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Protective Effects of L-Carnitine on Intestinal Ischemia/Reperfusion Injury in a Rat Model
BACKGROUND: Ischemia/reperfusion (IR) injury of the intestine is a major problem in abdominal pathological condition and is associated with a high morbidity and mortality. The purpose of the study is to determine whether the L-carnitine can prevent the harmful effects of small intestinal IR injury i...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elmer Press
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3140927/ https://www.ncbi.nlm.nih.gov/pubmed/21811534 http://dx.doi.org/10.4021/jocmr540w |
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author | Yuan, Yong Guo, Hao Zhang, Yi Zhou, Dong Gan, Ping Liang, Dao Ming Chen, Jia Yong |
author_facet | Yuan, Yong Guo, Hao Zhang, Yi Zhou, Dong Gan, Ping Liang, Dao Ming Chen, Jia Yong |
author_sort | Yuan, Yong |
collection | PubMed |
description | BACKGROUND: Ischemia/reperfusion (IR) injury of the intestine is a major problem in abdominal pathological condition and is associated with a high morbidity and mortality. The purpose of the study is to determine whether the L-carnitine can prevent the harmful effects of small intestinal IR injury in rats. METHODS: Thirty Sprague-Dawley rats were randomly divided into three groups. Sham operated group (S), for shamoperated, the IR group for rats submitted to 45-minute of intestinal ischemia and 2-hour reperfusion, and IR+L group for those IR group treated with L-carnitine before reperfusion. All the rats were given EmGFP labelled E. coli DH5α through gavage 2-hour before the operative procedure. Afterwards the bacterial translocation (BT) from mesenteric lymph nodes (MLN), liver, spleen, lung and portal vein blood were detected. And the colony forming units/g (CFU/g) were counted. The TNF-α, IL-1β, IL-6, and IL-10 in serum were measured by ELISA. The morphometric study was measured by Chius classification. RESULTS: The levels of BT were higher in the IR group than IR+L group (P < 0.05). The E. coli DH5α was hardly detected in the S group. The IR+L rats had enhancement of IL-10 and suppressed production of serum TNF-α, IL-1β and IL-6, compared to IR group rats (P < 0.05). The degree of pathological impairment in small intestine was lighter in IR+L than IR group (P < 0.05). CONCLUSIONS: The L-carnitine pretreatment has a positive effect on reducing levels of BT, on inhibiting secretion of proinflammatory cytokines, and on lessening intestinal mucosa injury during small intestinal IR injury. KEYWORDS: L-carnitine; Ischemia/reperfusion injury; Intestine |
format | Online Article Text |
id | pubmed-3140927 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Elmer Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-31409272011-08-02 Protective Effects of L-Carnitine on Intestinal Ischemia/Reperfusion Injury in a Rat Model Yuan, Yong Guo, Hao Zhang, Yi Zhou, Dong Gan, Ping Liang, Dao Ming Chen, Jia Yong J Clin Med Res Original Article BACKGROUND: Ischemia/reperfusion (IR) injury of the intestine is a major problem in abdominal pathological condition and is associated with a high morbidity and mortality. The purpose of the study is to determine whether the L-carnitine can prevent the harmful effects of small intestinal IR injury in rats. METHODS: Thirty Sprague-Dawley rats were randomly divided into three groups. Sham operated group (S), for shamoperated, the IR group for rats submitted to 45-minute of intestinal ischemia and 2-hour reperfusion, and IR+L group for those IR group treated with L-carnitine before reperfusion. All the rats were given EmGFP labelled E. coli DH5α through gavage 2-hour before the operative procedure. Afterwards the bacterial translocation (BT) from mesenteric lymph nodes (MLN), liver, spleen, lung and portal vein blood were detected. And the colony forming units/g (CFU/g) were counted. The TNF-α, IL-1β, IL-6, and IL-10 in serum were measured by ELISA. The morphometric study was measured by Chius classification. RESULTS: The levels of BT were higher in the IR group than IR+L group (P < 0.05). The E. coli DH5α was hardly detected in the S group. The IR+L rats had enhancement of IL-10 and suppressed production of serum TNF-α, IL-1β and IL-6, compared to IR group rats (P < 0.05). The degree of pathological impairment in small intestine was lighter in IR+L than IR group (P < 0.05). CONCLUSIONS: The L-carnitine pretreatment has a positive effect on reducing levels of BT, on inhibiting secretion of proinflammatory cytokines, and on lessening intestinal mucosa injury during small intestinal IR injury. KEYWORDS: L-carnitine; Ischemia/reperfusion injury; Intestine Elmer Press 2011-04 2011-04-04 /pmc/articles/PMC3140927/ /pubmed/21811534 http://dx.doi.org/10.4021/jocmr540w Text en Copyright © 2011, Yuan et al. http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Yuan, Yong Guo, Hao Zhang, Yi Zhou, Dong Gan, Ping Liang, Dao Ming Chen, Jia Yong Protective Effects of L-Carnitine on Intestinal Ischemia/Reperfusion Injury in a Rat Model |
title | Protective Effects of L-Carnitine on Intestinal Ischemia/Reperfusion Injury in a Rat Model |
title_full | Protective Effects of L-Carnitine on Intestinal Ischemia/Reperfusion Injury in a Rat Model |
title_fullStr | Protective Effects of L-Carnitine on Intestinal Ischemia/Reperfusion Injury in a Rat Model |
title_full_unstemmed | Protective Effects of L-Carnitine on Intestinal Ischemia/Reperfusion Injury in a Rat Model |
title_short | Protective Effects of L-Carnitine on Intestinal Ischemia/Reperfusion Injury in a Rat Model |
title_sort | protective effects of l-carnitine on intestinal ischemia/reperfusion injury in a rat model |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3140927/ https://www.ncbi.nlm.nih.gov/pubmed/21811534 http://dx.doi.org/10.4021/jocmr540w |
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