Keyword search (4,163 papers available)

"nap" Keyword-tagged Publications:

Title Authors PubMed ID
1 Habitual napping in older adults is accompanied by altered heat-loss rhythms across the circadian cycle and reduced coupling between pre-sleep thermoregulatory dynamics and sleep initiation Dourte M; Hammad G; de Haan S; Deantoni M; Reyt M; Baillet M; Lesoinne A; Muto V; Collette F; Vandewalle G; Peigneux P; Cajochen C; Schmidt C; 41797810
PSYCHOLOGY
2 Dopamine inhibits excitatory synaptic responses in layer I of the rat parasubiculum Carter F; Hobishi H; Chapman CA; 40818632
PSYCHOLOGY
3 Syngap1 regulates the synaptic drive and membrane excitability of Parvalbumin-positive interneurons in mouse auditory cortex Francavilla R; Chattopadhyaya B; Damo Kamda JL; Jadhav V; Kourrich S; Michaud JL; Di Cristo G; 40810392
CSBN
4 Progesterone and allopregnanolone facilitate excitatory synaptic transmission in the infralimbic cortex via activation of membrane progesterone receptors Rahaei N; Buynack LM; Kires L; Movasseghi Y; Chapman CA; 39722289
PSYCHOLOGY
5 The effects of acute exercise and a nap on heart rate variability and memory in young sedentary adults Mograss M; Frimpong E; Vilcourt F; Chouchou F; Zvionow T; Dang-Vu TT; 37855092
PERFORM
6 Inhibiting amyloid beta (1-42) peptide-induced mitochondrial dysfunction prevents the degradation of synaptic proteins in the entorhinal cortex Olajide OJ; La Rue C; Bergdahl A; Chapman CA; 36275011
HKAP
7 The effects of napping on night-time sleep in healthy young adults Melodee Mograss 35253300
PERFORM
8 G protein-coupled estrogen receptor-1 enhances excitatory synaptic responses in the entorhinal cortex Batallán Burrowes AA; Sundarakrishnan A; Bouhour C; Chapman CA; 34399010
PSYCHOLOGY
9 Are the Allergic Reactions of COVID-19 Vaccines Caused by mRNA Constructs or Nanocarriers? Immunological Insights Selvaraj G; Kaliamurthi S; Peslherbe GH; Wei DQ; 34021862
CHEMBIOCHEM
10 Neurobehavioral, neurochemical and synaptic plasticity perturbations during postnatal life of rats exposed to chloroquine in-utero Olajide OJ; Alliy ZO; Ojo DO; Osinubi OO; Bello SO; Ibrahim FE; Adukwu FO; Abikoye TO; Gbadamosi IT; Mutholib NY; Bamisi O; Ajiboye OJ; Okesina AA; Alli-Oluwafuyi A; Oyewole AL; Nafiu AB; Akinola O; 33845156
PSYCHOLOGY
11 Atrx Deletion in Neurons Leads to Sexually Dimorphic Dysregulation of miR-137 and Spatial Learning and Memory Deficits. Tamming RJ, Dumeaux V, Jiang Y, Shafiq S, Langlois L, Ellegood J, Qiu LR, Lerch JP, Bérubé NG 32610139
PERFORM
12 Exercising before a nap benefits memory better than napping or exercising alone. Mograss M, Crosetta M, Abi-Jaoude J, Frolova E, Robertson E, Pepin V, Dang-Vu TT 32236442
PERFORM
13 Heterosynaptic modulation of evoked synaptic potentials in layer II of the entorhinal cortex by activation of the parasubiculum. Sparks DW, Chapman CA 27146979
PSYCHOLOGY

 

Title:Heterosynaptic modulation of evoked synaptic potentials in layer II of the entorhinal cortex by activation of the parasubiculum.
Authors:Sparks DWChapman CA
Link:https://www.ncbi.nlm.nih.gov/pubmed/27146979?dopt=Abstract
DOI:10.1152/jn.00095.2016
Publication:Journal of neurophysiology
Keywords:Ihentorhinal cortexheterosynapticparasubiculumplasticity
PMID:27146979 Category:J Neurophysiol Date Added:2019-06-20
Dept Affiliation: PSYCHOLOGY
1 Centre for Studies in Behavioural Neurobiology, Department of Psychology, Concordia University, Montréal, Québec, Canada.
2 Centre for Studies in Behavioural Neurobiology, Department of Psychology, Concordia University, Montréal, Québec, Canada andrew.chapman@concordia.ca.

Description:

Heterosynaptic modulation of evoked synaptic potentials in layer II of the entorhinal cortex by activation of the parasubiculum.

J Neurophysiol. 2016 08 01;116(2):658-70

Authors: Sparks DW, Chapman CA

Abstract

The superficial layers of the entorhinal cortex receive sensory and associational cortical inputs and provide the hippocampus with the majority of its cortical sensory input. The parasubiculum, which receives input from multiple hippocampal subfields, sends its single major output projection to layer II of the entorhinal cortex, suggesting that it may modulate processing of synaptic inputs to the entorhinal cortex. Indeed, stimulation of the parasubiculum can enhance entorhinal responses to synaptic input from the piriform cortex in vivo. Theta EEG activity contributes to spatial and mnemonic processes in this region, and the current study assessed how stimulation of the parasubiculum with either single pulses or short, five-pulse, theta-frequency trains may modulate synaptic responses in layer II entorhinal stellate neurons evoked by stimulation of layer I afferents in vitro. Parasubicular stimulation pulses or trains suppressed responses to layer I stimulation at intervals of 5 ms, and parasubicular stimulation trains facilitated layer I responses at a train-pulse interval of 25 ms. This suggests that firing of parasubicular neurons during theta activity may heterosynaptically enhance incoming sensory inputs to the entorhinal cortex. Bath application of the hyperpolarization-activated cation current (Ih) blocker ZD7288 enhanced the facilitation effect, suggesting that cholinergic inhibition of Ih may contribute. In addition, repetitive pairing of parasubicular trains and layer I stimulation induced a lasting depression of entorhinal responses to layer I stimulation. These findings provide evidence that theta activity in the parasubiculum may promote heterosynaptic modulation effects that may alter sensory processing in the entorhinal cortex.

PMID: 27146979 [PubMed - indexed for MEDLINE]





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