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β-Amyloid1-42, HIV-1Ba-L (Clade B) Infection and Drugs of Abuse Induced Degeneration in Human Neuronal Cells and Protective Effects of Ashwagandha (Withania somnifera) and Its Constituent Withanolide A

https://doi.org/10.1371/journal.pone.0112818
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What this work says

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

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Potential medicinal plants for CNS disorders: an overview
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In vitro protective effects of Withania somnifera (L.) dunal root extract against hydrogen peroxide and β‐amyloid(1–42)‐induced cytotoxicity in differentiated PC12 cells
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Neuroprotective Effects of Withania somnifera Dunn. in Hippocampal Sub‐regions of Female Albino Rat
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The Comorbidity of HIV-Associated Neurocognitive Disorders and Alzheimer’s Disease: A Foreseeable Medical Challenge in Post-HAART Era
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Increased Accumulation of Intraneuronal Amyloid β in HIV-Infected Patients
inferredcites →https://doi.org/10.1016/0006-8993(90)91355-kopenalex-snapshot
β-Amyloid protein increases the vulnerability of cultured cortical neurons to excitotoxic damage
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Twenty Years of the Alzheimer’s Disease Amyloid Hypothesis: A Genetic Perspective
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Screening of selected Indian medicinal plants for acetylcholinesterase inhibitory activity
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A Hundred Years of Alzheimer's Disease Research
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The Genetics of Alzheimer Disease: Back to the Future
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A Mechanistic Approach to Preventing Schizophrenia in At-Risk Individuals
inferredcites →https://doi.org/10.1016/j.neuron.2013.04.014openalex-snapshot
Alzheimer’s Disease Risk Gene CD33 Inhibits Microglial Uptake of Amyloid Beta
inferredcites →https://doi.org/10.1016/j.pnpbp.2007.09.011openalex-snapshot
Withania somnifera: An Indian ginseng
inferredcites →https://doi.org/10.1016/s0002-9440(10)62493-5openalex-snapshot
Microtubule-Associated Protein 2, a Marker of Neuronal Differentiation, Induces Mitotic Defects, Inhibits Growth of Melanoma Cells, and Predicts Metastatic Potential of Cutaneous Melanoma
inferredcites →https://doi.org/10.1016/s0021-9258(18)48529-8openalex-snapshot
Assembly and aggregation properties of synthetic Alzheimer's A4/beta amyloid peptide analogs.
inferredcites →https://doi.org/10.1016/s0168-0102(02)00201-8openalex-snapshot
Involvement of oxidative stress in the enhancement of acetylcholinesterase activity induced by amyloid beta-peptide
inferredcites →https://doi.org/10.1016/s0304-3940(99)00282-7openalex-snapshot
Enhancement of MTT, a tetrazolium salt, exocytosis by amyloid β-protein and chloroquine in cultured rat astrocytes
inferredcites →https://doi.org/10.1016/s0378-8741(00)00213-0openalex-snapshot
Review on some plants of Indian traditional medicine with antioxidant activity
inferredcites →https://doi.org/10.1016/s0378-8741(98)00107-xopenalex-snapshot
Antistressor effect of Withania somnifera
inferredcites →https://doi.org/10.1021/bi990610fopenalex-snapshot
Plasmin Cleavage of the Amyloid β-Protein: Alteration of Secondary Structure and Stimulation of Tissue Plasminogen Activator Activity
inferredcites →https://doi.org/10.1038/nm1066openalex-snapshot
Protein aggregation and neurodegenerative disease
inferredcites →https://doi.org/10.1038/nrd2896openalex-snapshot
Alzheimer's disease: strategies for disease modification
inferredcites →https://doi.org/10.1038/nrn1495openalex-snapshot
Strategies for disease modification in Alzheimer's disease
inferredcites →https://doi.org/10.1038/sj.bjp.0706122openalex-snapshot
Neuritic regeneration and synaptic reconstruction induced by withanolide A
inferredcites →https://doi.org/10.1039/c0np00027bopenalex-snapshot
Natural products as a source of Alzheimer's drug leads
inferredcites →https://doi.org/10.1042/bj3110001openalex-snapshot
The toxicity in vitro of β-amyloid protein
inferredcites →https://doi.org/10.1046/j.1471-4159.1997.69062285.xopenalex-snapshot
Cytotoxic Amyloid Peptides Inhibit Cellular 3‐(4,5‐Dimethylthiazol‐2‐yl)‐2,5‐Diphenyltetrazolium Bromide (MTT) Reduction by Enhancing MTT Formazan Exocytosis
inferredcites →https://doi.org/10.1073/pnas.1112209109openalex-snapshot
Withania somnifera reverses Alzheimer's disease pathology by enhancing low-density lipoprotein receptor-related protein in liver
inferredcites →https://doi.org/10.1073/pnas.91.4.1470openalex-snapshot
Inhibition of PC12 cell redox activity is a specific,early indicator of the mechanism of beta-amyloid-mediated celldeath.
inferredcites →https://doi.org/10.1073/pnas.93.9.4147openalex-snapshot
Neurocytopathic effects of beta-amyloid-stimulated monocytes: a potential mechanism for central nervous system damage in Alzheimer disease.
inferredcites →https://doi.org/10.1074/jbc.m007579200openalex-snapshot
Degradation of the Alzheimer's Amyloid β Peptide by Endothelin-converting Enzyme
inferredcites →https://doi.org/10.1074/jbc.m008511200openalex-snapshot
Neprilysin Degrades Both Amyloid β Peptides 1–40 and 1–42 Most Rapidly and Efficiently among Thiorphan- and Phosphoramidon-sensitive Endopeptidases
inferredcites →https://doi.org/10.1074/jbc.m104068200openalex-snapshot
Angiotensin-converting Enzyme Degrades Alzheimer Amyloid β-Peptide (Aβ); Retards Aβ Aggregation, Deposition, Fibril Formation; and Inhibits Cytotoxicity
inferredcites →https://doi.org/10.1074/jbc.m602440200openalex-snapshot
Matrix Metalloproteinase-9 Degrades Amyloid-β Fibrils in Vitro and Compact Plaques in Situ
inferredcites →https://doi.org/10.1096/fj.04-2637fjeopenalex-snapshot
Intracellular Aβ42 activates p53 promoter: a pathway to neurodegeneration in Alzheimer's disease
inferredcites →https://doi.org/10.1097/00001756-200006260-00035openalex-snapshot
Dendrite extension by methanol extract of Ashwagandha (roots of Withania somnifera) in SK-N-SH cells
inferredcites →https://doi.org/10.1097/00001756-200211150-00008openalex-snapshot
Levels of ??-secretase BACE and ??-secretase ADAM10 mRNAs in Alzheimer hippocampus
inferredcites →https://doi.org/10.1097/00002030-200501280-00004openalex-snapshot
HIV-1 Tat inhibits neprilysin and elevates amyloid β
inferredcites →https://doi.org/10.1097/01.aids.0000161770.06158.5copenalex-snapshot
Brain deposition of beta-amyloid is a common pathologic feature in HIV positive patients
inferredcites →https://doi.org/10.1097/qad.0b013e32835a117copenalex-snapshot
Cerebral β-amyloid deposition predicts HIV-associated neurocognitive disorders in APOE ε4 carriers
inferredcites →https://doi.org/10.1111/j.1460-9568.2007.05797.xopenalex-snapshot
Involvement of astroglial ceramide in palmitic acid‐induced Alzheimer‐like changes in primary neurons
inferredcites →https://doi.org/10.1111/j.1471-4159.2012.07709.xopenalex-snapshot
Microbiosensor for Alzheimer’s disease diagnostics: detection of amyloid beta biomarkers
inferredcites →https://doi.org/10.1124/jpet.104.074450openalex-snapshot
β-Amyloid-Induced Neurodegeneration and Protection by Structurally Diverse Microtubule-Stabilizing Agents
inferredcites →https://doi.org/10.1126/science.1072994openalex-snapshot
The Amyloid Hypothesis of Alzheimer's Disease: Progress and Problems on the Road to Therapeutics
inferredcites →https://doi.org/10.1126/science.1566067openalex-snapshot
Alzheimer's Disease: The Amyloid Cascade Hypothesis
inferredcites →https://doi.org/10.1126/science.2218531openalex-snapshot
Neurotrophic and Neurotoxic Effects of Amyloid β Protein: Reversal by Tachykinin Neuropeptides
inferredcites →https://doi.org/10.1136/jnnp.65.1.29openalex-snapshot
Prevalence of Alzheimer plaques in AIDS
inferredcites →https://doi.org/10.1186/1756-6606-4-23openalex-snapshot
Antiretroviral medications disrupt microglial phagocytosis of β-amyloid and increase its production by neurons: Implications for HIV-associated neurocognitive disorders
inferredcites →https://doi.org/10.1248/cpb.50.760openalex-snapshot
Withanolide Derivatives from the Roots of Withania somnifera and Their Neurite Outgrowth Activities.
inferredcites →https://doi.org/10.1371/journal.pone.0077624openalex-snapshot
Ashwagandha (Withania somnifera) Reverses β-Amyloid1-42 Induced Toxicity in Human Neuronal Cells: Implications in HIV-Associated Neurocognitive Disorders (HAND)
inferredcites →https://doi.org/10.1523/jneurosci.13-04-01676.1993openalex-snapshot
Neurodegeneration induced by beta-amyloid peptides in vitro: the role of peptide assembly state
inferredcites →https://doi.org/10.1523/jneurosci.2381-04.2005openalex-snapshot
Nucleation-Dependent Polymerization Is an Essential Component of Amyloid-Mediated Neuronal Cell Death
inferredcites →https://doi.org/10.2174/138955706778560175openalex-snapshot
Intracellular Amyloid β-Protein and Its Associated Molecules in the Pathogenesis of Alzheimers Disease
inferredcites →https://doi.org/10.2174/156720508786898514openalex-snapshot
Intracellular Amyloid β-Protein As a Therapeutic Target for Treating Alzheimers Disease
inferredcites →https://doi.org/10.2174/156720512799015082openalex-snapshot
Editorial [Hot Topic: Progressive and Unconventional Pharmacotherapeutic Approaches to Alzheimers Disease Therapy (Guest Editors: Stuart Maudsley & Wayne Chadwick)]
inferredcites →https://doi.org/10.2478/s11658-007-0015-0openalex-snapshot
The neuroprotective effect of Withania somnifera root extract in MPTP-intoxicated mice: An analysis of behavioral and biochemical varibles

What points at this work

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

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Ashwagandha for Brain Health: Experimental Evidence for Its Neuroregenerative Activities
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Improving the inhibition of β-amyloid aggregation by withanolide and withanoside derivatives
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Astrocytic metabolic switch is a novel etiology for Cocaine and HIV-1 Tat-mediated neurotoxicity
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Distance-based β-amyloid protein detection on PADs for the scanning and subsequent follow-up of Alzheimer's disease in human urine samples
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Pharmacological evaluation of Ashwagandha highlighting its healthcare claims, safety, and toxicity aspects
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Withania somnifera (L.) Dunal ameliorates neurodegeneration and cognitive impairments associated with systemic inflammation
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Molecular and therapeutic insights into Withania somnifera (Ashwagandha) for cognition and neuroprotection
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