Sodium Salicylate Reduced Insulin Resistance in the Retina of a Type 2 Diabetic Rat Model
Sodium salicylate has been reported to reduce markers of diabetic retinopathy in a type 1 rat model. Because rates of type 2 diabetes are on the rise, we wanted to determine whether salicylate could improve insulin resistance in a type 2 rat model, as well as improve retinal function. We treated lea...
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Published in | PloS one Vol. 10; no. 4; p. e0125505 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
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14.04.2015
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Abstract | Sodium salicylate has been reported to reduce markers of diabetic retinopathy in a type 1 rat model. Because rates of type 2 diabetes are on the rise, we wanted to determine whether salicylate could improve insulin resistance in a type 2 rat model, as well as improve retinal function. We treated lean and obese BBZDR/Wor type 2 diabetic rats with salicylate in their chow for 2 months. Prior to salicylate treatment, rats underwent an electroretinogram to measure retinal function. After 2 months of treatment, rats underwent an additional electroretinogram prior to sacrifice. In addition to the animal model, we also treated retinal endothelial cells (REC) and rat Müller cells with salicylate and performed the same analyses as done for the rat retinal lysates. To investigate the role of salicylate in insulin signaling, we measured TNFα and caspase 3 levels by ELISA, as well as performed Western blotting for insulin receptor substrate 1, insulin receptor, SOCS3, and pro- and anti-apoptotic markers. Data demonstrated that salicylate significantly improved retinal function, as well as reduced TNFα and SOCS3-induced insulin resistance in all samples. Overall, results suggest that salicylate is effective in reducing insulin resistance in the retina of type 2 diabetic rat models. |
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AbstractList | Sodium salicylate has been reported to reduce markers of diabetic retinopathy in a type 1 rat model. Because rates of type 2 diabetes are on the rise, we wanted to determine whether salicylate could improve insulin resistance in a type 2 rat model, as well as improve retinal function. We treated lean and obese BBZDR/Wor type 2 diabetic rats with salicylate in their chow for 2 months. Prior to salicylate treatment, rats underwent an electroretinogram to measure retinal function. After 2 months of treatment, rats underwent an additional electroretinogram prior to sacrifice. In addition to the animal model, we also treated retinal endothelial cells (REC) and rat Müller cells with salicylate and performed the same analyses as done for the rat retinal lysates. To investigate the role of salicylate in insulin signaling, we measured TNFα and caspase 3 levels by ELISA, as well as performed Western blotting for insulin receptor substrate 1, insulin receptor, SOCS3, and pro- and anti-apoptotic markers. Data demonstrated that salicylate significantly improved retinal function, as well as reduced TNFα and SOCS3-induced insulin resistance in all samples. Overall, results suggest that salicylate is effective in reducing insulin resistance in the retina of type 2 diabetic rat models. Sodium salicylate has been reported to reduce markers of diabetic retinopathy in a type 1 rat model. Because rates of type 2 diabetes are on the rise, we wanted to determine whether salicylate could improve insulin resistance in a type 2 rat model, as well as improve retinal function. We treated lean and obese BBZDR/Wor type 2 diabetic rats with salicylate in their chow for 2 months. Prior to salicylate treatment, rats underwent an electroretinogram to measure retinal function. After 2 months of treatment, rats underwent an additional electroretinogram prior to sacrifice. In addition to the animal model, we also treated retinal endothelial cells (REC) and rat Müller cells with salicylate and performed the same analyses as done for the rat retinal lysates. To investigate the role of salicylate in insulin signaling, we measured TNF[alpha] and caspase 3 levels by ELISA, as well as performed Western blotting for insulin receptor substrate 1, insulin receptor, SOCS3, and pro- and anti-apoptotic markers. Data demonstrated that salicylate significantly improved retinal function, as well as reduced TNF[alpha] and SOCS3-induced insulin resistance in all samples. Overall, results suggest that salicylate is effective in reducing insulin resistance in the retina of type 2 diabetic rat models. Sodium salicylate has been reported to reduce markers of diabetic retinopathy in a type 1 rat model. Because rates of type 2 diabetes are on the rise, we wanted to determine whether salicylate could improve insulin resistance in a type 2 rat model, as well as improve retinal function. We treated lean and obese BBZDR/Wor type 2 diabetic rats with salicylate in their chow for 2 months. Prior to salicylate treatment, rats underwent an electroretinogram to measure retinal function. After 2 months of treatment, rats underwent an additional electroretinogram prior to sacrifice. In addition to the animal model, we also treated retinal endothelial cells (REC) and rat Müller cells with salicylate and performed the same analyses as done for the rat retinal lysates. To investigate the role of salicylate in insulin signaling, we measured TNFα and caspase 3 levels by ELISA, as well as performed Western blotting for insulin receptor substrate 1, insulin receptor, SOCS3, and pro- and anti-apoptotic markers. Data demonstrated that salicylate significantly improved retinal function, as well as reduced TNFα and SOCS3-induced insulin resistance in all samples. Overall, results suggest that salicylate is effective in reducing insulin resistance in the retina of type 2 diabetic rat models.Sodium salicylate has been reported to reduce markers of diabetic retinopathy in a type 1 rat model. Because rates of type 2 diabetes are on the rise, we wanted to determine whether salicylate could improve insulin resistance in a type 2 rat model, as well as improve retinal function. We treated lean and obese BBZDR/Wor type 2 diabetic rats with salicylate in their chow for 2 months. Prior to salicylate treatment, rats underwent an electroretinogram to measure retinal function. After 2 months of treatment, rats underwent an additional electroretinogram prior to sacrifice. In addition to the animal model, we also treated retinal endothelial cells (REC) and rat Müller cells with salicylate and performed the same analyses as done for the rat retinal lysates. To investigate the role of salicylate in insulin signaling, we measured TNFα and caspase 3 levels by ELISA, as well as performed Western blotting for insulin receptor substrate 1, insulin receptor, SOCS3, and pro- and anti-apoptotic markers. Data demonstrated that salicylate significantly improved retinal function, as well as reduced TNFα and SOCS3-induced insulin resistance in all samples. Overall, results suggest that salicylate is effective in reducing insulin resistance in the retina of type 2 diabetic rat models. |
Audience | Academic |
Author | Thakran, Shalini Steinle, Jena J. Jiang, Youde Walker, Robert J. Bheemreddy, Rajini Coppess, William |
AuthorAffiliation | 3 Department of Ophthalmology, University of Tennessee Health Science Center, Memphis, Tennessee, United States of America 5 Philder Smith College, Little Rock, Arkansas, United States of America 1 Department of Anatomy and Cell Biology, Wayne State University, Detroit, Michigan, United States of America 2 Department of Ophthalmology, Wayne State University, Detroit, Michigan, United States of America Children's Hospital Boston, UNITED STATES 4 VA Medical Center, Memphis, Tennessee, United States of America |
AuthorAffiliation_xml | – name: 1 Department of Anatomy and Cell Biology, Wayne State University, Detroit, Michigan, United States of America – name: Children's Hospital Boston, UNITED STATES – name: 5 Philder Smith College, Little Rock, Arkansas, United States of America – name: 3 Department of Ophthalmology, University of Tennessee Health Science Center, Memphis, Tennessee, United States of America – name: 4 VA Medical Center, Memphis, Tennessee, United States of America – name: 2 Department of Ophthalmology, Wayne State University, Detroit, Michigan, United States of America |
Author_xml | – sequence: 1 givenname: Youde surname: Jiang fullname: Jiang, Youde – sequence: 2 givenname: Shalini surname: Thakran fullname: Thakran, Shalini – sequence: 3 givenname: Rajini surname: Bheemreddy fullname: Bheemreddy, Rajini – sequence: 4 givenname: William surname: Coppess fullname: Coppess, William – sequence: 5 givenname: Robert J. surname: Walker fullname: Walker, Robert J. – sequence: 6 givenname: Jena J. surname: Steinle fullname: Steinle, Jena J. |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/25874611$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1111_ceo_14344 crossref_primary_10_2174_0929867324666170920144130 crossref_primary_10_1038_s41598_024_73337_4 crossref_primary_10_1155_2017_4832125 crossref_primary_10_1002_cbin_11015 crossref_primary_10_1371_journal_pone_0178236 crossref_primary_10_1002_ptr_5736 |
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Copyright | COPYRIGHT 2015 Public Library of Science 2015 Jiang et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. 2015 Jiang et al 2015 Jiang et al |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Competing Interests: The authors have declared that no competing interests exist. Conceived and designed the experiments: JS. Performed the experiments: YJ ST RB RW WC. Analyzed the data: YJ ST RB RW WC. Wrote the paper: ST RB JS. |
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Snippet | Sodium salicylate has been reported to reduce markers of diabetic retinopathy in a type 1 rat model. Because rates of type 2 diabetes are on the rise, we... |
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SubjectTerms | Animal models Animals Apoptosis Caspase Caspase 3 - analysis Caspase-3 Cells, Cultured Diabetes Diabetes mellitus Diabetes Mellitus, Type 2 - metabolism Diabetes Mellitus, Type 2 - pathology Diabetic retinopathy Disease Models, Animal Electroretinography Endothelial cells Endothelial Cells - cytology Endothelial Cells - drug effects Endothelial Cells - metabolism Enzyme-Linked Immunosorbent Assay Ependymoglial Cells - cytology Ependymoglial Cells - drug effects Ependymoglial Cells - metabolism Glucose - pharmacology Humans I-kappa B Proteins - metabolism Insulin Insulin - metabolism Insulin receptor substrate 1 Insulin Receptor Substrate Proteins - metabolism Insulin Resistance Intraocular Pressure - physiology Lysates Male Markers NF-KappaB Inhibitor alpha Nonsteroidal anti-inflammatory agents Obesity Phosphorylation - drug effects Rats Rats, Inbred BB Receptor, Insulin - metabolism Retina Retina - drug effects Retina - metabolism Retinopathy Salicylic acid Signal Transduction - drug effects Signaling Sodium Sodium salicylate Sodium Salicylate - pharmacology Substrates Suppressor of Cytokine Signaling 3 Protein Suppressor of Cytokine Signaling Proteins - metabolism Tumor Necrosis Factor-alpha - analysis Tumor necrosis factor-α Type 2 diabetes Western blotting |
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Title | Sodium Salicylate Reduced Insulin Resistance in the Retina of a Type 2 Diabetic Rat Model |
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