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SIM1-expressing paraventricular hypothalamus (PVH) neurons are key regulators of energy balance. Within the PVH population, melanocortin-4 receptor-expressing (PVH) neurons are known to regulate satiety and bodyweight, yet they account for only half of PVH neuron-mediated regulation. Here we report that PVH prodynorphin-expressing (PVH) neurons, which notably lack MC4Rs, function independently and additively with PVH neurons to account for the totality of PVH neuron-mediated satiety. Moreover, PVH neurons are necessary for prevention of obesity in an independent but equipotent manner to PVH neurons. While PVH and PVH neurons both project to the parabrachial complex (PB), they synaptically engage distinct efferent nodes, the pre-locus coeruleus (pLC), and central lateral parabrachial nucleus (cLPBN), respectively. PB-projecting PVH neurons, like PVH neurons, receive input from interoceptive ARC neurons, respond to caloric state, and are sufficient and necessary to control food intake. This expands the CNS satiety circuitry to include two non-overlapping PVH to hindbrain circuits.
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http://dx.doi.org/10.1016/j.neuron.2019.02.028 | DOI Listing |
Sci Adv
December 2024
Laboratory for Comparative Connectomics, RIKEN Center for Biosystems Dynamics Research, Kobe, Hyogo 650-0047, Japan.
Oxytocin (OT) neurons in the hypothalamic paraventricular nucleus (PVH) play an important role in various physiological and behavioral processes, including the initiation of milk ejection and the regulation of maternal behaviors. However, their activity patterns at the single-cell level remain poorly understood. Using microendoscopic Ca imaging in freely moving mouse dams, we demonstrate highly correlated pulsatile activity among individual OT neurons during lactation.
View Article and Find Full Text PDFbioRxiv
November 2024
Human and Evolutionary Biology Section, Department of Biological Sciences, Dornsife College of Letters, Arts and Sciences, University of Southern California, USA.
Oxytocin (OT) is a neuropeptide produced in the paraventricular (PVH) and supraoptic (SON) nuclei of the hypothalamus. Either peripheral or central administration of OT suppresses food intake through reductions in meal size. However, pharmacological approaches do not differentiate whether observed effects are mediated by OT neurons located in the PVH or in the SON.
View Article and Find Full Text PDFInt J Mol Sci
November 2024
Laboratory of Molecular Neuroendocrinology, Institute of Experimental Medicine, Hungarian Research Network, 1083 Budapest, Hungary.
Corticotropin-releasing hormone (CRH) neurons within the paraventricular hypothalamic nucleus (PVH) play a crucial role in initiating the neuroendocrine response to stress and are also pivotal in coordination of autonomic, metabolic, and behavioral stress reactions. Although the role of parvocellular CRH neurons in activation of the hypothalamic-pituitary-adrenal (HPA) axis is well established, the distribution and function of CRH-expressing neurons across the whole central nervous system are less understood. Stress responses activate complex neural networks, which differ depending on the type of stressor and on the sex of the individual.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
December 2024
Department of Molecular Physiology & Biophysics, Vanderbilt University, Nashville, TN 37232.
During postnatal life, leptin specifies neuronal inputs to the paraventricular nucleus of the hypothalamus (PVH) and activates agouti-related peptide (AgRP) neurons in the arcuate nucleus of the hypothalamus. Activity-dependent developmental mechanisms impact refinement of sensory circuits, but whether leptin-mediated postnatal neuronal activity specifies hypothalamic neural projections is largely unexplored. Here, we used chemogenetics to manipulate the activity of AgRP neurons during a discrete postnatal critical period and evaluated the development of AgRP inputs to the PVH and descending efferent outflow to the dorsal vagal complex (DVC).
View Article and Find Full Text PDFJ Integr Med
November 2024
Department of Rehabilitation Medicine, Huashan Hospital, Fudan University, Shanghai 200040, China; National Center for Neurological Disorders, Shanghai 200040, China; National Clinical Research Center for Geriatric Diseases, Shanghai 200040, China; School of Rehabilitation Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai 201203, China. Electronic address:
Objective: This study investigates the sleep-modulating effects of ginsenoside Rg1 (Rg1, CHO), a key bioactive component of ginseng, and elucidates its underlying mechanisms.
Methods: C57BL/6J mice were intraperitoneally administered doses of Rg1 ranging from 12.5 to 100 mg/kg.
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