Suchergebnisse - "Amyloid beta-Peptides toxicity"

Beneficial Effects of a Combination of Curcuma longa L. and Citrus junos Against Beta-Amyloid Peptide-Induced Neurodegeneration in Mice

Autoren: Mi Jeong, Kim Soo-Yeon, Park Yongjae, Kim et al.

Weitere Verfasser: Mi Jeong, Kim Soo-Yeon, Park Yongjae, Kim et al.

Quelle: Journal of Medicinal Food. 25:33-39

Schlagwörter: 0301 basic medicine, Citrus, Curcuma longa L, Mice, 03 medical and health sciences, Curcuma, Alzheimer Disease, Aβ peptide, Animals, cognitive function, 0303 health sciences, Amyloid beta-Peptides, Animal, Plant Extracts, brain-derived neurotrophic factor, Alzheimer Disease* / drug therapy, Alzheimer's disease, Citrus junos, Peptide Fragments, Disease Models, Animal, Amyloid beta-Peptides / toxicity, Disease Models, Alzheimer Disease* / genetics

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/35029510

Neuron-specific proteasome activation exerts cell non-autonomous protection against amyloid-beta (Aβ) proteotoxicity in Caenorhabditis elegans.

Autoren: Panagiotidou, Eleni Gioran, Anna Bano, Daniele et al.

Quelle: Redox Biology 65, 102817 (2023). doi:10.1016/j.redox.2023.102817

Schlagwörter: info:eu-repo/classification/ddc/570, Animals, Caenorhabditis elegans: genetics, Caenorhabditis elegans: metabolism, Proteasome Endopeptidase Complex: metabolism, Caenorhabditis elegans Proteins: genetics, Caenorhabditis elegans Proteins: metabolism, Amyloid beta-Peptides: toxicity, Amyloid beta-Peptides: metabolism, Neurons: metabolism, C. elegans, Cell non-autonomous regulation, Proteasome, Proteinopathies, Proteostasis, Proteasome Endopeptidase Complex, Caenorhabditis elegans Proteins, Amyloid beta-Peptides

Geographisches Schlagwort: DE

Relation: info:eu-repo/semantics/altIdentifier/issn/2213-2317; info:eu-repo/semantics/altIdentifier/pmid/pmid:37473700; https://pub.dzne.de/record/259961

Verfügbarkeit: https://pub.dzne.de/record/259961
https://pub.dzne.de/search?p=id:%22DZNE-2023-00814%22

Tokishakuyakusan ameliorates spatial memory deficits induced by ovariectomy combined with β-amyloid in rats

Autoren: Yuki Akiyoshi Kenichi Mishima Izzettin Hatip-Al-Khatib et al.

Quelle: Journal of Pharmacological Sciences, Vol 136, Iss 3, Pp 149-154 (2018)

Schlagwörter: 0301 basic medicine, ß-Amyloid, hippocampus, Chinese Herbal, Wistar, Acetylcholine/*metabolism, Amyloid beta-Peptides/*toxicity, Animals, Drugs, Chinese Herbal/administration & dosage/*pharmacology, Female, Hippocampus/*metabolism, Maze Learning/drug effects, Memory Disorders/*drug therapy/*etiology/psychology, Ovariectomy/*adverse effects, Rats, Wistar, Spatial Memory/*drug effects, Wistar rat, Hippocampus, radial arm maze test, rat, animal, Spatial Memory, 0303 health sciences, drug effect, Drugs, memory disorder, spatial memory, donepezil, 3. Good health, female, ovariectomy, β-Amyloid, dorsal hippocampus, Ovariectomy, animal experiment, RM1-950, psychology, Article, 03 medical and health sciences, Memory, drug mechanism, tokishakuyaku san, controlled study, maze test, Maze Learning, Tokishakuyakusan, Memory Disorders, nonhuman, Amyloid beta-Peptides, amyloid beta protein[1-42], animal model, acetylcholine, Acetylcholine, Rats, toki-shakuyaku-san, herbaceous agent, amyloid beta protein, Therapeutics. Pharmacology, metabolism, Drugs, Chinese Herbal

Dateibeschreibung: application/pdf

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/29478713
https://doaj.org/article/7bd873b4047640b1b927fab2c45a2b5b
https://core.ac.uk/display/153599206
https://kyushu-u.pure.elsevier.com/ja/publications/tokishakuyakusan-ameliorates-spatial-memory-deficits-induced-by-o
https://www.ncbi.nlm.nih.gov/pubmed/29478713
https://pubmed.ncbi.nlm.nih.gov/29478713/
https://www.sciencedirect.com/science/article/abs/pii/S1347861318300173
https://www.sciencedirect.com/science/article/pii/S1347861318300173
https://hdl.handle.net/11499/10839
https://doi.org/10.1016/j.jphs.2018.01.005
http://acikerisim.pau.edu.tr:8080/xmlui/handle/11499/10839

Study of the protective effects of nootropic agents against neuronal damage induced by amyloid-beta (fragment 25–35) in cultured hippocampal neurons

Autoren: Anna Stasiak-Barmuta Krzysztof Sendrowski Piotr Sobaniec et al.

Quelle: Pharmacological Reports. 67:326-331

Schlagwörter: 0301 basic medicine, Neurons - drug effects, Levetiracetam, Dose-response relationship, Peptide fragments - toxicity, Amyloid beta-peptides - toxicity, Nootropic agents - pharmacology, Apoptosis - drug effects, Primary Cell Culture, Apoptosis, Piracetam - analogs & derivatives, Hippocampus, 03 medical and health sciences, Neuroprotective agents - pharmacology, 0302 clinical medicine, Cell death - drug effects, Animals, Primary cell culture, Nootropic Agents, Neurons, Amyloid beta-Peptides, Hippocampus - cytology, Cell Death, Dose-Response Relationship, Drug, L-Lactate Dehydrogenase, L-lactate dehydrogenase - metabolism, drug, Piracetam, Peptide Fragments, Rats, 3. Good health, Neuroprotective Agents, Piracetam - pharmacology

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/25712658
https://europepmc.org/article/MED/25712658
https://www.sciencedirect.com/science/article/pii/S1734114014002977
https://link.springer.com/article/10.1016/j.pharep.2014.09.013
https://link.springer.com/content/pdf/10.1016/j.pharep.2014.09.013.pdf
https://pubmed.ncbi.nlm.nih.gov/25712658/
https://www.ncbi.nlm.nih.gov/pubmed/25712658

Constitutive cAMP response element binding protein (CREB) activation by Alzheimer's disease presenilin-driven inositol trisphosphate receptor (InsP 3 R) Ca 2+ signaling

Autoren: Mei, L Foskett, JK Müller, M et al.

Quelle: Proceedings of the National Academy of Sciences. 108:13293-13298

Schlagwörter: 0301 basic medicine, Amyloid Beta-Peptides - Toxicity, Transcription, Genetic, Mice, Transgenic, Transgenic, Mice, 03 medical and health sciences, Genetic - Drug Effects, Alzheimer Disease, Presenilin-1, Transcription, Genetic - Drug Effects, Animals, Humans, Inositol 1,4,5-Trisphosphate Receptors, Mutation - Genetics, Enzyme Activation - Drug Effects, Inositol 1,4,5-Trisphosphate Receptors - Metabolism, Calcium Signaling, Phosphorylation, Alzheimer Disease - Metabolism - Pathology, Cyclic AMP Response Element-Binding Protein, Calcium Signaling - Drug Effects, Amyloid beta-Peptides, Cell Death, Calcium-Calmodulin-Dependent Protein Kinase Type 4 - Metabolism, Brain, Phosphorylation - Drug Effects, Cyclic Amp Response Element-Binding Protein - Genetics - Metabolism, Brain - Drug Effects - Enzymology - Pathology, 3. Good health, Enzyme Activation, Mutation, Presenilin-1 - Metabolism, Cell Death - Drug Effects, Transcription, Calcium-Calmodulin-Dependent Protein Kinase Type 4

Zugangs-URL: http://www.pnas.org/content/108/32/13293.full.pdf
https://pubmed.ncbi.nlm.nih.gov/21784978
https://www.pnas.org/content/pnas/108/32/13293.full.pdf
https://www.pnas.org/content/108/32/13293.full.pdf
https://www.ncbi.nlm.nih.gov/pubmed/21784978
https://core.ac.uk/display/37999290
https://www.jstor.org/stable/pdfplus/27979184.pdf
http://ui.adsabs.harvard.edu/abs/2011PNAS..10813293M/abstract
http://hdl.handle.net/10722/171785

Protective effects of dibenzocyclooctadiene lignans from Schisandra chinensis against beta‐amyloid and homocysteine neurotoxicity in PC12 cells

Autoren: Song, JX Lin, X Wong, RNS et al.

Quelle: Phytotherapy Research. 25:435-443

Schlagwörter: 0301 basic medicine, Amyloid Beta-Peptides - Toxicity, Apoptosis - Drug Effects, Caspase 3 - Metabolism, Apoptosis, Dioxoles, PC12 Cells, Lignans, Cyclooctanes, 03 medical and health sciences, Animals, Polycyclic Compounds, Lignans - Pharmacology, Homocysteine, Schisandra, bcl-2-Associated X Protein, Amyloid beta-Peptides, Peptide Fragments - Toxicity, Caspase 3, Schisandra - Chemistry, Neuroprotective Agents - Pharmacology, Homocysteine - Toxicity, Peptide Fragments, Rats, 3. Good health, Neuroprotective Agents, Reactive Oxygen Species - Metabolism, Cyclooctanes - Pharmacology, Bcl-2-Associated X Protein - Metabolism, Reactive Oxygen Species, Pc12 Cells

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/20740476
https://pubmed.ncbi.nlm.nih.gov/20740476/
https://scholars.hkbu.edu.hk/en/publications/protective-effects-of-dibenzocyclooctadiene-lignans-from-schisand-2
https://europepmc.org/article/MED/20740476
https://www.ncbi.nlm.nih.gov/pubmed/20740476
https://hub.hku.hk/handle/10722/179457
https://onlinelibrary.wiley.com/doi/10.1002/ptr.3269
http://hdl.handle.net/10722/179457

Inhibition of cytotoxicity and amyloid fibril formation by a D-amino acid peptide that specifically binds to Alzheimer's disease amyloid peptide

Autoren: Luitgard Nagel-Steger T. van Groen Jan Stöhr et al.

Quelle: Protein engineering design and selection 21, 241-246 (2008). doi:10.1093/protein/gzm054

Schlagwörter: D-amino acid peptide, 0301 basic medicine, Cytotoxins: toxicity, Polymers, Cell Death: drug effects, Polymers: metabolism, Protein Structure, Secondary: drug effects, Peptides: chemistry, A beta, PC12 Cells, Protein Structure, Secondary, Substrate Specificity, 03 medical and health sciences, Cytotoxins: metabolism, Amyloid beta-Peptides: toxicity, Animals, Benzothiazoles, Peptides: pharmacology, Amyloid beta-Peptides, thioflavin T, Cell Death, Cytotoxins: antagonists & inhibitors, Cytotoxins, aggregation, Amyloid beta-Peptides: metabolism, Alzheimer's disease, Rats, 3. Good health, Amyloid beta-Peptides: antagonists & inhibitors, Microscopy, Electron, Thiazoles, Spectrometry, Fluorescence, Peptides: metabolism, Thiazoles: metabolism, cytotoxicity, Peptides, Protein Binding

Zugangs-URL: https://academic.oup.com/peds/article-pdf/21/4/241/4340411/gzm054.pdf
https://pubmed.ncbi.nlm.nih.gov/18252750
https://academic.oup.com/peds/article/21/4/241/1506642
https://core.ac.uk/display/34881025
https://europepmc.org/article/MED/18252750
https://pubmed.ncbi.nlm.nih.gov/18252750/
http://www.ncbi.nlm.nih.gov/pubmed/18252750
https://paperity.org/p/41791237/inhibition-of-cytotoxicity-and-amyloid-fibril-formation-by-a-d-amino-acid-peptide-that
https://juser.fz-juelich.de/record/338

Characterizing the neuroprotective effects of alkaline extract of Lycium barbarum on β-amyloid peptide neurotoxicity

Autoren: Yuen, WH Ho, YS Yu, MS et al.

Quelle: Brain Research. 1158:123-134

Schlagwörter: 0301 basic medicine, Amyloid Beta-Peptides - Toxicity, Indoles, Cells, Caspase 3 - Metabolism, Indoles - Diagnostic Use, Cell Count, Lycium - Chemistry, Dose-Response Relationship, Rats, Sprague-Dawley, 03 medical and health sciences, Cerebral Cortex - Cytology, Analysis Of Variance, Animals, Drug Interactions, Cells, Cultured, Cerebral Cortex, Neurons, Analysis of Variance, 0303 health sciences, Cultured, Amyloid beta-Peptides, Peptide Fragments - Toxicity, Dose-Response Relationship, Drug, L-Lactate Dehydrogenase, Drugs, Chinese Herbal - Pharmacology, Caspase 3, Mammalian, Neuroprotective Agents - Pharmacology, Drugs, Signal Transduction - Drug Effects, Lycium, Embryo, Mammalian, Peptide Fragments, Rats, 3. Good health, Neuroprotective Agents, L-Lactate Dehydrogenase - Metabolism, Embryo, Sprague-Dawley, Drug, Chinese Herbal - Pharmacology, Neurons - Drug Effects, Drugs, Chinese Herbal, Signal Transduction

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/17568570
https://core.ac.uk/display/37970695
http://hub.hku.hk/handle/10722/149671
http://www.sciencedirect.com/science/article/pii/S0006899307010220
https://research.polyu.edu.hk/en/publications/characterizing-the-neuroprotective-effects-of-alkaline-extract-of
https://www.ncbi.nlm.nih.gov/pubmed/17568570
https://www.sciencedirect.com/science/article/pii/S0006899307010220
http://hdl.handle.net/10722/149671

New polysaccharide from Nerium indicum protects neurons via stress kinase signaling pathway

Autoren: Chang, RCC Yuen, WH Fang, JN et al.

Quelle: Brain Research. 1153:221-230

Schlagwörter: 0301 basic medicine, L-Lactate Dehydrogenase - metabolism, Neurons - drug effects, Indoles - diagnostic use, Indoles, Plant Structures - chemistry, Dose-Response Relationship, Rats, Sprague-Dawley, 03 medical and health sciences, Polysaccharides, Signal Transduction - drug effects, Polysaccharides - pharmacology, Animals, Cerebral Cortex - cytology, Drug Interactions, Nerium, Mitogen-Activated Protein Kinases - metabolism, Cerebral Cortex, Neurons, Analysis of Variance, 0303 health sciences, Amyloid beta-Peptides, Dose-Response Relationship, Drug, L-Lactate Dehydrogenase, Caspase 3, Mammalian, Nerium - chemistry, Amyloid beta-Peptides - toxicity, Embryo, Mammalian, Rats, 3. Good health, Caspase 3 - metabolism, Embryo, Sprague-Dawley, Drug, Mitogen-Activated Protein Kinases, Plant Structures, Signal Transduction

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/17475226
http://www.sciencedirect.com/science/article/pii/S0006899307007585
https://pubmed.ncbi.nlm.nih.gov/17475226/
https://www.ncbi.nlm.nih.gov/pubmed/17475226
https://europepmc.org/article/MED/17475226
https://core.ac.uk/display/37901521
http://hub.hku.hk/handle/10722/67796
http://hdl.handle.net/10722/67796

Exceptional in vivo catabolism of neurodegeneration-related aggregates

Autoren: Angéla Földi Bence Galik János Kálmán et al.

Quelle: Acta Neuropathol Commun
Acta Neuropathologica Communications, Vol 6, Iss 1, Pp 1-12 (2018)

Schlagwörter: 0301 basic medicine, tumor, Amyloid beta-peptides - metabolism, Caenorhabditis elegans - metabolism, Kaplan-Meier estimate, Amyloid beta-peptides - toxicity, Rotifera, Kaplan-Meier Estimate, Lobosea - metabolism, Beta-amyloid, Klinikai orvostudományok, Platyhelminths - metabolism, Protein Aggregation, Pathological, RC0321 Neuroscience. Biological psychiatry. Neuropsychiatry / idegkórtan, Oligohymenophorea - metabolism, Alpha-synuclein, 03 medical and health sciences, Species Specificity, Neurodegenerative diseases - metabolism, Cell Line, Tumor, Tardigrada, Animals, Humans, Lobosea, RC346-429, Caenorhabditis elegans, Species specificity, Amyloid beta-Peptides, neurológia, Lifespan, Tardigrada - metabolism, RZ Other systems of medicine / orvostudomány egyéb területei, Research, Catabolism, Neurodegenerative Diseases, Orvostudományok, Rotifera - metabolism, Metabolism, Platyhelminths, pszichiátria, pathological - metabolism, Oligohymenophorea, Prion, Neurology. Diseases of the nervous system, Protein aggregation, Cell line, Bdelloid rotifer

Dateibeschreibung: application/pdf; text

Zugangs-URL: https://actaneurocomms.biomedcentral.com/track/pdf/10.1186/s40478-018-0507-3
https://pubmed.ncbi.nlm.nih.gov/29378654
https://doaj.org/article/2f34904feeef404aa7d56b238521b8a3
https://actaneurocomms.biomedcentral.com/articles/10.1186/s40478-018-0507-3
http://real.mtak.hu/73710/
https://europepmc.org/articles/PMC5789616
https://link.springer.com/article/10.1186/s40478-018-0507-3
https://www.ncbi.nlm.nih.gov/pubmed/29378654
https://link.springer.com/content/pdf/10.1186%2Fs40478-018-0507-3.pdf

Novel neuroprotective effects of the aqueous extracts from Verbena officinalis Linn

Autoren: Chang, RCC Yu, MS Lai, SW et al.

Quelle: Neuropharmacology. 50:641-650

Schlagwörter: 0301 basic medicine, Time Factors, Indoles - diagnostic use, Indoles, MAP Kinase Kinase 4, Cells, DDT - toxicity, Plant Extracts - chemistry - isolation & purification - pharmacology, Neuroprotective Agents - chemistry - isolation & purification - pharmacology, MAP Kinase Kinase 4 - metabolism, DDT, Dose-Response Relationship, Rats, Sprague-Dawley, 03 medical and health sciences, Animals, Cerebral Cortex - cytology, Drug Interactions, Phosphorylation, Peptide Fragments - toxicity, Cells, Cultured, Caspases - metabolism, Neurons - cytology - drug effects, Cerebral Cortex, Neurons, 0303 health sciences, Cultured, Amyloid beta-Peptides, Dose-Response Relationship, Drug, Caspase 3, Plant Extracts, Mammalian, Verbena - chemistry, Phosphorylation - drug effects, Amyloid beta-Peptides - toxicity, Interferons - pharmacology, Protein Kinases - metabolism, Embryo, Mammalian, Peptide Fragments, Rats, 3. Good health, Neuroprotective Agents, Embryo, Caspases, Sprague-Dawley, Interferons, Drug, Protein Kinases

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/16406021
https://www.ncbi.nlm.nih.gov/pubmed/16406021
https://www.sciencedirect.com/science/article/pii/S0028390805003953
http://hub.hku.hk/handle/10722/67790
https://pubmed.ncbi.nlm.nih.gov/16406021/
https://core.ac.uk/display/37901518
https://europepmc.org/article/MED/16406021
http://hdl.handle.net/10722/67790

Modulation of calcium/calmodulin kinase‐II provides partial neuroprotection against beta‐amyloid peptide toxicity

Autoren: KC Suen Kwok-Fai So Jacques Hugon et al.

Quelle: European Journal of Neuroscience. 19:2047-2055

Schlagwörter: 0301 basic medicine, Cells, Neurons - drug effects - enzymology, Rats, Sprague-Dawley, 03 medical and health sciences, Enzyme Activation - drug effects - physiology, Animals, Enzyme Inhibitors, Peptide Fragments - toxicity, Cells, Cultured, Caspases - metabolism, Neurons, Cultured, Amyloid beta-Peptides, Amyloid beta-Peptides - toxicity, Peptide Fragments, Rats, Enzyme Activation, Neuroprotective Agents, Caspases, Calcium-Calmodulin-Dependent Protein Kinases, Sprague-Dawley, Calcium-Calmodulin-Dependent Protein Kinases - antagonists & inhibitors - metabolism, Enzyme Inhibitors - pharmacology, Calcium-Calmodulin-Dependent Protein Kinase Type 2, Neuroprotective Agents - antagonists & inhibitors - metabolism

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/15090032
http://doi.wiley.com/10.1111/j.0953-816X.2004.03245.x
https://www.ncbi.nlm.nih.gov/pubmed/15090032
https://pubmed.ncbi.nlm.nih.gov/15090032/
http://hub.hku.hk/handle/10722/67890
https://europepmc.org/abstract/MED/15090032
https://onlinelibrary.wiley.com/doi/10.1111/j.0953-816X.2004.03245.x
http://hdl.handle.net/10722/67890

Involvement of double‐stranded RNA‐dependent protein kinase and phosphorylation of eukaryotic initiation factor‐2α in neuronal degeneration

Autoren: Chang, RCC Ma, CH Elyaman, W et al.

Quelle: Journal of Neurochemistry. 83:1215-1225

Schlagwörter: 0301 basic medicine, Amyloid Beta-Peptides - Toxicity, Apoptosis - Drug Effects, Eukaryotic Initiation Factor-2, Apoptosis, Cell Count, Inbred C57bl, Rats, Sprague-Dawley, Mice, Neuroblastoma, eIF-2 Kinase, 03 medical and health sciences, Genistein - Toxicity, Animals, Humans, Phosphorylation, Calcimycin, Quercetin - Toxicity, Neurons, 0303 health sciences, Amyloid beta-Peptides, Peptide Fragments - Toxicity, Eif-2 Kinase - Metabolism, Ionophores, Calcimycin - Toxicity, Phosphorylation - Drug Effects, Genistein, Ionophores - Toxicity, Peptide Fragments, Neuroblastoma - Metabolism - Pathology, Rats, Mice, Inbred C57bl, Mice, Inbred C57BL, Eukaryotic Initiation Factor-2 - Metabolism, Neurons - Drug Effects - Metabolism - Pathology, Calcium, Quercetin, Sprague-Dawley, Calcium - Metabolism

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/12437593
https://europepmc.org/article/MED/12437593
https://hub.hku.hk/handle/10722/149608
http://onlinelibrary.wiley.com/doi/10.1046/j.1471-4159.2002.01237.x/abstract
https://core.ac.uk/display/37970637
https://www.ncbi.nlm.nih.gov/pubmed/12437593
https://pubmed.ncbi.nlm.nih.gov/12437593/
http://hdl.handle.net/10722/149608

Neuroprotective and neurorescuing effects of isoform‐specific nitric oxide synthase inhibitors, nitric oxide scavenger, and antioxidant against beta‐amyloid toxicity

Autoren: Quirion, R Law, A Gauthier, S

Quelle: British Journal of Pharmacology. 133:1114-1124

Schlagwörter: 0301 basic medicine, Amyloid Beta-Peptides - Toxicity, Time Factors, Cell Survival - Drug Effects, Benzoates, Nitroarginine, Antioxidants, Rats, Sprague-Dawley, Enzyme Inhibitors, Cells, Cultured, Cerebral Cortex, 0303 health sciences, Cultured, Imidazoles, Isoenzymes - Antagonists & Inhibitors, Oxidants, 3. Good health, Isoenzymes, Neuroprotective Agents, Lysine - Analogs & Derivatives - Pharmacology, Imidazoles - Pharmacology, Drug, Chromans - Pharmacology, Cerebral Cortex - Cytology - Drug Effects - Metabolism, Enzyme Inhibitors - Pharmacology, Cell Survival, Cells, Thiourea - Analogs & Derivatives - Pharmacology, Oxidants - Pharmacology, Nitric Oxide, Benzoates - Pharmacology, Dose-Response Relationship, 03 medical and health sciences, Citrulline - Analogs & Derivatives - Pharmacology, Animals, Chromans, Nitric Oxide Synthase - Antagonists & Inhibitors, Nitrates - Pharmacology, Nitroarginine - Pharmacology, Amyloid beta-Peptides, Nitrates, Peptide Fragments - Toxicity, Dose-Response Relationship, Drug, Lysine, Neuroprotective Agents - Pharmacology, Rats, Antioxidants - Pharmacology, Nitric Oxide - Antagonists & Inhibitors - Metabolism, Citrulline, Sprague-Dawley, Nitric Oxide Synthase

Zugangs-URL: https://europepmc.org/articles/pmc1572883?pdf=render
https://pubmed.ncbi.nlm.nih.gov/11487523
https://bpspubs.onlinelibrary.wiley.com/doi/full/10.1038/sj.bjp.0704179
https://core.ac.uk/display/37999529
https://europepmc.org/article/MED/11487523
http://onlinelibrary.wiley.com/doi/10.1038/sj.bjp.0704179/abstract
https://www.ncbi.nlm.nih.gov/pubmed/11487523
http://hub.hku.hk/handle/10722/171902
http://hdl.handle.net/10722/171902

The effect of age on the response of the rat brains to continuous β-amyloid infusion

Autoren: Nag, S Tang, F

Quelle: Brain Research. 889:303-307

Schlagwörter: Neurotoxins - Toxicity, Brain Chemistry, Male, 0301 basic medicine, Amyloid Beta-Peptides - Toxicity, Aging, Choline O-Acetyltransferase - Metabolism, Amyloid beta-Peptides, Intraventricular, Brain Chemistry - Drug Effects, Neurotoxins, Brain, Brain - Drug Effects - Growth & Development, Injections, Choline O-Acetyltransferase, Rats, Aging - Physiology, Rats, Sprague-Dawley, 03 medical and health sciences, Maze Learning - Drug Effects, 0302 clinical medicine, Animals, Sprague-Dawley, Maze Learning, Injections, Intraventricular

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/11166723
https://www.ncbi.nlm.nih.gov/pubmed/11166723
http://europepmc.org/abstract/MED/11166723
http://hub.hku.hk/handle/10722/171700
https://www.sciencedirect.com/science/article/abs/pii/S0006899300031723
http://hdl.handle.net/10722/171700

Inhibition of cytotoxicity and amyloid fibril formation by a D-amino acid peptide that specifically binds to Alzheimer's disease amyloid peptide

Autoren: Wiesehan, K. Stöhr, J. Nagel-Steger, K. et al.

Quelle: Protein engineering design and selection 21, 241 - 246 (2008). doi:10.1093/protein/gzm054

Schlagwörter: info:eu-repo/classification/ddc/540, Amyloid beta-Peptides: antagonists & inhibitors, Amyloid beta-Peptides: metabolism, Amyloid beta-Peptides: toxicity, Animals, Cell Death: drug effects, Cytotoxins: antagonists & inhibitors, Cytotoxins: metabolism, Cytotoxins: toxicity, Microscopy, Electron, PC12 Cells, Peptides: chemistry, Peptides: metabolism, Peptides: pharmacology, Polymers: metabolism, Protein Binding, Protein Structure, Secondary: drug effects, Rats, Spectrometry, Fluorescence, Substrate Specificity, Thiazoles: metabolism, Amyloid beta-Peptides, Cytotoxins, Peptides, Polymers, Thiazoles, thioflavin T

Geographisches Schlagwort: DE

Relation: info:eu-repo/semantics/altIdentifier/hdl/2128/25408; info:eu-repo/semantics/altIdentifier/issn/1741-0126; info:eu-repo/semantics/altIdentifier/wos/WOS:000254295200003; info:eu-repo/semantics/altIdentifier/pmid/pmid:18252750

Verfügbarkeit: https://juser.fz-juelich.de/record/338
https://juser.fz-juelich.de/search?p=id:%22PreJuSER-338%22

Neuroprotective effects of the active principles from selected Chinese medicinal herbs on b-amyloid-induced toxicity in PC12 cells.

Weitere Verfasser: Hoi, Chu Peng. Chinese University of Hong Kong Graduate School. Division of Pharmacy.

Schlagwörter: Alzheimer's disease--Chemotherapy, Neuroprotective agents, Herbs--Therapeutic use, Herbs--Therapeutic use--China, Amyloid beta-protein--Toxicology, Pheochromocytoma--Effect of drugs on, Alzheimer Disease--drug therapy, Neuroprotective Agents--pharmacology, Drugs, Chinese Herbal, Amyloid beta-Peptides--toxicity, PC12 Cells--drug effects

Geographisches Schlagwort: China

Dateibeschreibung: print; xiii, 103 leaves : ill. (some col.); 30 cm.

Relation: cuhk:325928; http://library.cuhk.edu.hk/record=b5896706

Verfügbarkeit: http://library.cuhk.edu.hk/record=b5896706
https://repository.lib.cuhk.edu.hk/en/item/cuhk-325928

Potential human transmission of amyloid β pathology: surveillance and risks

Autoren: Lauwers, Elsa Lalli, Giovanna Ivinson, Adrian J et al.

Quelle: The lancet / Neurology 19(10), 872 - 878 (2020). doi:10.1016/S1474-4422(20)30238-6

Schlagwörter: info:eu-repo/classification/ddc/610, Alzheimer Disease: etiology, Alzheimer Disease: metabolism, Alzheimer Disease: pathology, Amyloid beta-Peptides: metabolism, Amyloid beta-Peptides: toxicity, Animals, Creutzfeldt-Jakob Syndrome: metabolism, Creutzfeldt-Jakob Syndrome: pathology, Creutzfeldt-Jakob Syndrome: transmission, Humans, Neurodegenerative Diseases: etiology, Neurodegenerative Diseases: metabolism, Neurodegenerative Diseases: pathology, Parkinson Disease: etiology, Parkinson Disease: metabolism, Parkinson Disease: pathology, Population Surveillance, Risk Factors

Geographisches Schlagwort: DE

Relation: info:eu-repo/semantics/altIdentifier/pmid/pmid:32949547; info:eu-repo/semantics/altIdentifier/issn/1474-4465; info:eu-repo/semantics/altIdentifier/issn/1474-4422; https://pub.dzne.de/record/164429

Verfügbarkeit: https://pub.dzne.de/record/164429
https://pub.dzne.de/search?p=id:%22DZNE-2022-00981%22

β-Amyloid Clustering around ASC Fibrils Boosts Its Toxicity in Microglia

Autoren: Friker, Lea L. Scheiblich, Hannah Hochheiser, Inga V. et al.

Quelle: Cell reports 30(11), 3743 - 3754.e6 (2020). doi:10.1016/j.celrep.2020.02.025

Schlagwörter: info:eu-repo/classification/ddc/610, Amyloid beta-Peptides: metabolism, Amyloid beta-Peptides: toxicity, Amyloid beta-Peptides: ultrastructure, Animals, CARD Signaling Adaptor Proteins: metabolism, Caspase 1: metabolism, Cells, Cultured, Humans, Inflammasomes: metabolism, Interleukin-1beta: metabolism, Mice, Inbred C57BL, Microglia: drug effects, Microglia: metabolism, Microglia: pathology, Models, Biological, NLR Family, Pyrin Domain-Containing 3 Protein: metabolism, Proteolysis: drug effects, Pyroptosis: drug effects, Signal Transduction: drug effects, Toll-Like Receptor 2: metabolism, Toll-Like Receptor 4: metabolism

Geographisches Schlagwort: DE

Relation: info:eu-repo/semantics/altIdentifier/issn/2211-1247; info:eu-repo/semantics/altIdentifier/issn/2639-1856; info:eu-repo/semantics/altIdentifier/pmid/pmid:32187546; https://pub.dzne.de/record/151661

Verfügbarkeit: https://pub.dzne.de/record/151661
https://pub.dzne.de/search?p=id:%22DZNE-2020-01240%22

Coenzyme Q10 protects SHSY5Y neuronal cells from beta amyloid toxicity and oxygen-glucose deprivation by inhibiting the opening of the mitochondrial permeability transition pore

Autoren: Yang, ES Li, G Zou, LY et al.

Schlagwörter: Amyloid Beta-Peptides - Toxicity, Tumor, Lactate Dehydrogenases - Secretion, Cell Hypoxia - Physiology, Ubiquinone - Analogs & Derivatives - Antagonists & Inhibitors - Pharmacology, Coenzymes, Cell Survival - Drug Effects, Atractyloside - Pharmacology, Cell Line, Neuroblastoma, Mitochondrial Membrane Transport Proteins - Antagonists & Inhibitors, Cell Line, Tumor, Superoxides - Metabolism, Humans, Fluoresceins - Diagnostic Use, Glucose - Deficiency, Neurons - Drug Effects

Zugangs-URL: http://hdl.handle.net/10722/155331