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Low-Level Laser Therapy with 670 nm Alleviates Diabetic Retinopathy in an Experimental Model

PURPOSE: To evaluate the effects of low-level laser therapy (LLLT) on the retina with diabetic retinopathy (DR). METHODS: Eight Wistar rats were used as a control group, and 64 rats were injected intraperitoneally with 55 mg/kg of streptozotocin to induce diabetes and served as a diabetic group. Aft...

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Autores principales: Ahmed, Salwa Abdelkawi, Ghoneim, Dina Fouad, Morsy, Mona Ebrahim, Hassan, Aziza Ahmed, Mahmoud, Abdel Rahman Hassan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8365584/
https://www.ncbi.nlm.nih.gov/pubmed/34409224
http://dx.doi.org/10.4103/joco.joco_29_20
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author Ahmed, Salwa Abdelkawi
Ghoneim, Dina Fouad
Morsy, Mona Ebrahim
Hassan, Aziza Ahmed
Mahmoud, Abdel Rahman Hassan
author_facet Ahmed, Salwa Abdelkawi
Ghoneim, Dina Fouad
Morsy, Mona Ebrahim
Hassan, Aziza Ahmed
Mahmoud, Abdel Rahman Hassan
author_sort Ahmed, Salwa Abdelkawi
collection PubMed
description PURPOSE: To evaluate the effects of low-level laser therapy (LLLT) on the retina with diabetic retinopathy (DR). METHODS: Eight Wistar rats were used as a control group, and 64 rats were injected intraperitoneally with 55 mg/kg of streptozotocin to induce diabetes and served as a diabetic group. After the establishment of the DR, the rats were separated into (a) 32 rats with DR; did not receive any treatment, (b) 32 rats with DR were exposed to 670 nm LLLT for 6 successive weeks (2 sessions/week). The retinal protein was analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, total antioxidant capacity (TAC), hydrogen peroxide (H(2)O(2)), and histological examination. RESULTS: LLLT improved retinal proteins such as neurofilament (NF) proteins (200 KDa, 160 KDa, and 86 KDa), neuron-specific enolase (NSE) (46 KDa). Moreover, the percentage changes in TAC were 46.8% (P < 0.001), 14.5% (P < 0.01), 4.8% and 1.6% (P > 0.05), and in H(2)O(2,) they were 30% (P < 0.001), 25% (P < 0.001), 20% (P < 0.01), and 5% (P > 0.05) after 1, 2, 4, and 6 weeks, compared with the control. DR displayed swelling and disorganization in the retinal ganglion cells (RGCs) and photoreceptors, congestion of the capillaries in the nerve fiber layer, thickening of the endothelial cells’ capillaries, and edema of the outer segment of the photoreceptors layer. The improvement of the retinal structure was achieved after LLLT. CONCLUSION: LLLT could modulate retinal proteins such as NSE and NFs, improve the RGCs, photoreceptors, and reduce the oxidative stress that originated in the retina from diabetes-induced DR.
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spelling pubmed-83655842021-08-17 Low-Level Laser Therapy with 670 nm Alleviates Diabetic Retinopathy in an Experimental Model Ahmed, Salwa Abdelkawi Ghoneim, Dina Fouad Morsy, Mona Ebrahim Hassan, Aziza Ahmed Mahmoud, Abdel Rahman Hassan J Curr Ophthalmol Original Article PURPOSE: To evaluate the effects of low-level laser therapy (LLLT) on the retina with diabetic retinopathy (DR). METHODS: Eight Wistar rats were used as a control group, and 64 rats were injected intraperitoneally with 55 mg/kg of streptozotocin to induce diabetes and served as a diabetic group. After the establishment of the DR, the rats were separated into (a) 32 rats with DR; did not receive any treatment, (b) 32 rats with DR were exposed to 670 nm LLLT for 6 successive weeks (2 sessions/week). The retinal protein was analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, total antioxidant capacity (TAC), hydrogen peroxide (H(2)O(2)), and histological examination. RESULTS: LLLT improved retinal proteins such as neurofilament (NF) proteins (200 KDa, 160 KDa, and 86 KDa), neuron-specific enolase (NSE) (46 KDa). Moreover, the percentage changes in TAC were 46.8% (P < 0.001), 14.5% (P < 0.01), 4.8% and 1.6% (P > 0.05), and in H(2)O(2,) they were 30% (P < 0.001), 25% (P < 0.001), 20% (P < 0.01), and 5% (P > 0.05) after 1, 2, 4, and 6 weeks, compared with the control. DR displayed swelling and disorganization in the retinal ganglion cells (RGCs) and photoreceptors, congestion of the capillaries in the nerve fiber layer, thickening of the endothelial cells’ capillaries, and edema of the outer segment of the photoreceptors layer. The improvement of the retinal structure was achieved after LLLT. CONCLUSION: LLLT could modulate retinal proteins such as NSE and NFs, improve the RGCs, photoreceptors, and reduce the oxidative stress that originated in the retina from diabetes-induced DR. Wolters Kluwer - Medknow 2021-07-05 /pmc/articles/PMC8365584/ /pubmed/34409224 http://dx.doi.org/10.4103/joco.joco_29_20 Text en Copyright: © 2021 Journal of Current Ophthalmology https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Ahmed, Salwa Abdelkawi
Ghoneim, Dina Fouad
Morsy, Mona Ebrahim
Hassan, Aziza Ahmed
Mahmoud, Abdel Rahman Hassan
Low-Level Laser Therapy with 670 nm Alleviates Diabetic Retinopathy in an Experimental Model
title Low-Level Laser Therapy with 670 nm Alleviates Diabetic Retinopathy in an Experimental Model
title_full Low-Level Laser Therapy with 670 nm Alleviates Diabetic Retinopathy in an Experimental Model
title_fullStr Low-Level Laser Therapy with 670 nm Alleviates Diabetic Retinopathy in an Experimental Model
title_full_unstemmed Low-Level Laser Therapy with 670 nm Alleviates Diabetic Retinopathy in an Experimental Model
title_short Low-Level Laser Therapy with 670 nm Alleviates Diabetic Retinopathy in an Experimental Model
title_sort low-level laser therapy with 670 nm alleviates diabetic retinopathy in an experimental model
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8365584/
https://www.ncbi.nlm.nih.gov/pubmed/34409224
http://dx.doi.org/10.4103/joco.joco_29_20
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