Aminoguanidine Prevents the Oxidative Stress, Inhibiting Elements of Inflammation, Endothelial Activation, Mesenchymal Markers, and Confers a Renoprotective Effect in Renal Ischemia and Reperfusion Injury
Oxidative stress produces macromolecules dysfunction and cellular damage. Renal ischemia-reperfusion injury (IRI) induces oxidative stress, inflammation, epithelium and endothelium damage, and cessation of renal function. The IRI is an inevitable process during kidney transplantation. Preliminary st...
| Published in: | Antioxidants |
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| Main Authors: | , , , , , , , |
| Format: | Article |
| Language: | English |
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MDPI AG
2021-10-01
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| Online Access: | https://www.mdpi.com/2076-3921/10/11/1724 |
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| author | Consuelo Pasten Mauricio Lozano Jocelyn Rocco Flavio Carrión Cristobal Alvarado Jéssica Liberona Luis Michea Carlos E. Irarrázabal |
| author_facet | Consuelo Pasten Mauricio Lozano Jocelyn Rocco Flavio Carrión Cristobal Alvarado Jéssica Liberona Luis Michea Carlos E. Irarrázabal |
| author_sort | Consuelo Pasten |
| collection | DOAJ |
| container_title | Antioxidants |
| description | Oxidative stress produces macromolecules dysfunction and cellular damage. Renal ischemia-reperfusion injury (IRI) induces oxidative stress, inflammation, epithelium and endothelium damage, and cessation of renal function. The IRI is an inevitable process during kidney transplantation. Preliminary studies suggest that aminoguanidine (AG) is an antioxidant compound. In this study, we investigated the antioxidant effects of AG (50 mg/kg, intraperitoneal) and its association with molecular pathways activated by IRI (30 min/48 h) in the kidney. The antioxidant effect of AG was studied measuring GSSH/GSSG ratio, GST activity, lipoperoxidation, iNOS, and Hsp27 levels. In addition, we examined the effect of AG on elements associated with cell survival, inflammation, endothelium, and mesenchymal transition during IRI. AG prevented lipid peroxidation, increased GSH levels, and recovered the GST activity impaired by IRI. AG was associated with inhibition of iNOS, Hsp27, endothelial activation (VE-cadherin, PECAM), mesenchymal markers (vimentin, fascin, and HSP47), and inflammation (IL-1β, IL-6, Foxp3, and IL-10) upregulation. In addition, AG reduced kidney injury (NGAL, clusterin, Arg-2, and TFG-β1) and improved kidney function (glomerular filtration rate) during IRI. In conclusion, we found new evidence of the antioxidant properties of AG as a renoprotective compound during IRI. Therefore, AG is a promising compound to treat the deleterious effect of renal IRI. |
| format | Article |
| id | doaj-art-fee9d9f49e0143bd846d5ad3c90ca4e8 |
| institution | Directory of Open Access Journals |
| issn | 2076-3921 |
| language | English |
| publishDate | 2021-10-01 |
| publisher | MDPI AG |
| record_format | Article |
| spelling | doaj-art-fee9d9f49e0143bd846d5ad3c90ca4e82025-08-19T23:23:55ZengMDPI AGAntioxidants2076-39212021-10-011011172410.3390/antiox10111724Aminoguanidine Prevents the Oxidative Stress, Inhibiting Elements of Inflammation, Endothelial Activation, Mesenchymal Markers, and Confers a Renoprotective Effect in Renal Ischemia and Reperfusion InjuryConsuelo Pasten0Mauricio Lozano1Jocelyn Rocco2Flavio Carrión3Cristobal Alvarado4Jéssica Liberona5Luis Michea6Carlos E. Irarrázabal7Laboratorio de Fisiología Integrativa y Molecular, Programa de Fisiología, Centro de Investigación e Innovación Biomédica, Universidad de los Andes, Santiago 7620157, ChileLaboratorio de Fisiología Integrativa y Molecular, Programa de Fisiología, Centro de Investigación e Innovación Biomédica, Universidad de los Andes, Santiago 7620157, ChileLaboratorio de Fisiología Integrativa y Molecular, Programa de Fisiología, Centro de Investigación e Innovación Biomédica, Universidad de los Andes, Santiago 7620157, ChileFacultad de Ciencias de la Salud, Universidad del Alba, Santiago 7620157, ChileClinical Research Unit, Hospital Las Higueras, Talcahuano 4260000, ChileInstituto de Ciencias Biomédicas, School of Medicine, Universidad de Chile, Santiago 7620157, ChileInstituto de Ciencias Biomédicas, School of Medicine, Universidad de Chile, Santiago 7620157, ChileLaboratorio de Fisiología Integrativa y Molecular, Programa de Fisiología, Centro de Investigación e Innovación Biomédica, Universidad de los Andes, Santiago 7620157, ChileOxidative stress produces macromolecules dysfunction and cellular damage. Renal ischemia-reperfusion injury (IRI) induces oxidative stress, inflammation, epithelium and endothelium damage, and cessation of renal function. The IRI is an inevitable process during kidney transplantation. Preliminary studies suggest that aminoguanidine (AG) is an antioxidant compound. In this study, we investigated the antioxidant effects of AG (50 mg/kg, intraperitoneal) and its association with molecular pathways activated by IRI (30 min/48 h) in the kidney. The antioxidant effect of AG was studied measuring GSSH/GSSG ratio, GST activity, lipoperoxidation, iNOS, and Hsp27 levels. In addition, we examined the effect of AG on elements associated with cell survival, inflammation, endothelium, and mesenchymal transition during IRI. AG prevented lipid peroxidation, increased GSH levels, and recovered the GST activity impaired by IRI. AG was associated with inhibition of iNOS, Hsp27, endothelial activation (VE-cadherin, PECAM), mesenchymal markers (vimentin, fascin, and HSP47), and inflammation (IL-1β, IL-6, Foxp3, and IL-10) upregulation. In addition, AG reduced kidney injury (NGAL, clusterin, Arg-2, and TFG-β1) and improved kidney function (glomerular filtration rate) during IRI. In conclusion, we found new evidence of the antioxidant properties of AG as a renoprotective compound during IRI. Therefore, AG is a promising compound to treat the deleterious effect of renal IRI.https://www.mdpi.com/2076-3921/10/11/1724aminoguanidineantioxidantsoxidative stressischemia-reperfusion injuryrenal protection |
| spellingShingle | Consuelo Pasten Mauricio Lozano Jocelyn Rocco Flavio Carrión Cristobal Alvarado Jéssica Liberona Luis Michea Carlos E. Irarrázabal Aminoguanidine Prevents the Oxidative Stress, Inhibiting Elements of Inflammation, Endothelial Activation, Mesenchymal Markers, and Confers a Renoprotective Effect in Renal Ischemia and Reperfusion Injury aminoguanidine antioxidants oxidative stress ischemia-reperfusion injury renal protection |
| title | Aminoguanidine Prevents the Oxidative Stress, Inhibiting Elements of Inflammation, Endothelial Activation, Mesenchymal Markers, and Confers a Renoprotective Effect in Renal Ischemia and Reperfusion Injury |
| title_full | Aminoguanidine Prevents the Oxidative Stress, Inhibiting Elements of Inflammation, Endothelial Activation, Mesenchymal Markers, and Confers a Renoprotective Effect in Renal Ischemia and Reperfusion Injury |
| title_fullStr | Aminoguanidine Prevents the Oxidative Stress, Inhibiting Elements of Inflammation, Endothelial Activation, Mesenchymal Markers, and Confers a Renoprotective Effect in Renal Ischemia and Reperfusion Injury |
| title_full_unstemmed | Aminoguanidine Prevents the Oxidative Stress, Inhibiting Elements of Inflammation, Endothelial Activation, Mesenchymal Markers, and Confers a Renoprotective Effect in Renal Ischemia and Reperfusion Injury |
| title_short | Aminoguanidine Prevents the Oxidative Stress, Inhibiting Elements of Inflammation, Endothelial Activation, Mesenchymal Markers, and Confers a Renoprotective Effect in Renal Ischemia and Reperfusion Injury |
| title_sort | aminoguanidine prevents the oxidative stress inhibiting elements of inflammation endothelial activation mesenchymal markers and confers a renoprotective effect in renal ischemia and reperfusion injury |
| topic | aminoguanidine antioxidants oxidative stress ischemia-reperfusion injury renal protection |
| url | https://www.mdpi.com/2076-3921/10/11/1724 |
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