Background: Hippocampus is an important target for estrogen action. It is severely affected in patients of Alzheimer's disease. Much of the current research related to estrogen and brain function is focused in two directions.
Purpose: By attempting to lacalize localizing ERs in GABAergic neurons of the hippocampus we tried to test the hypothesis that the action of estrogen in maintaining the neuronal plasticity and more specially the spine density of pyramidal neurons is through GABAergic neurons.
Methods: The present study was planned to demonstrate the detailed immunoreactive (IR) distribution pattern of estrogen receptors (ER) in GABAergic neurons of hippocampus. The study was conducted in adult female Wistar rats in estrous phase. 30 µm thick cryostat sections of hippocampal region were obtained from perfusion fixed (with 4% buffered Para formaldehyde) adult female rats (n = 15). The sections were processed free- floating for immunolocalization using the PAP protocol. First they were immunostained for ER using, mouse monoclonal anti-ER-α antibody with DAB as chromogen. Subsequently the same sections were immunostained for GABA using rabbit monoclonal anti-GABA antibody respectively with 9 amino 3 ethyl carbazole (AEC) as chromogen.
Results: The results showed ER were colocalised in GABAergic neurons in all the subfields of hippocampus with obvious variations. In Cornua ammonis (CA) maximum co-localised neurons were seen in CA3 region.
Conclusions: The view is strengthened by our results as it was established through previous studies that the immediate target neurons of estrogen in hippocampus is the GABAergic neurons.
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http://dx.doi.org/10.5214/ans.0972.7531.190305 | DOI Listing |
J Comp Neurol
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Graduate Program in Molecular and Systems Pharmacology, Emory University, Atlanta, Georgia, USA.
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Department of Cell and Developmental Biology, Institute of Life Sciences, The Hebrew University of Jerusalem, Jerusalem, Israel.
The mesopontine tegmental anesthesia area (MPTA) is a focal brainstem locus which, when exposed to GABAergic agents, induces brain-state transitioning from wakefulness to unconsciousness. Correspondingly, MPTA lesions render animals relatively insensitive to GABAergic anesthetics delivered systemically. Using chemogenetics, we recently identified a neuronal subpopulation within the MPTA whose excitation induces this same pro-anesthetic effect.
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German Center for Neurodegenerative Diseases (DZNE), Helmholtz Association of German Research Centers, Magdeburg, Germany; Center for Behavioral Brain Sciences (CBBS), Magdeburg, Germany; Medical Faculty, Otto-von-Guericke University, Magdeburg, Germany. Electronic address:
The neural extracellular matrix (ECM) accumulates in the form of perineuronal nets (PNNs), particularly around fast-spiking GABAergic interneurons in the cortex and hippocampus, but also around synapses and in association with the axon initial segments (AIS) and nodes of Ranvier. Increasing evidence highlights the role of Neurocan (Ncan), a brain-specific component of ECM, in the pathophysiology of neuropsychiatric disorders like bipolar disorder and schizophrenia. Ncan localizes at PNNs, perisynaptically, and at the nodes of Ranvier and the AIS, highlighting its potential role in regulating axonal excitability.
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January 2025
The Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California San Francisco, San Francisco, CA, USA.
The development of the human neocortex is highly dynamic, involving complex cellular trajectories controlled by gene regulation. Here we collected paired single-nucleus chromatin accessibility and transcriptome data from 38 human neocortical samples encompassing both the prefrontal cortex and the primary visual cortex. These samples span five main developmental stages, ranging from the first trimester to adolescence.
View Article and Find Full Text PDFJ Neurosci
January 2025
Bowles Center for Alcohol Studies, University of North Carolina School of Medicine, Chapel Hill, NC, USA; Department of Pharmacology, University of North Carolina School of Medicine, Chapel Hill, NC, USA, 27599.
Blunted sensitivity to ethanol's aversive effects can increase motivation to consume ethanol; yet, the neurobiological circuits responsible for encoding these aversive properties are not fully understood. Plasticity in cells projecting from the anterior insular cortex (aIC) to the basolateral amygdala (BLA) is critical for taste aversion learning and retrieval, suggesting this circuit's potential involvement in modulating the aversive properties of ethanol. Here, we tested the hypothesis that GABAergic currents onto aIC-BLA projections would be facilitated as a consequence of retrieval of an ethanol-conditioned taste aversion (CTA).
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