Anti-epileptic effect of Ganoderma lucidum polysaccharides by inhibition of intracellular calcium accumulation and stimulation of expression of CaMKII a in epileptic hippocampal neurons
dc.contributor.author | Wang, Shu-Qiu | en |
dc.contributor.author | Li, Xiao-Jie | en |
dc.contributor.author | Qiu, Hong-Bin | en |
dc.contributor.author | Jiang, Zhi-Mei | en |
dc.contributor.author | Simon, Maria | en |
dc.contributor.author | Ma, Xiao-Ru | en |
dc.contributor.author | Liu, Lei | en |
dc.contributor.author | Li, Jun-Xing | en |
dc.contributor.author | Wang, Fang-Fang | en |
dc.contributor.author | Liang, Yan-Feng | en |
dc.contributor.author | Wu, Jia-Mei | en |
dc.contributor.author | Di, Wei-Hua | en |
dc.contributor.author | Zhou, Shaobo | en |
dc.date.accessioned | 2017-09-25T11:39:07Z | |
dc.date.available | 2017-09-25T11:39:07Z | |
dc.date.issued | 2014-07-10 | |
dc.identifier.citation | Wang SQ, Li, XJ, Q HB, Jiang ZM, Simon M, Ma XR, Liu L, Li JX, Wang FF, LIang YF, Wu JM, Di WH, Zou S (2014) 'Anti-epileptic effect of Ganoderma lucidum polysaccharides by inhibition of intracellular calcium accumulation and stimulation of expression of CaMKII a in epileptic hippocampal neurons', PLoS ONE, 9 (7) e102161. | en |
dc.identifier.issn | 1932-6203 | |
dc.identifier.pmid | 25010576 | |
dc.identifier.doi | 10.1371/journal.pone.0102161 | |
dc.identifier.uri | http://hdl.handle.net/10547/622234 | |
dc.description.abstract | Purpose: To investigate the mechanism of the anti-epileptic effect of Ganoderma lucidum polysaccharides (GLP), the changes of intracellular calcium and CaMK II a expression in a model of epileptic neurons were investigated. Method: Primary hippocampal neurons were divided into: 1) Control group, neurons were cultured with Neurobasal medium, for 3 hours; 2) Model group I: neurons were incubated with Mg2+ free medium for 3 hours; 3) Model group II: neurons were incubated with Mg2+ free medium for 3 hours then cultured with the normal medium for a further 3 hours; 4) GLP group I: neurons were incubated with Mg2+ free medium containing GLP (0.375 mg/ml) for 3 hours; 5) GLP group II: neurons were incubated with Mg2+ free medium for 3 hours then cultured with a normal culture medium containing GLP for a further 3 hours. The CaMK II a protein expression was assessed by Western-blot. Ca2+ turnover in neurons was assessed using Fluo-3/AM which was added into the replacement medium and Ca2+ turnover was observed under a laser scanning confocal microscope. Results: The CaMK II a expression in the model groups was less than in the control groups, however, in the GLP groups, it was higher than that observed in the model group. Ca2+ fluorescence intensity in GLP group I was significantly lower than that in model group I after 30 seconds, while in GLP group II, it was reduced significantly compared to model group II after 5 minutes. Conclusion: GLP may inhibit calcium overload and promote CaMK II a expression to protect epileptic neurons | |
dc.language.iso | en | en |
dc.publisher | PLOS | en |
dc.relation.url | http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0102161 | en |
dc.rights | Green - can archive pre-print and post-print or publisher's version/PDF | |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
dc.subject | epilepsy | en |
dc.subject | Ganoderma lucidum | en |
dc.title | Anti-epileptic effect of Ganoderma lucidum polysaccharides by inhibition of intracellular calcium accumulation and stimulation of expression of CaMKII a in epileptic hippocampal neurons | en |
dc.type | Article | en |
dc.contributor.department | Jiamusi University | en |
dc.contributor.department | University of Bedfordshire | en |
dc.identifier.journal | PLoS ONE | en |
dc.identifier.pmcid | PMC4092074 | |
dc.date.updated | 2017-09-25T11:16:36Z | |
dc.description.note | open access | |
html.description.abstract | Purpose: To investigate the mechanism of the anti-epileptic effect of Ganoderma lucidum polysaccharides (GLP), the changes of intracellular calcium and CaMK II a expression in a model of epileptic neurons were investigated. Method: Primary hippocampal neurons were divided into: 1) Control group, neurons were cultured with Neurobasal medium, for 3 hours; 2) Model group I: neurons were incubated with Mg2+ free medium for 3 hours; 3) Model group II: neurons were incubated with Mg2+ free medium for 3 hours then cultured with the normal medium for a further 3 hours; 4) GLP group I: neurons were incubated with Mg2+ free medium containing GLP (0.375 mg/ml) for 3 hours; 5) GLP group II: neurons were incubated with Mg2+ free medium for 3 hours then cultured with a normal culture medium containing GLP for a further 3 hours. The CaMK II a protein expression was assessed by Western-blot. Ca2+ turnover in neurons was assessed using Fluo-3/AM which was added into the replacement medium and Ca2+ turnover was observed under a laser scanning confocal microscope. Results: The CaMK II a expression in the model groups was less than in the control groups, however, in the GLP groups, it was higher than that observed in the model group. Ca2+ fluorescence intensity in GLP group I was significantly lower than that in model group I after 30 seconds, while in GLP group II, it was reduced significantly compared to model group II after 5 minutes. Conclusion: GLP may inhibit calcium overload and promote CaMK II a expression to protect epileptic neurons |