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Central amygdala (CeA) neurons expressing protein kinase Cδ (PKCδ) or somatostatin (Som) differentially modulate diverse behaviors. The underlying features supporting cell-type-specific function in the CeA, however, remain unknown. Using whole-cell patch-clamp electrophysiology in acute mouse brain slices and biocytin-based neuronal reconstructions, we demonstrate that neuronal morphology and relative excitability are two distinguishing features between Som and PKCδ neurons in the laterocapsular subdivision of the CeA (CeLC). Som neurons, for example, are more excitable, compact, and with more complex dendritic arborizations than PKCδ neurons. Cell size, intrinsic membrane properties, and anatomic localization were further shown to correlate with cell-type-specific differences in excitability. Lastly, in the context of neuropathic pain, we show a shift in the excitability equilibrium between PKCδ and Som neurons, suggesting that imbalances in the relative output of these cells underlie maladaptive changes in behaviors. Together, our results identify fundamentally important distinguishing features of PKCδ and Som cells that support cell-type-specific function in the CeA.
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http://dx.doi.org/10.1523/ENEURO.0402-20.2020 | DOI Listing |
J Neurosci
September 2025
Center for Studies in Behavioural Neurobiology, Department of Psychology, Concordia University, Montreal, QC, Canada, H4B 1R6
Adaptive behavior depends on a dynamic balance between acquisition and extinction memories. Male and female rodents differ in extinction learning rates, suggestion potential sex-based differences in this balance. In males, deletion of extinction-recruited neurons in the central nucleus (CN) of the amygdala impairs extinction retrieval, shifting behavior toward acquisition (Lay et al.
View Article and Find Full Text PDFPLoS One
September 2025
Escuela Nacional de Estudios Superiores Unidad Juriquilla, Campus UNAM-Juriquilla, Universidad Nacional Autónoma de México, Querétaro, Querétaro, Mexico.
In the adult brain, neurogenesis primarily occurs in the dentate gyrus of the hippocampus (DG) and the olfactory bulbs, with new cells migrating from the subventricular zone. Additionally, small amounts of cell proliferation have been observed in the preoptic area (POA) and the amygdala (AMG), regions involved in the control of male sexual behavior. Sexual activity induces a reward state mediated by opioids, and our group previously demonstrated that neurogenesis induced by paced mating is opioid dependent in female rats.
View Article and Find Full Text PDFNeuroimage Rep
September 2025
Department of Endocrinology, Amsterdam University Medical Centers, location VUMC, Amsterdam, the Netherlands.
People with obesity tend to have altered functional connectivity of reward-related areas in the brain, contributing to overeating and weight gain. The gut-brain axis may function as a mediating factor, with gut-derived short-chain fatty acids (SCFAs) as possible intermediates in the relationship between microbiota and functional connectivity. We investigated the influence of SCFA turnover on resting state functional connectivity in healthy individuals with extremely high and extremely low levels of intestinal SCFA turnover.
View Article and Find Full Text PDF3 Biotech
September 2025
Department of Anatomy, Kasturba Medical College Mangalore, Manipal Academy of Higher Education, Manipal, India.
Neuroinflammation is known to be a contributing factor for several neurological disorders as well as cognitive dysfunction. Different signalling pathways, and a variety of supporting cells of CNS are suggested to be involved in the progression of neurodegeneration. Among the factors contributing to neuroinflammation, peripheral inflammation takes a lead role according to recent research, since persistent peripheral inflammation is believed to disrupt the blood-brain barrier (BBB).
View Article and Find Full Text PDFMol Psychiatry
August 2025
Department of Life Sciences, Korea University, Seoul, 02841, Republic of Korea.
Compulsive eating behavior, characterized by the excessive intake of palatable high-sugar and high-fat foods despite negative consequences, may be associated with dysfunctional dopamine system, specifically involving the dopamine D2 receptors (D2Rs). Here, we demonstrate that D2Rs regulate insulin receptor (InsR) signaling in the central amygdala, and this interaction plays a critical role in the persistent, compulsive-like palatable food-seeking behavior. The specific ablation of D2Rs in the CeA markedly enhances compulsive-like eating despite adverse consequences.
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