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GHS-R1a Deletion Selectively Reduces Inhibitory Drive of Dca1 Pyramidal Neurons to Improve Memory and Prevent LPS-Induced Memory Impairment

https://doi.org/10.2139/ssrn.3944544
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inferredcites →https://doi.org/10.1002/cne.10905openalex-extracted
Green fluorescent protein expression and colocalization with calretinin, parvalbumin, and somatostatin in the GAD67‐GFP knock‐in mouse
inferredcites →https://doi.org/10.1002/hipo.20086openalex-extracted
Chronic LPS exposure produces changes in intrinsic membrane properties and a sustained IL-β-dependent increase in GABAergic inhibition in hippocampal CA1 pyramidal neurons
inferredcites →https://doi.org/10.1007/s00125-012-2509-1openalex-extracted
Ghrelin contributes to derangements of glucose metabolism induced by rapamycin in mice
inferredcites →https://doi.org/10.1007/s00213-014-3817-6openalex-extracted
Ghrelin increases memory consolidation through hippocampal mechanisms dependent on glutamate release and NR2B-subunits of the NMDA receptor
inferredcites →https://doi.org/10.1016/j.bbr.2012.03.012openalex-extracted
Growth hormone secretagogue receptor (GHS-R1a) knockout mice exhibit improved spatial memory and deficits in contextual memory
inferredcites →https://doi.org/10.1016/j.bbrc.2003.11.150openalex-extracted
Differential role of the hippocampus, amygdala, and dorsal raphe nucleus in regulating feeding, memory, and anxiety-like behavioral responses to ghrelin
inferredcites →https://doi.org/10.1016/j.biopsych.2014.10.021openalex-extracted
Ghrelin’s Role in the Hypothalamic-Pituitary-Adrenal Axis Stress Response: Implications for Mood Disorders
inferredcites →https://doi.org/10.1016/j.brainres.2013.10.022openalex-extracted
Ghrelin but not nesfatin-1 affects certain forms of learning and memory in both rats and mice
inferredcites →https://doi.org/10.1016/j.cell.2015.10.062openalex-extracted
Hippocampal Dopamine/DRD1 Signaling Dependent on the Ghrelin Receptor
inferredcites →https://doi.org/10.1016/j.cmet.2018.02.008openalex-extracted
The Homeostatic Force of Ghrelin
inferredcites →https://doi.org/10.1016/j.molmet.2020.101004openalex-extracted
Metabolic insights from a GHSR-A203E mutant mouse model
inferredcites →https://doi.org/10.1016/j.neulet.2017.10.012openalex-extracted
Local infusion of ghrelin into the lateral amygdala blocks extinction of conditioned taste aversion in rats
inferredcites →https://doi.org/10.1016/j.neuropharm.2018.12.022openalex-extracted
A ghrelin receptor and oxytocin receptor heterocomplex impairs oxytocin mediated signalling
inferredcites →https://doi.org/10.1016/j.neuroscience.2013.10.063openalex-extracted
Ghrelin administration enhances neurogenesis but impairs spatial learning and memory in adult mice
inferredcites →https://doi.org/10.1016/j.physbeh.2010.10.017openalex-extracted
Signaling through the ghrelin receptor modulates hippocampal function and meal anticipation in mice
inferredcites →https://doi.org/10.1016/j.pneurobio.2020.101881openalex-extracted
Frontal eye field neurons selectively signal the reward value of prior actions
inferredcites →https://doi.org/10.1016/j.tins.2006.08.005openalex-extracted
Learning, aging and intrinsic neuronal plasticity
inferredcites →https://doi.org/10.1016/j.tins.2010.10.001openalex-extracted
The extra-hypothalamic actions of ghrelin on neuronal function
inferredcites →https://doi.org/10.1016/j.xcrm.2020.100120openalex-extracted
Unacylated-Ghrelin Impairs Hippocampal Neurogenesis and Memory in Mice and Is Altered in Parkinson’s Dementia in Humans
inferredcites →https://doi.org/10.1016/s0006-291x(02)02740-7openalex-extracted
Ghrelin increases anxiety-like behavior and memory retention in rats
inferredcites →https://doi.org/10.1016/s0169-328x(97)00071-5openalex-extracted
Distribution of mRNA encoding the growth hormone secretagogue receptor in brain and peripheral tissues
inferredcites →https://doi.org/10.1038/45230openalex-extracted
Ghrelin is a growth-hormone-releasing acylated peptide from stomach
inferredcites →https://doi.org/10.1038/ncomms2439openalex-extracted
Peptide hormone ghrelin enhances neuronal excitability by inhibition of Kv7/KCNQ channels
inferredcites →https://doi.org/10.1038/nn1656openalex-extracted
Ghrelin controls hippocampal spine synapse density and memory performance
inferredcites →https://doi.org/10.1038/nrn1248openalex-extracted
The other side of the engram: experience-driven changes in neuronal intrinsic excitability
inferredcites →https://doi.org/10.1038/s41598-019-42286-8openalex-extracted
Neuroinflammation induced by lipopolysaccharide causes cognitive impairment in mice
inferredcites →https://doi.org/10.1073/pnas.1313798111openalex-extracted
Ghrelin triggers the synaptic incorporation of AMPA receptors in the hippocampus
inferredcites →https://doi.org/10.1074/jbc.m112.382473openalex-extracted
Promiscuous Dimerization of the Growth Hormone Secretagogue Receptor (GHS-R1a) Attenuates Ghrelin-mediated Signaling
inferredcites →https://doi.org/10.1074/jbc.m114.581397openalex-extracted
G Protein and β-Arrestin Signaling Bias at the Ghrelin Receptor
inferredcites →https://doi.org/10.1085/jgp.201511383openalex-extracted
Constitutive and ghrelin-dependent GHSR1a activation impairs CaV2.1 and CaV2.2 currents in hypothalamic neurons
inferredcites →https://doi.org/10.1101/lm.4.2.230openalex-extracted
Brief theta-burst stimulation induces a transcription-dependent late phase of LTP requiring cAMP in area CA1 of the mouse hippocampus.
inferredcites →https://doi.org/10.1111/j.1460-9568.2010.07491.xopenalex-extracted
Local infusion of ghrelin enhanced hippocampal synaptic plasticity and spatial memory through activation of phosphoinositide 3-kinase in the dentate gyrus of adult rats
inferredcites →https://doi.org/10.1111/jne.12677openalex-extracted
Brain accessibility delineates the central effects of circulating ghrelin
inferredcites →https://doi.org/10.1113/jphysiol.1987.sp016517openalex-extracted
Action potential repolarization and a fast after‐hyperpolarization in rat hippocampal pyramidal cells.
inferredcites →https://doi.org/10.1124/mol.109.056101openalex-extracted
Growth Hormone Secretagogues and Growth Hormone Releasing Peptides Act As Orthosteric Super-Agonists but Not Allosteric Regulators for Activation of the G Protein Gαo1 by the Ghrelin Receptor
inferredcites →https://doi.org/10.1126/science.273.5277.974openalex-extracted
A Receptor in Pituitary and Hypothalamus That Functions in Growth Hormone Release
inferredcites →https://doi.org/10.1126/scisignal.abb1953openalex-extracted
Ligand-independent activity of the ghrelin receptor modulates AMPA receptor trafficking and supports memory formation
inferredcites →https://doi.org/10.1126/scitranslmed.aav6278openalex-extracted
Disrupted hippocampal growth hormone secretagogue receptor 1α interaction with dopamine receptor D1 plays a role in Alzheimer′s disease
inferredcites →https://doi.org/10.1152/ajpendo.00576.2011openalex-extracted
Ablation of ghrelin receptor in leptin-deficient ob/ob mice has paradoxical effects on glucose homeostasis when compared with ablation of ghrelin in ob/ob mice
inferredcites →https://doi.org/10.1186/s13041-016-0270-yopenalex-extracted
Disrupted-in-schizophrenia1 (DISC1) L100P mutation alters synaptic transmission and plasticity in the hippocampus and causes recognition memory deficits
inferredcites →https://doi.org/10.1210/en.2008-1638openalex-extracted
In Vivo Characterization of High Basal Signaling from the Ghrelin Receptor
inferredcites →https://doi.org/10.1210/me.2003-0069openalex-extracted
High Constitutive Signaling of the Ghrelin Receptor—Identification of a Potent Inverse Agonist
inferredcites →https://doi.org/10.1371/journal.pone.0016391openalex-extracted
Ablations of Ghrelin and Ghrelin Receptor Exhibit Differential Metabolic Phenotypes and Thermogenic Capacity during Aging
inferredcites →https://doi.org/10.1371/journal.pone.0065422openalex-extracted
Ghrelin Modulates Lateral Amygdala Neuronal Firing and Blocks Acquisition for Conditioned Taste Aversion
inferredcites →https://doi.org/10.1371/journal.pone.0098180openalex-extracted
Unacylated Ghrelin Suppresses Ghrelin-Induced Neuronal Activity in the Hypothalamus and Brainstem of Male Rats
inferredcites →https://doi.org/10.1523/jneurosci.0384-09.2009openalex-extracted
The Fast and Slow Afterhyperpolarizations Are Differentially Modulated in Hippocampal Neurons by Aging and Learning
inferredcites →https://doi.org/10.18632/aging.103802openalex-extracted
Both ghrelin deletion and unacylated ghrelin overexpression preserve muscles in aging mice
inferredcites →https://doi.org/10.3233/jad-2010-100873openalex-extracted
Expression of the Ghrelin and Neurotensin Systems is Altered in the Temporal Lobe of Alzheimer's Disease Patients
inferredcites →https://doi.org/10.3389/fnins.2020.614828openalex-extracted
Acylated Ghrelin as a Multi-Targeted Therapy for Alzheimer's and Parkinson's Disease
inferredcites →https://doi.org/10.3390/ijms18030638openalex-extracted
Is Ghrelin Synthesized in the Central Nervous System?
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