Lateral Hypothalamic Area Glutamatergic Neurons and Their Projections to the Lateral Habenula Regulate Feeding and Reward

Autor: Pranish A. Kantak, Grace A. Blair, Marcus L. Basiri, Garret D. Stuber, Maaike M.H. van Swieten, Alice M. Stamatakis
Jazyk: angličtina
Rok vydání: 2016
Předmět:
Male
0301 basic medicine
endocrine system
Vesicular Inhibitory Amino Acid Transport Proteins
Genetic Vectors
Glutamic Acid
Mice
Transgenic

Context (language use)
Biology
Optogenetics
Mice
03 medical and health sciences
Glutamatergic
chemistry.chemical_compound
0302 clinical medicine
Bacterial Proteins
Reward
Postsynaptic potential
Neural Pathways
Biological neural network
Animals
Neurotransmitter
Fluorescent Dyes
Neurons
Habenula
Caspase 3
General Neuroscience
Articles
Feeding Behavior
Mice
Inbred C57BL

Luminescent Proteins
030104 developmental biology
chemistry
Hypothalamic Area
Lateral

Exploratory Behavior
Vesicular Glutamate Transport Protein 2
Excitatory postsynaptic potential
Conditioning
Operant

Neuroscience
030217 neurology & neurosurgery
hormones
hormone substitutes
and hormone antagonists
DOI: 10.17615/h9yr-1584
Popis: The overconsumption of calorically dense, highly palatable foods is thought to be a major contributor to the worldwide obesity epidemic; however, the precise neural circuits that directly regulate hedonic feeding remain elusive. Here, we show that lateral hypothalamic area (LHA) glutamatergic neurons, and their projections to the lateral habenula (LHb), negatively regulate the consumption of palatable food. Genetic ablation of LHA glutamatergic neurons increased daily caloric intake and produced weight gain in mice that had access to a high-fat diet, while not altering general locomotor activity. Anterior LHA glutamatergic neurons send a functional glutamatergic projection to the LHb, a brain region involved in processing aversive stimuli and negative reward prediction outcomes. Pathway-specific, optogenetic stimulation of glutamatergic LHA-LHb circuit resulted in detectable glutamate-mediated EPSCs as well as GABA-mediated IPSCs, although the net effect of neurotransmitter release was to increase the firing of most LHb neurons.In vivooptogenetic inhibition of LHA-LHb glutamatergic fibers produced a real-time place preference, whereas optogenetic stimulation of LHA-LHb glutamatergic fibers had the opposite effect. Furthermore, optogenetic inhibition of LHA-LHb glutamatergic fibers acutely increased the consumption of a palatable liquid caloric reward. Collectively, these results demonstrate that LHA glutamatergic neurons are well situated to bidirectionally regulate feeding and potentially other behavioral states via their functional circuit connectivity with the LHb and potentially other brain regions.SIGNIFICANCE STATEMENTIn this study, we show that the genetic ablation of LHA glutamatergic neurons enhances caloric intake. Some of these LHA glutamatergic neurons project to the lateral habenula, a brain area important for generating behavioral avoidance. Optogenetic stimulation of this circuit has net excitatory effects on postsynaptic LHb neurons. This is the first study to characterize the functional connectivity and behavioral relevance of this circuit within the context of feeding and reward-related behavior.
Databáze: OpenAIRE