Acute inhibition of hunger-sensing AgRP neurons promotes context-specific learning in mice
Objective: An environmental context, which reliably predicts food availability, can increase the appetitive food drive within the same environment context. However, hunger is required for the development of such a context-induced feeding (CIF) response, suggesting the neural circuits sensitive to hu...
Main Authors: | , , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Elsevier
2023-11-01
|
Series: | Molecular Metabolism |
Subjects: | |
Online Access: | http://www.sciencedirect.com/science/article/pii/S2212877823001370 |
_version_ | 1797677693016211456 |
---|---|
author | Felicia Reed Alex Reichenbach Harry Dempsey Rachel E. Clarke Mathieu Mequinion Romana Stark Sasha Rawlinson Claire J. Foldi Sarah H. Lockie Zane B. Andrews |
author_facet | Felicia Reed Alex Reichenbach Harry Dempsey Rachel E. Clarke Mathieu Mequinion Romana Stark Sasha Rawlinson Claire J. Foldi Sarah H. Lockie Zane B. Andrews |
author_sort | Felicia Reed |
collection | DOAJ |
description | Objective: An environmental context, which reliably predicts food availability, can increase the appetitive food drive within the same environment context. However, hunger is required for the development of such a context-induced feeding (CIF) response, suggesting the neural circuits sensitive to hunger link an internal energy state with a particular environment context. Since Agouti related peptide (AgRP) neurons are activated by energy deficit, we hypothesised that AgRP neurons are both necessary and sufficient to drive CIF. Methods: To examine the role of AgRP neurons in the CIF process, we used fibre photometry with GCaMP7f, chemogenetic activation of AgRP neurons, as well as optogenetic control of AgRP neurons to facilitate acute temporal control not permitted with chemogenetics. Results: A CIF response at test was only observed when mice were fasted during context training and AgRP population activity at test showed an attenuated inhibitory response to food, suggesting increased food-seeking and/or decreased satiety signalling drives the increased feeding response at test. Intriguingly, chemogenetic activation of AgRP neurons during context training did not increase CIF, suggesting precise temporal firing properties may be required. Indeed, termination of AgRP neuronal photostimulation during context training (ON–OFF in context), in the presence or absence of food, increased CIF. Moreover, photoinhibition of AgRP neurons during context training in fasted mice was sufficient to drive a subsequent CIF in the absence of food. Conclusions: Our results suggest that AgRP neurons regulate the acquisition of CIF when the acute inhibition of AgRP activity is temporally matched to context exposure. These results establish acute AgRP inhibition as a salient neural event underscoring the effect of hunger on associative learning. |
first_indexed | 2024-03-11T22:48:54Z |
format | Article |
id | doaj.art-973cd8944ea749ea8909dbb84cd9dea6 |
institution | Directory Open Access Journal |
issn | 2212-8778 |
language | English |
last_indexed | 2024-03-11T22:48:54Z |
publishDate | 2023-11-01 |
publisher | Elsevier |
record_format | Article |
series | Molecular Metabolism |
spelling | doaj.art-973cd8944ea749ea8909dbb84cd9dea62023-09-22T04:38:37ZengElsevierMolecular Metabolism2212-87782023-11-0177101803Acute inhibition of hunger-sensing AgRP neurons promotes context-specific learning in miceFelicia Reed0Alex Reichenbach1Harry Dempsey2Rachel E. Clarke3Mathieu Mequinion4Romana Stark5Sasha Rawlinson6Claire J. Foldi7Sarah H. Lockie8Zane B. Andrews9Monash Biomedicine Discovery Institute and Department of Physiology, Monash University, Clayton, 3800, Victoria, AustraliaMonash Biomedicine Discovery Institute and Department of Physiology, Monash University, Clayton, 3800, Victoria, AustraliaMonash Biomedicine Discovery Institute and Department of Physiology, Monash University, Clayton, 3800, Victoria, AustraliaDepartment of Neurosciences, Medical University of South Carolina, Charleston, SC, 29425, USAMonash Biomedicine Discovery Institute and Department of Physiology, Monash University, Clayton, 3800, Victoria, AustraliaMonash Biomedicine Discovery Institute and Department of Physiology, Monash University, Clayton, 3800, Victoria, AustraliaMonash Biomedicine Discovery Institute and Department of Physiology, Monash University, Clayton, 3800, Victoria, AustraliaMonash Biomedicine Discovery Institute and Department of Physiology, Monash University, Clayton, 3800, Victoria, AustraliaMonash Biomedicine Discovery Institute and Department of Physiology, Monash University, Clayton, 3800, Victoria, AustraliaMonash Biomedicine Discovery Institute and Department of Physiology, Monash University, Clayton, 3800, Victoria, Australia; Corresponding author.Objective: An environmental context, which reliably predicts food availability, can increase the appetitive food drive within the same environment context. However, hunger is required for the development of such a context-induced feeding (CIF) response, suggesting the neural circuits sensitive to hunger link an internal energy state with a particular environment context. Since Agouti related peptide (AgRP) neurons are activated by energy deficit, we hypothesised that AgRP neurons are both necessary and sufficient to drive CIF. Methods: To examine the role of AgRP neurons in the CIF process, we used fibre photometry with GCaMP7f, chemogenetic activation of AgRP neurons, as well as optogenetic control of AgRP neurons to facilitate acute temporal control not permitted with chemogenetics. Results: A CIF response at test was only observed when mice were fasted during context training and AgRP population activity at test showed an attenuated inhibitory response to food, suggesting increased food-seeking and/or decreased satiety signalling drives the increased feeding response at test. Intriguingly, chemogenetic activation of AgRP neurons during context training did not increase CIF, suggesting precise temporal firing properties may be required. Indeed, termination of AgRP neuronal photostimulation during context training (ON–OFF in context), in the presence or absence of food, increased CIF. Moreover, photoinhibition of AgRP neurons during context training in fasted mice was sufficient to drive a subsequent CIF in the absence of food. Conclusions: Our results suggest that AgRP neurons regulate the acquisition of CIF when the acute inhibition of AgRP activity is temporally matched to context exposure. These results establish acute AgRP inhibition as a salient neural event underscoring the effect of hunger on associative learning.http://www.sciencedirect.com/science/article/pii/S2212877823001370AgRP neuronsPhotometryOptogeneticsChemogeneticsHungerConditioning |
spellingShingle | Felicia Reed Alex Reichenbach Harry Dempsey Rachel E. Clarke Mathieu Mequinion Romana Stark Sasha Rawlinson Claire J. Foldi Sarah H. Lockie Zane B. Andrews Acute inhibition of hunger-sensing AgRP neurons promotes context-specific learning in mice Molecular Metabolism AgRP neurons Photometry Optogenetics Chemogenetics Hunger Conditioning |
title | Acute inhibition of hunger-sensing AgRP neurons promotes context-specific learning in mice |
title_full | Acute inhibition of hunger-sensing AgRP neurons promotes context-specific learning in mice |
title_fullStr | Acute inhibition of hunger-sensing AgRP neurons promotes context-specific learning in mice |
title_full_unstemmed | Acute inhibition of hunger-sensing AgRP neurons promotes context-specific learning in mice |
title_short | Acute inhibition of hunger-sensing AgRP neurons promotes context-specific learning in mice |
title_sort | acute inhibition of hunger sensing agrp neurons promotes context specific learning in mice |
topic | AgRP neurons Photometry Optogenetics Chemogenetics Hunger Conditioning |
url | http://www.sciencedirect.com/science/article/pii/S2212877823001370 |
work_keys_str_mv | AT feliciareed acuteinhibitionofhungersensingagrpneuronspromotescontextspecificlearninginmice AT alexreichenbach acuteinhibitionofhungersensingagrpneuronspromotescontextspecificlearninginmice AT harrydempsey acuteinhibitionofhungersensingagrpneuronspromotescontextspecificlearninginmice AT racheleclarke acuteinhibitionofhungersensingagrpneuronspromotescontextspecificlearninginmice AT mathieumequinion acuteinhibitionofhungersensingagrpneuronspromotescontextspecificlearninginmice AT romanastark acuteinhibitionofhungersensingagrpneuronspromotescontextspecificlearninginmice AT sasharawlinson acuteinhibitionofhungersensingagrpneuronspromotescontextspecificlearninginmice AT clairejfoldi acuteinhibitionofhungersensingagrpneuronspromotescontextspecificlearninginmice AT sarahhlockie acuteinhibitionofhungersensingagrpneuronspromotescontextspecificlearninginmice AT zanebandrews acuteinhibitionofhungersensingagrpneuronspromotescontextspecificlearninginmice |