Protective effects of piceatannol on retinal ganglion cells in experimental glaucoma rats
10.13389/j.cnki.rao.2017.0133
- VernacularTitle:白皮杉醇对青光眼大鼠视网膜神经节细胞的保护作用
- Author:
Qian DU
;
Xu HOU
;
Jianbo LI
;
Fengren ZHOU
;
Chen DU
- Keywords:
piceatannol;
retinal ganglion cells;
MARK signaling pathway
- From:
Recent Advances in Ophthalmology
2017;37(6):527-530,547
- CountryChina
- Language:Chinese
-
Abstract:
Objective To investigate the protective effects of piceatannol on retinal ganglion cells (RGCs) in rats with glaucoma.Methods Forty rats were randomly divided into 4 groups:control group,model group,low dose piceatannol treatment group and high dose piceatannol treatment group.Photocoagulation method was used to establish the experimental glaucoma model in rats,and then rats were given 100 mg· kg-1 or 200 mg · kg-1 of piceatannol by gavage.The intraocular pressure was measured before and after the model was established.Rat retinal ganglion cells were labeled and counted using FG staining.Retinal tissue pathological morphology was observed by HE staining.The protein expression of p-JNK,p-c-Jun,p-ERK,p-p38 MAPK and TNF-α were measured by western blot.Results Compared with control group,the intraocular pressure,the protein expressions of p-JNK,p-c-Jun p-ERK,p-p38 MAPK and TNF-α were significantly increased in model group (all P < 0.05).However,the number of RGCs were lower in model group(P <0.05).Furthermore,there were cavitation and edema changes in retinal tissue of model group.Compared with model group,piceatannol treatment markediy increased the number of RGCs(P =0.003,0.002),improved the pathological morphology of retinal tissue,and reduced the protein expressions of p-JNK,p-c-Jun p-ERK,p-p38 MAPK and TNF-α (all P < 0.05),especially for the high concentration.Conclusion Piceatannol can protect against RGCs injury in glaucoma rats,and the mechanism may be associated with inhibition of MARK signaling pathway.