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Expression of the Ghrelin and Neurotensin Systems is Altered in the Temporal Lobe of Alzheimer's Disease Patients

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/cne.903170306openalex-snapshot
Distribution of neurotensin immunoreactivity within the human amygdaloid complex: A comparison with acetylcholinesterase‐ and Nissl‐stained tissue sections
inferredcites →https://doi.org/10.1002/jnr.22088openalex-snapshot
Desacyl‐ghrelin and synthetic GH‐secretagogues modulate the production of inflammatory cytokines in mouse microglia cells stimulated by β‐amyloid fibrils
inferredcites →https://doi.org/10.1002/psc.1177openalex-snapshot
Ghrelin—a novel generation of anti‐obesity drug: design, pharmacomodulation and biological activity of ghrelin analogues
inferredcites →https://doi.org/10.1007/bf00308809openalex-snapshot
Neuropathological stageing of Alzheimer-related changes
inferredcites →https://doi.org/10.1007/s11064-006-9125-8openalex-snapshot
Systemic and Brain Metabolic Dysfunction as a New Paradigm for Approaching Alzheimer’s Dementia
inferredcites →https://doi.org/10.1016/0006-8993(90)90372-iopenalex-snapshot
Reduction of neurotensin immunoreactivity in the amygdala in Alzheimer's disease
inferredcites →https://doi.org/10.1016/0022-510x(83)90114-4openalex-snapshot
Post mortem levels of thyrotropin-releasing hormone and neurotensin in the amygdala in Alzheimer's disease, schizophrenia and depression
inferredcites →https://doi.org/10.1016/0022-510x(83)90196-xopenalex-snapshot
Neuropeptides in Alzheimer type dementia
inferredcites →https://doi.org/10.1016/0022-510x(85)90157-1openalex-snapshot
Neurotensin immunoreactivity in post-mortem brain is increased in Down's syndrome but not in Alzheimer-type dementia
inferredcites →https://doi.org/10.1016/0026-0495(91)90139-nopenalex-snapshot
Reduced hypothalamic neurotensin concentrations in the genetically obese diabetic ( ) mouse: Possible relationship to obesity
inferredcites →https://doi.org/10.1016/0167-0115(89)90254-1openalex-snapshot
Neuropeptides in Alzheimer's disease: a postmortem study
inferredcites →https://doi.org/10.1016/0306-4522(90)90246-zopenalex-snapshot
Alzheimer's disease: Changes in hippocampal N-methyl-d-aspartate, quisqualate, neurotensin, adenosine, benzodiazepine, serotonin and opioid receptors—an autoradiographic study
inferredcites →https://doi.org/10.1016/j.bbr.2009.03.031openalex-snapshot
Intraamygdaloid microinjection of acylated-ghrelin influences passive avoidance learning
inferredcites →https://doi.org/10.1016/j.bbrc.2003.11.150openalex-snapshot
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.biocel.2006.11.007openalex-snapshot
Over-expression of the truncated ghrelin receptor polypeptide attenuates the constitutive activation of phosphatidylinositol-specific phospholipase C by ghrelin receptors but has no effect on ghrelin-stimulated extracellular signal-regulated kinase 1/2 activity
inferredcites →https://doi.org/10.1016/j.biocel.2007.04.020openalex-snapshot
Ghrelin: A new peptide regulating growth hormone release and food intake
inferredcites →https://doi.org/10.1016/j.brainresbull.2009.10.003openalex-snapshot
Role of intraamygdaloid acylated-ghrelin in spatial learning
inferredcites →https://doi.org/10.1016/j.cell.2008.01.017openalex-snapshot
Identification of the Acyltransferase that Octanoylates Ghrelin, an Appetite-Stimulating Peptide Hormone
inferredcites →https://doi.org/10.1016/j.cellsig.2006.11.011openalex-snapshot
The truncated ghrelin receptor polypeptide (GHS-R1b) acts as a dominant-negative mutant of the ghrelin receptor
inferredcites →https://doi.org/10.1016/j.cytogfr.2009.07.006openalex-snapshot
New insights into the molecular complexity of the ghrelin gene locus
inferredcites →https://doi.org/10.1016/j.neurobiolaging.2006.10.010openalex-snapshot
Age-dependent decline of neprilysin in Alzheimer's disease and normal brain: Inverse correlation with Aβ levels
inferredcites →https://doi.org/10.1016/j.neuroscience.2008.03.015openalex-snapshot
Decreased memory for novel object recognition in chronically food-restricted mice is reversed by acute ghrelin administration
inferredcites →https://doi.org/10.1016/j.nlm.2008.12.008openalex-snapshot
Central ghrelin increases anxiety in the Open Field test and impairs retention memory in a passive avoidance task in neonatal chicks
inferredcites →https://doi.org/10.1016/j.peptides.2007.06.002openalex-snapshot
β-Lactotensin, a neurotensin agonist peptide derived from bovine β-lactoglobulin, enhances memory consolidation in mice
inferredcites →https://doi.org/10.1016/j.peptides.2007.06.030openalex-snapshot
Over-expression of neurotensin high-affinity receptor 1 (NTS1) in relation with its ligand neurotensin (NT) and nuclear ß-catenin in inflammatory bowel disease-related oncogenesis
inferredcites →https://doi.org/10.1016/j.peptides.2008.03.020openalex-snapshot
Role of ghrelin axis in colorectal cancer: A novel association
inferredcites →https://doi.org/10.1016/j.pneurobio.2009.07.002openalex-snapshot
Somatostatin, Alzheimer's disease and cognition: An old story coming of age?
inferredcites →https://doi.org/10.1016/j.regpep.2006.11.012openalex-snapshot
Selective serotonin reuptake inhibitor (fluoxetine) decreases the effects of ghrelin on memory retention and food intake
inferredcites →https://doi.org/10.1016/j.yfrne.2009.10.008openalex-snapshot
Ghrelin in the regulation of body weight and metabolism
inferredcites →https://doi.org/10.1016/s0006-291x(02)02740-7openalex-snapshot
Ghrelin increases anxiety-like behavior and memory retention in rats
inferredcites →https://doi.org/10.1016/s0006-8993(02)03271-7openalex-snapshot
Targeted inactivation of the neurotensin type 1 receptor reveals its role in body temperature control and feeding behavior but not in analgesia
inferredcites →https://doi.org/10.1016/s0165-6147(99)01357-7openalex-snapshot
Neurotensin and neurotensin receptors
inferredcites →https://doi.org/10.1016/s0306-4522(03)00460-3openalex-snapshot
Protein and mRNA levels of nicotinic receptors in brain of tobacco using controls and patients with Alzheimer's disease
inferredcites →https://doi.org/10.1037/0735-7044.120.5.1093openalex-snapshot
Microinfusions of neurotensin antagonist SR 48692 within the nucleus accumbens core impair spatial learning in rats.
inferredcites →https://doi.org/10.1038/nn1656openalex-snapshot
Ghrelin controls hippocampal spine synapse density and memory performance
inferredcites →https://doi.org/10.1073/pnas.0800708105openalex-snapshot
Ghrelin octanoylation mediated by an orphan lipid transferase
inferredcites →https://doi.org/10.1073/pnas.0903499106openalex-snapshot
Neurotensin induces IL-6 secretion in mouse preadipocytes and adipose tissues during 2,4,6,-trinitrobenzensulphonic acid-induced colitis
inferredcites →https://doi.org/10.1074/jbc.m407676200openalex-snapshot
Common Structural Basis for Constitutive Activity of the Ghrelin Receptor Family
inferredcites →https://doi.org/10.1074/jbc.m600223200openalex-snapshot
Ghrelin and the Growth Hormone Secretagogue Receptor Constitute a Novel Autocrine Pathway in Astrocytoma Motility
inferredcites →https://doi.org/10.1080/09513590500519385openalex-snapshot
Plasma levels of neuropeptides in Alzheimer's disease
inferredcites →https://doi.org/10.1097/mco.0b013e32829fb37copenalex-snapshot
Influence of ghrelin on food intake and energy homeostasis
inferredcites →https://doi.org/10.1111/j.1471-4159.2007.04805.xopenalex-snapshot
Neurotensin type 2 receptor is involved in fear memory in mice
inferredcites →https://doi.org/10.1111/j.1471-4159.2008.05698.xopenalex-snapshot
Human ProNGF: biological effects and binding profiles at TrkA, P75 NTR and sortilin
inferredcites →https://doi.org/10.1111/j.1749-6632.1992.tb27343.xopenalex-snapshot
Distribution of Neurotensin Receptors in Mammalian Brain
inferredcites →https://doi.org/10.1152/physrev.2001.81.2.741openalex-snapshot
Alzheimer's Disease: Genes, Proteins, and Therapy
inferredcites →https://doi.org/10.1158/0008-5472.can-06-1349openalex-snapshot
The Neuromedin U-Growth Hormone Secretagogue Receptor 1b/Neurotensin Receptor 1 Oncogenic Signaling Pathway as a Therapeutic Target for Lung Cancer
inferredcites →https://doi.org/10.1159/000086983openalex-snapshot
Loss of Growth Hormone Secretagogue Receptor 1a and Overexpression of Type 1b Receptor Transcripts in Human Adrenocortical Tumors
inferredcites →https://doi.org/10.1159/000107132openalex-snapshot
Quantitative Morphometric Analysis of Basal Forebrain Neurons Expressing β-Nerve Growth Factor Receptors in Normal and Alzheimer's Disease Brains
inferredcites →https://doi.org/10.1210/jc.2008-1826openalex-snapshot
Expression Analysis of Dopamine Receptor Subtypes in Normal Human Pituitaries, Nonfunctioning Pituitary Adenomas and Somatotropinomas, and the Association between Dopamine and Somatostatin Receptors with Clinical Response to Octreotide-LAR in Acromegaly
inferredcites →https://doi.org/10.1523/jneurosci.2269-05.2005openalex-snapshot
Anorexigenic Hormones Leptin, Insulin, and α-Melanocyte-Stimulating Hormone Directly Induce Neurotensin (NT) Gene Expression in Novel NT-Expressing Cell Models
inferredcites →https://doi.org/10.1523/jneurosci.4734-03.2004openalex-snapshot
Dysregulation in the Suicide Brain: mRNA Expression of Corticotropin-Releasing Hormone Receptors and GABAAReceptor Subunits in Frontal Cortical Brain Region
inferredcites →https://doi.org/10.1530/eje.1.02313openalex-snapshot
Quantitative analysis of somatostatin receptor subtype (SSTR1–5) gene expression levels in somatotropinomas and non-functioning pituitary adenomas
inferredcites →https://doi.org/10.1677/joe.0.175r001openalex-snapshot
Plasma ghrelin concentrations in elderly subjects: comparison with anorexic and obese patients
inferredcites →https://doi.org/10.3233/jad-2008-13302openalex-snapshot
An Integrated and Unifying Hypothesis for the Metabolic Basis of Sporadic Alzheimer's Disease
inferredcites →https://doi.org/10.3233/jad-2010-1385openalex-snapshot
Expression of Somatostatin, Cortistatin, and Their Receptors, as well as Dopamine Receptors, but not of Neprilysin, are Reduced in the Temporal Lobe of Alzheimer's Disease Patients

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.3944544openalex-extracted
GHS-R1a Deletion Selectively Reduces Inhibitory Drive of Dca1 Pyramidal Neurons to Improve Memory and Prevent LPS-Induced Memory Impairment
inferred← citeshttps://doi.org/10.1002/glia.24062openalex-snapshot
Neurotensin receptor 2 is induced in astrocytes and brain endothelial cells in relation to neuroinflammation following pilocarpine‐induced seizures in rats
inferred← citeshttps://doi.org/10.1002/jnr.22731openalex-snapshot
Epigenetic control of somatostatin and cortistatin expression by β amyloid peptide
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Dietary fat alters the expression of cortistatin and ghrelin systems in the PBMCs of elderly subjects: Putative implications in the postprandial inflammatory response
inferred← citeshttps://doi.org/10.1007/978-1-4939-0823-3_10openalex-snapshot
Ghrelin and Memory
inferred← citeshttps://doi.org/10.1007/s00005-014-0287-9openalex-snapshot
Ghrelin Gene Products in Acute and Chronic Inflammation
inferred← citeshttps://doi.org/10.1007/s11011-013-9412-4openalex-snapshot
Neurodegenerative disease and obesity: what is the role of weight loss and bariatric interventions?
inferred← citeshttps://doi.org/10.1007/s11064-022-03784-wopenalex-snapshot
Intestinal Flora Affect Alzheimer's Disease by Regulating Endogenous Hormones
inferred← citeshttps://doi.org/10.1007/s12035-015-9227-xopenalex-snapshot
Effects of Ghrelin on the Proteolytic Pathways of Alzheimer’s Disease Neuronal Cells
inferred← citeshttps://doi.org/10.1007/s12035-016-9729-1openalex-snapshot
Ghrelin and Neurodegenerative Disorders—a Review
inferred← citeshttps://doi.org/10.1007/s12264-024-01302-2openalex-snapshot
Loss of TET Activity in the Postnatal Mouse Brain Perturbs Synaptic Gene Expression and Impairs Cognitive Function
inferred← citeshttps://doi.org/10.1007/s12603-012-0058-4openalex-snapshot
Ghrelin and leptin secretion in patients with moderate Alzheimer's disease
inferred← citeshttps://doi.org/10.1007/s40520-014-0203-5openalex-snapshot
Glucose impairment and ghrelin gene variants are associated to cognitive dysfunction
inferred← citeshttps://doi.org/10.1016/bs.vh.2021.11.008openalex-snapshot
Ghrelin-O-acyltransferase (GOAT) acylates ghrelin in the hippocampus
inferred← citeshttps://doi.org/10.1016/j.arr.2019.100945openalex-snapshot
Ghrelin in Alzheimer’s disease: Pathologic roles and therapeutic implications
inferred← citeshttps://doi.org/10.1016/j.arr.2020.101187openalex-snapshot
A new understanding of GHSR1a——independent of ghrelin activation
inferred← citeshttps://doi.org/10.1016/j.bbr.2021.113270openalex-snapshot
Differential expression levels of the hippocampal ghrelin and its receptor mRNA during memory consolidation
inferred← citeshttps://doi.org/10.1016/j.conb.2022.102655openalex-snapshot
Ghrelin system in Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.encep.2017.10.012openalex-snapshot
The effects of ghrelin on sleep, appetite, and memory, and its possible role in depression: A review of the literature
inferred← citeshttps://doi.org/10.1016/j.jpsychires.2018.10.011openalex-snapshot
Ghrelin cascade changes in the peripheral blood of Japanese patients with Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.lfs.2015.05.002openalex-snapshot
The role of leptin in the sporadic form of Alzheimer's disease. Interactions with the adipokines amylin, ghrelin and the pituitary hormone prolactin
inferred← citeshttps://doi.org/10.1016/j.lungcan.2017.05.006openalex-snapshot
The components of somatostatin and ghrelin systems are altered in neuroendocrine lung carcinoids and associated to clinical-histological features
inferred← citeshttps://doi.org/10.1016/j.mce.2011.05.002openalex-snapshot
Ghrelin axis genes, peptides and receptors: Recent findings and future challenges
inferred← citeshttps://doi.org/10.1016/j.mehy.2015.01.018openalex-snapshot
Potential ghrelin-mediated benefits and risks of hydrogen water
inferred← citeshttps://doi.org/10.1016/j.nbd.2014.08.026openalex-snapshot
Ghrelin: A link between ageing, metabolism and neurodegenerative disorders
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2016.12.010openalex-snapshot
The neurological effects of ghrelin in brain diseases: Beyond metabolic functions
inferred← citeshttps://doi.org/10.1016/j.neuropharm.2017.12.025openalex-snapshot
Leptin and ghrelin: Sewing metabolism onto neurodegeneration
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2011.07.063openalex-snapshot
Investigation of the presence of ghrelin in the central nervous system of the rat and mouse
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2013.02.062openalex-snapshot
Leptin and ghrelin prevent hippocampal dysfunction induced by Aβ oligomers
inferred← citeshttps://doi.org/10.1016/j.npep.2018.09.002openalex-snapshot
Potential roles of neurotensin on cognition in conditions of obese-insulin resistance
inferred← citeshttps://doi.org/10.1016/j.npep.2020.102112openalex-snapshot
Regulatory effects of ghrelin on endoplasmic reticulum stress, oxidative stress, and autophagy: Therapeutic potential
inferred← citeshttps://doi.org/10.1016/j.peptides.2011.09.019openalex-snapshot
Role of ghrelin system in neuroprotection and cognitive functions: Implications in Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.phrs.2012.06.006openalex-snapshot
Novel domain-selective ACE-inhibiting activity of synthetic growth hormone secretagogues
inferred← citeshttps://doi.org/10.1016/j.phrs.2018.01.018openalex-snapshot
Synaptic plasticity modulation by circulating peptides and metaplasticity: Involvement in Alzheimer’s disease
inferred← citeshttps://doi.org/10.1016/j.psyneuen.2014.11.013openalex-snapshot
Ghrelin in psychiatric disorders – A review
inferred← citeshttps://doi.org/10.1016/j.regpep.2013.07.004openalex-snapshot
Ghrelin stimulates synaptic formation in cultured cortical networks in a dose-dependent manner
inferred← citeshttps://doi.org/10.1016/j.yfrne.2013.08.001openalex-snapshot
Estrogen: A master regulator of bioenergetic systems in the brain and body
inferred← citeshttps://doi.org/10.1021/acs.analchem.5c04297openalex-snapshot
Spatially Mapping Neuropeptide Isomers via MALDI Trapped Ion Mobility MS Imaging
inferred← citeshttps://doi.org/10.1021/acschemneuro.4c00075openalex-snapshot
Native Mass Spectrometry-Centric Approaches Revealed That Neuropeptides Frequently Interact with Amyloid-β
inferred← citeshttps://doi.org/10.1038/s41598-018-31783-xopenalex-snapshot
Ghrelin expression is associated with a favorable outcome in male breast cancer
inferred← citeshttps://doi.org/10.1042/bsr20250362openalex-snapshot
Integrative role of orexigenic peptides in neuroprotection and neurodegenerative disease modulation
inferred← citeshttps://doi.org/10.1080/07391102.2019.1602078openalex-snapshot
Identification of novel small molecule non-peptidomimetic inhibitor for prolyl oligopeptidase through in silico and in vitro approaches
inferred← citeshttps://doi.org/10.1093/cercor/bhac230openalex-snapshot
GHSR1a deficiency suppresses inhibitory drive on dCA1 pyramidal neurons and contributes to memory reinforcement
inferred← citeshttps://doi.org/10.1111/ggi.13275openalex-snapshot
Effect of rivastigmine on plasma butyrylcholine esterase activity and plasma ghrelin levels in patients with dementia in Alzheimer’s disease
inferred← citeshttps://doi.org/10.1111/jdi.12580openalex-snapshot
Ghrelin is a possible new predictor associated with executive function in patients with type 2 diabetes mellitus
inferred← citeshttps://doi.org/10.1111/jnc.12142openalex-snapshot
Comprehensive gene expression analyses of the rat prefrontal cortex after oxysterol treatment
inferred← citeshttps://doi.org/10.1111/jnc.14244openalex-snapshot
Endogenous ghrelin‐O‐acyltransferase ( GOAT ) acylates local ghrelin in the hippocampus
inferred← citeshttps://doi.org/10.1111/jne.12138openalex-snapshot
Protective Effect of Leptin and Ghrelin against Toxicity Induced by Amyloid‐β Oligomers in a Hypothalamic cell Line
inferred← citeshttps://doi.org/10.1111/jphp.12010openalex-snapshot
Semagacestat, a γ-secretase inhibitor, activates the growth hormone secretagogue (GHS-R1a) receptor
inferred← citeshttps://doi.org/10.1126/scitranslmed.aav6278openalex-snapshot
Disrupted hippocampal growth hormone secretagogue receptor 1α interaction with dopamine receptor D1 plays a role in Alzheimer′s disease
inferred← citeshttps://doi.org/10.1159/000333075openalex-snapshot
Genetic Association between Ghrelin Polymorphisms and Alzheimer’s Disease in a Japanese Population
inferred← citeshttps://doi.org/10.11606/t.5.2015.tde-11052015-114427openalex-snapshot
Mudança cognitiva em obesos com comprometimento cognitivo leve submetidos à perda intencional de peso
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Multiple roles of ghrelin in breast cancer
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Ghrelin accelerates synapse formation and activity development in cultured cortical networks
inferred← citeshttps://doi.org/10.1210/clinem/dgab516openalex-snapshot
In1-Ghrelin Splicing Variant as a Key Element in the Pathophysiological Association Between Obesity and Prostate Cancer
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Glucagon-Like Peptide-2 Directly Regulates Hypothalamic Neurons Expressing Neuropeptides Linked to Appetite Control in Vivo and in Vitro
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A Novel Human Ghrelin Variant (In1-Ghrelin) and Ghrelin-O-Acyltransferase Are Overexpressed in Breast Cancer: Potential Pathophysiological Relevance
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Ghrelin is a prognostic marker and a potential therapeutic target in breast cancer
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Acylated Ghrelin Administration Inhibits Sleeve Gastrectomy - Induced Hippocampal Oxidative Stress, Apoptosis and Tau-Hyperphosphorylation by Activating the PI3K/Akt Pathway
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Reinstating plasticity and memory in a tauopathy mouse model with an acetyltransferase activator
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Cloning of a novel insulin-regulated ghrelin transcript in prostate cancer
inferred← citeshttps://doi.org/10.1530/joe-13-0391openalex-snapshot
Ghrelin gene products, receptors, and GOAT enzyme: biological and pathophysiological insight
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In1-ghrelin, a splice variant of ghrelin gene, is associated with the evolution and aggressiveness of human neuroendocrine tumors: Evidence from clinical, cellular and molecular parameters
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Serum Ghrelin in Mild Cognitive Impairment and Alzheimer's Disease A Systematic Review and Meta-analysis
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Ghrelin as a Neuroprotective and Palliative Agent in Alzheimer's and Parkinson's Disease
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Metabolic Dysfunction in Alzheimers Disease and Related Neurodegenerative Disorders
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Energy Metabolism, Adult Neurogenesis and their Possible Roles in Alzheimer's Disease: A Brief Overview
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Zinc-mediated Neurotransmission in Alzheimer's Disease: A Potential Role of the GPR39 in Dementia
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Interactions of Growth Hormone, Insulin-Like Growth Factor-1, and Ghrelin with the Blood-Brain Barrier
inferred← citeshttps://doi.org/10.23889/suthesis.58915openalex-snapshot
Characterisation of the ghrelinergic system in human models of neurodegenerative diseases
inferred← citeshttps://doi.org/10.3233/jad-132417openalex-snapshot
Impaired Hippocampal Neurogenesis and its Enhancement with Ghrelin in 5XFAD Mice
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Increased Serum Acylated Ghrelin Levels in Patients with Mild Cognitive Impairment
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Adiposity and Cognitive Decline: Underlying Mechanisms
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Cognitive Enhancers (Nootropics). Part 1: Drugs Interacting with Receptors
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FARELERDE SKOPOLAMİNLE BOZULMUŞ ÖĞRENME VE BELLEK ÜZERİNE NÖROTENSİN AGONİSTİ PD149163’ÜN ETKİSİ
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Systems-Level G Protein-Coupled Receptor Therapy Across a Neurodegenerative Continuum by the GLP-1 Receptor System
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Synchronizing an aging brain: can entraining circadian clocks by food slow Alzheimer’s disease?
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The Potential Roles of Ghrelin in Metabolic Syndrome and Secondary Symptoms of Alzheimer’s Disease
inferred← citeshttps://doi.org/10.3389/fnins.2020.614828openalex-snapshot
Acylated Ghrelin as a Multi-Targeted Therapy for Alzheimer's and Parkinson's Disease
inferred← citeshttps://doi.org/10.3389/fnins.2023.1130730openalex-snapshot
The potential of the gut microbiome for identifying Alzheimer’s disease diagnostic biomarkers and future therapies
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Molecular pathogenesis of Alzheimer's disease onset in a mouse model: effects of cannabidiol treatment
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Neuropeptides Exert Neuroprotective Effects in Alzheimer's Disease
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Ghrelin’s role in sleep and sleep deprivation: a narrative review
inferred← citeshttps://doi.org/10.3390/biomedicines10081946openalex-snapshot
Arc Regulates Transcription of Genes for Plasticity, Excitability and Alzheimer’s Disease
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The Role of Ghrelin in Neuroprotection after Ischemic Brain Injury
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The Anti-Apoptotic Role of Neurotensin
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The Role of Probiotics in Modulating the Gut Microbiome in Alzheimer’s Disease: A Review
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Is Ghrelin Synthesized in the Central Nervous System?
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MK-0677, a Ghrelin Agonist, Alleviates Amyloid Beta-Related Pathology in 5XFAD Mice, an Animal Model of Alzheimer’s Disease
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Design and Experimental Evaluation of a Peptide Antagonist against Amyloid β(1–42) Interactions with Calmodulin and Calbindin-D28k
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The Aggravating Role of Failing Neuropeptide Networks in the Development of Sporadic Alzheimer’s Disease
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Beyond Hunger: The Structure, Signaling, and Systemic Roles of Ghrelin
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Pro- and Anti-Inflammatory Neuropeptides and Glia: The Balance Between Neuroprotection and Neuroinflammation
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Alzheimer’s Disease and Metabolic Dysfunction: No Association Between L72m Ghlr Variant in Brazilian Population
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Improved Serum Leptin and Ghrelin Following Bariatric Surgery Predict Better Postoperative Cognitive Function
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Ghrelin Levels in Elderly, Diabetic Patients with Mild Cognitive Impairment
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Insulin resistance as the molecular link between diabetes and Alzheimer's disease
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Gut Microbiome and Brain-Gut Axis in Autism — Aberrant Development of Gut-Brain Communication and Reward Circuitry
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Différences mâles/femelles dans les effets de l'éthanol sur la plasticité hippocampique chez le rat adolescent : rôle des œstrogènes
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