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Scutellarin protects against Aβ-induced learning and memory deficits in rats: involvement of nicotinic acetylcholine receptors and cholinesterase

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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/ana.410220206openalex-snapshot
Cholinesterases within neurofibrillary tangles related to age and Alzheimer's disease
inferredcites →https://doi.org/10.1002/jnr.10391openalex-snapshot
In vivo conversion of racemized β‐amyloid ([ D ‐Ser26]Aβ1–40) to truncated and toxic fragments ([ D ‐Ser26]Aβ25–35/40) and fragment presence in the brains of Alzheimer's patients
inferredcites →https://doi.org/10.1002/jnr.21463openalex-snapshot
Decreased nicotinic receptors and cognitive deficit in rats intracerebroventricularly injected with beta‐amyloid peptide(1‐42) and fed a high‐cholesterol diet
inferredcites →https://doi.org/10.1007/bf00307630openalex-snapshot
Senile plaques: staining for acetylcholinesterase and A4 protein: a comparative study in the hippocampus and entorhinal cortex
inferredcites →https://doi.org/10.1007/s00702-008-0022-yopenalex-snapshot
Tetrahydrofurobenzofuran cymserine, a potent butyrylcholinesterase inhibitor and experimental Alzheimer drug candidate, enzyme kinetic analysis
inferredcites →https://doi.org/10.1007/s007020100017openalex-snapshot
Suppressed expression of nicotinic acetylcholine receptors by nanomolar β-amyloid peptides in PC12 cells
inferredcites →https://doi.org/10.1016/0006-2952(61)90145-9openalex-snapshot
A new and rapid colorimetric determination of acetylcholinesterase activity
inferredcites →https://doi.org/10.1016/0165-0270(84)90007-4openalex-snapshot
Developments of a water-maze procedure for studying spatial learning in the rat
inferredcites →https://doi.org/10.1016/b978-0-12-547620-1.50003-5openalex-snapshot
WITHDRAWN: Dedication
inferredcites →https://doi.org/10.1016/c2009-0-63235-9openalex-snapshot
The Rat Brain in Stereotaxic Coordinates
inferredcites →https://doi.org/10.1016/j.bbr.2004.04.012openalex-snapshot
β-Amyloid (1–42)-induced learning and memory deficits in mice: involvement of oxidative burdens in the hippocampus and cerebral cortex
inferredcites →https://doi.org/10.1016/j.ejphar.2003.08.026openalex-snapshot
Amnesia induced by β-amyloid fragments is counteracted by cannabinoid CB1 receptor blockade
inferredcites →https://doi.org/10.1016/j.febslet.2009.11.036openalex-snapshot
Neuronal nicotinic acetylcholine receptor–cholesterol crosstalk in Alzheimer's disease
inferredcites →https://doi.org/10.1016/j.lfs.2003.09.074openalex-snapshot
Protection against hydrogen peroxide-induced cytotoxicity in PC12 cells by scutellarin
inferredcites →https://doi.org/10.1016/j.neuint.2010.08.001openalex-snapshot
Amyloid precursor protein gene mutated at Swedish 670/671 sites in vitro induces changed expression of nicotinic acetylcholine receptors and neurotoxicity
inferredcites →https://doi.org/10.1016/s0006-3223(00)01116-1openalex-snapshot
Nicotinic receptor abnormalities in Alzheimer’s disease
inferredcites →https://doi.org/10.1016/s0006-8993(02)03571-0openalex-snapshot
Selective changes in the levels of nicotinic acetylcholine receptor protein and of corresponding mRNA species in the brains of patients with Parkinson’s disease
inferredcites →https://doi.org/10.1016/s0026-895x(25)13162-3openalex-snapshot
Commonly occurring plant flavonoids have estrogenic activity.
inferredcites →https://doi.org/10.1016/s0091-3057(03)00128-xopenalex-snapshot
Plants used in Chinese and Indian traditional medicine for improvement of memory and cognitive function
inferredcites →https://doi.org/10.1016/s0166-2236(98)01361-7openalex-snapshot
Acetylcholine in mind: a neurotransmitter correlate of consciousness?
inferredcites →https://doi.org/10.1016/s0197-4580(02)00230-0openalex-snapshot
Acetylcholinesterase promotes beta-amyloid plaques in cerebral cortex
inferredcites →https://doi.org/10.1016/s0301-0082(99)00045-3openalex-snapshot
Neuronal nicotinic receptors in the human brain
inferredcites →https://doi.org/10.1021/jf051985copenalex-snapshot
Effects of Naturally Occurring Compounds on Fibril Formation and Oxidative Stress of β-Amyloid
inferredcites →https://doi.org/10.1021/jf063299zopenalex-snapshot
Flavonoids Possess Neuroprotective Effects on Cultured Pheochromocytoma PC12 Cells: A Comparison of Different Flavonoids in Activating Estrogenic Effect and in Preventing β-Amyloid-Induced Cell Death
inferredcites →https://doi.org/10.1038/nrd2314openalex-snapshot
Therapies for Alzheimer's disease
inferredcites →https://doi.org/10.1046/j.1471-4159.2000.0740237.xopenalex-snapshot
Decreased Protein Levels of Nicotinic Receptor Subunits in the Hippocampus and Temporal Cortex of Patients with Alzheimer’s Disease
inferredcites →https://doi.org/10.1055/s-0028-1088368openalex-snapshot
Protective Effects of Scutellarin Against Cerebral Ischemia in Rats: Evidence for Inhibition of the Apoptosis-Inducing Factor Pathway
inferredcites →https://doi.org/10.1055/s-0029-1185776openalex-snapshot
Estrogenic and Neuroprotective Properties of Scutellarin fromErigeron breviscapus: A Drug against Postmenopausal Symptoms and Alzheimer's Disease
inferredcites →https://doi.org/10.1074/jbc.m006406200openalex-snapshot
The Neuroprotective Effects of Phytoestrogens on Amyloid β Protein-induced Toxicity Are Mediated by Abrogating the Activation of Caspase Cascade in Rat Cortical Neurons
inferredcites →https://doi.org/10.1097/fjc.0b013e3180cbd0e7openalex-snapshot
Protective Effects of Scutellarin and Breviscapine on Brain and Heart Ischemia in Rats
inferredcites →https://doi.org/10.1101/lm.69204openalex-snapshot
The Cholinergic Lesion of Alzheimer's Disease: Pivotal Factor or Side Show?
inferredcites →https://doi.org/10.1111/j.1745-7254.2007.00502.xopenalex-snapshot
Effects of scutellarin on PKC? in PC12 cell injury induced by oxygen and glucose deprivation
inferredcites →https://doi.org/10.1124/jpet.105.098640openalex-snapshot
Effects of a Novel Cognitive Enhancer, Spiro[imidazo-[1,2-a]pyridine-3,2-indan]-2(3 H)-one (ZSET1446), on Learning Impairments Induced by Amyloid-β1–40 in the Rat
inferredcites →https://doi.org/10.1124/pr.108.000562openalex-snapshot
Nicotinic Acetylcholine Receptor Signalling: Roles in Alzheimer’s Disease and Amyloid Neuroprotection
inferredcites →https://doi.org/10.1146/annurev.pharmtox.47.120505.105214openalex-snapshot
Nicotinic Acetylcholine Receptors and Nicotinic Cholinergic Mechanisms of the Central Nervous System
inferredcites →https://doi.org/10.1196/annals.1254.007openalex-snapshot
Nicotinic Acetylcholine Receptors of Muscles and Nerves
inferredcites →https://doi.org/10.1212/wnl.43.2.301openalex-snapshot
Long‐term and high‐dose piracetam treatment of Alzheimer's disease
inferredcites →https://doi.org/10.1212/wnl.54.2.295openalex-snapshot
Estrogen for Alzheimer’s disease in women
inferredcites →https://doi.org/10.1248/bpb.29.1880openalex-snapshot
Protective Effects of Breviscapine on Ischemic Vascular Dementia in Rats
inferredcites →https://doi.org/10.1358/dot.2004.40.8.850473openalex-snapshot
Butyrylcholinesterase, cholinergic neurotransmission and the pathology of Alzheimer's disease
inferredcites →https://doi.org/10.1385/jmn:30:1:19openalex-snapshot
Ispronicline: A Novel α4β2 Nicotinic Acetylcholine Receptor-Selective Agonist With Cognition-Enhancing and Neuroprotective Properties
inferredcites →https://doi.org/10.14712/18059694.2018.95openalex-snapshot
Acetylcholinesterase and Butyrylcholinesterase – Important Enzymes of Human Body
inferredcites →https://doi.org/10.2174/138955705774329546openalex-snapshot
New Anti-Alzheimer Drugs from Biodiversity: The Role of the Natural Acetylcholinesterase Inhibitors
inferredcites →https://doi.org/10.3233/jad-2010-1283openalex-snapshot
Cholinesterase Activity and mRNA Level of Nicotinic Acetylcholine Receptors (α4 and β2 Subunits) in Blood of Elderly Chinese Diagnosed as Alzheimer's Disease
inferredcites →https://doi.org/10.3389/fnagi.2010.00008openalex-snapshot
Intracellular accumulation of amyloid-beta – a predictor for synaptic dysfunction and neuron loss in Alzheimer’s disease
inferredcites →https://doi.org/10.3389/neuro.24.003.2010openalex-snapshot
Oxidative stress mediates the pathogenic effect of different Alzheimer’s disease risk factors
inferredcites →https://doi.org/10.55782/ane-2004-1495openalex-snapshot
Alzheimer's disease and acetylcholine receptors

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.4702812openalex-extracted
HSPA8 and 3,4,5-Tricaffeoylquinic Acid May Be Essential Hub Genes and Active Components for the Treatment of Alzheimer's Disease with Erigeron Breviscapus (Vant.) Hand-Mazz by Regulating Ferroptosis: A Study Based on WGCNA, Network Pharmacology, Molecular Docking, and Molecular Dynamics Simulations
inferred← citeshttps://doi.org/10.1007/978-3-030-94753-8_8-1openalex-snapshot
Scutellarin: Bioactivities, Pharmacology, and Development as Promising Therapeutic Agents and Nutraceuticals
inferred← citeshttps://doi.org/10.1007/s00702-017-1797-5openalex-snapshot
Neurotrophic function of phytochemicals for neuroprotection in aging and neurodegenerative disorders: modulation of intracellular signaling and gene expression
inferred← citeshttps://doi.org/10.1007/s12017-016-8394-xopenalex-snapshot
Scutellarin as a Potential Therapeutic Agent for Microglia-Mediated Neuroinflammation in Cerebral Ischemia
inferred← citeshttps://doi.org/10.1007/s12668-025-02386-4openalex-snapshot
Development and Fabrication of Mesoporous Silica Nanoparticle Loaded in Situ Nasal Gel of Scutellarin for Alzheimer’s Disease
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.103980openalex-snapshot
Synthesis, pharmacological evaluation and mechanistic study of scutellarin methyl ester -4′-dipeptide conjugates for the treatment of hypoxic-ischemic encephalopathy (HIE) in rat pups
inferred← citeshttps://doi.org/10.1016/j.etp.2012.05.003openalex-snapshot
The neurotoxicity of β-amyloid peptide toward rat brain is associated with enhanced oxidative stress, inflammation and apoptosis, all of which can be attenuated by scutellarin
inferred← citeshttps://doi.org/10.1016/j.intimp.2017.11.033openalex-snapshot
Scutellarin alleviates lipopolysaccharide-induced cognitive deficits in the rat: Insights into underlying mechanisms
inferred← citeshttps://doi.org/10.1016/j.intimp.2020.106943openalex-snapshot
Scutellarin protects against lipopolysaccharide-induced behavioral deficits by inhibiting neuroinflammation and microglia activation in rats
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.138698openalex-snapshot
Integrated bioinformatics, network pharmacology, molecular docking, and molecular dynamics simulation to explore the potential pharmacological mechanism of Erigeron breviscapus (Vant.) Hand-Mazz regulating ferroptosis for the treatment of Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.neuint.2016.04.007openalex-snapshot
Scutellarin promotes microglia-mediated astrogliosis coupled with improved behavioral function in cerebral ischemia
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2015.04.017openalex-snapshot
Selective activation of α7 nicotinic acetylcholine receptor by PHA-543613 improves Aβ25–35-mediated cognitive deficits in mice
inferred← citeshttps://doi.org/10.1016/j.pharmthera.2018.05.006openalex-snapshot
Clinical benefits and pharmacology of scutellarin: A comprehensive review
inferred← citeshttps://doi.org/10.1016/j.tice.2021.101624openalex-snapshot
Metanil yellow promotes oxidative stress, astrogliosis, and apoptosis in the cerebellar cortex of adult male rat with possible protective effect of scutellarin: A histological and immunohistochemical study
inferred← citeshttps://doi.org/10.1016/j.yexcr.2019.111546openalex-snapshot
Effect of α7nAChR on learning and memory dysfunction in a rat model of diffuse axonal injury
inferred← citeshttps://doi.org/10.1039/c9fo00058eopenalex-snapshot
Essential oil of Schisandra chinensis ameliorates cognitive decline in mice by alleviating inflammation
inferred← citeshttps://doi.org/10.1042/bcj20190705openalex-snapshot
Scutellarin inhibits the uninduced and metal-induced aggregation of α-Synuclein and disaggregates preformed fibrils: implications for Parkinson's disease
inferred← citeshttps://doi.org/10.1111/cns.70069openalex-snapshot
Alterations in Neuronal Nicotinic Acetylcholine Receptors in the Pathogenesis of Various Cognitive Impairments
inferred← citeshttps://doi.org/10.1142/s0192415x18500167openalex-snapshot
Pharmacological Effects of Scutellarin, An Active Component of GenusScutellariaandErigeron: A Systematic Review
inferred← citeshttps://doi.org/10.1142/s0192415x18500635openalex-snapshot
Scutellarin Ameliorates Learning and Memory Deficit via Suppressing β-Amyloid Formation and Microglial Activation in Rats with Chronic Cerebral Hypoperfusion
inferred← citeshttps://doi.org/10.1142/s0192415x21500312openalex-snapshot
Effect of Sutellarin on Neurogenesis in Neonatal Hypoxia–Ischemia Rat Model: Potential Mechanisms of Action
inferred← citeshttps://doi.org/10.1155/2013/507091openalex-snapshot
Functional Recovery after Scutellarin Treatment in Transient Cerebral Ischemic Rats: A Pilot Study with18F-Fluorodeoxyglucose MicroPET
inferred← citeshttps://doi.org/10.1155/2021/8820406openalex-snapshot
[Retracted] Natural Products for Neurodegeneration: Regulating Neurotrophic Signals
inferred← citeshttps://doi.org/10.1186/s13020-021-00517-zopenalex-snapshot
Scutellarin ameliorates neonatal hypoxic-ischemic encephalopathy associated with GAP43-dependent signaling pathway
inferred← citeshttps://doi.org/10.14670/hh-18-239openalex-snapshot
Microglia mediated neuroinflammation - signaling regulation and therapeutic considerations with special reference to some natural compounds.
inferred← citeshttps://doi.org/10.2174/0118746098373086251201095903openalex-snapshot
Recent Alzheimer’s Research Targets Amyloid-β with Novel Phytochemicals and Pharmacological Strategies for Therapy
inferred← citeshttps://doi.org/10.2174/1389200221666201217093255openalex-snapshot
Metabolism and Pharmacological Mechanisms of Active Ingredients in Erigeron breviscapus
inferred← citeshttps://doi.org/10.3389/fphar.2019.01035openalex-snapshot
Xanthoceraside Could Ameliorate Alzheimer’s Disease Symptoms of Rats by Affecting the Gut Microbiota Composition and Modulating the Endogenous Metabolite Levels
inferred← citeshttps://doi.org/10.3389/fphar.2022.877872openalex-snapshot
Erigeron breviscapus (Vant.) Hand-Mazz.: A Promising Natural Neuroprotective Agent for Alzheimer’s Disease
inferred← citeshttps://doi.org/10.3389/fphar.2024.1470879openalex-snapshot
Scutellarin: pharmacological effects and therapeutic mechanisms in chronic diseases
inferred← citeshttps://doi.org/10.3389/fphar.2026.1707688openalex-snapshot
Multi-target intervention mechanisms and prospects of the traditional Chinese medicine Scutellaria baicalensis georgi in Alzheimer’s disease
inferred← citeshttps://doi.org/10.3390/molecules19055748openalex-snapshot
In Vitro Inhibitory Effects of Scutellarin on Six Human/Rat Cytochrome P450 Enzymes and P-glycoprotein
inferred← citeshttps://doi.org/10.3390/molecules23040869openalex-snapshot
Scutellarin Mitigates Aβ-Induced Neurotoxicity and Improves Behavior Impairments in AD Mice
inferred← citeshttps://doi.org/10.3969/j.issn.1673-5374.2012.15.002openalex-snapshot
Wendan decoction improves learning and memory deficits in a rat model of schizophrenia.
inferred← citeshttps://doi.org/10.6084/m9.figshare.16829326openalex-snapshot
Additional file 1 of Scutellarin ameliorates neonatal hypoxic-ischemic encephalopathy associated with GAP43-dependent signaling pathway
inferred← citeshttps://doi.org/10.61958/ndtj4325openalex-snapshot
Scutellarin promotes neuronal function repair in oxygen-glucose deprivation neuronal model by regulating netrin-1 and associated with 3-kinase and protein kinase B
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