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The effect of Ankaferd blood stopper on liver damage in experimental obstructive jaundice
BACKGROUND/AIMS: To evaluate the potential protective effects of Ankaferd blood stopper (ABS) in an experimental obstructive jaundice (OJ) model. MATERIALS AND METHODS: The study included 26 female rats, which were divided into 3 groups. The sham group, consisting of 10 rats, (group 1) only received...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Scientific and Technological Research Council of Turkey
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8283441/ https://www.ncbi.nlm.nih.gov/pubmed/32979898 http://dx.doi.org/10.3906/sag-2007-298 |
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author | KOŞMAZ, Koray DURHAN, Abdullah SÜLEYMAN, Marlen ÜNAL, Yılmaz BOSTANCI, Mustafa Taner YİĞİT HASKARACA, Tuğba ERSAK, Can ŞENEŞ, Mehmet KUŞABBİ, İlknur Alkan ESER, Eylem Pınar HÜCÜMENOĞLU, Sema |
author_facet | KOŞMAZ, Koray DURHAN, Abdullah SÜLEYMAN, Marlen ÜNAL, Yılmaz BOSTANCI, Mustafa Taner YİĞİT HASKARACA, Tuğba ERSAK, Can ŞENEŞ, Mehmet KUŞABBİ, İlknur Alkan ESER, Eylem Pınar HÜCÜMENOĞLU, Sema |
author_sort | KOŞMAZ, Koray |
collection | PubMed |
description | BACKGROUND/AIMS: To evaluate the potential protective effects of Ankaferd blood stopper (ABS) in an experimental obstructive jaundice (OJ) model. MATERIALS AND METHODS: The study included 26 female rats, which were divided into 3 groups. The sham group, consisting of 10 rats, (group 1) only received solely laparotomy. In the control group, consisting of 8 rats, (group 2), ligation was applied to the biliary tract and no treatment was implemented. In the treatment group, consisting of 8 rats, (group 3), following ligation of biliary tract, 0.5 mL/day ABS was given for 10 days. Liver tissue and blood samples were taken for histopathological and biochemical examination. RESULTS: Compared to group 2, group 3 had higher aspartate aminotransferase (AST), total oxidant status (TOS) malondialdehyde (MDA), fluorescent oxidant products (FOP), and lower expression of albumin and total antioxidant status (TAS) (P < 0.05). In histopathological analysis, the mean scores of all histopathological parameters (fibrosis, portal inflammation, confluent necrosis, interphase activity, bile duct proliferation) have statistical significance between group 2 and group 3 (P < 005). CONCLUSIONS: ABS has promising results in the treatment of experimental OJ because of its antioxidant and antiinflammatory properties. It may be used in clinical practice after more extensive studies about the effects of ABS on OJ. |
format | Online Article Text |
id | pubmed-8283441 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Scientific and Technological Research Council of Turkey |
record_format | MEDLINE/PubMed |
spelling | pubmed-82834412021-08-02 The effect of Ankaferd blood stopper on liver damage in experimental obstructive jaundice KOŞMAZ, Koray DURHAN, Abdullah SÜLEYMAN, Marlen ÜNAL, Yılmaz BOSTANCI, Mustafa Taner YİĞİT HASKARACA, Tuğba ERSAK, Can ŞENEŞ, Mehmet KUŞABBİ, İlknur Alkan ESER, Eylem Pınar HÜCÜMENOĞLU, Sema Turk J Med Sci Article BACKGROUND/AIMS: To evaluate the potential protective effects of Ankaferd blood stopper (ABS) in an experimental obstructive jaundice (OJ) model. MATERIALS AND METHODS: The study included 26 female rats, which were divided into 3 groups. The sham group, consisting of 10 rats, (group 1) only received solely laparotomy. In the control group, consisting of 8 rats, (group 2), ligation was applied to the biliary tract and no treatment was implemented. In the treatment group, consisting of 8 rats, (group 3), following ligation of biliary tract, 0.5 mL/day ABS was given for 10 days. Liver tissue and blood samples were taken for histopathological and biochemical examination. RESULTS: Compared to group 2, group 3 had higher aspartate aminotransferase (AST), total oxidant status (TOS) malondialdehyde (MDA), fluorescent oxidant products (FOP), and lower expression of albumin and total antioxidant status (TAS) (P < 0.05). In histopathological analysis, the mean scores of all histopathological parameters (fibrosis, portal inflammation, confluent necrosis, interphase activity, bile duct proliferation) have statistical significance between group 2 and group 3 (P < 005). CONCLUSIONS: ABS has promising results in the treatment of experimental OJ because of its antioxidant and antiinflammatory properties. It may be used in clinical practice after more extensive studies about the effects of ABS on OJ. The Scientific and Technological Research Council of Turkey 2021-06-28 /pmc/articles/PMC8283441/ /pubmed/32979898 http://dx.doi.org/10.3906/sag-2007-298 Text en Copyright © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Article KOŞMAZ, Koray DURHAN, Abdullah SÜLEYMAN, Marlen ÜNAL, Yılmaz BOSTANCI, Mustafa Taner YİĞİT HASKARACA, Tuğba ERSAK, Can ŞENEŞ, Mehmet KUŞABBİ, İlknur Alkan ESER, Eylem Pınar HÜCÜMENOĞLU, Sema The effect of Ankaferd blood stopper on liver damage in experimental obstructive jaundice |
title | The effect of Ankaferd blood stopper on liver damage in experimental obstructive jaundice |
title_full | The effect of Ankaferd blood stopper on liver damage in experimental obstructive jaundice |
title_fullStr | The effect of Ankaferd blood stopper on liver damage in experimental obstructive jaundice |
title_full_unstemmed | The effect of Ankaferd blood stopper on liver damage in experimental obstructive jaundice |
title_short | The effect of Ankaferd blood stopper on liver damage in experimental obstructive jaundice |
title_sort | effect of ankaferd blood stopper on liver damage in experimental obstructive jaundice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8283441/ https://www.ncbi.nlm.nih.gov/pubmed/32979898 http://dx.doi.org/10.3906/sag-2007-298 |
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