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Background: Numerous studies demonstrate that anesthetic-induced unconsciousness is accompanied by activation of hypothalamic sleep-promoting neurons, which occurs through both pre- and postsynaptic mechanisms. However, the correlation between drug exposure, neuronal activation, and onset of hypnosis remains incompletely understood. Moreover, the degree to which anesthetics activate both endogenous populations of γ-aminobutyric acid (GABA)ergic sleep-promoting neurons within the ventrolateral preoptic (VLPO) and median preoptic nuclei remains unknown.
Methods: Mice were exposed to oxygen, hypnotic doses of isoflurane or halothane, or 1,2-dichlorohexafluorocyclobutane (F6), a nonimmobilizer. Hypothalamic brain slices prepared from anesthetic-naive mice were also exposed to oxygen, volatile anesthetics, or F6 ex vivo, both in the presence and absence of tetrodotoxin. Double-label immunohistochemistry was performed to quantify the number of c-Fos-immunoreactive nuclei in the GABAergic subpopulation of neurons in the VLPO and the median preoptic areas to test the hypothesis that volatile anesthetics, but not nonimmobilizers, activate sleep-promoting neurons in both nuclei.
Results: In vivo exposure to isoflurane and halothane doubled the fraction of active, c-Fos-expressing GABAergic neurons in the VLPO, whereas F6 failed to affect VLPO c-Fos expression. Both in the presence and absence of tetrodotoxin, isoflurane dose-dependently increased c-Fos expression in GABAergic neurons ex vivo, whereas F6 failed to alter expression. In GABAergic neurons of the median preoptic area, c-Fos expression increased with isoflurane and F6, but not with halothane exposure.
Conclusions: Anesthetic unconsciousness is not accompanied by global activation of all putative sleep-promoting neurons. However, within the VLPO hypnotic doses of volatile anesthetics, but not nonimmobilizers, activate putative sleep-promoting neurons, correlating with the appearance of the hypnotic state.
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http://dx.doi.org/10.1097/ALN.0000000000000383 | DOI Listing |
Anesthesiology
August 2025
Department of Anesthesiology, Affiliated Hospital of Zunyi Medical University, 563000, Zunyi, Guizhou, China.
Background: General anesthesia induces both unconsciousness and respiratory depression, but whether these effects share a common neural substrate remains unclear. The parafacial zone (PZ), a GABAergic sleep-promoting region, has been proposed to modulate respiration. This study investigates whether PZ GABAergic neurons function as a common neural node coordinating anesthetic-induced unconsciousness and respiratory suppression.
View Article and Find Full Text PDFCurr Biol
August 2025
Brain Plasticity Unit, CNRS, ESPCI-Paris, PSL Research University, Paris 75005, France. Electronic address:
The cerebral structures orchestrating the daily cycles of wake, rapid eye movement (REM), and non-rapid eye movement (NREM) sleep have been identified in remarkable detail. However, the mechanisms by which they dynamically adapt to environmental challenges remain to be fully understood. Here, we show that the prefrontal cortex (PFC), a key hub in stress regulation, modulates sleep architecture through direct projections to the ventrolateral preoptic nucleus (VLPO), a major sleep center.
View Article and Find Full Text PDFCurr Neuropharmacol
July 2025
Department of Translational Research and New Technologies in Medicine and Surgery, University of Pisa, Pisa, Italy.
Introduction: Exogenous melatonin (exo-MLT) is a sleep-promoting agent that modulates key sleep-wake neurotransmitters.
Methods: This scoping review analyzed 623 studies retrieved from PubMed/MEDLINE and ISI/ Web of Science, applying PRISMA methodology to ensure rigorous inclusion criteria. After screening, 58 original research papers were analyzed for exo-MLT's effects on gamma-aminobutyric acid (GABA), serotonin, dopamine, glutamine, norepinephrine, epinephrine, orexin, acetylcholine, adenosine, glycine, galanin, and histamine.
iScience
July 2025
Institute of Molecular Biology, Academia Sinica, Taipei 115, Taiwan.
Animals exhibit diverse behavioral adaptations to predation, driving coevolution across the Tree of Life. Using as a genetic model organism, we investigated how nematodes respond to predation by the nematode-trapping fungus . Fungal trapping induces quiescence in , characterized by a rapid cessation of pharyngeal pumping and movement.
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June 2025
Department of Neurology, Johns Hopkins University, Baltimore, MD, USA.
Prolonged wakefulness leads to persistent, deep recovery sleep (RS). However, the neuronal circuits that mediate this process remain elusive. From a circuit screen in mice, we identified a group of thalamic nucleus reuniens (RE) neurons activated during sleep deprivation (SD) and required for sleep homeostasis.
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