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Luo Tong Formula Alleviates Diabetic Retinopathy in Rats Through Micro-200b Target

Aim: Diabetic retinopathy (DR) is a serious complication of diabetes (DM). Luo Tong formula (LTF) exerts protective effects against DR in rats, but its underlying mechanism remains unknown. Methods: Sprague-Dawley rats injected with streptozotocin (STZ) were used as an experimental diabetes model. L...

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Autores principales: Pang, Bing, Ni, Qing, Di, Sha, Du, Li-juan, Qin, Ya-li, Li, Qing-wei, Li, Min, Tong, Xiao-lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7723456/
https://www.ncbi.nlm.nih.gov/pubmed/33324202
http://dx.doi.org/10.3389/fphar.2020.551766
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author Pang, Bing
Ni, Qing
Di, Sha
Du, Li-juan
Qin, Ya-li
Li, Qing-wei
Li, Min
Tong, Xiao-lin
author_facet Pang, Bing
Ni, Qing
Di, Sha
Du, Li-juan
Qin, Ya-li
Li, Qing-wei
Li, Min
Tong, Xiao-lin
author_sort Pang, Bing
collection PubMed
description Aim: Diabetic retinopathy (DR) is a serious complication of diabetes (DM). Luo Tong formula (LTF) exerts protective effects against DR in rats, but its underlying mechanism remains unknown. Methods: Sprague-Dawley rats injected with streptozotocin (STZ) were used as an experimental diabetes model. LTF or calcium dobesilate (CaD) was administered to diabetic rats via gastric gavage. After the 12 weeks of treatment, blood and tissue samples were collected to determine serum glucose and retinal structure. Blood samples were collected for blood glucose and hemorheology analysis. Gene or protein expression levels were evaluated by immunohistochemistry, western blotting and/or quantitative real-time polymerase chain reaction (PCR). Results: DM rats exhibits significantly increased blood retinal-barrier (BRB) breakdown and VEGF/VEGFR expression in the retina, and decreased miR-200b and tight junction ZO-1/Occludin/ Claudin-5 genes expression, as well as Ang-1/Tie-2 expressions in the retina compared to normal control group. LTF treatment significantly moderated histological abnormalities in diabetic rats, independent of blood glucose level; improved some hemorrheological parameters; decreased the expressions of VEGF/VEGFR and BRB breakdown, significantly increased PEDF and tight junction proteins ZO-1/Occludin, as well as increased retinal miR-200b expression compared to non-treatment diabetic rats. Moreover, LTF prevented the reduction in Ang-1/Tie-2 expression. Conclusions: LTF treatment ameliorated DR through its repair vascular and attenuate vascular leakage. A mechanism involving miR-200b may contribute to benefit effects.
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spelling pubmed-77234562020-12-14 Luo Tong Formula Alleviates Diabetic Retinopathy in Rats Through Micro-200b Target Pang, Bing Ni, Qing Di, Sha Du, Li-juan Qin, Ya-li Li, Qing-wei Li, Min Tong, Xiao-lin Front Pharmacol Pharmacology Aim: Diabetic retinopathy (DR) is a serious complication of diabetes (DM). Luo Tong formula (LTF) exerts protective effects against DR in rats, but its underlying mechanism remains unknown. Methods: Sprague-Dawley rats injected with streptozotocin (STZ) were used as an experimental diabetes model. LTF or calcium dobesilate (CaD) was administered to diabetic rats via gastric gavage. After the 12 weeks of treatment, blood and tissue samples were collected to determine serum glucose and retinal structure. Blood samples were collected for blood glucose and hemorheology analysis. Gene or protein expression levels were evaluated by immunohistochemistry, western blotting and/or quantitative real-time polymerase chain reaction (PCR). Results: DM rats exhibits significantly increased blood retinal-barrier (BRB) breakdown and VEGF/VEGFR expression in the retina, and decreased miR-200b and tight junction ZO-1/Occludin/ Claudin-5 genes expression, as well as Ang-1/Tie-2 expressions in the retina compared to normal control group. LTF treatment significantly moderated histological abnormalities in diabetic rats, independent of blood glucose level; improved some hemorrheological parameters; decreased the expressions of VEGF/VEGFR and BRB breakdown, significantly increased PEDF and tight junction proteins ZO-1/Occludin, as well as increased retinal miR-200b expression compared to non-treatment diabetic rats. Moreover, LTF prevented the reduction in Ang-1/Tie-2 expression. Conclusions: LTF treatment ameliorated DR through its repair vascular and attenuate vascular leakage. A mechanism involving miR-200b may contribute to benefit effects. Frontiers Media S.A. 2020-10-30 /pmc/articles/PMC7723456/ /pubmed/33324202 http://dx.doi.org/10.3389/fphar.2020.551766 Text en Copyright © 2020 Pang, Ni, Di, Du, Qin, Li, Li and Tong http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Pang, Bing
Ni, Qing
Di, Sha
Du, Li-juan
Qin, Ya-li
Li, Qing-wei
Li, Min
Tong, Xiao-lin
Luo Tong Formula Alleviates Diabetic Retinopathy in Rats Through Micro-200b Target
title Luo Tong Formula Alleviates Diabetic Retinopathy in Rats Through Micro-200b Target
title_full Luo Tong Formula Alleviates Diabetic Retinopathy in Rats Through Micro-200b Target
title_fullStr Luo Tong Formula Alleviates Diabetic Retinopathy in Rats Through Micro-200b Target
title_full_unstemmed Luo Tong Formula Alleviates Diabetic Retinopathy in Rats Through Micro-200b Target
title_short Luo Tong Formula Alleviates Diabetic Retinopathy in Rats Through Micro-200b Target
title_sort luo tong formula alleviates diabetic retinopathy in rats through micro-200b target
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7723456/
https://www.ncbi.nlm.nih.gov/pubmed/33324202
http://dx.doi.org/10.3389/fphar.2020.551766
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