CX3CR1 mediates the neuroprotective effect of triptolide on 1-methyl-4-phenylpyridinium-induced hemiparkinson rats
10.3969/j.issn.1000-4718.2015.04.015
- VernacularTitle:CX3CR1参与雷公藤内酯对MPP＋帕金森病大鼠多巴胺能神经元的保护作用
- Author:
Ziyi ZHOU
;
Junpeng GAO
;
Jun XIANG
;
Yiping CHEN
;
Yefeng CAI
;
Enli LUO
;
Dingfang CAI
- Publication Type:Journal Article
- Keywords:
Parkinson’ s disease;
Microglia;
Triptolide;
Dopaminergic neuron
- From:
Chinese Journal of Pathophysiology
2015;33(4):659-663
- CountryChina
- Language:Chinese
-
Abstract:
[ ABSTRACT] AIM:To investigate the effect of triptolide on the inhibition of microglial activation in 1-methyl-4-phenyl pyridinium ( MPP+)-induced hemiparkinson disease rats.METHODS:The rat model of Parkinson disease was es-tablished by intranigral injection of MPP +.The rats were randomly divided into sham group, MPP+group, triptolide group and vehicle group.The survival of dopaminergic neurons was detected by the immunofluorescence of tyrosine hydroxylase ( TH) in the substantia nigra ( SN) .The activation of microglia was determined by immunofluorescence of OX-42 ( micro-glia marker) in the SN.The expression of chemokine receptor CX3CR1 in SN was measured by Western blotting.RE-SULTS:Intranigral injection of MPP+increased the fluorescence intensity of the microglial marker, and promoted DA neu-ron degenerative death.Immunohistological analysis showed that the OX-42 density was decreased (P<0.01) and tyrosine hydroxylase (TH) positive neurons were increased in the triptolide group (P<0.01).The expression of CX3CR1 was lower in triptolide group than that in model group (P<0.05).CONCLUSION:Triptolide may improve PA neurons func-tion in MPP+-induced rats through inhibiting CX3CR1 expression and microglial activation.
