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Protective effect of Naoxintong against cerebral ischemia reperfusion injury in mice.

Authors :
Xue, Jing
Zhang, Xiangjian
Zhang, Cong
Kang, Ning
Liu, Xiaoxia
Yu, Jingying
Zhang, Nan
Wang, Hong
Zhang, Lan
Chen, Rong
Cui, Lili
Wang, Lina
Wang, Xiaolu
Source :
Journal of Ethnopharmacology. Apr2016, Vol. 182, p181-189. 9p.
Publication Year :
2016

Abstract

Ethnopharmacological relevance Naoxintong (NXT), a renowned traditional Chinese medicine in China, has been used for the treatment of acute and chronic cardio-cerebrovascular diseases in clinic for more than 20 years. Aim of the study To evaluate the potential neuroprotective effect of NXT against ischemia reperfusion (I/R) injury in mice and investigate the underlying mechanisms. Materials and methods Focal cerebral I/R injury in adult male CD-1 mice was induced by transient middle cerebral artery occlusion (tMCAO) for 1 h followed by reperfusion for 23 h. Mice were randomly divided into five groups: Sham group; tMCAO group; Vehicle group; NXT-treated groups at doses of 0.36 g/kg and 0.54 g/kg. The effects of NXT on murine neurological function were estimated by neurological defect scores, infarct volume and brain water content at 24 h after tMCAO. Immunohistochemistry and Western blot were used to detect the expression of LOX-1, pERK1/2 and NF-κB at 24 h after tMCAO. qRT-PCR was used to detect the expression of LOX-1 and NF-κB at 24 h after tMCAO. Results Compared with Vehicle group, 0.54 g/kg group of NXT significantly ameliorated neurological outcome, infarction volume and brain water content, decreased the expression of LOX-1, pERK1/2 and NF-κB ( P <0.05). Conclusion NXT protected the mice brain against I/R injury, and this protection maybe associated with the down-regulation of LOX-1, pERK1/2 and NF-κB expression. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03788741
Volume :
182
Database :
Academic Search Index
Journal :
Journal of Ethnopharmacology
Publication Type :
Academic Journal
Accession number :
113666241
Full Text :
https://doi.org/10.1016/j.jep.2016.02.022