| Literature DB >> 30291956 |
Soo Jung Shin1, Yuon Jeong1, Seong Gak Jeon1, Sujin Kim1, Seong-Kyung Lee1, Hong Seok Choi1, Cheong Su Im1, Seong Hee Kim1, Soo Hwan Kim2, Jae Ho Park3, Jin-Il Kim4, Jwa-Jin Kim5, Minho Moon6.
Abstract
One of the pathological hallmarks of Alzheimer's disease (AD) is the abnormal aggregation of amyloid beta (Aβ) peptides. Uncaria rhynchophylla (UR), one of the Uncaria species, has long been used to treat neurodegenerative disease. In particular, it has been reported that UR inhibits aggregation of Aβ in vitro. However, little is known about the histological effects of UR treatment on Aβ pathology in AD animal models. In the present study, we investigated the effect of UR on Aβ aggregation, Aβ-mediated pathologies and adult hippocampal neurogenesis in the brain of 5XFAD mice. First, using the thioflavin T assay and amyloid staining, we demonstrated that UR treatment effectively inhibited Aβ aggregation and accumulation in the cortex and subiculum. Second, immunofluorescence staining showed that administration of UR attenuated gliosis and neurodegeneration in the subiculum and cortex. Third, UR treatment ameliorated impaired adult hippocampal neurogenesis. The present results indicate that UR significantly alleviates Aβ deposition and Aβ-mediated neuropathology in the brain in 5XFAD mice, suggesting the potency of UR as a preventive and therapeutic agent for AD.Entities:
Keywords: Adult hippocampal neurogenesis; Alzheimer's disease; Amyloid beta; Neurodegeneration; Neuroinflammation; Uncaria rhynchophylla
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Year: 2018 PMID: 30291956 DOI: 10.1016/j.neuint.2018.10.003
Source DB: PubMed Journal: Neurochem Int ISSN: 0197-0186 Impact factor: 3.921