International journal of molecular sciences, 2018-12, Vol.19 (12), p.4026
2018
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- Autor(en) / Beteiligte
- Titel
- Jowiseungchungtang Inhibits Amyloid-β Aggregation and Amyloid-β-Mediated Pathology in 5XFAD Mice
- Ist Teil von
- International journal of molecular sciences, 2018-12, Vol.19 (12), p.4026
- Ort / Verlag
- Switzerland: MDPI AG
- Erscheinungsjahr
- 2018
- Quelle
- EZB-FREE-00999 freely available EZB journals
- Beschreibungen/Notizen
- Alzheimer's disease (AD) is a neurodegenerative disease, which is accompanied by memory loss and cognitive dysfunction. Although a number of trials to treat AD are in progress, there are no drugs available that inhibit the progression of AD. As the aggregation of amyloid-β (Aβ) peptides in the brain is considered to be the major pathology of AD, inhibition of Aβ aggregation could be an effective strategy for AD treatment. Jowiseungchungtang (JWS) is a traditional oriental herbal formulation that has been shown to improve cognitive function in patients or animal models with dementia. However, there are no reports examining the effects of JWS on Aβ aggregation. Thus, we investigated whether JWS could protect against both Aβ aggregates and Aβ-mediated pathology such as neuroinflammation, neurodegeneration, and impaired adult neurogenesis in 5 five familial Alzheimer's disease mutations (5XFAD) mice, an animal model for AD. In an in vitro thioflavin T assay, JWS showed a remarkable anti-Aβ aggregation effect. Histochemical analysis indicated that JWS had inhibitory effects on Aβ aggregation, Aβ-induced pathologies, and improved adult hippocampal neurogenesis in vivo. Taken together, these results suggest the therapeutic possibility of JWS for AD targeting Aβ aggregation, Aβ-mediated neurodegeneration, and impaired adult hippocampal neurogenesis.
- Sprache
- Englisch
- Identifikatoren
- ISSN: 1422-0067, 1661-6596eISSN: 1422-0067DOI: 10.3390/ijms19124026Titel-ID: cdi_doaj_primary_oai_doaj_org_article_adce800b42684ca38ad0ed81dc775cb6
- Format
- –
- Schlagworte
- 5XFAD mice, Administration, Oral, adult hippocampal neurogenesis, Alzheimer Disease - drug therapy, Alzheimer Disease - genetics, Alzheimer Disease - metabolism, Alzheimer's disease, Amyloid beta-Peptides - metabolism, amyloid-β, Animal cognition, Animal models, Animals, Brain, Clinical trials, Cognitive ability, Dementia disorders, Disease Models, Animal, Drugs, Chinese Herbal - administration & dosage, Drugs, Chinese Herbal - pharmacology, Enzymes, Female, Hippocampus, Hippocampus - cytology, Hippocampus - drug effects, Hippocampus - metabolism, Histochemical analysis, Humans, Hypotheses, Inflammation, jowiseungchungtang, Memory, Mice, Mutation, Neurodegeneration, Neurogenesis, neuroinflammation, Neurotoxicity, Pathology, Peptides, Protein Aggregates - drug effects, β-Amyloid