期刊文献+

High glucose levels impact visual response properties of retinal ganglion cells in C57 mice—An in vitro physiological study 被引量:5

High glucose levels impact visual response properties of retinal ganglion cells in C57 mice—An in vitro physiological study
原文传递
导出
摘要 This study investigated visual response properties of retinal ganglion cells(RGCs) under high glucose levels. Extracellular single-unit responses of RGCs from mouse retinas were recorded. And the eyecup was prepared as a flat mount in a recording chamber and superfused with Ames medium. The averaged RF size of the ON RGCs(34.1±2.9, n=14) was significantly smaller than the OFF RGCs under the HG(49.3±0.3, n=12)(P<0.0001) conditions. The same reduction pattern was also observed in the osmotic control group(HM) between ON and OFF RGCs(P<0.0001). The averaged luminance threshold(LT) of ON RGCs increased significantly under HG or HM(HG: P<0.0001; HM: P<0.0002). OFF RGCs exhibited a similar response pattern under the same conditions(HG: P<0.01; HM: P<0.0002). The averaged contrast gain of ON cells was significantly lower than that of OFF cells with the HM treatment(P<0.015, unpaired Student's t test). The averaged contrast gain of ON cells was significantly higher than OFF cells with the HG treatment(P<0.0001). The present results suggest that HG reduced receptive field center size, suppressed luminance threshold, and attenuated contrast gain of RGCs. The impact of HG on ON and OFF RGCs may be mediated via different mechanisms. This study investigated visual response properties of retinal ganglion cells(RGCs) under high glucose levels. Extracellular single-unit responses of RGCs from mouse retinas were recorded. And the eyecup was prepared as a flat mount in a recording chamber and superfused with Ames medium. The averaged RF size of the ON RGCs(34.1±2.9, n=14) was significantly smaller than the OFF RGCs under the HG(49.3±0.3, n=12)(P〈0.0001) conditions. The same reduction pattern was also observed in the osmotic control group(HM) between ON and OFF RGCs(P〈0.0001). The averaged luminance threshold(LT) of ON RGCs increased significantly under HG or HM(HG: P〈0.0001; HM: P〈0.0002). OFF RGCs exhibited a similar response pattern under the same conditions(HG: P〈0.01; HM: P〈0.0002). The averaged contrast gain of ON cells was significantly lower than that of OFF cells with the HM treatment(P〈0.015, unpaired Student's t test). The averaged contrast gain of ON cells was significantly higher than OFF cells with the HG treatment(P〈0.0001). The present results suggest that HG reduced receptive field center size, suppressed luminance threshold, and attenuated contrast gain of RGCs. The impact of HG on ON and OFF RGCs may be mediated via different mechanisms.
出处 《Science China(Life Sciences)》 SCIE CAS CSCD 2017年第12期1428-1435,共8页 中国科学(生命科学英文版)
基金 supported by the National Basic Research Program of China(2015CB351806 to Mingliang Pu) the National Science Foundation of China(31571091 to Mingliang Pu) the Science and Technology Planning Project of China Hunan Provincial Science and Technology Department(2015SK2046 to Chunxia Xiao)
关键词 retinal ganglion cells high glucose high mannitol receptive field center size luminance threshold contrast threshold retinal ganglion cells, high glucose, high mannitol, receptive field center size, luminance threshold, contrast threshold
作者简介 Corresponding authors (Chunxia Xiao, email: xiaochunxia-2006@163.com);Corresponding authors (Mingliang Pu, email: mpu@bjmu.edu.cn,mp_scl@yahoo.com)
  • 相关文献

参考文献5

二级参考文献156

  • 1Hiroaki Itamochi.Targeted therapies in epithelial ovarian cancer: Molecular mechanisms of action[J].World Journal of Biological Chemistry,2010,1(7):209-220. 被引量:14
  • 2Osborne NN, Casson RJ, Wood JPM, Chidlow G, Graham M, Melena J. Retinal ischemia: mechanisms of damage and potential therapeutic strategies. Prog Retin Eye Res, 2004, 23: 91-147.
  • 3Buchi ER. Cell death in the rat retina after a pressure-induced ischaemia-reperfusion insult: an electron microscopic study. I. Ganglion cell layer and inner nuclear layer. Exp Eye Res, 1992, 55: 605-613.
  • 4Lafuente MP, Villegas-Perez MP, Selles-Navarro I, MayorTorroglosa S, de Imperial JM, Vidal-Sanz M. Retinal ganglion cell death after acute retinal ischemia is an ongoing process whose severity and duration depends on the duration of the insult. Neuroscience, 2002, 109: 157-168.
  • 5Nucci C, Tartaglione R, Rombola L, Morrone LA, Fazzi E, Bagetta G. Neurochemical evidence to implicate elevated glutamate in the mechanisms of high intraocular pressure (IOP)-induced retinal ganglion cell death in rat. Neurotoxicology, 2005, 26: 935-941.
  • 6Yamamoto H, Schmidt-Kastner R, Hamasaki DI, Yamamoto H, Parel JM. Complex neurodegeneration in retina following moderate ischemia induced by bilateral common carotid artery occlusion in Wistar rats. Exp Eye Res, 2006, 82: 767-779.
  • 7Bringmann A, Francke M, Pannicke T, Biedermann B, Faude F, Enzmann V, Wiedemann P, Reichelt W, Reichenbach A. Human Muller glial cells: altered potassium channel activity in proliferative vitreoretinopathy. Invest Ophthalmol Vis Sci, 1999,40: 3316-3323.
  • 8Kim lB, Kim KY, Joo CK, Lee MY, Oh SJ, Chung JW, Chun MH. Reaction of Muller cells after increased intraocular pressure in the rat retina. Exp Brain Res, 1998, 121: 419-424.
  • 9Da T, Verkman AS. Aquaporin-4 gene disruption in mice protects against impaired retinal function and cell death after ischemia. Invest Ophthalmol Vis Sci, 2004, 45: 4477-4483.
  • 10Yanoff M, Fine BS, Brucker AJ, Eagle Jr. Ralph C. Pathology of human cystoid macular edema. Surv Ophthalmol, 1984, 28(Suppl): 505-511.

共引文献44

同被引文献14

引证文献5

二级引证文献8

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部