Cargando…

Anti-Fibrotic Effect of Natural Toxin Bee Venom on Animal Model of Unilateral Ureteral Obstruction

Progressive renal fibrosis is the final common pathway for all kidney diseases leading to chronic renal failure. Bee venom (BV) has been widely used as a traditional medicine for various diseases. However, the precise mechanism of BV in ameliorating the renal fibrosis is not fully understood. To inv...

Descripción completa

Detalles Bibliográficos
Autores principales: An, Hyun Jin, Kim, Kyung Hyun, Lee, Woo Ram, Kim, Jung Yeon, Lee, Sun Jae, Pak, Sok Cheon, Han, Sang Mi, Park, Kwan Kyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4488681/
https://www.ncbi.nlm.nih.gov/pubmed/26035488
http://dx.doi.org/10.3390/toxins7061917
_version_ 1782379202819915776
author An, Hyun Jin
Kim, Kyung Hyun
Lee, Woo Ram
Kim, Jung Yeon
Lee, Sun Jae
Pak, Sok Cheon
Han, Sang Mi
Park, Kwan Kyu
author_facet An, Hyun Jin
Kim, Kyung Hyun
Lee, Woo Ram
Kim, Jung Yeon
Lee, Sun Jae
Pak, Sok Cheon
Han, Sang Mi
Park, Kwan Kyu
author_sort An, Hyun Jin
collection PubMed
description Progressive renal fibrosis is the final common pathway for all kidney diseases leading to chronic renal failure. Bee venom (BV) has been widely used as a traditional medicine for various diseases. However, the precise mechanism of BV in ameliorating the renal fibrosis is not fully understood. To investigate the therapeutic effects of BV against unilateral ureteral obstruction (UUO)-induced renal fibrosis, BV was given intraperitoneally after ureteral ligation. At seven days after UUO surgery, the kidney tissues were collected for protein analysis and histologic examination. Histological observation revealed that UUO induced a considerable increase in the number of infiltrated inflammatory cells. However, BV treatment markedly reduced these reactions compared with untreated UUO mice. The expression levels of TNF-α and IL-1β were significantly reduced in BV treated mice compared with UUO mice. In addition, treatment with BV significantly inhibited TGF-β1 and fibronectin expression in UUO mice. Moreover, the expression of α-SMA was markedly withdrawn after treatment with BV. These findings suggest that BV attenuates renal fibrosis and reduces inflammatory responses by suppression of multiple growth factor-mediated pro-fibrotic genes. In conclusion, BV may be a useful therapeutic agent for the prevention of fibrosis that characterizes progression of chronic kidney disease.
format Online
Article
Text
id pubmed-4488681
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-44886812015-07-06 Anti-Fibrotic Effect of Natural Toxin Bee Venom on Animal Model of Unilateral Ureteral Obstruction An, Hyun Jin Kim, Kyung Hyun Lee, Woo Ram Kim, Jung Yeon Lee, Sun Jae Pak, Sok Cheon Han, Sang Mi Park, Kwan Kyu Toxins (Basel) Article Progressive renal fibrosis is the final common pathway for all kidney diseases leading to chronic renal failure. Bee venom (BV) has been widely used as a traditional medicine for various diseases. However, the precise mechanism of BV in ameliorating the renal fibrosis is not fully understood. To investigate the therapeutic effects of BV against unilateral ureteral obstruction (UUO)-induced renal fibrosis, BV was given intraperitoneally after ureteral ligation. At seven days after UUO surgery, the kidney tissues were collected for protein analysis and histologic examination. Histological observation revealed that UUO induced a considerable increase in the number of infiltrated inflammatory cells. However, BV treatment markedly reduced these reactions compared with untreated UUO mice. The expression levels of TNF-α and IL-1β were significantly reduced in BV treated mice compared with UUO mice. In addition, treatment with BV significantly inhibited TGF-β1 and fibronectin expression in UUO mice. Moreover, the expression of α-SMA was markedly withdrawn after treatment with BV. These findings suggest that BV attenuates renal fibrosis and reduces inflammatory responses by suppression of multiple growth factor-mediated pro-fibrotic genes. In conclusion, BV may be a useful therapeutic agent for the prevention of fibrosis that characterizes progression of chronic kidney disease. MDPI 2015-05-29 /pmc/articles/PMC4488681/ /pubmed/26035488 http://dx.doi.org/10.3390/toxins7061917 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
An, Hyun Jin
Kim, Kyung Hyun
Lee, Woo Ram
Kim, Jung Yeon
Lee, Sun Jae
Pak, Sok Cheon
Han, Sang Mi
Park, Kwan Kyu
Anti-Fibrotic Effect of Natural Toxin Bee Venom on Animal Model of Unilateral Ureteral Obstruction
title Anti-Fibrotic Effect of Natural Toxin Bee Venom on Animal Model of Unilateral Ureteral Obstruction
title_full Anti-Fibrotic Effect of Natural Toxin Bee Venom on Animal Model of Unilateral Ureteral Obstruction
title_fullStr Anti-Fibrotic Effect of Natural Toxin Bee Venom on Animal Model of Unilateral Ureteral Obstruction
title_full_unstemmed Anti-Fibrotic Effect of Natural Toxin Bee Venom on Animal Model of Unilateral Ureteral Obstruction
title_short Anti-Fibrotic Effect of Natural Toxin Bee Venom on Animal Model of Unilateral Ureteral Obstruction
title_sort anti-fibrotic effect of natural toxin bee venom on animal model of unilateral ureteral obstruction
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4488681/
https://www.ncbi.nlm.nih.gov/pubmed/26035488
http://dx.doi.org/10.3390/toxins7061917
work_keys_str_mv AT anhyunjin antifibroticeffectofnaturaltoxinbeevenomonanimalmodelofunilateralureteralobstruction
AT kimkyunghyun antifibroticeffectofnaturaltoxinbeevenomonanimalmodelofunilateralureteralobstruction
AT leewooram antifibroticeffectofnaturaltoxinbeevenomonanimalmodelofunilateralureteralobstruction
AT kimjungyeon antifibroticeffectofnaturaltoxinbeevenomonanimalmodelofunilateralureteralobstruction
AT leesunjae antifibroticeffectofnaturaltoxinbeevenomonanimalmodelofunilateralureteralobstruction
AT paksokcheon antifibroticeffectofnaturaltoxinbeevenomonanimalmodelofunilateralureteralobstruction
AT hansangmi antifibroticeffectofnaturaltoxinbeevenomonanimalmodelofunilateralureteralobstruction
AT parkkwankyu antifibroticeffectofnaturaltoxinbeevenomonanimalmodelofunilateralureteralobstruction