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Dendropanax morbifera Léveille extract ameliorates cadmium-induced impairment in memory and hippocampal neurogenesis in rats

Cited 21 time in Web of Science Cited 21 time in Scopus
Authors

Kim, Woosuk; Yim, Hee Sun; Yoo, Dae Young; Jung, Hyo Young; Kim, Jong Whi; Choi, Jung Hoon; Yoon, Yeo Sung; Kim, Dae Won; Hwang, In Koo

Issue Date
2016-11-09
Publisher
BioMed Central
Citation
BMC Complementary and Alternative Medicine, 16(1):452
Keywords
Dendropanax morbifera extractCadmiumNeurogenesisMemoryAcetylcholinesterase
Description
This article is distributed under the terms of the Creative Commons Attribution 4.0
International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and
reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to
the Creative Commons license, and indicate if changes were made.
Abstract
Abstract

Background
Cadmium leads to learning and memory impairment. Dendropanax morbifera Léveille stem extract (DMS) reduces cadmium-induced oxidative stress in the hippocampus. We investigated the effects of DMS on cadmium-induced impairments in memory in rats.


Methods
Cadmium (2mg/kg), with or without DMS (100mg/kg), was orally administered to 7-week-old Sprague-Dawley rats for 28days. Galantamine (5mg/kg), an acetylcholinesterase inhibitor, was intraperitoneally administered as a positive control. A novel-object recognition test was conducted 2h after the final administration. Cell proliferation and neuroblast differentiation were assessed by immunohistochemistry for Ki67 and doublecortin, respectively. Acetylcholinesterase activity in the synaptosomes of the hippocampus was also measured based on the formation of 5,5′-dithio-bis-acid nitrobenzoic acid.


Results
An increase in the preferential exploration time of new objects was observed in both vehicle-treated and cadmium-treated rats. In addition, DMS administration increased cell proliferation and neuroblast differentiation in the dentate gyrus of vehicle-treated and cadmium-treated rats. Acetylcholinesterase activity in the hippocampal synaptosomes was also significantly higher in the DMS-treated group than in the vehicle-treated group. The effect of DMS on cadmium-induced memory impairment and cell proliferation in the hippocampus was comparable to that of galantamine.


Conclusions
These results suggest that DMS ameliorates cadmium-induced memory impairment via increase in cell proliferation, neuroblast differentiation, and acetylcholinesterase activity in the hippocampus. The consumption of DMS may reduce cadmium-induced neurotoxicity in animals or humans.
Language
English
URI
https://hdl.handle.net/10371/100446
DOI
https://doi.org/10.1186/s12906-016-1435-z
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