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The effects of a hirudin/liposome complex on a diabetic nephropathy rat model

BACKGROUND: Hirudin, an extract from Hirudo spp., is an anticoagulant used to treat a variety of renal diseases, including diabetic nephropathy (DN). Currently, hirudin has to be used at high dosages to treat DN because it poorly targets the kidneys, although at high dosages it can have severe side...

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Autores principales: Wang, Hongwu, Cui, Huantian, Lin, Lan, Ji, Yue, Ni, Qing, Li, Junchen, Pang, Jianli, Bing, Gongyan, Bian, Yuhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6554961/
https://www.ncbi.nlm.nih.gov/pubmed/31170978
http://dx.doi.org/10.1186/s12906-019-2531-7
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author Wang, Hongwu
Cui, Huantian
Lin, Lan
Ji, Yue
Ni, Qing
Li, Junchen
Pang, Jianli
Bing, Gongyan
Bian, Yuhong
author_facet Wang, Hongwu
Cui, Huantian
Lin, Lan
Ji, Yue
Ni, Qing
Li, Junchen
Pang, Jianli
Bing, Gongyan
Bian, Yuhong
author_sort Wang, Hongwu
collection PubMed
description BACKGROUND: Hirudin, an extract from Hirudo spp., is an anticoagulant used to treat a variety of renal diseases, including diabetic nephropathy (DN). Currently, hirudin has to be used at high dosages to treat DN because it poorly targets the kidneys, although at high dosages it can have severe side effects. Developing a targeted drug delivery system for hirudin, then, could boost its positive therapeutic effects while lowering the risk of side effects. Liposomes have been demonstrated to have significant renal targeting potential, but here we show that a hirudin-loaded liposome is an effective delivery method for patients with DN. METHOD: In this study, we prepared a hirudin/liposome complex and tested its efficacy by injecting it into a rat model. We then compared the renal accumulation of hirudin between complex-injected rat models and rat models that received injections of hirudin alone. We also investigated the mechanisms behind the complex’s effects. RESULT: The hirudin/liposome complex increased the accumulation of hirudin in kidney tissues and relieved the renal injury in DN rat models. Moreover, the hirudin/liposome complex down-regulated the expression of TGF-β1 and VEGF in the kidneys. CONCLUSION: We demonstrated that a hirudin/liposome complex can have a significant positive effect on DN. The mechanism may be that the complex inhibits the expression of VEGF and TGF-β1.
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spelling pubmed-65549612019-06-10 The effects of a hirudin/liposome complex on a diabetic nephropathy rat model Wang, Hongwu Cui, Huantian Lin, Lan Ji, Yue Ni, Qing Li, Junchen Pang, Jianli Bing, Gongyan Bian, Yuhong BMC Complement Altern Med Research Article BACKGROUND: Hirudin, an extract from Hirudo spp., is an anticoagulant used to treat a variety of renal diseases, including diabetic nephropathy (DN). Currently, hirudin has to be used at high dosages to treat DN because it poorly targets the kidneys, although at high dosages it can have severe side effects. Developing a targeted drug delivery system for hirudin, then, could boost its positive therapeutic effects while lowering the risk of side effects. Liposomes have been demonstrated to have significant renal targeting potential, but here we show that a hirudin-loaded liposome is an effective delivery method for patients with DN. METHOD: In this study, we prepared a hirudin/liposome complex and tested its efficacy by injecting it into a rat model. We then compared the renal accumulation of hirudin between complex-injected rat models and rat models that received injections of hirudin alone. We also investigated the mechanisms behind the complex’s effects. RESULT: The hirudin/liposome complex increased the accumulation of hirudin in kidney tissues and relieved the renal injury in DN rat models. Moreover, the hirudin/liposome complex down-regulated the expression of TGF-β1 and VEGF in the kidneys. CONCLUSION: We demonstrated that a hirudin/liposome complex can have a significant positive effect on DN. The mechanism may be that the complex inhibits the expression of VEGF and TGF-β1. BioMed Central 2019-06-06 /pmc/articles/PMC6554961/ /pubmed/31170978 http://dx.doi.org/10.1186/s12906-019-2531-7 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Wang, Hongwu
Cui, Huantian
Lin, Lan
Ji, Yue
Ni, Qing
Li, Junchen
Pang, Jianli
Bing, Gongyan
Bian, Yuhong
The effects of a hirudin/liposome complex on a diabetic nephropathy rat model
title The effects of a hirudin/liposome complex on a diabetic nephropathy rat model
title_full The effects of a hirudin/liposome complex on a diabetic nephropathy rat model
title_fullStr The effects of a hirudin/liposome complex on a diabetic nephropathy rat model
title_full_unstemmed The effects of a hirudin/liposome complex on a diabetic nephropathy rat model
title_short The effects of a hirudin/liposome complex on a diabetic nephropathy rat model
title_sort effects of a hirudin/liposome complex on a diabetic nephropathy rat model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6554961/
https://www.ncbi.nlm.nih.gov/pubmed/31170978
http://dx.doi.org/10.1186/s12906-019-2531-7
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