our understanding of neuronal control mechanisms of whole-body insulin sensitivity and glucose metabolism.

Additional information

How to cite this article: Ruud, J. et al. Neuronal control of peripheral insulin sensitivity and glucose metabolism. Nat. Commun. 8, 15259 doi: 10.1038/ncomms15259 (2017).

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J.R. held a postdoctoral fellowship from the Swedish Research Council (2013-530). J.C.B. was supported by a grant from the DFG (BR 1492/7-1), received funding by the DFG within the framework of the TRR134 and within the Excellence Initiative by German Federal and State Governments (CECAD), from the European Union Seventh Framework Program (FP7/2007-2013) under grant agreement 266408, and in part by the Helmholtz Alliance (Imaging and Curing Environmental Metabolic Diseases [ICEMED]) through the Initiative and Networking Fund of the Helmholtz Association. The authors are thankful to Servier Medical Art for providing access to designed medical elements (, supporting the generation of graphical items in this publication. We apologize to all colleagues whose important contributions could not be cited due to space limitations.

Author information


  1. Department of Neuronal Control of Metabolism, Max Planck Institute for Metabolism Research, Gleueler Strasse 50, 50931 Cologne, Germany

    • Johan Ruud
    • , Sophie M. Steculorum
    •  & Jens C. Brüning
  2. Policlinic for Endocrinology, Diabetes and Preventive Medicine (PEDP), University Hospital Cologne, Kerpener Strasse 26, 50924 Cologne, Germany

    • Johan Ruud
    • , Sophie M. Steculorum
    •  & Jens C. Brüning
  3. Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases (CECAD) and Center for Molecular Medicine Cologne (CMMC), University of Cologne, Joseph-Stelzmann-Strasse 26, 50931 Cologne, Germany

    • Johan Ruud
    • , Sophie M. Steculorum
    •  & Jens C. Brüning
  4. National Center for Diabetes Research (DZD), Ingolstädter Land Strasse 1, 85764 Neuherberg, Germany

    • Jens C. Brüning


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The authors declare no competing financial interests.

Corresponding author

Correspondence to Jens C. Brüning.

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