Low glutathione peroxidase in rdl mouse retina increases oxidative stress and proteases

被引:20
作者
Ahuja-Jensen, Poonam
Johnsen-Soriano, Siv
Ahuja, Satpal [1 ]
Bosch-Morell, Francisco
Sancho-Tello, Maria
Romero, Francisco Javier
Abrahamson, Magnus
van Veen, Theo
机构
[1] Lund Univ, Klin Gatan, Wallenberg Retina Ctr, Dept Ophthalmol, S-22007 Lund, Sweden
[2] Lund Univ, Univ Hosp, Dept Lab Med, Div Clin Chem & Pharmacol, S-22007 Lund, Sweden
[3] Cardenal Herrera CEU Univ, Valencia 46113, Spain
[4] Mediterranean Ophthalmol Fdn, Valencia 46113, Spain
关键词
cysteine protease; glutathione system; malondialdehyde; oxidative stress; rd1; mice; retinal degeneration;
D O I
10.1097/WNR.0b013e3280c1e344
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Malondialdehyde, reduced glutathione, glutathione peroxidase, glutathione reductase and cysteine protease cathepsins at postnatal (PN) days 2, 7, 14, 21 and 28 in controls (wt) and the retinal degeneration 1 (rd1) mouse model for retinitis pigmentosa retinas were measured to determine oxidative stress. In PN28 wt and PN2 rd1 retinas, elevated malondialdehyde and low glutathione peroxidase activity indicate higher oxidative load, despite higher reduced glutathione in PN2 rd1 retinas. This is due to physiological exposure to light and retinal vascular/neural restructuring, respectively. Compared with wt retinas, relatively high malondialdehyde at PN2 and cathepsin levels at PN14, 21 and 28 in rd1 retinas indicate that cells of the residual inner retina also contribute to the oxidative stress and retinal degeneration.
引用
收藏
页码:797 / 801
页数:5
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