Spirulina maxima Extract Ameliorates Learning and Memory Impairments via Inhibiting GSK-3 beta Phosphorylation Induced by Intracerebroventricular Injection of Amyloid-beta 1-42 in Miceopen access
- Authors
- Koh, Eun-Jeong; Kim, Kui-Jin; Song, Ji-Hyeon; Choi, Jia; Lee, Hyeon Yong; Kang, Do-Hyung; Heo, Ho Jin; Lee, Boo-Yong
- Issue Date
- Nov-2017
- Publisher
- Multidisciplinary Digital Publishing Institute (MDPI)
- Keywords
- cognitive impairment; Spirulina maxima 70% ethanol extract (SM70EE); amyloid precursor protein (APP) processing; oxidative stress; glycogen synthase kinase-3 beta (GSK-3)
- Citation
- International Journal of Molecular Sciences, v.18, no.11
- Indexed
- SCIE
SCOPUS
- Journal Title
- International Journal of Molecular Sciences
- Volume
- 18
- Number
- 11
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/13373
- DOI
- 10.3390/ijms18112401
- ISSN
- 1661-6596
1422-0067
- Abstract
- Spirulina maxima, a microalga containing high levels of protein and many polyphenols, including chlorophyll a and C-phycocyanin, has antioxidant and anti-inflammatory therapeutic effects. However, the mechanisms where by Spirulina maxima ameliorates cognitive disorders induced by amyloid-beta 1-42 (A beta(1-42)) are not fully understood. In this study, we investigated whether a 70% ethanol extract of Spirulina maxima (SM70EE) ameliorated cognitive impairments induced by an intracerebroventricular injection of A beta(1-42) in mice. SM70EE increased the step-through latency time in the passive avoidance test and decreased the escape latency time in the Morris water maze test in A beta(1-42)-injected mice. SM70EE reduced hippocampal A beta(1-42) levels and inhibited amyloid precursor protein processing-associated factors in A beta(1-42)-injected mice. Additionally, acetylcholinesterase activity was suppressed by SM70EE in A beta(1-42)-injected mice. Hippocampal glutathione levels were examined to determine the effects of SM70EE on oxidative stress in A beta(1-42)-injected mice. SM70EE increased the levels of glutathione and its associated factors that were reduced in A beta(1-42)-injected mice. SM70EE also promoted activation of the brain-derived neurotrophic factor/phosphatidylinositol-3 kinase/serine/threonine protein kinase signaling pathway and inhibited glycogen synthase kinase-3 phosphorylation. These findings suggested that SM70EE ameliorated A beta(1-42)-induced cognitive impairments by inhibiting the increased phosphorylation of glycogen synthase kinase-3 caused by intracerebroventricular injection of A beta(1-42) in mice.
- Files in This Item
- There are no files associated with this item.
- Appears in
Collections - ETC > Journal Articles

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.