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Homeostatic scaling is a non-Hebbian form of neural plasticity that maintains neuronal excitability and informational content of synaptic arrays in the face of changes of network activity. Here, we demonstrate that homeostatic scaling is dependent on group I metabotropic glutamate receptor activation that is mediated by the immediate early gene Homer1a. Homer1a is transiently upregulated during increases in network activity and evokes agonist-independent signaling of group I mGluRs that scales down the expression of synaptic AMPA receptors. Homer1a effects are dynamic and play a role in the induction of scaling. Similar to mGluR-LTD, Homer1a-dependent scaling involves a reduction of tyrosine phosphorylation of GluA2 (GluR2), but is distinct in that it exploits a unique signaling property of group I mGluR to confer cell-wide, agonist-independent activation of the receptor. These studies reveal an elegant interplay of mechanisms that underlie Hebbian and non-Hebbian plasticity.
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http://dx.doi.org/10.1016/j.neuron.2010.11.008 | DOI Listing |
Sleep Adv
June 2025
Sleep and Performance Research Center, Washington State University, Spokane, WA, United States.
Study Objectives: There are large individual differences in the homeostatic response to sleep deprivation, as reflected in slow wave sleep (SWS) and electroencephalogram (EEG) spectral power, which have largely been left unexplained. Recent evidence suggests the possible involvement of the activity-regulated cytoskeleton-associated protein () gene. Here we assessed the effects of the "c.
View Article and Find Full Text PDFMol Psychiatry
August 2025
Graduate Institute of Mind Brain and Consciousness, Taipei Medical University, Taipei, Taiwan.
Background: Major depressive disorder (MDD) is a severe affective disorder with largely unknown neurobiology-partly due to the heterogeneity and often contradictory nature of existing findings.
Methods: To address this challenge, we conducted a systematic umbrella review of neuroimaging meta-analyses to identify the most consistent brain alterations associated with prototypical MDD. Data on intrinsic activity, task-based activation, and grey/white matter structure were organized by mapping alterations onto large-scale brain networks and categorizing them by early and chronic illness stages.
Eur Child Adolesc Psychiatry
August 2025
Departamento de Investigación en Enfermedades Mentales, Instituto de Investigación Marqués de Valdecilla (IDIVAL), Santander, 39011, España.
This study examines the effects of SARS-CoV-2-induced maternal immune activation (MIA) on early neurodevelopment, focusing on sex-specific vulnerabilities related to early behavioral and regulatory functions, which may be precursors to later developmental or cognitive challenges. A total of 107 mother-infant dyads from the COGESTCOV-19 study were analyzed to assess neurodevelopmental outcomes in male and female infants at six weeks using the Neonatal Behavioral Assessment Scale (NBAS). Maternal and newborn cytokine levels-specifically interleukin-6 (IL-6), interleukin-10 (IL-10), and the IL-6/IL-10 ratio-were measured at the first prenatal visit at the time of study enrolment and at birth to evaluate inflammatory responses and homeostatic balance.
View Article and Find Full Text PDFCureus
July 2025
Department of Obstetrics and Gynecology, University Medical Center of Johannes Gutenberg University Mainz, Mainz, DEU.
Psychosexual impairments in women with polycystic ovary syndrome (PCOS), often linked to depression, low self-esteem, and negative body image, significantly reduce quality of life. Although metabolic dysfunctions such as insulin resistance and obesity are key features of PCOS, their impact on psychosexual health remains poorly understood. This cross-sectional study aimed to examine the association between metabolic markers and psychosexual functioning in PCOS patients.
View Article and Find Full Text PDFEssays Biochem
August 2025
Department of Biochemistry and Molecular Biology, Seoul National University College of Medicine, Seoul, 03080, South Korea.
The 26S proteasome is a multi-subunit protease complex that degrades most eukaryotic cellular proteins. It not only regulates individual protein's half-lives but also maintains proteome homeostasis and modulates immunological responses. During conditions involving large-scale proteome remodeling, such as fibrosis and cellular differentiation, the 26S proteasome plays a central role in the rapid removal of excess cytosolic proteins.
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