Photobiomodulation Mitigates Diabetes-Induced Retinopathy by Direct and Indirect Mechanisms: Evidence from Intervention Studies in Pigmented Mice

被引:49
|
作者
Saliba, Alexandra [1 ,2 ]
Du, Yunpeng [1 ]
Liu, Haitao [1 ]
Patel, Shyam [3 ]
Roberts, Robin [3 ]
Berkowitz, Bruce A. [3 ,4 ]
Kern, Timothy S. [1 ,5 ]
机构
[1] Case Western Reserve Univ, Cleveland, OH 44106 USA
[2] Univ Catolica Brasilia, Brasilia, DF, Brazil
[3] Wayne State Univ, Dept Anat & Cell Biol, Detroit, MI USA
[4] Wayne State Univ, Dept Ophthalmol, Detroit, MI USA
[5] Cleveland Vet Affairs Med Ctr, Res Serv 151, Cleveland, OH USA
来源
PLOS ONE | 2015年 / 10卷 / 10期
关键词
MANGANESE-ENHANCED MRI; NEAR-INFRARED LIGHT; MESENCHYMAL STEM-CELLS; LASER IRRADIATION; MOUSE MODEL; OXIDATIVE STRESS; HEME OXYGENASE-1; BONE-MARROW; ION DEMAND; IN-VIVO;
D O I
10.1371/journal.pone.0139003
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Objective Daily application of far-red light from the onset of diabetes mitigated diabetes-induced abnormalities in retinas of albino rats. Here, we test the hypothesis that photobiomodulation (PBM) is effective in diabetic, pigmented mice, even when delayed until weeks after onset of diabetes. Direct and indirect effects of PBM on the retina also were studied. Methods Diabetes was induced in C57Bl/6J mice using streptozotocin. Some diabetics were exposed to PBM therapy (4 min/day; 670 nm) daily. In one study, mice were diabetic for 4 weeks before initiation of PBM for an additional 10 weeks. Retinal oxidative stress, inflammation, and retinal function were measured. In some mice, heads were covered with a lead shield during PBM to prevent direct illumination of the eye, or animals were treated with an inhibitor of heme oxygenase-1. In a second study, PBM was initiated immediately after onset of diabetes, and administered daily for 2 months. These mice were examined using manganese-enhanced MRI to assess effects of PBM on transretinal calcium channel function in vivo. Results PBM intervention improved diabetes-induced changes in superoxide generation, leukostasis, expression of ICAM-1, and visual performance. PBM acted in part remotely from the retina because the beneficial effects were achieved even with the head shielded from the light therapy, and because leukocyte-mediated cytotoxicity of retinal endothelial cells was less in diabetics treated with PBM. SnPP+PBM significantly reduced iNOS expression compared to PBM alone, but significantly exacerbated leukostasis. In study 2, PBM largely mitigated diabetes-induced retinal calcium channel dysfunction in all retinal layers. Conclusions PBM induces retinal protection against abnormalities induced by diabetes in pigmented animals, and even as an intervention. Beneficial effects on the retina likely are mediated by both direct and indirect mechanisms. PBM is a novel non-pharmacologic treatment strategy to inhibit early changes of diabetic retinopathy.
引用
收藏
页数:14
相关论文
共 1 条