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Oral High-Dose Ankaferd Administration Effects on Gastrointestinal System

Background and aims: Ankaferd Blood Stopper (ABS) is a herbal extract obtained from five different plants. It has a therapeutic potential for the management of external hemorrhage and controlling gastrointestinal bleeding. However, ABS's effects are not unknown on gastrointestinal systems. The...

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Autores principales: Akbal, Erdem, Köklü, Seyfettin, Astarcı, Hesna Müzeyyen, Koçak, Erdem, Karaca, Gökhan, Beyazıt, Yavuz, Topcu, Güler, Acar, Bilgehan, Ergün, Dilek, Haznedaroğlu, İbrahim Celalettin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3590606/
https://www.ncbi.nlm.nih.gov/pubmed/23471574
http://dx.doi.org/10.7150/ijms.4875
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author Akbal, Erdem
Köklü, Seyfettin
Astarcı, Hesna Müzeyyen
Koçak, Erdem
Karaca, Gökhan
Beyazıt, Yavuz
Topcu, Güler
Acar, Bilgehan
Ergün, Dilek
Haznedaroğlu, İbrahim Celalettin
author_facet Akbal, Erdem
Köklü, Seyfettin
Astarcı, Hesna Müzeyyen
Koçak, Erdem
Karaca, Gökhan
Beyazıt, Yavuz
Topcu, Güler
Acar, Bilgehan
Ergün, Dilek
Haznedaroğlu, İbrahim Celalettin
author_sort Akbal, Erdem
collection PubMed
description Background and aims: Ankaferd Blood Stopper (ABS) is a herbal extract obtained from five different plants. It has a therapeutic potential for the management of external hemorrhage and controlling gastrointestinal bleeding. However, ABS's effects are not unknown on gastrointestinal systems. The aim of this study was to assess the effect of short- and long-term systemic exposure and gastrointestinal safety following the oral administration of high-dose ABS in rats. Methods: Eighteen healthy adult male rats were included into the study. The rats were divided into 4 groups: group A was fed with high dose ABS (2ml/Kg) for one week, group B for one month, group C for three months and group D's diet did not contain any ABS. On termination of the ABS treatment, the gastrointestinal system from the esophagus to the anus and the liver were surgically removed and histological investigated. Results: During the study period, there was no mortality; signs of intoxication in any of the studied groups. No gastrointestinal tissue fibrosis, dysplasia, or metaplasia was detectable in any of the groups. The stomach had a normal morphology in all groups. However, the other gastrointestinal tract sections showed mucosal inflammation, goblet cell decrements, and intra-epithelial lymphocyte infiltration. The most common changes were mucosal inflammation in all rats in group B and C. Frequency of inflammation was greater in groups B and C in comparison to group A (P= 0.001). Loss of goblet cell and intra-epithelial lymphocyte infiltration were not significantly different between groups A and B (P=0.308 and P=0.189, respectively). However, there was significantly higher intra-epithelial lymphocyte infiltration in group C than in group A (P=0.04). Histopathological examination of the liver showed no inflammation, fibrosis, bile duct destruction or proliferation in any of the groups. However, each groups revealed vascular dilatation and erythrocyte accumulation at the sinusoidal structures of the liver. Conclusions: ABS seems to be a safe agent and it can be used for hemorrhage originated from gastric lesions. Further work needs to be done to establish whether ABS leads to be used to stop gastrointestinal bleeding.
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spelling pubmed-35906062013-03-07 Oral High-Dose Ankaferd Administration Effects on Gastrointestinal System Akbal, Erdem Köklü, Seyfettin Astarcı, Hesna Müzeyyen Koçak, Erdem Karaca, Gökhan Beyazıt, Yavuz Topcu, Güler Acar, Bilgehan Ergün, Dilek Haznedaroğlu, İbrahim Celalettin Int J Med Sci Research Paper Background and aims: Ankaferd Blood Stopper (ABS) is a herbal extract obtained from five different plants. It has a therapeutic potential for the management of external hemorrhage and controlling gastrointestinal bleeding. However, ABS's effects are not unknown on gastrointestinal systems. The aim of this study was to assess the effect of short- and long-term systemic exposure and gastrointestinal safety following the oral administration of high-dose ABS in rats. Methods: Eighteen healthy adult male rats were included into the study. The rats were divided into 4 groups: group A was fed with high dose ABS (2ml/Kg) for one week, group B for one month, group C for three months and group D's diet did not contain any ABS. On termination of the ABS treatment, the gastrointestinal system from the esophagus to the anus and the liver were surgically removed and histological investigated. Results: During the study period, there was no mortality; signs of intoxication in any of the studied groups. No gastrointestinal tissue fibrosis, dysplasia, or metaplasia was detectable in any of the groups. The stomach had a normal morphology in all groups. However, the other gastrointestinal tract sections showed mucosal inflammation, goblet cell decrements, and intra-epithelial lymphocyte infiltration. The most common changes were mucosal inflammation in all rats in group B and C. Frequency of inflammation was greater in groups B and C in comparison to group A (P= 0.001). Loss of goblet cell and intra-epithelial lymphocyte infiltration were not significantly different between groups A and B (P=0.308 and P=0.189, respectively). However, there was significantly higher intra-epithelial lymphocyte infiltration in group C than in group A (P=0.04). Histopathological examination of the liver showed no inflammation, fibrosis, bile duct destruction or proliferation in any of the groups. However, each groups revealed vascular dilatation and erythrocyte accumulation at the sinusoidal structures of the liver. Conclusions: ABS seems to be a safe agent and it can be used for hemorrhage originated from gastric lesions. Further work needs to be done to establish whether ABS leads to be used to stop gastrointestinal bleeding. Ivyspring International Publisher 2013-03-02 /pmc/articles/PMC3590606/ /pubmed/23471574 http://dx.doi.org/10.7150/ijms.4875 Text en © Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited.
spellingShingle Research Paper
Akbal, Erdem
Köklü, Seyfettin
Astarcı, Hesna Müzeyyen
Koçak, Erdem
Karaca, Gökhan
Beyazıt, Yavuz
Topcu, Güler
Acar, Bilgehan
Ergün, Dilek
Haznedaroğlu, İbrahim Celalettin
Oral High-Dose Ankaferd Administration Effects on Gastrointestinal System
title Oral High-Dose Ankaferd Administration Effects on Gastrointestinal System
title_full Oral High-Dose Ankaferd Administration Effects on Gastrointestinal System
title_fullStr Oral High-Dose Ankaferd Administration Effects on Gastrointestinal System
title_full_unstemmed Oral High-Dose Ankaferd Administration Effects on Gastrointestinal System
title_short Oral High-Dose Ankaferd Administration Effects on Gastrointestinal System
title_sort oral high-dose ankaferd administration effects on gastrointestinal system
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3590606/
https://www.ncbi.nlm.nih.gov/pubmed/23471574
http://dx.doi.org/10.7150/ijms.4875
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