Cargando…
Suramin: A Potential Therapy for Diabetic Nephropathy
OBJECTIVE: To determine whether delayed administration of a single dose of suramin, a drug that has been used extensively in humans to treat trypanosomiasis, attenuates renal injury in a leptin receptor deficient C57BLKS/J db/db type 2 diabetic nephropathy (T2DN) mouse model. RESEARCH DESIGN AND MET...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3767615/ https://www.ncbi.nlm.nih.gov/pubmed/24040012 http://dx.doi.org/10.1371/journal.pone.0073655 |
_version_ | 1782283672712380416 |
---|---|
author | Korrapati, Midhun C. Howell, Lauren H. Shaner, Brooke E. Megyesi, Judit K. Siskind, Leah J. Schnellmann, Rick G. |
author_facet | Korrapati, Midhun C. Howell, Lauren H. Shaner, Brooke E. Megyesi, Judit K. Siskind, Leah J. Schnellmann, Rick G. |
author_sort | Korrapati, Midhun C. |
collection | PubMed |
description | OBJECTIVE: To determine whether delayed administration of a single dose of suramin, a drug that has been used extensively in humans to treat trypanosomiasis, attenuates renal injury in a leptin receptor deficient C57BLKS/J db/db type 2 diabetic nephropathy (T2DN) mouse model. RESEARCH DESIGN AND METHODS: Groups of female non-diabetic (control) db/m and diabetic db/db mice of 8 and 16 weeks of age, respectively, were treated with suramin (10 mg/kg) or saline i.v. All animals were euthanized one week later. Measurements in mice 1 week following treatment included the following: body weight; blood glucose; urinary protein excretion; pathological lesions in glomeruli and proximal tubules; changes in protein expression of pro-inflammatory transcription factor nuclear factor κB (NF-κB) and intracellular adhesion molecule-1 (ICAM-1), profibrotic transforming growth factor-β1 (TGF-β1), phospho-SMAD-3 and alpha-smooth muscle actin (α-SMA); and immunohistochemical analysis of leukocyte infiltration and collagen 1A2 (COL1A2) deposition. RESULTS: Immunoblot analysis revealed increased NF-κB, ICAM-1, TGF-β1, phospho-SMAD-3, and α-SMA proteins in both 9 and 17 week db/db mice as compared to db/m control mice. Immunohistochemical analysis revealed moderate leukocyte infiltration and collagen 1A2 (COL1A2) deposition in 9 week db/db mice that was increased in the 17 week db/db mice. Importantly, suramin significantly decreased expression of all these markers in 9 week db/db mice and partially decreased in 17 week db/db mice without altering body weight, blood glucose or urinary protein excretion. There was no difference in creatinine clearance between 9 week db/m and db/db mice ± suramin. Importantly, in the 17 week db/db mice suramin intervention reversed the impaired creatinine clearance and overt histological damage. CONCLUSIONS: Delayed administration of a single dose of suramin in a model of T2DN attenuated inflammation and fibrosis as well as improved renal function, supporting the use of suramin in T2DN. |
format | Online Article Text |
id | pubmed-3767615 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37676152013-09-13 Suramin: A Potential Therapy for Diabetic Nephropathy Korrapati, Midhun C. Howell, Lauren H. Shaner, Brooke E. Megyesi, Judit K. Siskind, Leah J. Schnellmann, Rick G. PLoS One Research Article OBJECTIVE: To determine whether delayed administration of a single dose of suramin, a drug that has been used extensively in humans to treat trypanosomiasis, attenuates renal injury in a leptin receptor deficient C57BLKS/J db/db type 2 diabetic nephropathy (T2DN) mouse model. RESEARCH DESIGN AND METHODS: Groups of female non-diabetic (control) db/m and diabetic db/db mice of 8 and 16 weeks of age, respectively, were treated with suramin (10 mg/kg) or saline i.v. All animals were euthanized one week later. Measurements in mice 1 week following treatment included the following: body weight; blood glucose; urinary protein excretion; pathological lesions in glomeruli and proximal tubules; changes in protein expression of pro-inflammatory transcription factor nuclear factor κB (NF-κB) and intracellular adhesion molecule-1 (ICAM-1), profibrotic transforming growth factor-β1 (TGF-β1), phospho-SMAD-3 and alpha-smooth muscle actin (α-SMA); and immunohistochemical analysis of leukocyte infiltration and collagen 1A2 (COL1A2) deposition. RESULTS: Immunoblot analysis revealed increased NF-κB, ICAM-1, TGF-β1, phospho-SMAD-3, and α-SMA proteins in both 9 and 17 week db/db mice as compared to db/m control mice. Immunohistochemical analysis revealed moderate leukocyte infiltration and collagen 1A2 (COL1A2) deposition in 9 week db/db mice that was increased in the 17 week db/db mice. Importantly, suramin significantly decreased expression of all these markers in 9 week db/db mice and partially decreased in 17 week db/db mice without altering body weight, blood glucose or urinary protein excretion. There was no difference in creatinine clearance between 9 week db/m and db/db mice ± suramin. Importantly, in the 17 week db/db mice suramin intervention reversed the impaired creatinine clearance and overt histological damage. CONCLUSIONS: Delayed administration of a single dose of suramin in a model of T2DN attenuated inflammation and fibrosis as well as improved renal function, supporting the use of suramin in T2DN. Public Library of Science 2013-09-09 /pmc/articles/PMC3767615/ /pubmed/24040012 http://dx.doi.org/10.1371/journal.pone.0073655 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. |
spellingShingle | Research Article Korrapati, Midhun C. Howell, Lauren H. Shaner, Brooke E. Megyesi, Judit K. Siskind, Leah J. Schnellmann, Rick G. Suramin: A Potential Therapy for Diabetic Nephropathy |
title | Suramin: A Potential Therapy for Diabetic Nephropathy |
title_full | Suramin: A Potential Therapy for Diabetic Nephropathy |
title_fullStr | Suramin: A Potential Therapy for Diabetic Nephropathy |
title_full_unstemmed | Suramin: A Potential Therapy for Diabetic Nephropathy |
title_short | Suramin: A Potential Therapy for Diabetic Nephropathy |
title_sort | suramin: a potential therapy for diabetic nephropathy |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3767615/ https://www.ncbi.nlm.nih.gov/pubmed/24040012 http://dx.doi.org/10.1371/journal.pone.0073655 |
work_keys_str_mv | AT korrapatimidhunc suraminapotentialtherapyfordiabeticnephropathy AT howelllaurenh suraminapotentialtherapyfordiabeticnephropathy AT shanerbrookee suraminapotentialtherapyfordiabeticnephropathy AT megyesijuditk suraminapotentialtherapyfordiabeticnephropathy AT siskindleahj suraminapotentialtherapyfordiabeticnephropathy AT schnellmannrickg suraminapotentialtherapyfordiabeticnephropathy |