Amygdala aromatase controls food intake, reward, and thermoregulation

Objective: Estrogens play a pivotal role in energy balance control, by acting on its CNS receptors. It is generally assumed that the gonads are the main source of estradiol for these receptors. However, aromatase, the sole enzyme responsible for estradiol synthesis, is also present in the brain, and...

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Main Authors: Ivana Maric, Jennifer E. Richard, Lilly Taing, Suyeun Byun, Lorena Lopez-Ferreras, Yifan Qiu, Karolina P. Skibicka
Format: Article
Language:English
Published: Elsevier 2025-09-01
Series:Molecular Metabolism
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Online Access:http://www.sciencedirect.com/science/article/pii/S2212877825001097
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author Ivana Maric
Jennifer E. Richard
Lilly Taing
Suyeun Byun
Lorena Lopez-Ferreras
Yifan Qiu
Karolina P. Skibicka
author_facet Ivana Maric
Jennifer E. Richard
Lilly Taing
Suyeun Byun
Lorena Lopez-Ferreras
Yifan Qiu
Karolina P. Skibicka
author_sort Ivana Maric
collection DOAJ
description Objective: Estrogens play a pivotal role in energy balance control, by acting on its CNS receptors. It is generally assumed that the gonads are the main source of estradiol for these receptors. However, aromatase, the sole enzyme responsible for estradiol synthesis, is also present in the brain, and its role in energy balance remains largely unexplored. Methods and Results: We identified high aromatase expression in the neurons of rat amygdala and investigated whether brain-derived estradiol, particularly within the amygdala, plays a role in energy balance and food reward control. Both whole brain chronic pharmacological inhibition of aromatase with a clinically utilized inhibitor, Letrozole, and a virogenetic approach to manipulate aromatase specifically in the amygdala were used in adult male and female rats, in conjunction with an array of measurements assessing feeding behavior and thermoregulation. Our results show that inhibition of brain aromatase results in increased food intake and body weight gain in females, but reduced food intake in males. This was driven by opposing effects on food preference for a high-fat diet. Amygdala aromatase knockdown was sufficient to increase feeding and body weight in lean and obese females, with increased visceral adiposity; effects not observed in males. Even in the absence of ovarian steroids, which already results in obesity, loss of amygdala aromatase further exacerbated weight gain and hyperphagia on an obesogenic diet. In females, hyperphagia was driven by increased meal size and increased food-motivated behavior, with increased preference for fat-rich but not sucrose-rich foods. Loss of amygdala aromatase also led to disrupted thermoregulation, with increased temperature in males but reduced in females, linked to alteration in brown adipose tissue thermogenesis. Conclusions: Collectively, our data reveal that estradiol synthesis in the brain is necessary for body weight and feeding behavior control, as well as thermoregulation, in a sex specific manner. Our findings may have translational and clinical relevance, as aromatase inhibitors are widely used in the clinic, and aromatase has recently been found in the human amygdala.
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spelling doaj-art-2e17b35803654abb83dd963e1a80b7cd2025-08-20T03:38:58ZengElsevierMolecular Metabolism2212-87782025-09-019910220210.1016/j.molmet.2025.102202Amygdala aromatase controls food intake, reward, and thermoregulationIvana Maric0Jennifer E. Richard1Lilly Taing2Suyeun Byun3Lorena Lopez-Ferreras4Yifan Qiu5Karolina P. Skibicka6Institute for Neuroscience and Physiology, University of Gothenburg, Gothenburg, Sweden; Department of Nutritional Sciences, Pennsylvania State University, University Park, PA, United StatesInstitute for Neuroscience and Physiology, University of Gothenburg, Gothenburg, SwedenInstitute for Neuroscience and Physiology, University of Gothenburg, Gothenburg, SwedenDepartment of Nutritional Sciences, Pennsylvania State University, University Park, PA, United StatesInstitute for Neuroscience and Physiology, University of Gothenburg, Gothenburg, Sweden; Instituto de Biomedicina and Departamento de Biología Molecular, Universidad de León, León, SpainColumbia University Irving Medical Center, NY, NY, United StatesInstitute for Neuroscience and Physiology, University of Gothenburg, Gothenburg, Sweden; Department of Nutritional Sciences, Pennsylvania State University, University Park, PA, United States; Corresponding author. Department of Nutritional Sciences, College of Health and Human Development, The Pennsylvania State University, 110 Chandlee Laboratory, University Park, PA, 16802, United States.Objective: Estrogens play a pivotal role in energy balance control, by acting on its CNS receptors. It is generally assumed that the gonads are the main source of estradiol for these receptors. However, aromatase, the sole enzyme responsible for estradiol synthesis, is also present in the brain, and its role in energy balance remains largely unexplored. Methods and Results: We identified high aromatase expression in the neurons of rat amygdala and investigated whether brain-derived estradiol, particularly within the amygdala, plays a role in energy balance and food reward control. Both whole brain chronic pharmacological inhibition of aromatase with a clinically utilized inhibitor, Letrozole, and a virogenetic approach to manipulate aromatase specifically in the amygdala were used in adult male and female rats, in conjunction with an array of measurements assessing feeding behavior and thermoregulation. Our results show that inhibition of brain aromatase results in increased food intake and body weight gain in females, but reduced food intake in males. This was driven by opposing effects on food preference for a high-fat diet. Amygdala aromatase knockdown was sufficient to increase feeding and body weight in lean and obese females, with increased visceral adiposity; effects not observed in males. Even in the absence of ovarian steroids, which already results in obesity, loss of amygdala aromatase further exacerbated weight gain and hyperphagia on an obesogenic diet. In females, hyperphagia was driven by increased meal size and increased food-motivated behavior, with increased preference for fat-rich but not sucrose-rich foods. Loss of amygdala aromatase also led to disrupted thermoregulation, with increased temperature in males but reduced in females, linked to alteration in brown adipose tissue thermogenesis. Conclusions: Collectively, our data reveal that estradiol synthesis in the brain is necessary for body weight and feeding behavior control, as well as thermoregulation, in a sex specific manner. Our findings may have translational and clinical relevance, as aromatase inhibitors are widely used in the clinic, and aromatase has recently been found in the human amygdala.http://www.sciencedirect.com/science/article/pii/S2212877825001097Ingestive behaviorSex differencesEnergy balanceFood motivationGonadectomy
spellingShingle Ivana Maric
Jennifer E. Richard
Lilly Taing
Suyeun Byun
Lorena Lopez-Ferreras
Yifan Qiu
Karolina P. Skibicka
Amygdala aromatase controls food intake, reward, and thermoregulation
Molecular Metabolism
Ingestive behavior
Sex differences
Energy balance
Food motivation
Gonadectomy
title Amygdala aromatase controls food intake, reward, and thermoregulation
title_full Amygdala aromatase controls food intake, reward, and thermoregulation
title_fullStr Amygdala aromatase controls food intake, reward, and thermoregulation
title_full_unstemmed Amygdala aromatase controls food intake, reward, and thermoregulation
title_short Amygdala aromatase controls food intake, reward, and thermoregulation
title_sort amygdala aromatase controls food intake reward and thermoregulation
topic Ingestive behavior
Sex differences
Energy balance
Food motivation
Gonadectomy
url http://www.sciencedirect.com/science/article/pii/S2212877825001097
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AT suyeunbyun amygdalaaromatasecontrolsfoodintakerewardandthermoregulation
AT lorenalopezferreras amygdalaaromatasecontrolsfoodintakerewardandthermoregulation
AT yifanqiu amygdalaaromatasecontrolsfoodintakerewardandthermoregulation
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