Kaempferide prevents cognitive decline via attenuation of oxidative stress and enhancement of brain‐derived neurotrophic factor/tropomyosin receptor kinase B/cAMP response element‐binding signaling pathway. (30th January 2019)

• Record Type: Journal Article
• Authors: Yan, Tingxu; He, Bosai; Xu, Mengjie; Wu, Bo; Xiao, Feng; Bi, Kaishun; Jia, Ying
• Is Part Of: Phytotherapy research. Volume 33:Number 4(2019)
• Page Start: 1065
• Page End: 1073
• Publication Date: 2019-01-30
• Subjects: Alzheimer's disease -- BDNF/TrkB/CREB -- kaempferide -- oxidative stress; Materia medica, Vegetable -- Periodicals; Botany, Medical -- Periodicals; Medicinal plants -- Periodicals; Plant Extracts -- therapeutic use -- Periodicals; Plants, Medicinal -- Periodicals; 581.634
• DOI: 10.1002/ptr.6300
• Languages: English
• ISSNs: 0951-418X

Abstract

Abstract : Kaempferide (KF) is a compound of flavonoids from Alpinae oxyphylla Miq, and the herb itself is used as a classical tonic agent. This paper aims to investigate the effects of KF on cognitive function impairment and neurodegeneration in the mouse model of Alzheimer's disease induced by intracerebroventricular (ICV) injection of Aβ1–42 . The mice were treated with KF at doses of 0.02 and 0.2 mg/kg/day (ICV) for five consecutive days after Aβ1–42 exposures. The behavioral test results showed that KF could prevent cognitive decline in mice induced by Aβ1–42 as assessed by the locomotor activity test, Y‐maze test, and Morris water maze test. Furthermore, the activities of superoxide dismutase and malondialdehyde in the hippocampus and cerebral cortex were elevated by KF administration. Results of hippocampus slices showed that neurons were integrated and regularly arranged in the groups, which were administered along with KF. In addition, we found KF could boost brain‐derived neurotrophic factor (BDNF)/tropomyosin receptor kinase B (TrkB)/cAMP response element‐binding (CREB) protein signal in the hippocampus. All results illustrated that KF could exert neuroprotective effects at least partly through alleviating oxidative stress and enhancing the BDNF/TrkB/CREB pathway in Aβ1–42 ‐induced mice.