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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...

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Autores principales: Lee, Yong-Kook, Lee, Joon-Yeop, Kim, Jun-Seup, Won, Ki-Bum, Kang, Hyeok-Joo, Jang, Tae-jung, Tak, Woo-Taek, Lee, Jeong-Ho
Formato: Texto
Lenguaje:English
Publicado: The Korean Academy of Medical Sciences 2009
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.
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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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