Keyword search (4,164 papers available)

"alpha" Keyword-tagged Publications:

Title Authors PubMed ID
1 Assessing in silico tools for accurate pathogenicity prediction in CHD nucleosome remodelers Rabouhi N; Guindon S; Coleman EA; van Heesbeen HJ; Greenwood CMT; Lu T; Campeau PM; 40907936
ENCS
2 Sound degradation type differentially affects neural indicators of cognitive workload and speech tracking Gagné N; Greenlaw KM; Coffey EBJ; 40412301
PSYCHOLOGY
3 AP-1 contributes to endosomal targeting of ubiquitin ligase RNF13 via a secondary and novel non-canonical binding motif Cabana VC; Sénécal AM; Bouchard AY; Kourrich S; Cappadocia L; Lussier MP; 39206621
CSBN
4 Social network dynamics, infant loss, and gut microbiota composition in female Colobus vellerosus during time periods with alpha male challenges Samartino S; Christie D; Penna A; Sicotte P; Ting N; Wikberg E; 38735025
BIOLOGY
5 Age of Acquisition Modulates Alpha Power During Bilingual Speech Comprehension in Noise Grant AM; Kousaie S; Coulter K; Gilbert AC; Baum SR; Gracco V; Titone D; Klein D; Phillips NA; 35548507
CRDH
6 Estrogen receptors observed at extranuclear neuronal sites and in glia in the nucleus accumbens core and shell of the female rat: Evidence for localization to catecholaminergic and GABAergic neurons Almey A; Milner TA; Brake WG; 35397175
CSBN
7 The stress induced caleosin, RD20/CLO3, acts as a negative regulator of GPA1 in Arabidopsis Brunetti SC; Arseneault MKM; Wright JA; Wang Z; Ehdaeivand MR; Lowden MJ; Rivoal J; Khalil HB; Garg G; Gulick PJ; 34599731
BIOLOGY
8 Data-driven beamforming technique to attenuate ballistocardiogram artefacts in electroencephalography-functional magnetic resonance imaging without detecting cardiac pulses in electrocardiography recordings Uji M; Cross N; Pomares FB; Perrault AA; Jegou A; Nguyen A; Aydin U; Lina JM; Dang-Vu TT; Grova C; 34101939
PERFORM
9 How cerebral cortex protects itself from interictal spikes: The alpha/beta inhibition mechanism Pellegrino G; Hedrich T; Sziklas V; Lina JM; Grova C; Kobayashi E; 34002916
PERFORM
10 Effects of pH on an IDP conformational ensemble explored by molecular dynamics simulation. Lindsay RJ, Mansbach RA, Gnanakaran S, Shen T 33581430
PHYSICS
11 Estrogen receptor α and G-protein coupled estrogen receptor 1 are localized to GABAergic neurons in the dorsal striatum. Almey A, Milner TA, Brake WG 27080432
PSYCHOLOGY

 

Title:Estrogen receptors observed at extranuclear neuronal sites and in glia in the nucleus accumbens core and shell of the female rat: Evidence for localization to catecholaminergic and GABAergic neurons
Authors:Almey AMilner TABrake WG
Link:https://pubmed.ncbi.nlm.nih.gov/35397175/
DOI:10.1002/cne.25320
Publication:The Journal of comparative neurology
Keywords:G-protein coupled estrogen receptor 1electron microscopyestrogen receptor alphaestrogen receptor betaventral striatumγ-aminobutyric acid
PMID:35397175 Category: Date Added:2022-04-09
Dept Affiliation: CSBN
1 Department of Psychology, Centre for Studies in Behavioral Neurobiology (CSBN), Concordia University, Montreal, Canada.
2 Feil Family Brain and Mind Research Institute, Weill Cornell Medicine, New York City, New York, USA.
3 Harold and Margaret Milliken Hatch Laboratory of Neuroendocrinology, The Rockefeller University, New York City, New York, USA.

Description:

Estrogens affect dopamine-dependent diseases/behavior and have rapid effects on dopamine release and receptor availability in the nucleus accumbens (NAc). Low levels of nuclear estrogen receptor (ER) a and ERß are seen in the NAc, which cannot account for the rapid effects of estrogens in this region. G-protein coupled ER 1 (GPER1) is observed at low levels in the NAc shell, which also likely does not account for the array of estrogens' effects in this region. Prior studies demonstrated membrane-associated ERs in the dorsal striatum; these experiments extend those findings to the NAc core and shell. Single- and dual-immunolabeling electron microscopy determined whether ERa, ERß, and GPER1 are at extranuclear sites in the NAc core and shell and whether ERa and GPER1 were localized to catecholaminergic or ?-aminobutyric acid-ergic (GABAergic) neurons. All three ERs are observed, almost exclusively, at extranuclear sites in the NAc, and similarly distributed in the core and shell. ERa, ERß, and GPER1 are primarily in axons and axon terminals suggesting that estrogens affect transmission in the NAc via presynaptic mechanisms. About 10% of these receptors are found on glia. A small proportion of ERa and GPER1 are localized to catecholaminergic terminals, suggesting that binding at these ERs alters release of catecholamines, including dopamine. A larger proportion of ERa and GPER1 are localized to GABAergic dendrites and terminals, suggesting that estrogens alter GABAergic transmission to indirectly affect dopamine transmission in the NAc. Thus, the localization of ERs could account for the rapid effects of estrogen in the NAc.





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