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Anti-dementia Activity of Nobiletin, a Citrus Flavonoid: A Review of Animal Studies

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出版社

KOREAN COLL NEUROPSYCHOPHARMACOLOGY
DOI: 10.9758/cpn.2014.12.2.75

关键词

Nobiletin; Alzheimer's disease; Memory; Amyloid beta; Hyperphosphorylated tau; Oxidative stress; Cholinergic neurodegeneration

资金

  1. Grants for Project Research (Development of Fundamental Technology for Analysis and Evaluation of Functional Agricultural Products and Functional Foods) from the Ministry of Agriculture, Forestry, and Fisheries of Japan
  2. Grants for Strategic Research Program for Brain Sciences from the Ministry of Education, Culture, Sports, Science and Technology of Japan
  3. Japan Society for the Promotion of Science [22390046, 23659135, 23790290, 24111518]
  4. Smoking Research Foundation
  5. Brain Research Center from the 21st Century Frontier Research Program - Ministry of Science and Technology, Republic of Korea [2012k001115]
  6. Grants-in-Aid for Scientific Research [24111518, 23659135, 23790290] Funding Source: KAKEN

向作者/读者索取更多资源

Alzheimer's disease (AD), the most common form of dementia among the elderly, is characterized by the progressive decline of cognitive function and has a detrimental impact worldwide. Despite intensive laboratory and clinical research over the last three decades, pharmacological options for the prevention and effective long-term treatment of AD are not currently available. Consequently, successful therapeutic and preventive treatments for AD are needed. When researching materials from natural resources having anti dementia drug activity, we identified nobiletin, a polymethoxylated flavone from the peel of Citrus depressa. Nobiletin exhibited memory-improving effects in various animal models of dementia and exerted a wide range of beneficial effects against pathological features of AD including amyloid-beta (A beta) pathology, tau hyperphosphorylation, oxidative stress, cholinergic neurodegeneration and dysfunction of synaptic plasticity related signaling, suggesting this natural compound could become a novel drug for the treatment and prevention of AD.

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