Suppression of diabetic retinopathy with GLUT1 siRNA

• Published in: Scientific reports 2017-08, Vol.7 (1), p.7437-10, Article 7437
• Main Authors: You, Zhi-Peng, Zhang, Yu-Lan, Shi, Ke, Shi, Lu, Zhang, Yue-Zhi, Zhou, Yue, Wang, Chang-yun
• Format: Article
• Language: English
• Subjects: 13/1; 13/51; 64/60; 692/163/2743; 692/699/2743/137/138; 82/80; 96/63; Animals; Cones; Diabetes; Diabetes mellitus; Diabetes Mellitus, Experimental - complications; Diabetes Mellitus, Experimental - genetics; Diabetes Mellitus, Experimental - metabolism; Diabetic retinopathy; Diabetic Retinopathy - genetics; Diabetic Retinopathy - metabolism; Diabetic Retinopathy - therapy; Electroretinograms; Electroretinography; Glucose; Glucose - metabolism; Glucose transport; Glucose transporter; Glucose Transporter Type 1 - antagonists & inhibitors; Glucose Transporter Type 1 - genetics; Humanities and Social Sciences; Immunoblotting; Intercellular adhesion molecule 1; Intercellular Adhesion Molecule-1 - metabolism; Intravitreal Injections; Leakage; Male; Mice; multidisciplinary; Oncogene Proteins - metabolism; Retina; Retina - metabolism; Retinal degeneration; Retinopathy; RNA, Small Interfering - administration & dosage; RNA, Small Interfering - pharmacology; Science; Science (multidisciplinary); siRNA; Transcriptional Regulator ERG - metabolism; Treatment Outcome; Tumor Necrosis Factor-alpha - metabolism; Tumor necrosis factor-α
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-017-07942-x

To investigate the effect of glucose transporter-1 (GLUT1) inhibition on diabetic retinopathy, we divided forty-eight mice into scrambled siRNA, diabetic scrambled siRNA, and GLUT1 siRNA (intravitreally injected) groups. Twenty-one weeks after diabetes induction, we calculated retinal glucose concentrations, used electroretinography (ERG) and histochemical methods to assess photoreceptor degeneration, and conducted immunoblotting, leukostasis and vascular leakage assays to estimate microangiopathy. The diabetic scrambled siRNA and GLUT1 siRNA exhibited higher glucose concentrations than scrambled siRNA, but GLUT1 siRNA group concentrations were only 50.05% of diabetic scrambled siRNA due to downregulated GLUT1 expression. The diabetic scrambled siRNA and GLUT1 siRNA had lower ERG amplitudes and ONL thicknesses than scrambled siRNA. However, compared with diabetic scrambled siRNA, GLUT1 siRNA group amplitudes and thicknesses were higher. Diabetic scrambled siRNA cones were more loosely arranged and had shorter outer segments than GLUT1 siRNA cones. ICAM-1 and TNF-α expression levels, adherent leukocyte numbers, fluorescence leakage areas and extravasated Evans blue in diabetic scrambled siRNA were higher than those in scrambled siRNA. However, these parameters in the GLUT1 siRNA were lower than diabetic scrambled siRNA. Together, these results demonstrate that GLUT1 siRNA restricted glucose transport by inhibiting GLUT1 expression, which decreased retinal glucose concentrations and ameliorated diabetic retinopathy.