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1.
Nature ; 620(7974): 643-650, 2023 Aug.
Article in English | MEDLINE | ID: mdl-37437602

ABSTRACT

In addition to its canonical function of protection from pathogens, the immune system can also alter behaviour1,2. The scope and mechanisms of behavioural modifications by the immune system are not yet well understood. Here, using mouse models of food allergy, we show that allergic sensitization drives antigen-specific avoidance behaviour. Allergen ingestion activates brain areas involved in the response to aversive stimuli, including the nucleus of tractus solitarius, parabrachial nucleus and central amygdala. Allergen avoidance requires immunoglobulin E (IgE) antibodies and mast cells but precedes the development of gut allergic inflammation. The ability of allergen-specific IgE and mast cells to promote avoidance requires cysteinyl leukotrienes and growth and differentiation factor 15. Finally, a comparison of C57BL/6 and BALB/c mouse strains revealed a strong effect of the genetic background on the avoidance behaviour. These findings thus point to antigen-specific behavioural modifications that probably evolved to promote niche selection to avoid unfavourable environments.


Subject(s)
Allergens , Avoidance Learning , Food Hypersensitivity , Animals , Mice , Allergens/immunology , Avoidance Learning/physiology , Central Amygdaloid Nucleus/physiology , Disease Models, Animal , Food Hypersensitivity/genetics , Food Hypersensitivity/immunology , Immunoglobulin E/immunology , Intestines/immunology , Mast Cells/immunology , Mice, Inbred BALB C , Mice, Inbred C57BL , Parabrachial Nucleus/physiology , Solitary Nucleus/physiology
2.
Biol Psychiatry ; 91(10): 907-914, 2022 05 15.
Article in English | MEDLINE | ID: mdl-35397878

ABSTRACT

Over the course of a lifetime, the perinatal period plays an outsized role in the function of physiological systems. Here, we discuss how neurons that regulate energy metabolism contribute to the infant's relationship with the mother. We focus our discussion on Agrp neurons, which are located in the arcuate nucleus of the hypothalamus. These neurons heavily regulate energy metabolism. Because offspring transition from a period of dependence on the caregiver to independence, we discuss the importance of the caregiver-offspring relationship for the function of Agrp neurons. We present evidence that in the adult, Agrp neurons motivate the animal to eat, while in the neonate, they motivate the offspring to seek the proximity of the caregiver. We specifically highlight the peculiarities in the development of Agrp neurons and how they relate to the regulation of metabolism and behavior over the course of a lifetime. In sum, this review considers the unique insights that ontogenetic studies can offer toward our understanding of complex biological systems, such as the regulation of energy metabolism and mother-infant attachment.


Subject(s)
Energy Metabolism , Hunger , Agouti-Related Protein/metabolism , Animals , Energy Metabolism/physiology , Humans , Hunger/physiology , Infant , Mother-Child Relations , Neurons/physiology
3.
Cell ; 178(1): 44-59.e7, 2019 06 27.
Article in English | MEDLINE | ID: mdl-31104844

ABSTRACT

Hypothalamic Agrp neurons regulate food ingestion in adult mice. Whether these neurons are functional before animals start to ingest food is unknown. Here, we studied the functional ontogeny of Agrp neurons during breastfeeding using postnatal day 10 mice. In contrast to adult mice, we show that isolation from the nursing nest, not milk deprivation or ingestion, activated Agrp neurons. Non-nutritive suckling and warm temperatures blunted this effect. Using in vivo fiber photometry, neonatal Agrp neurons showed a rapid increase in activity upon isolation from the nest, an effect rapidly diminished following reunion with littermates. Neonates unable to release GABA from Agrp neurons expressed blunted emission of isolation-induced ultrasonic vocalizations. Chemogenetic overactivation of these neurons further increased emission of these ultrasonic vocalizations, but not milk ingestion. We uncovered important functional properties of hypothalamic Agrp neurons during mouse development, suggesting these neurons facilitate offspring-to-caregiver bonding.


Subject(s)
Agouti-Related Protein/metabolism , Feeding Behavior/physiology , Hypothalamus/cytology , Neurons/metabolism , Agouti-Related Protein/genetics , Animals , Animals, Newborn , Eating/physiology , Maternal Behavior/physiology , Mice , Mice, Knockout , Milk , Proto-Oncogene Proteins c-fos/metabolism , Social Isolation , Sucking Behavior/physiology , Temperature , Vocalization, Animal/physiology , gamma-Aminobutyric Acid/metabolism
4.
Pharmacol Res ; 141: 303-309, 2019 03.
Article in English | MEDLINE | ID: mdl-30610962

ABSTRACT

Hypothalamic Agrp neurons are critical regulators of food intake in adult mice. In addition to food intake, these neurons have been involved in other cognitive processes, such as the manifestation of stereotyped behaviors. Here, we evaluated the extent to which Agrp neurons modulate mouse behavior in spatial memory-related tasks. We found that activation of Agrp neurons did not affect spatial learning but altered behavioral flexibility using a modified version of the Barnes Maze task. Furthermore, using the Y-maze test to probe working memory, we found that chemogenetic activation of Agrp neurons reduced spontaneous alternation behavior mediated by the neuropeptide Y receptor-5 signaling. These findings suggest novel functional properties of Agrp neurons in memory-related cognitive processes.


Subject(s)
Agouti-Related Protein/metabolism , Hypothalamus/physiology , Memory , Neurons/metabolism , Animals , Cognition , Eating , Female , Male , Maze Learning , Mice , Neuropeptide Y/metabolism
5.
Nat Commun ; 10(1): 311, 2019 01 18.
Article in English | MEDLINE | ID: mdl-30659173

ABSTRACT

The type of nutrient utilized by the organism at any given time-substrate utilization-is a critical component of energy metabolism. The neuronal mechanisms involved in the regulation of substrate utilization in mammals are largely unknown. Here, we found that activation of hypothalamic Agrp neurons rapidly altered whole-body substrate utilization, increasing carbohydrate utilization, while decreasing fat utilization. These metabolic changes occurred even in the absence of caloric ingestion and were coupled to increased lipogenesis. Accordingly, inhibition of fatty acid synthase-a key enzyme that mediates lipogenesis-blunted the effects of Agrp neuron activation on substrate utilization. In pair-fed conditions during positive energy balance, activation of Agrp neurons improved metabolic efficiency, and increased weight gain and adiposity. Conversely, ablation of Agrp neurons impaired fat mass accumulation. These results suggest Agrp neurons regulate substrate utilization, contributing to lipogenesis and fat mass accumulation during positive energy balance.


Subject(s)
Adiposity/physiology , Agouti-Related Protein/metabolism , Carbohydrate Metabolism , Neurons/metabolism , Animals , Capsaicin/pharmacology , Energy Metabolism/physiology , Hypothalamus/metabolism , Lipogenesis/physiology , Mice , Mice, Knockout , Neurons/drug effects , Weight Gain/physiology
7.
Cell ; 160(6): 1222-32, 2015 Mar 12.
Article in English | MEDLINE | ID: mdl-25748653

ABSTRACT

The nervous system evolved to coordinate flexible goal-directed behaviors by integrating interoceptive and sensory information. Hypothalamic Agrp neurons are known to be crucial for feeding behavior. Here, however, we show that these neurons also orchestrate other complex behaviors in adult mice. Activation of Agrp neurons in the absence of food triggers foraging and repetitive behaviors, which are reverted by food consumption. These stereotypic behaviors that are triggered by Agrp neurons are coupled with decreased anxiety. NPY5 receptor signaling is necessary to mediate the repetitive behaviors after Agrp neuron activation while having minor effects on feeding. Thus, we have unmasked a functional role for Agrp neurons in controlling repetitive behaviors mediated, at least in part, by neuropeptidergic signaling. The findings reveal a new set of behaviors coupled to the energy homeostasis circuit and suggest potential therapeutic avenues for diseases with stereotypic behaviors.


Subject(s)
Hypothalamus/physiology , Neurons/physiology , Stereotyped Behavior , Agouti-Related Protein/metabolism , Animals , Anxiety/metabolism , Behavior, Animal/drug effects , Capsaicin/administration & dosage , Feeding Behavior/drug effects , Female , GABA Antagonists/administration & dosage , Hypothalamus/cytology , Male , Neurons/classification , Stereotyped Behavior/drug effects , TRPV Cation Channels/metabolism
8.
Cell ; 159(2): 306-17, 2014 Oct 09.
Article in English | MEDLINE | ID: mdl-25303527

ABSTRACT

Induction of beige cells causes the browning of white fat and improves energy metabolism. However, the central mechanism that controls adipose tissue browning and its physiological relevance are largely unknown. Here, we demonstrate that fasting and chemical-genetic activation of orexigenic AgRP neurons in the hypothalamus suppress the browning of white fat. O-linked ß-N-acetylglucosamine (O-GlcNAc) modification of cytoplasmic and nuclear proteins regulates fundamental cellular processes. The levels of O-GlcNAc transferase (OGT) and O-GlcNAc modification are enriched in AgRP neurons and are elevated by fasting. Genetic ablation of OGT in AgRP neurons inhibits neuronal excitability through the voltage-dependent potassium channel, promotes white adipose tissue browning, and protects mice against diet-induced obesity and insulin resistance. These data reveal adipose tissue browning as a highly dynamic physiological process under central control, in which O-GlcNAc signaling in AgRP neurons is essential for suppressing thermogenesis to conserve energy in response to fasting.


Subject(s)
Adipose Tissue, Brown/metabolism , Diet , N-Acetylglucosaminyltransferases/metabolism , Neurons/metabolism , Adipose Tissue, White/metabolism , Agouti-Related Protein/metabolism , Animals , Fasting , Female , Ghrelin/metabolism , Hypothalamus/cytology , Hypothalamus/metabolism , Insulin Resistance , Male , Mice, Inbred C57BL , Mice, Knockout , N-Acetylglucosaminyltransferases/genetics , Obesity/metabolism , Obesity/prevention & control
9.
Nat Neurosci ; 17(7): 908-10, 2014 Jul.
Article in English | MEDLINE | ID: mdl-24880214

ABSTRACT

We found that leptin receptors were expressed in hypothalamic astrocytes and that their conditional deletion led to altered glial morphology and synaptic inputs onto hypothalamic neurons involved in feeding control. Leptin-regulated feeding was diminished, whereas feeding after fasting or ghrelin administration was elevated in mice with astrocyte-specific leptin receptor deficiency. These data reveal an active role of glial cells in hypothalamic synaptic remodeling and control of feeding by leptin.


Subject(s)
Astrocytes/physiology , Eating/physiology , Hypothalamus/physiology , Leptin/physiology , Nerve Net/physiology , Neurons/physiology , Signal Transduction/physiology , Animals , Cell Count , Excitatory Postsynaptic Potentials/physiology , Glial Fibrillary Acidic Protein/genetics , Glial Fibrillary Acidic Protein/metabolism , Hypothalamus/cytology , Immunohistochemistry , In Situ Hybridization , Leptin/genetics , Male , Melanocortins/physiology , Mice , Mice, Knockout , Microscopy, Electron , Primary Cell Culture , Pro-Opiomelanocortin/physiology , Pulmonary Gas Exchange/physiology , RNA, Messenger/biosynthesis , RNA, Messenger/genetics , Real-Time Polymerase Chain Reaction
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