Homeostatic and Hedonic Signals Differentially Regulate cFos Activation in PVN MC4R, PVN pro-TRH, PBN vGlut2, and PBN CRF Neuronal Populations

Background: The high worldwide prevalence of obesity, with palatable food hyperphagia as its main etiological factor, justifies studying neural circuit alterations under conditions such as chronic stress and exposure to high-energy diets, which elevate palatable food preference and body weight. Short-term intake of palatable food, acting as a satiety stimulus, activates melanocortin-4 receptor-expressing neurons in the paraventricular hypothalamic nucleus (PVNMC4R) and those from the caudo-lateral region of the parabrachial nucleus (PBN). It remains unclear whether stress targets this circuit, reducing satiety, or whether 2-week palatable diet exposure alters anorexigenic cells’ responsiveness to stress, such as MC4R, pro-thyrotropin-releasing hormone (pro-TRH), vesicular glutamate transporter 2 (vGlut2), and corticotropin-releasing factor (CRF)-expressing neurons. Methods: Male adult Wistar rats subjected to isolation stress or group-housed and fed with chow or palatable food for 2 weeks were fasted and then re-fed for 2 h with chow or chocolate milk. Using immunohistochemical analyses, we determined the circuit responsiveness to stimuli, identifying the cFos-indicated activation of anterior and medial PVN-MC4R, PVN-pro-TRH, PBN-vGlut2, and PBN-CRF-expressing cells. We also analyzed VTA tyrosine hydroxylase and accumbal type-2 dopamine receptor expression, where PBN neurons’ activity impacts and modulates the food-rewarding properties of DAergic circuit responses. Results: PVNMC4R+cFos cells responded differently depending on food type, diet duration, combination, and nature of stimuli (homeostatic/hedonic); their responsiveness pattern was similar to PBNvGlut2+cFos and different from anterior PVNpro-TRH+cFos cells. Conclusions: The results suggest that 2-week palatable diet exposure changes satiety-circuit cells’ responsiveness, showing enhanced activity when stress and palatable food are combined, which seemed associated with their higher food intake.

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Journal
Brain Sciences
Published
2026-10-15
DOI
https://doi.org/10.3390/brainsci16101111
Primary Topic
Regulation of Appetite and Obesity
Type
article
Field-Weighted Citation Impact
0.00

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article

Homeostatic and Hedonic Signals Differentially Regulate cFos Activation in PVN MC4R, PVN pro-TRH, PBN vGlut2, and PBN CRF Neuronal Populations

Elena Alvarez‐Salas, Estefania Espítia‐Bautista, Patricia de Gortari, Cinthia García-Luna et al.
Brain Sciences
Regulation of Appetite and Obesity
article

Homeostatic and Hedonic Signals Differentially Regulate cFos Activation in PVN MC4R, PVN pro-TRH, PBN vGlut2, and PBN CRF Neuronal Populations

Elena Alvarez‐Salas, Estefania Espítia‐Bautista, Patricia de Gortari, Cinthia García-Luna, Javier Berjon, Paulina Soberanes-Chávez
article en

Abstract

Background: The high worldwide prevalence of obesity, with palatable food hyperphagia as its main etiological factor, justifies studying neural circuit alterations under conditions such as chronic stress and exposure to high-energy diets, which elevate palatable food preference and body weight. Short-term intake of palatable food, acting as a satiety stimulus, activates melanocortin-4 receptor-expressing neurons in the paraventricular hypothalamic nucleus (PVNMC4R) and those from the caudo-lateral region of the parabrachial nucleus (PBN). It remains unclear whether stress targets this circuit, reducing satiety, or whether 2-week palatable diet exposure alters anorexigenic cells’ responsiveness to stress, such as MC4R, pro-thyrotropin-releasing hormone (pro-TRH), vesicular glutamate transporter 2 (vGlut2), and corticotropin-releasing factor (CRF)-expressing neurons. Methods: Male adult Wistar rats subjected to isolation stress or group-housed and fed with chow or palatable food for 2 weeks were fasted and then re-fed for 2 h with chow or chocolate milk. Using immunohistochemical analyses, we determined the circuit responsiveness to stimuli, identifying the cFos-indicated activation of anterior and medial PVN-MC4R, PVN-pro-TRH, PBN-vGlut2, and PBN-CRF-expressing cells. We also analyzed VTA tyrosine hydroxylase and accumbal type-2 dopamine receptor expression, where PBN neurons’ activity impacts and modulates the food-rewarding properties of DAergic circuit responses. Results: PVNMC4R+cFos cells responded differently depending on food type, diet duration, combination, and nature of stimuli (homeostatic/hedonic); their responsiveness pattern was similar to PBNvGlut2+cFos and different from anterior PVNpro-TRH+cFos cells. Conclusions: The results suggest that 2-week palatable diet exposure changes satiety-circuit cells’ responsiveness, showing enhanced activity when stress and palatable food are combined, which seemed associated with their higher food intake.

Brain SciencesVol. 16(10)
Instituto Nacional de Psiquiatría Ramón de la Fuente Muñiz (MX)
Consejo Nacional de Ciencia y Tecnología
Good health and well-being
Openalex Percentile: Top 18%
Regulation of Appetite and Obesity
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