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The Effect of Silymarin on Mesenteric Ischemia-Reperfusion Injury

OBJECTIVE: To examine the effect of silymarin (SM), a mixture of flavonoids and polyphenols extracted from Silybum marianum, on mesenteric ischemia-reperfusion (I-R) injury in a rat model. MATERIALS AND METHODS: Fifty rats were randomly divided into 5 groups (n = 10). Group 1 was sham operated, whil...

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Autores principales: Demir, M., Amanvermez, R., Kamalı Polat, A., Karabıçak, İ., Çınar, H., Kesicioğlu, T., Polat, C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5586953/
https://www.ncbi.nlm.nih.gov/pubmed/24356575
http://dx.doi.org/10.1159/000356860
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author Demir, M.
Amanvermez, R.
Kamalı Polat, A.
Karabıçak, İ.
Çınar, H.
Kesicioğlu, T.
Polat, C.
author_facet Demir, M.
Amanvermez, R.
Kamalı Polat, A.
Karabıçak, İ.
Çınar, H.
Kesicioğlu, T.
Polat, C.
author_sort Demir, M.
collection PubMed
description OBJECTIVE: To examine the effect of silymarin (SM), a mixture of flavonoids and polyphenols extracted from Silybum marianum, on mesenteric ischemia-reperfusion (I-R) injury in a rat model. MATERIALS AND METHODS: Fifty rats were randomly divided into 5 groups (n = 10). Group 1 was sham operated, while groups 2-5 were subjected to mesenteric I-R lasting 1 h. Group 2 received isotonic sodium chloride, group 3 received SM (100 mg/kg/day) for 7 days before I-R, group 4 received SM for 7 days after I-R, and group 5 received SM for 7 days both before and after I-R. The rats were sacrificed by exsanguination in groups 1-3 at the 24th hour and groups 4 and 5 were sacrificed on the 7th day of reperfusion. Blood and intestinal specimens were taken for biochemical and pathological evaluations. RESULTS: Serum superoxide dismutase (SOD) and heat shock protein 70 levels were significantly higher in group 2 (5.24 ± 1.76 U/l and 261.4 ± 16.8 ng/ml) compared to the sham group (2.08 ± 1.76 U/l and 189.9 ± 28.7 ng/ml) (p < 0.001 and p < 0.0001, respectively). However, SOD activity and the extent and severity of the histopathological lesions were significantly less in groups 3 [3.11 ± 1.18 U/l, 1.0 (range 0.0-2.0)], 4 [2.15 ± 0.87 U/l, 1.0 (range 1.0-3.0)], and 5 [1.80 ± 0.61 U/l, 0.5 (range 0.0-2.0)], treated with SM, than in group 2 [5.24 ± 1.76 U/l, 2.0 (range 2.0-3.0)] (p = 0.002, p < 0.001, and p = 0.0001; p < 0.001, p = 0.007, and p = 0.0001, respectively). Also, TNF-α levels were lower in the SM-supplemented groups compared to group 2. Serum thiobarbituric acid-reactive substance concentrations were low in the pre-/posttreatment groups treated with SM compared to group 2. No statistical difference was observed for protein carbonyls between the groups. CONCLUSION: Our findings suggest that SM therapy may attenuate the oxidative and intestinal damage induced by I-R injuries.
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spelling pubmed-55869532017-11-01 The Effect of Silymarin on Mesenteric Ischemia-Reperfusion Injury Demir, M. Amanvermez, R. Kamalı Polat, A. Karabıçak, İ. Çınar, H. Kesicioğlu, T. Polat, C. Med Princ Pract Original Paper OBJECTIVE: To examine the effect of silymarin (SM), a mixture of flavonoids and polyphenols extracted from Silybum marianum, on mesenteric ischemia-reperfusion (I-R) injury in a rat model. MATERIALS AND METHODS: Fifty rats were randomly divided into 5 groups (n = 10). Group 1 was sham operated, while groups 2-5 were subjected to mesenteric I-R lasting 1 h. Group 2 received isotonic sodium chloride, group 3 received SM (100 mg/kg/day) for 7 days before I-R, group 4 received SM for 7 days after I-R, and group 5 received SM for 7 days both before and after I-R. The rats were sacrificed by exsanguination in groups 1-3 at the 24th hour and groups 4 and 5 were sacrificed on the 7th day of reperfusion. Blood and intestinal specimens were taken for biochemical and pathological evaluations. RESULTS: Serum superoxide dismutase (SOD) and heat shock protein 70 levels were significantly higher in group 2 (5.24 ± 1.76 U/l and 261.4 ± 16.8 ng/ml) compared to the sham group (2.08 ± 1.76 U/l and 189.9 ± 28.7 ng/ml) (p < 0.001 and p < 0.0001, respectively). However, SOD activity and the extent and severity of the histopathological lesions were significantly less in groups 3 [3.11 ± 1.18 U/l, 1.0 (range 0.0-2.0)], 4 [2.15 ± 0.87 U/l, 1.0 (range 1.0-3.0)], and 5 [1.80 ± 0.61 U/l, 0.5 (range 0.0-2.0)], treated with SM, than in group 2 [5.24 ± 1.76 U/l, 2.0 (range 2.0-3.0)] (p = 0.002, p < 0.001, and p = 0.0001; p < 0.001, p = 0.007, and p = 0.0001, respectively). Also, TNF-α levels were lower in the SM-supplemented groups compared to group 2. Serum thiobarbituric acid-reactive substance concentrations were low in the pre-/posttreatment groups treated with SM compared to group 2. No statistical difference was observed for protein carbonyls between the groups. CONCLUSION: Our findings suggest that SM therapy may attenuate the oxidative and intestinal damage induced by I-R injuries. S. Karger AG 2014-02 2013-12-18 /pmc/articles/PMC5586953/ /pubmed/24356575 http://dx.doi.org/10.1159/000356860 Text en Copyright © 2013 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article licensed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported license (CC BY-NC) (www.karger.com/OA-license), applicable to the online version of the article only. Distribution permitted for non-commercial purposes only.
spellingShingle Original Paper
Demir, M.
Amanvermez, R.
Kamalı Polat, A.
Karabıçak, İ.
Çınar, H.
Kesicioğlu, T.
Polat, C.
The Effect of Silymarin on Mesenteric Ischemia-Reperfusion Injury
title The Effect of Silymarin on Mesenteric Ischemia-Reperfusion Injury
title_full The Effect of Silymarin on Mesenteric Ischemia-Reperfusion Injury
title_fullStr The Effect of Silymarin on Mesenteric Ischemia-Reperfusion Injury
title_full_unstemmed The Effect of Silymarin on Mesenteric Ischemia-Reperfusion Injury
title_short The Effect of Silymarin on Mesenteric Ischemia-Reperfusion Injury
title_sort effect of silymarin on mesenteric ischemia-reperfusion injury
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5586953/
https://www.ncbi.nlm.nih.gov/pubmed/24356575
http://dx.doi.org/10.1159/000356860
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