Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 10/2014, Volume 111, Issue 41, pp. 14870 - 14875
Mucopolysaccharidosis type IIIB (MPS 1IIB, Sanfilippo syndrome type B) is a lysosomal storage disease characterized by profound intellectual disability,...
Proteins | Enzymes | Brain | Receptors | Neurons | Enzyme replacement therapy | Liver | Mucopolysaccharidoses | Sulfates | Vehicles | SANFILIPPO-SYNDROME | RECOMBINANT | MULTIDISCIPLINARY SCIENCES | DISEASE | SYNDROME TYPE-B | REPLACEMENT THERAPY | LYSOSOMAL STORAGE | MICE | GROWTH-FACTOR-II | MANNOSE 6-PHOSPHATE RECEPTOR | ALPHA-N-ACETYLGLUCOSAMINIDASE | Neurons - pathology | Cricetulus | Humans | Recombinant Fusion Proteins - therapeutic use | Injections, Intraventricular | Mucopolysaccharidosis III - pathology | Mucopolysaccharidosis III - drug therapy | Heparitin Sulfate - metabolism | Drug Delivery Systems | Brain - metabolism | Endocytosis | Neurons - metabolism | Recombinant Fusion Proteins - administration & dosage | CHO Cells | Fibroblasts - metabolism | Biomarkers - metabolism | Acetylglucosaminidase - therapeutic use | Cricetinae | Lysosome-Associated Membrane Glycoproteins - metabolism | beta-N-Acetylhexosaminidases - metabolism | Insulin-Like Growth Factor II - therapeutic use | Liver - metabolism | Cells, Cultured | Fibroblasts - pathology | Animals | Brain - pathology | Protein Binding | Mice | Biological Sciences
Proteins | Enzymes | Brain | Receptors | Neurons | Enzyme replacement therapy | Liver | Mucopolysaccharidoses | Sulfates | Vehicles | SANFILIPPO-SYNDROME | RECOMBINANT | MULTIDISCIPLINARY SCIENCES | DISEASE | SYNDROME TYPE-B | REPLACEMENT THERAPY | LYSOSOMAL STORAGE | MICE | GROWTH-FACTOR-II | MANNOSE 6-PHOSPHATE RECEPTOR | ALPHA-N-ACETYLGLUCOSAMINIDASE | Neurons - pathology | Cricetulus | Humans | Recombinant Fusion Proteins - therapeutic use | Injections, Intraventricular | Mucopolysaccharidosis III - pathology | Mucopolysaccharidosis III - drug therapy | Heparitin Sulfate - metabolism | Drug Delivery Systems | Brain - metabolism | Endocytosis | Neurons - metabolism | Recombinant Fusion Proteins - administration & dosage | CHO Cells | Fibroblasts - metabolism | Biomarkers - metabolism | Acetylglucosaminidase - therapeutic use | Cricetinae | Lysosome-Associated Membrane Glycoproteins - metabolism | beta-N-Acetylhexosaminidases - metabolism | Insulin-Like Growth Factor II - therapeutic use | Liver - metabolism | Cells, Cultured | Fibroblasts - pathology | Animals | Brain - pathology | Protein Binding | Mice | Biological Sciences
Journal Article
Nature Chemical Biology, ISSN 1552-4450, 08/2008, Volume 4, Issue 8, pp. 483 - 490
Pathological hyperphosphorylation of the microtubule-associated protein tau is characteristic of Alzheimer's disease (AD) and the associated tauopathies. The...
D-GLUCOSAMINIDASE | BETA-N-ACETYLGLUCOSAMINIDASE | NEUROFIBRILLARY TANGLES | NUCLEAR | BIOCHEMISTRY & MOLECULAR BIOLOGY | HYPERPHOSPHORYLATION | NAG-THIAZOLINE | CYTOSOLIC PROTEINS | GLYCOSYLATION | PUGNAC | ACETYL | Brain Chemistry - drug effects | Cerebral Cortex - enzymology | Humans | Enzyme Inhibitors - pharmacology | Rats | tau Proteins - metabolism | beta-N-Acetylhexosaminidases - antagonists & inhibitors | Enzyme Inhibitors - therapeutic use | Cerebral Cortex - metabolism | Hippocampus - metabolism | Animals | beta-N-Acetylhexosaminidases - physiology | Hippocampus - enzymology | Phosphorylation - drug effects | Tauopathies - drug therapy | Proteins | Biochemistry | Inhibitor drugs | Alzheimers disease | Chemical synthesis | Rodents
D-GLUCOSAMINIDASE | BETA-N-ACETYLGLUCOSAMINIDASE | NEUROFIBRILLARY TANGLES | NUCLEAR | BIOCHEMISTRY & MOLECULAR BIOLOGY | HYPERPHOSPHORYLATION | NAG-THIAZOLINE | CYTOSOLIC PROTEINS | GLYCOSYLATION | PUGNAC | ACETYL | Brain Chemistry - drug effects | Cerebral Cortex - enzymology | Humans | Enzyme Inhibitors - pharmacology | Rats | tau Proteins - metabolism | beta-N-Acetylhexosaminidases - antagonists & inhibitors | Enzyme Inhibitors - therapeutic use | Cerebral Cortex - metabolism | Hippocampus - metabolism | Animals | beta-N-Acetylhexosaminidases - physiology | Hippocampus - enzymology | Phosphorylation - drug effects | Tauopathies - drug therapy | Proteins | Biochemistry | Inhibitor drugs | Alzheimers disease | Chemical synthesis | Rodents
Journal Article
Phytomedicine, ISSN 0944-7113, 12/2016, Volume 23, Issue 14, pp. 1706 - 1715
Nicolson & Sivadasan (Araceae) is a traditional Chinese medicinal herb possessing detumescent, detoxifying, and anti-inflammatory activities. It is used in...
Typhonium blumei | Typhonium roxburghii | Anti-allergic | Anti-inflammatory | Fatty acids | Calcium influx | Fatty Acids - therapeutic use | Calcium - metabolism | Humans | Drugs, Chinese Herbal - pharmacology | Phosphatidylinositol 3-Kinases - metabolism | Anti-Allergic Agents - pharmacology | Mast Cells - metabolism | Anti-Inflammatory Agents - therapeutic use | Phosphorylation - drug effects | Phytotherapy | Drugs, Chinese Herbal - therapeutic use | Neutrophils - metabolism | Histamine Release - drug effects | Cell Line | Araceae - chemistry | Phospholipase C gamma - metabolism | Cytokines - metabolism | Signal Transduction | Anti-Inflammatory Agents - pharmacology | beta-N-Acetylhexosaminidases - metabolism | Interleukin-4 - metabolism | Fatty Acids - analysis | Rats | Mast Cells - drug effects | Anti-Allergic Agents - therapeutic use | Animals | Receptors, IgE - metabolism | Cell Degranulation - drug effects | Fatty Acids - pharmacology
Typhonium blumei | Typhonium roxburghii | Anti-allergic | Anti-inflammatory | Fatty acids | Calcium influx | Fatty Acids - therapeutic use | Calcium - metabolism | Humans | Drugs, Chinese Herbal - pharmacology | Phosphatidylinositol 3-Kinases - metabolism | Anti-Allergic Agents - pharmacology | Mast Cells - metabolism | Anti-Inflammatory Agents - therapeutic use | Phosphorylation - drug effects | Phytotherapy | Drugs, Chinese Herbal - therapeutic use | Neutrophils - metabolism | Histamine Release - drug effects | Cell Line | Araceae - chemistry | Phospholipase C gamma - metabolism | Cytokines - metabolism | Signal Transduction | Anti-Inflammatory Agents - pharmacology | beta-N-Acetylhexosaminidases - metabolism | Interleukin-4 - metabolism | Fatty Acids - analysis | Rats | Mast Cells - drug effects | Anti-Allergic Agents - therapeutic use | Animals | Receptors, IgE - metabolism | Cell Degranulation - drug effects | Fatty Acids - pharmacology
Journal Article
American Journal of Physiology - Heart and Circulatory Physiology, ISSN 0363-6135, 11/2010, Volume 299, Issue 5, pp. H1715 - H1727
Laczy B, Marsh SA, Brocks CA, Wittmann I, Chatham JC. Inhibition of O-GlcNAcase in perfused rat hearts by NAG-thiazolines at the time of reperfusion is...
Ischemia-reperfusion | O-GlcNAcase | Protein O-glcnacylation | Cardioprotection | Hexosamine biosynthesis | CARDIAC & CARDIOVASCULAR SYSTEMS | PHYSIOLOGY | GLCNACYLATION | MYOCARDIAL PROTECTION | INJURY | ISCHEMIA | ischemia-reperfusion | protein O-GlcNAcylation | hexosamine biosynthesis | PROTECTS NEONATAL CARDIOMYOCYTES | INSULIN-RESISTANCE | cardioprotection | PERIPHERAL VASCULAR DISEASE | PROTEINS | EXPRESSION | LINKED N-ACETYLGLUCOSAMINE | beta-N-Acetylhexosaminidases - metabolism | Enzyme Inhibitors - pharmacology | Rats | Acetylglucosamine - pharmacology | Acetylglucosamine - therapeutic use | Male | beta-N-Acetylhexosaminidases - antagonists & inhibitors | Thiazoles - therapeutic use | Enzyme Inhibitors - therapeutic use | Rats, Sprague-Dawley | Acetylglucosamine - metabolism | Myocardial Reperfusion Injury - metabolism | Animals | Desmin - metabolism | Myocardium - metabolism | Acetylglucosamine - analogs & derivatives | Models, Animal | Thiazoles - pharmacology | Myocardial Reperfusion Injury - prevention & control
Ischemia-reperfusion | O-GlcNAcase | Protein O-glcnacylation | Cardioprotection | Hexosamine biosynthesis | CARDIAC & CARDIOVASCULAR SYSTEMS | PHYSIOLOGY | GLCNACYLATION | MYOCARDIAL PROTECTION | INJURY | ISCHEMIA | ischemia-reperfusion | protein O-GlcNAcylation | hexosamine biosynthesis | PROTECTS NEONATAL CARDIOMYOCYTES | INSULIN-RESISTANCE | cardioprotection | PERIPHERAL VASCULAR DISEASE | PROTEINS | EXPRESSION | LINKED N-ACETYLGLUCOSAMINE | beta-N-Acetylhexosaminidases - metabolism | Enzyme Inhibitors - pharmacology | Rats | Acetylglucosamine - pharmacology | Acetylglucosamine - therapeutic use | Male | beta-N-Acetylhexosaminidases - antagonists & inhibitors | Thiazoles - therapeutic use | Enzyme Inhibitors - therapeutic use | Rats, Sprague-Dawley | Acetylglucosamine - metabolism | Myocardial Reperfusion Injury - metabolism | Animals | Desmin - metabolism | Myocardium - metabolism | Acetylglucosamine - analogs & derivatives | Models, Animal | Thiazoles - pharmacology | Myocardial Reperfusion Injury - prevention & control
Journal Article
Neurobiology of Aging, ISSN 0197-4580, 2013, Volume 34, Issue 1, pp. 275 - 285
Abstract Deposition of β-amyloid (Aβ) as senile plaques and disrupted glucose metabolism are two main characteristics of Alzheimer's disease (AD). It is...
Neurology | Internal Medicine | Alzheimer's disease (AD) | O-GlcNAcylation | Nicastrin | NButGT | 5XFAD transgenic mouse | β-Amyloid (Aβ) | 3T3-L1 ADIPOCYTES | GAMMA-SECRETASE COMPLEX | ALZHEIMERS-DISEASE | GLYCOSYLATION | NEUROSCIENCES | GERIATRICS & GERONTOLOGY | beta-Amyloid (A beta) | GLCNACASE INHIBITOR | INSULIN-RESISTANCE | IN-VIVO | PRECURSOR PROTEIN | TRANSGENIC MICE | Gene Expression Regulation, Enzymologic - drug effects | Alzheimer Disease - complications | Humans | Fear - drug effects | Dose-Response Relationship, Drug | Transfection | Bridged Bicyclo Compounds, Heterocyclic - therapeutic use | Amyloid beta-Peptides - metabolism | HEK293 Cells | Disease Models, Animal | Memory Disorders - enzymology | Peptide Fragments - metabolism | Enzyme-Linked Immunosorbent Assay | Conditioning (Psychology) - drug effects | beta-N-Acetylhexosaminidases - metabolism | Alzheimer Disease - drug therapy | Presenilin-1 - genetics | Mice, Transgenic | Maze Learning - drug effects | Mutation - genetics | Enzyme Inhibitors - therapeutic use | Plaque, Amyloid - drug therapy | Amyloid Precursor Protein Secretases - metabolism | Amyloid beta-Protein Precursor - genetics | Animals | Memory Disorders - drug therapy | Memory Disorders - etiology | Analysis of Variance | Presenilin-2 - genetics | Mice | Alzheimer Disease - genetics
Neurology | Internal Medicine | Alzheimer's disease (AD) | O-GlcNAcylation | Nicastrin | NButGT | 5XFAD transgenic mouse | β-Amyloid (Aβ) | 3T3-L1 ADIPOCYTES | GAMMA-SECRETASE COMPLEX | ALZHEIMERS-DISEASE | GLYCOSYLATION | NEUROSCIENCES | GERIATRICS & GERONTOLOGY | beta-Amyloid (A beta) | GLCNACASE INHIBITOR | INSULIN-RESISTANCE | IN-VIVO | PRECURSOR PROTEIN | TRANSGENIC MICE | Gene Expression Regulation, Enzymologic - drug effects | Alzheimer Disease - complications | Humans | Fear - drug effects | Dose-Response Relationship, Drug | Transfection | Bridged Bicyclo Compounds, Heterocyclic - therapeutic use | Amyloid beta-Peptides - metabolism | HEK293 Cells | Disease Models, Animal | Memory Disorders - enzymology | Peptide Fragments - metabolism | Enzyme-Linked Immunosorbent Assay | Conditioning (Psychology) - drug effects | beta-N-Acetylhexosaminidases - metabolism | Alzheimer Disease - drug therapy | Presenilin-1 - genetics | Mice, Transgenic | Maze Learning - drug effects | Mutation - genetics | Enzyme Inhibitors - therapeutic use | Plaque, Amyloid - drug therapy | Amyloid Precursor Protein Secretases - metabolism | Amyloid beta-Protein Precursor - genetics | Animals | Memory Disorders - drug therapy | Memory Disorders - etiology | Analysis of Variance | Presenilin-2 - genetics | Mice | Alzheimer Disease - genetics
Journal Article
Journal of Ethnopharmacology, ISSN 0378-8741, 09/2013, Volume 149, Issue 2, pp. 471 - 477
The root bark of Turcz. is widely used as a medicinal herb for treatment of skin diseases such as eczema, pruritus and urticaria in China, Japan and Korea. We...
Traditional Chinese medicine | Allergy | Dictamnus dasycarpus | Inflammation | Mast cell | Contact dermatitis | CHEMISTRY, MEDICINAL | IFN-GAMMA | MAST-CELLS | MECHANISMS | HUMAN KERATINOCYTES | PLANT SCIENCES | INTEGRATIVE & COMPLEMENTARY MEDICINE | PHARMACOLOGY & PHARMACY | TNF-ALPHA | SKIN | HISTAMINE | Dictamnus dasycmpus | T-LYMPHOCYTES | HYPERSENSITIVITY | ALKALOIDS | Tumor Necrosis Factor-alpha - metabolism | Dictamnus | Plant Extracts - pharmacology | Solvents - chemistry | Male | Anti-Allergic Agents - pharmacology | Interferon-gamma - metabolism | Dermatitis, Allergic Contact - pathology | Histamine - metabolism | Plant Roots | Anti-Inflammatory Agents - therapeutic use | Methanol - chemistry | Dermatitis, Allergic Contact - drug therapy | Anti-Inflammatory Agents - pharmacology | beta-N-Acetylhexosaminidases - metabolism | Dinitrofluorobenzene | Edema - drug therapy | Plant Bark | Anti-Allergic Agents - therapeutic use | Animals | Dermatitis, Allergic Contact - etiology | Cell Proliferation - drug effects | Ear - pathology | Mice | Mice, Inbred BALB C | Edema - pathology | Plant Extracts - therapeutic use | Mitogen-Activated Protein Kinases - metabolism | Medicine, Herbal | Anti-inflammatory drugs | Medicine, Botanic | Skin care products
Traditional Chinese medicine | Allergy | Dictamnus dasycarpus | Inflammation | Mast cell | Contact dermatitis | CHEMISTRY, MEDICINAL | IFN-GAMMA | MAST-CELLS | MECHANISMS | HUMAN KERATINOCYTES | PLANT SCIENCES | INTEGRATIVE & COMPLEMENTARY MEDICINE | PHARMACOLOGY & PHARMACY | TNF-ALPHA | SKIN | HISTAMINE | Dictamnus dasycmpus | T-LYMPHOCYTES | HYPERSENSITIVITY | ALKALOIDS | Tumor Necrosis Factor-alpha - metabolism | Dictamnus | Plant Extracts - pharmacology | Solvents - chemistry | Male | Anti-Allergic Agents - pharmacology | Interferon-gamma - metabolism | Dermatitis, Allergic Contact - pathology | Histamine - metabolism | Plant Roots | Anti-Inflammatory Agents - therapeutic use | Methanol - chemistry | Dermatitis, Allergic Contact - drug therapy | Anti-Inflammatory Agents - pharmacology | beta-N-Acetylhexosaminidases - metabolism | Dinitrofluorobenzene | Edema - drug therapy | Plant Bark | Anti-Allergic Agents - therapeutic use | Animals | Dermatitis, Allergic Contact - etiology | Cell Proliferation - drug effects | Ear - pathology | Mice | Mice, Inbred BALB C | Edema - pathology | Plant Extracts - therapeutic use | Mitogen-Activated Protein Kinases - metabolism | Medicine, Herbal | Anti-inflammatory drugs | Medicine, Botanic | Skin care products
Journal Article
Laboratory Investigation, ISSN 0023-6837, 10/2012, Volume 92, Issue 10, pp. 1472 - 1482
Cromolyn, widely characterized as a 'mast cell stabilizer', has been used in mice to investigate the biological roles of mast cells in vivo. However, it is not...
mouse | DSCG | rat | cromolyn | mast cell | anaphylaxis | disodium cromoglycate | NEDOCROMIL SODIUM | MEDICINE, RESEARCH & EXPERIMENTAL | IMMEDIATE HYPERSENSITIVITY REACTIONS | ANTIALLERGIC DRUGS | BONE-MARROW | HISTAMINE-RELEASE | DEFICIENT MICE | PATHOLOGY | MEDIATOR RELEASE | BREAST-CANCER | DISODIUM-CROMOGLYCATE | GENE-EXPRESSION | Species Specificity | Humans | Tumor Necrosis Factor-alpha - blood | Peritoneum - drug effects | Male | Cromolyn Sodium - therapeutic use | Dose-Response Relationship, Drug | Cromolyn Sodium - pharmacology | Peritoneum - cytology | Mast Cells - metabolism | Female | Chemokine CCL2 - metabolism | Anti-Asthmatic Agents - pharmacology | Passive Cutaneous Anaphylaxis - drug effects | Chymases - blood | Anaphylaxis - drug therapy | beta-N-Acetylhexosaminidases - metabolism | Immunoglobulin E - metabolism | Mice, Inbred C57BL | Rats | Mice, Transgenic | Mast Cells - drug effects | Chymases - secretion | Animals | Evans Blue | Analysis of Variance | Histamine - blood | Leukocytes - drug effects | Mice | Anaphylaxis - metabolism | Leukocytes - metabolism | Extravasation of Diagnostic and Therapeutic Materials
mouse | DSCG | rat | cromolyn | mast cell | anaphylaxis | disodium cromoglycate | NEDOCROMIL SODIUM | MEDICINE, RESEARCH & EXPERIMENTAL | IMMEDIATE HYPERSENSITIVITY REACTIONS | ANTIALLERGIC DRUGS | BONE-MARROW | HISTAMINE-RELEASE | DEFICIENT MICE | PATHOLOGY | MEDIATOR RELEASE | BREAST-CANCER | DISODIUM-CROMOGLYCATE | GENE-EXPRESSION | Species Specificity | Humans | Tumor Necrosis Factor-alpha - blood | Peritoneum - drug effects | Male | Cromolyn Sodium - therapeutic use | Dose-Response Relationship, Drug | Cromolyn Sodium - pharmacology | Peritoneum - cytology | Mast Cells - metabolism | Female | Chemokine CCL2 - metabolism | Anti-Asthmatic Agents - pharmacology | Passive Cutaneous Anaphylaxis - drug effects | Chymases - blood | Anaphylaxis - drug therapy | beta-N-Acetylhexosaminidases - metabolism | Immunoglobulin E - metabolism | Mice, Inbred C57BL | Rats | Mice, Transgenic | Mast Cells - drug effects | Chymases - secretion | Animals | Evans Blue | Analysis of Variance | Histamine - blood | Leukocytes - drug effects | Mice | Anaphylaxis - metabolism | Leukocytes - metabolism | Extravasation of Diagnostic and Therapeutic Materials
Journal Article
MOLECULAR PSYCHIATRY, ISSN 1359-4184, 02/2015, Volume 20, Issue 1, pp. 109 - 117
Certain mutant Alzheimer's amyloid-beta (A beta) peptides (that is, Dutch mutant APP(E693Q)) form complexes with gangliosides (GA beta). These mutant A beta...
PROTEIN | GM1 GANGLIOSIDE | CHOLESTEROL | PSYCHIATRY | ALZHEIMERS-DISEASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | SANDHOFF-DISEASE | NEUROSCIENCES | GLUCOCEREBROSIDASE | TAY-SACHS | MUTATIONS | PHARMACOLOGICAL CHAPERONE | BRAIN | Alzheimer Disease - complications | Humans | Cognition Disorders - metabolism | Dose-Response Relationship, Drug | Time Factors | Antipsychotic Agents - therapeutic use | Cognition Disorders - etiology | Gangliosides - metabolism | Amyloid beta-Peptides - metabolism | Gangliosides - therapeutic use | Disease Models, Animal | Fibroblasts - metabolism | beta-N-Acetylhexosaminidases - metabolism | Mice, Inbred C57BL | Cells, Cultured | Cognition Disorders - drug therapy | Maze Learning - drug effects | Mutation - genetics | Amyloid beta-Protein Precursor - genetics | Animals | Recognition (Psychology) - drug effects | Fibroblasts - drug effects | Blood-Testis Barrier - drug effects | Mice | Alzheimer Disease - genetics
PROTEIN | GM1 GANGLIOSIDE | CHOLESTEROL | PSYCHIATRY | ALZHEIMERS-DISEASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | SANDHOFF-DISEASE | NEUROSCIENCES | GLUCOCEREBROSIDASE | TAY-SACHS | MUTATIONS | PHARMACOLOGICAL CHAPERONE | BRAIN | Alzheimer Disease - complications | Humans | Cognition Disorders - metabolism | Dose-Response Relationship, Drug | Time Factors | Antipsychotic Agents - therapeutic use | Cognition Disorders - etiology | Gangliosides - metabolism | Amyloid beta-Peptides - metabolism | Gangliosides - therapeutic use | Disease Models, Animal | Fibroblasts - metabolism | beta-N-Acetylhexosaminidases - metabolism | Mice, Inbred C57BL | Cells, Cultured | Cognition Disorders - drug therapy | Maze Learning - drug effects | Mutation - genetics | Amyloid beta-Protein Precursor - genetics | Animals | Recognition (Psychology) - drug effects | Fibroblasts - drug effects | Blood-Testis Barrier - drug effects | Mice | Alzheimer Disease - genetics
Journal Article
Journal of Nutrition, ISSN 0022-3166, 05/2013, Volume 143, Issue 5, pp. 632 - 639
Resveratrol is a phytoalexin abundantly found in red grape skin and is effective in antitumor and antiinflammation associated with immune responses. This study...
ALLERGIC INFLAMMATION | ACTIVATION | NUTRITION & DIETETICS | FC-EPSILON-RI | RBL-2H3 CELLS | DISEASES | PHOSPHORYLATION | KINASE | PICEATANNOL | RECEPTOR | RELEASE | Phosphorylation | Vitis - chemistry | Stilbenes - therapeutic use | Plant Extracts - pharmacology | Protein-Tyrosine Kinases - metabolism | Skin - metabolism | Anaphylaxis - prevention & control | CD24 Antigen - metabolism | Male | Intracellular Signaling Peptides and Proteins - metabolism | Stilbenes - pharmacology | Dose-Response Relationship, Drug | Histamine - metabolism | Mast Cells - metabolism | Anaphylaxis - immunology | Chemokine CCL2 - metabolism | Phytotherapy | Chemokine CXCL2 - metabolism | Syk Kinase | Edema - prevention & control | Histamine Release - drug effects | Skin - immunology | Phospholipase C gamma - metabolism | Edema - immunology | Dinitrophenols | beta-N-Acetylhexosaminidases - metabolism | Immunoglobulin E - metabolism | Rats | Mast Cells - drug effects | Passive Cutaneous Anaphylaxis | Serum Albumin | Animals | Basophils | Inflammation - prevention & control | Mice | Mice, Inbred BALB C | Anaphylaxis - metabolism | Dietary Supplements | Plant Extracts - therapeutic use | Skin - drug effects | Physiological aspects | Care and treatment | Mast cells | Anaphylaxis | Resveratrol
ALLERGIC INFLAMMATION | ACTIVATION | NUTRITION & DIETETICS | FC-EPSILON-RI | RBL-2H3 CELLS | DISEASES | PHOSPHORYLATION | KINASE | PICEATANNOL | RECEPTOR | RELEASE | Phosphorylation | Vitis - chemistry | Stilbenes - therapeutic use | Plant Extracts - pharmacology | Protein-Tyrosine Kinases - metabolism | Skin - metabolism | Anaphylaxis - prevention & control | CD24 Antigen - metabolism | Male | Intracellular Signaling Peptides and Proteins - metabolism | Stilbenes - pharmacology | Dose-Response Relationship, Drug | Histamine - metabolism | Mast Cells - metabolism | Anaphylaxis - immunology | Chemokine CCL2 - metabolism | Phytotherapy | Chemokine CXCL2 - metabolism | Syk Kinase | Edema - prevention & control | Histamine Release - drug effects | Skin - immunology | Phospholipase C gamma - metabolism | Edema - immunology | Dinitrophenols | beta-N-Acetylhexosaminidases - metabolism | Immunoglobulin E - metabolism | Rats | Mast Cells - drug effects | Passive Cutaneous Anaphylaxis | Serum Albumin | Animals | Basophils | Inflammation - prevention & control | Mice | Mice, Inbred BALB C | Anaphylaxis - metabolism | Dietary Supplements | Plant Extracts - therapeutic use | Skin - drug effects | Physiological aspects | Care and treatment | Mast cells | Anaphylaxis | Resveratrol
Journal Article
Biochemical and Biophysical Research Communications, ISSN 0006-291X, 03/2014, Volume 445, Issue 3, pp. 549 - 555
Previous studies demonstrated that derived crude antigens suppress development of allergic responses. We investigated the effects of venom allergen-like...
Clonochis sinensis | Clonochis sinensis venom allergen-like (CsVAL) proteins | RBL-2H3 rat mast cell | Contact hypersensitivity | MAST-CELL ACTIVATION | IGE | BIOCHEMISTRY & MOLECULAR BIOLOGY | AIRWAY INFLAMMATION | MEDIATE | MODEL | RESPONSES | BIOPHYSICS | MICE | EXPRESSION | Anti-Allergic Agents - immunology | Cell Line | Mast Cells - immunology | Dermatitis, Contact - pathology | Helminth Proteins - therapeutic use | Rats | beta-N-Acetylhexosaminidases - immunology | Mast Cells - drug effects | Anti-Allergic Agents - therapeutic use | Antigens, Helminth - immunology | Clonorchis sinensis - immunology | Dermatitis, Contact - immunology | Animals | Immunoglobulin E - immunology | Antigens, Helminth - therapeutic use | Dermatitis, Contact - drug therapy | Helminth Proteins - immunology | Female | Mice, Inbred BALB C | Skin - drug effects | Skin - pathology | Cell Degranulation - drug effects | Skin - immunology | Allergens | Allergy | Peptides | Allergic reaction | Venom
Clonochis sinensis | Clonochis sinensis venom allergen-like (CsVAL) proteins | RBL-2H3 rat mast cell | Contact hypersensitivity | MAST-CELL ACTIVATION | IGE | BIOCHEMISTRY & MOLECULAR BIOLOGY | AIRWAY INFLAMMATION | MEDIATE | MODEL | RESPONSES | BIOPHYSICS | MICE | EXPRESSION | Anti-Allergic Agents - immunology | Cell Line | Mast Cells - immunology | Dermatitis, Contact - pathology | Helminth Proteins - therapeutic use | Rats | beta-N-Acetylhexosaminidases - immunology | Mast Cells - drug effects | Anti-Allergic Agents - therapeutic use | Antigens, Helminth - immunology | Clonorchis sinensis - immunology | Dermatitis, Contact - immunology | Animals | Immunoglobulin E - immunology | Antigens, Helminth - therapeutic use | Dermatitis, Contact - drug therapy | Helminth Proteins - immunology | Female | Mice, Inbred BALB C | Skin - drug effects | Skin - pathology | Cell Degranulation - drug effects | Skin - immunology | Allergens | Allergy | Peptides | Allergic reaction | Venom
Journal Article
Bioscience, Biotechnology, and Biochemistry, ISSN 0916-8451, 09/2011, Volume 75, Issue 9, pp. 1644 - 1648
Peanut skin contains large amounts of polyphenols having antiallergic effects. We found that a peanut-skin extract (PSE) inhibits the degranulation induced by...
procyanidin | degranulation | polyphenol | rat basophilic leukemia (RBL)-2H3 | peanut skin | Degranulation | Peanut skin | Polyphenol | Procyanidin | Rat basophilic leukemia (RBL)-2H3 | GRAPE SEEDS | BIOCHEMISTRY & MOLECULAR BIOLOGY | FOOD SCIENCE & TECHNOLOGY | MAST-CELLS | RATS | HISTAMINE-RELEASE | CATECHINS | CHROMATOGRAPHY | DIMERS | AFFINITY IGE RECEPTOR | POLYPHENOLS | ALLERGY | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | CHEMISTRY, APPLIED | Arachis - chemistry | Hypersensitivity - prevention & control | Plant Extracts - chemistry | Tetradecanoylphorbol Acetate - pharmacology | beta-N-Acetylhexosaminidases - analysis | Calcium - metabolism | Plant Extracts - pharmacology | Polyphenols - pharmacology | Hypersensitivity - immunology | Anti-Allergic Agents - pharmacology | Hydroquinones - pharmacology | Hypersensitivity - drug therapy | Tetradecanoylphorbol Acetate - antagonists & inhibitors | Proanthocyanidins - chemistry | Signal Transduction - immunology | Proanthocyanidins - pharmacology | Anti-Allergic Agents - chemistry | Catechin - therapeutic use | Seeds - chemistry | Catechin - pharmacology | Leukemia, Basophilic, Acute - metabolism | Hydroquinones - antagonists & inhibitors | Leukemia, Basophilic, Acute - pathology | Magnetic Resonance Spectroscopy | Rats | Proanthocyanidins - therapeutic use | Cell Degranulation - immunology | beta-N-Acetylhexosaminidases - secretion | Anti-Allergic Agents - therapeutic use | Animals | Leukemia, Basophilic, Acute - immunology | Signal Transduction - drug effects | Polyphenols - chemistry | Cell Line, Tumor | Polyphenols - therapeutic use | Plant Extracts - therapeutic use | Catechin - chemistry | Cell Degranulation - drug effects | Antiallergics
procyanidin | degranulation | polyphenol | rat basophilic leukemia (RBL)-2H3 | peanut skin | Degranulation | Peanut skin | Polyphenol | Procyanidin | Rat basophilic leukemia (RBL)-2H3 | GRAPE SEEDS | BIOCHEMISTRY & MOLECULAR BIOLOGY | FOOD SCIENCE & TECHNOLOGY | MAST-CELLS | RATS | HISTAMINE-RELEASE | CATECHINS | CHROMATOGRAPHY | DIMERS | AFFINITY IGE RECEPTOR | POLYPHENOLS | ALLERGY | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | CHEMISTRY, APPLIED | Arachis - chemistry | Hypersensitivity - prevention & control | Plant Extracts - chemistry | Tetradecanoylphorbol Acetate - pharmacology | beta-N-Acetylhexosaminidases - analysis | Calcium - metabolism | Plant Extracts - pharmacology | Polyphenols - pharmacology | Hypersensitivity - immunology | Anti-Allergic Agents - pharmacology | Hydroquinones - pharmacology | Hypersensitivity - drug therapy | Tetradecanoylphorbol Acetate - antagonists & inhibitors | Proanthocyanidins - chemistry | Signal Transduction - immunology | Proanthocyanidins - pharmacology | Anti-Allergic Agents - chemistry | Catechin - therapeutic use | Seeds - chemistry | Catechin - pharmacology | Leukemia, Basophilic, Acute - metabolism | Hydroquinones - antagonists & inhibitors | Leukemia, Basophilic, Acute - pathology | Magnetic Resonance Spectroscopy | Rats | Proanthocyanidins - therapeutic use | Cell Degranulation - immunology | beta-N-Acetylhexosaminidases - secretion | Anti-Allergic Agents - therapeutic use | Animals | Leukemia, Basophilic, Acute - immunology | Signal Transduction - drug effects | Polyphenols - chemistry | Cell Line, Tumor | Polyphenols - therapeutic use | Plant Extracts - therapeutic use | Catechin - chemistry | Cell Degranulation - drug effects | Antiallergics
Journal Article
Journal of Ethnopharmacology, ISSN 0378-8741, 06/2012, Volume 142, Issue 1, pp. 253 - 258
The dried root of Aiton (Sophorae radix, SR) has long been used in traditional medicine for the treatment of fever and swelling in eastern countries. The...
Traditional Chinese medicine | Allergy | Inflammation | Mast cell | Contact dermatitis | Sophora flavescens | CHEMISTRY, MEDICINAL | FLAVONOIDS | PROLIFERATION | MECHANISMS | DELAYED-TYPE HYPERSENSITIVITY | HUMAN KERATINOCYTES | FIBROBLASTS | PLANT SCIENCES | INHIBITION | ELICITATION | INTEGRATIVE & COMPLEMENTARY MEDICINE | ROOTS | PHARMACOLOGY & PHARMACY | HISTAMINE | Sophora | Dermatitis, Allergic Contact - immunology | Plant Extracts - pharmacology | Male | Anti-Allergic Agents - pharmacology | Plant Roots | Histamine Release | Tumor Necrosis Factor-alpha - immunology | Anti-Inflammatory Agents - therapeutic use | Phytotherapy | Dermatitis, Allergic Contact - drug therapy | Cell Line | Edema - immunology | Anti-Inflammatory Agents - pharmacology | Rats | Mast Cells - physiology | Dinitrofluorobenzene | Edema - drug therapy | beta-N-Acetylhexosaminidases - immunology | Mast Cells - drug effects | Anti-Allergic Agents - therapeutic use | Animals | Interferon-gamma - immunology | Cell Line, Tumor | Mice | Mice, Inbred BALB C | Edema - chemically induced | Edema - pathology | Plant Extracts - therapeutic use | Cell Degranulation - drug effects | Skin | Medicine, Chinese | Dermatitis
Traditional Chinese medicine | Allergy | Inflammation | Mast cell | Contact dermatitis | Sophora flavescens | CHEMISTRY, MEDICINAL | FLAVONOIDS | PROLIFERATION | MECHANISMS | DELAYED-TYPE HYPERSENSITIVITY | HUMAN KERATINOCYTES | FIBROBLASTS | PLANT SCIENCES | INHIBITION | ELICITATION | INTEGRATIVE & COMPLEMENTARY MEDICINE | ROOTS | PHARMACOLOGY & PHARMACY | HISTAMINE | Sophora | Dermatitis, Allergic Contact - immunology | Plant Extracts - pharmacology | Male | Anti-Allergic Agents - pharmacology | Plant Roots | Histamine Release | Tumor Necrosis Factor-alpha - immunology | Anti-Inflammatory Agents - therapeutic use | Phytotherapy | Dermatitis, Allergic Contact - drug therapy | Cell Line | Edema - immunology | Anti-Inflammatory Agents - pharmacology | Rats | Mast Cells - physiology | Dinitrofluorobenzene | Edema - drug therapy | beta-N-Acetylhexosaminidases - immunology | Mast Cells - drug effects | Anti-Allergic Agents - therapeutic use | Animals | Interferon-gamma - immunology | Cell Line, Tumor | Mice | Mice, Inbred BALB C | Edema - chemically induced | Edema - pathology | Plant Extracts - therapeutic use | Cell Degranulation - drug effects | Skin | Medicine, Chinese | Dermatitis
Journal Article
Neurochemical Research, ISSN 0364-3190, 6/2012, Volume 37, Issue 6, pp. 1335 - 1343
Sandhoff Disease (SD) involves the CNS accumulation of ganglioside GM2 and asialo-GM2 (GA2) due to inherited defects in the β-subunit gene of β-hexosaminidase...
Biochemistry, general | Neurochemistry | Neurology | Neurosciences | Biomedicine | Stem cell | Sandhoff disease | Gangliosides | Cell Biology | Substrate reduction therapy | NERVOUS-SYSTEM | COMPLEX GANGLIOSIDES | BIOCHEMISTRY & MOLECULAR BIOLOGY | LYSOSOMAL STORAGE | BRAIN GANGLIOSIDE | THIN-LAYER CHROMATOGRAPHY | NEUROSCIENCES | N-BUTYLDEOXYNOJIRIMYCIN | MOUSE MODELS | GM1 GANGLIOSIDOSIS | TAY-SACHS | DISEASE MICE | 1-Deoxynojirimycin - therapeutic use | Animals | G(M2) Ganglioside | Hexosaminidase B - metabolism | Sandhoff Disease - drug therapy | Sandhoff Disease - therapy | Neural Stem Cells - transplantation | 1-Deoxynojirimycin - analogs & derivatives | Mice | beta-N-Acetylhexosaminidases - genetics | Stem cell research | Enzymes | Brain | Genes | Analysis | Stem cells | Physiological aspects | Transplantation | Health aspects | Drugs | beta N- double prime Acetylhexosaminidase | Central nervous system | Cortex | Ganglioside GM2 | Data processing | Neural stem cells | beta -Galactosidase | Sugar
Biochemistry, general | Neurochemistry | Neurology | Neurosciences | Biomedicine | Stem cell | Sandhoff disease | Gangliosides | Cell Biology | Substrate reduction therapy | NERVOUS-SYSTEM | COMPLEX GANGLIOSIDES | BIOCHEMISTRY & MOLECULAR BIOLOGY | LYSOSOMAL STORAGE | BRAIN GANGLIOSIDE | THIN-LAYER CHROMATOGRAPHY | NEUROSCIENCES | N-BUTYLDEOXYNOJIRIMYCIN | MOUSE MODELS | GM1 GANGLIOSIDOSIS | TAY-SACHS | DISEASE MICE | 1-Deoxynojirimycin - therapeutic use | Animals | G(M2) Ganglioside | Hexosaminidase B - metabolism | Sandhoff Disease - drug therapy | Sandhoff Disease - therapy | Neural Stem Cells - transplantation | 1-Deoxynojirimycin - analogs & derivatives | Mice | beta-N-Acetylhexosaminidases - genetics | Stem cell research | Enzymes | Brain | Genes | Analysis | Stem cells | Physiological aspects | Transplantation | Health aspects | Drugs | beta N- double prime Acetylhexosaminidase | Central nervous system | Cortex | Ganglioside GM2 | Data processing | Neural stem cells | beta -Galactosidase | Sugar
Journal Article
Journal of Neurochemistry, ISSN 0022-3042, 06/2010, Volume 113, Issue 6, pp. 1525 - 1535
J. Neurochem. (2010) 113, 1525–1535. Sandhoff disease is an autosomal recessive, neurodegenerative disease involving the storage of brain ganglioside GM2 and...
GA2 | ketogenic diet | lysosomal storage disease | GM2 | Sandhoff disease | ganglioside | Ganglioside | Lysosomal storage disease | Ketogenic diet | BONE-MARROW-TRANSPLANTATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | LYSOSOMAL STORAGE | THIN-LAYER CHROMATOGRAPHY | NEUROSCIENCES | MOUSE MODELS | AUDIOGENIC-SEIZURES | GANGLIOSIDE CONTENT | KETONE-BODIES | CEREBELLAR-ATAXIA | CALORIC RESTRICTION | GAUCHERS-DISEASE | Chromatography, High Pressure Liquid - methods | Sandhoff Disease - pathology | Body Weight - drug effects | G(M2) Ganglioside - metabolism | Myelin Sheath - metabolism | Brain - metabolism | 1-Deoxynojirimycin - therapeutic use | Sandhoff Disease - drug therapy | 1-Deoxynojirimycin - analogs & derivatives | beta-N-Acetylhexosaminidases - genetics | Brain - cytology | Purkinje Cells - metabolism | 3-Hydroxybutyric Acid - blood | Chromatography, Thin Layer - methods | Diet, Ketogenic - methods | Mice, Knockout | beta-N-Acetylhexosaminidases - deficiency | Blood Glucose - drug effects | Brain - drug effects | Sandhoff Disease - diet therapy | Eating - drug effects | Animals | Analysis of Variance | Lipid Metabolism - drug effects | Mice | Purkinje Cells - pathology | Physiological aspects | Nervous system diseases | Gangliosides | Analysis | Organic acids | Biochemistry | Genetic disorders | Diet | Rodents | Neurological disorders
GA2 | ketogenic diet | lysosomal storage disease | GM2 | Sandhoff disease | ganglioside | Ganglioside | Lysosomal storage disease | Ketogenic diet | BONE-MARROW-TRANSPLANTATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | LYSOSOMAL STORAGE | THIN-LAYER CHROMATOGRAPHY | NEUROSCIENCES | MOUSE MODELS | AUDIOGENIC-SEIZURES | GANGLIOSIDE CONTENT | KETONE-BODIES | CEREBELLAR-ATAXIA | CALORIC RESTRICTION | GAUCHERS-DISEASE | Chromatography, High Pressure Liquid - methods | Sandhoff Disease - pathology | Body Weight - drug effects | G(M2) Ganglioside - metabolism | Myelin Sheath - metabolism | Brain - metabolism | 1-Deoxynojirimycin - therapeutic use | Sandhoff Disease - drug therapy | 1-Deoxynojirimycin - analogs & derivatives | beta-N-Acetylhexosaminidases - genetics | Brain - cytology | Purkinje Cells - metabolism | 3-Hydroxybutyric Acid - blood | Chromatography, Thin Layer - methods | Diet, Ketogenic - methods | Mice, Knockout | beta-N-Acetylhexosaminidases - deficiency | Blood Glucose - drug effects | Brain - drug effects | Sandhoff Disease - diet therapy | Eating - drug effects | Animals | Analysis of Variance | Lipid Metabolism - drug effects | Mice | Purkinje Cells - pathology | Physiological aspects | Nervous system diseases | Gangliosides | Analysis | Organic acids | Biochemistry | Genetic disorders | Diet | Rodents | Neurological disorders
Journal Article