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作 者:Bing-Wen Lu Yu-Xiang Liang Jin-Feng Liu Zhong-Qing Sun Kwok-Fai So Kin Chiu
机构地区:[1]Department of Ophthalmology,Li Ka Shing Faculty of Medicine,The University of Hong Kong,Hong Kong,China [2]State Key Laboratory of Brain and Cognitive Sciences,The University of Hong Kong,Hong Kong,China [3]Department of Psychology,Faculty of Social Sciences,The University of Hong Kong,Hong Kong,China [4]Guangdong-Hongkong-Macao(GHM)Institute of CNS Regeneration,Ministry of Education,CNS Regeneration Collaborative Joint Laboratory,Jinan University,Guangzhou,China
出 处:《Advances in Ophthalmology Practice and Research》2023年第2期47-54,共8页眼科实践与研究新进展(英文)
基 金:supported by Midstream Research Programme for Universities,Hong Kong to Kin Chiu(Project No:MRP-092–17X).
摘 要:Background:Artesunate(ART),a member of the artemisinin family,possesses multi-properties,including antiinflammation,anti-oxidation,and anti-tumor.ART was recently reported to show anti-neovascularization effect on the cornea,iris,and retina.Compared to the expensive anti-VEGF treatment,this versatile,economical treatment option is attractive in the ophthalmic field.The safety and toxicity profile of ART intravitreal application are in utmost need.Methods:In this study,immortalized microglial(IMG)cells were treated with ART to determine the safe concentrations without inducing overt inflammatory reactions.Reverse transcription-polymerase chain reaction analysis was used to detect the cytokine expressions in IMG cells in response to ART stimulation.Various doses of ART were intravitreally injected into the right eyes of C57BL/6 mice.Retinal function was tested by electroretinogram,and retinal ganglion cell(RGC)survival was evaluated by counting Brn3a stained cells in flat-mounted retinas at 7 days after ART injection.Results:ART below 5μM was safe for IMG cells in vitro.Both 2.5 and 5μM ART treatment increased IL-10 gene expression in IMG cells while not changing IL-1β,IL-6,TNF-α,and Arg-1.In the in vivo study,intravitreal injection of ART below 100μM did not cause deterioration in the retinal function and RGC survival of the mouse eyes,while 1 mM ART treatment significantly attenuated both the scotopic and photopic b-wave amplitudes and impaired RGC survival.In addition,treatment with ART of 25,50,and 100μM significantly decreased TNF-αgene expression while ART of 100μM significantly increased IL-10 in the mouse retina.Conclusions:Intravitreal injection of 100μM ART could downregulate TNF-αwhile upregulate IL-10 in the mouse retina without causing retinal functional deterioration and RGC loss.ART might be used as anti-inflammatory agent for retinal disorders.
关 键 词:ARTESUNATE SAFETY RETINA MICROGLIA
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