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The Breakdown of Preformed Peritoneal Advanced Glycation End Products by Intraperitoneal Alagebrium
It has been demonstrated that inhibitors of advanced glycation end products (AGE), such as aminoguanidine, can suppress peritoneal AGE in rats on peritoneal dialysis (PD). However, it is unknown whether late administration of a putative cross-link breaker, alagebrium, could reverse peritoneal AGE. W...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Korean Academy of Medical Sciences
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2633188/ https://www.ncbi.nlm.nih.gov/pubmed/19194551 http://dx.doi.org/10.3346/jkms.2009.24.S1.S189 |
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author | Lee, Yong-Kook Lee, Joon-Yeop Kim, Jun-Seup Won, Ki-Bum Kang, Hyeok-Joo Jang, Tae-jung Tak, Woo-Taek Lee, Jeong-Ho |
author_facet | Lee, Yong-Kook Lee, Joon-Yeop Kim, Jun-Seup Won, Ki-Bum Kang, Hyeok-Joo Jang, Tae-jung Tak, Woo-Taek Lee, Jeong-Ho |
author_sort | Lee, Yong-Kook |
collection | PubMed |
description | It has been demonstrated that inhibitors of advanced glycation end products (AGE), such as aminoguanidine, can suppress peritoneal AGE in rats on peritoneal dialysis (PD). However, it is unknown whether late administration of a putative cross-link breaker, alagebrium, could reverse peritoneal AGE. We therefore compared alagebrium with aminoguanidine in their ability to reverse peritoneal AGE in rats on PD. Male Sprague-Dawley rats were randomly divided into 3 groups: group I dialyzed with 4.25% glucose solution for all exchanges; group II dialyzed with 4.25% glucose solution containing aminoguanidine, and group III dialyzed with 4.25% glucose solution containing alagebrium for last 8 weeks of 12-week dialysis period. Dialysis exchanges were performed 2 times a day for 12 weeks. Immunohistochemistry was performed using a monoclonal anti-AGE antibody. One-hour PET was performed for comparison of transport characteristics. The immunolabelling of AGE in peritoneal membrane was markedly decreased in the alagebrium group. Consistent with this, the alagebrium group exhibited significantly higher D/Do glucose and lower D/P urea, suggesting low peritoneal membrane transport. But there were no significant differences between the control and the aminoguanidine group. These results suggest that the alagebrium may be the optimal therapeutic approach, compared with treatment with inhibitors of AGE formation, in rats on PD. |
format | Text |
id | pubmed-2633188 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | The Korean Academy of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-26331882009-02-03 The Breakdown of Preformed Peritoneal Advanced Glycation End Products by Intraperitoneal Alagebrium Lee, Yong-Kook Lee, Joon-Yeop Kim, Jun-Seup Won, Ki-Bum Kang, Hyeok-Joo Jang, Tae-jung Tak, Woo-Taek Lee, Jeong-Ho J Korean Med Sci Original Article It has been demonstrated that inhibitors of advanced glycation end products (AGE), such as aminoguanidine, can suppress peritoneal AGE in rats on peritoneal dialysis (PD). However, it is unknown whether late administration of a putative cross-link breaker, alagebrium, could reverse peritoneal AGE. We therefore compared alagebrium with aminoguanidine in their ability to reverse peritoneal AGE in rats on PD. Male Sprague-Dawley rats were randomly divided into 3 groups: group I dialyzed with 4.25% glucose solution for all exchanges; group II dialyzed with 4.25% glucose solution containing aminoguanidine, and group III dialyzed with 4.25% glucose solution containing alagebrium for last 8 weeks of 12-week dialysis period. Dialysis exchanges were performed 2 times a day for 12 weeks. Immunohistochemistry was performed using a monoclonal anti-AGE antibody. One-hour PET was performed for comparison of transport characteristics. The immunolabelling of AGE in peritoneal membrane was markedly decreased in the alagebrium group. Consistent with this, the alagebrium group exhibited significantly higher D/Do glucose and lower D/P urea, suggesting low peritoneal membrane transport. But there were no significant differences between the control and the aminoguanidine group. These results suggest that the alagebrium may be the optimal therapeutic approach, compared with treatment with inhibitors of AGE formation, in rats on PD. The Korean Academy of Medical Sciences 2009-01 2009-01-29 /pmc/articles/PMC2633188/ /pubmed/19194551 http://dx.doi.org/10.3346/jkms.2009.24.S1.S189 Text en Copyright © 2009 The Korean Academy of Medical Sciences http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Lee, Yong-Kook Lee, Joon-Yeop Kim, Jun-Seup Won, Ki-Bum Kang, Hyeok-Joo Jang, Tae-jung Tak, Woo-Taek Lee, Jeong-Ho The Breakdown of Preformed Peritoneal Advanced Glycation End Products by Intraperitoneal Alagebrium |
title | The Breakdown of Preformed Peritoneal Advanced Glycation End Products by Intraperitoneal Alagebrium |
title_full | The Breakdown of Preformed Peritoneal Advanced Glycation End Products by Intraperitoneal Alagebrium |
title_fullStr | The Breakdown of Preformed Peritoneal Advanced Glycation End Products by Intraperitoneal Alagebrium |
title_full_unstemmed | The Breakdown of Preformed Peritoneal Advanced Glycation End Products by Intraperitoneal Alagebrium |
title_short | The Breakdown of Preformed Peritoneal Advanced Glycation End Products by Intraperitoneal Alagebrium |
title_sort | breakdown of preformed peritoneal advanced glycation end products by intraperitoneal alagebrium |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2633188/ https://www.ncbi.nlm.nih.gov/pubmed/19194551 http://dx.doi.org/10.3346/jkms.2009.24.S1.S189 |
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