Cargando…

Ginsenoside Ameliorates Cognitive Dysfunction in Type 2 Diabetic Goto-Kakizaki Rats

BACKGROUND: Ginsenoside is the major bioactive component of ginseng, which has been proven to be a neuroprotective drug. The aim of this study was to evaluate the therapeutic effect of ginsenoside in a diabetic Goto-Kakizaki (GK) rat model. MATERIAL/METHODS: Twenty GK rats were randomly divided into...

Descripción completa

Detalles Bibliográficos
Autores principales: Tian, Zhiyan, Ren, Ning, Wang, Jinhua, Zhang, Danhong, Zhou, Yuying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6027254/
https://www.ncbi.nlm.nih.gov/pubmed/29886506
http://dx.doi.org/10.12659/MSM.907417
_version_ 1783336569014321152
author Tian, Zhiyan
Ren, Ning
Wang, Jinhua
Zhang, Danhong
Zhou, Yuying
author_facet Tian, Zhiyan
Ren, Ning
Wang, Jinhua
Zhang, Danhong
Zhou, Yuying
author_sort Tian, Zhiyan
collection PubMed
description BACKGROUND: Ginsenoside is the major bioactive component of ginseng, which has been proven to be a neuroprotective drug. The aim of this study was to evaluate the therapeutic effect of ginsenoside in a diabetic Goto-Kakizaki (GK) rat model. MATERIAL/METHODS: Twenty GK rats were randomly divided into a diabetic model (DM) group (n=10) and a ginsenoside + DM group (n=10); Wistar rats with the same age and body weight were used as the control (CON) group (n=10). Food and water intake, body weight, and blood fasting plasma glucose were measured. The Morris water maze test was used to detect learning and memory functions of the rats. Superoxide dismutase (SOD), malondialdehyde (MDA), and inflammatory cytokines (TNF-α, IL-1β, and IL-6) in the hippocampus were analyzed after ginsenoside treatment. RESULTS: The blood glucose, body weight, Morris correlation index, SOD, MDA, and other test results were increased in the diabetic rats. Ginsenoside ameliorated diabetic cognitive decline. CONCLUSIONS: The possible mechanism was related to inhibiting brain oxidative/nitrosative damage and affecting the expression of the cytokines IL-1β, IL-6, and TNF-α.
format Online
Article
Text
id pubmed-6027254
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher International Scientific Literature, Inc.
record_format MEDLINE/PubMed
spelling pubmed-60272542018-07-09 Ginsenoside Ameliorates Cognitive Dysfunction in Type 2 Diabetic Goto-Kakizaki Rats Tian, Zhiyan Ren, Ning Wang, Jinhua Zhang, Danhong Zhou, Yuying Med Sci Monit Animal Study BACKGROUND: Ginsenoside is the major bioactive component of ginseng, which has been proven to be a neuroprotective drug. The aim of this study was to evaluate the therapeutic effect of ginsenoside in a diabetic Goto-Kakizaki (GK) rat model. MATERIAL/METHODS: Twenty GK rats were randomly divided into a diabetic model (DM) group (n=10) and a ginsenoside + DM group (n=10); Wistar rats with the same age and body weight were used as the control (CON) group (n=10). Food and water intake, body weight, and blood fasting plasma glucose were measured. The Morris water maze test was used to detect learning and memory functions of the rats. Superoxide dismutase (SOD), malondialdehyde (MDA), and inflammatory cytokines (TNF-α, IL-1β, and IL-6) in the hippocampus were analyzed after ginsenoside treatment. RESULTS: The blood glucose, body weight, Morris correlation index, SOD, MDA, and other test results were increased in the diabetic rats. Ginsenoside ameliorated diabetic cognitive decline. CONCLUSIONS: The possible mechanism was related to inhibiting brain oxidative/nitrosative damage and affecting the expression of the cytokines IL-1β, IL-6, and TNF-α. International Scientific Literature, Inc. 2018-06-10 /pmc/articles/PMC6027254/ /pubmed/29886506 http://dx.doi.org/10.12659/MSM.907417 Text en © Med Sci Monit, 2018 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Animal Study
Tian, Zhiyan
Ren, Ning
Wang, Jinhua
Zhang, Danhong
Zhou, Yuying
Ginsenoside Ameliorates Cognitive Dysfunction in Type 2 Diabetic Goto-Kakizaki Rats
title Ginsenoside Ameliorates Cognitive Dysfunction in Type 2 Diabetic Goto-Kakizaki Rats
title_full Ginsenoside Ameliorates Cognitive Dysfunction in Type 2 Diabetic Goto-Kakizaki Rats
title_fullStr Ginsenoside Ameliorates Cognitive Dysfunction in Type 2 Diabetic Goto-Kakizaki Rats
title_full_unstemmed Ginsenoside Ameliorates Cognitive Dysfunction in Type 2 Diabetic Goto-Kakizaki Rats
title_short Ginsenoside Ameliorates Cognitive Dysfunction in Type 2 Diabetic Goto-Kakizaki Rats
title_sort ginsenoside ameliorates cognitive dysfunction in type 2 diabetic goto-kakizaki rats
topic Animal Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6027254/
https://www.ncbi.nlm.nih.gov/pubmed/29886506
http://dx.doi.org/10.12659/MSM.907417
work_keys_str_mv AT tianzhiyan ginsenosideamelioratescognitivedysfunctionintype2diabeticgotokakizakirats
AT renning ginsenosideamelioratescognitivedysfunctionintype2diabeticgotokakizakirats
AT wangjinhua ginsenosideamelioratescognitivedysfunctionintype2diabeticgotokakizakirats
AT zhangdanhong ginsenosideamelioratescognitivedysfunctionintype2diabeticgotokakizakirats
AT zhouyuying ginsenosideamelioratescognitivedysfunctionintype2diabeticgotokakizakirats