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Cited 33 time in webofscience Cited 40 time in scopus
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Ethyl acetate fraction from Hibiscus sabdariffa L. attenuates diabetes-associated cognitive impairment in mice

Authors
Seung, Tae WanPark, Seon KyeongKang, Jin YongKim, Jong MinPark, Sang HyunKwon, Bong SeokLee, Chang JunKang, Jeong EunKim, Dae OkLee, UkHeo, Ho Jin
Issue Date
Mar-2018
Publisher
Elsevier BV
Keywords
Hibiscus sabdariffa L.; Streptozotocin; Diabetes mellitus; Cognitive function
Citation
Food Research International, v.105, pp 589 - 598
Pages
10
Indexed
SCI
SCIE
SCOPUS
Journal Title
Food Research International
Volume
105
Start Page
589
End Page
598
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/11840
DOI
10.1016/j.foodres.2017.11.063
ISSN
0963-9969
1873-7145
Abstract
The ameliorating effects of the ethyl acetate fraction from Hibiscus sabdariffa L. (EFHS)(2) against diabetes mellitus (DM)(3) and DM-induced cognitive impairment were investigated on streptozotocin (STZ)(4)-induced DM mice. The EFHS groups showed improved hyperglycemia and glucose tolerance compared to the STZ group. Furthermore, their liver and kidney function and lipid metabolic imbalance in the blood serum were effectively recovered. The EFHS groups significantly ameliorated STZ-induced cognitive impairment in Y-maze, passive avoidance, and Morris water maze (MWM)(6) tests. The EFHS groups showed significant improvement in the antioxidant and cholinergic systems of the brain tissue. In addition, EFHS had an excellent ameliorating effect on protein expression levels from the tau hyperphosphorylation pathways, such as phospho-c-Jun N-terminal kinases (p-JNK),(6) phospho-tau (p-tau),(7) and cleaved poly (ADP-ribose) polymerase (c-PARP).(8) The main compounds of EFHS were identified as various phenolic compounds, including hibiscus acid, caffeoylquinic acid (CQA)(9) isomers, and quercetin derivates. Therefore, EFHS containing various physiologically active materials can potentially be used for improving DM-induced cognitive impairment via its antioxidant activity, improvement of the cholinergic system, and hyperphosphorylation tau signaling.
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