Comparison of the Effects of Sodium Nitroprusside and L-Carnitine in Experimental Ischemia-Reperfusion Injury in Rats
Abstract Aim The aim of this study was to evaluate the protective effect of sodium nitroprusside (SNP) as a nitric oxide (NO) donor and L-carnitine intraperitoneal administration to treat experimental ischemia-reperfusion (I/R) in rats. Materials and methods Rats were divided into four groups, each...
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Published in | Transplantation proceedings Vol. 39; no. 10; pp. 2997 - 3001 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.12.2007
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Subjects | |
Online Access | Get full text |
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Summary: | Abstract Aim The aim of this study was to evaluate the protective effect of sodium nitroprusside (SNP) as a nitric oxide (NO) donor and L-carnitine intraperitoneal administration to treat experimental ischemia-reperfusion (I/R) in rats. Materials and methods Rats were divided into four groups, each one consisting of 10 animals. Group 1 was subjected to a sham operation. In group 2, an I/R process was applied to the rats. In group 3, SNP (5 mg/kg) and in group 4, L-carnitine (500 mg/kg) was administered in addition to the I/R process. Ileal tissue samples were obtained for analysis of tissue malonyl dialdehyde (MDA) and for histopathologic examination. Results By histopathologic examination, the I/R group showed a significant difference from the SNP and L-carnitine groups ( P < .05). There was no difference between the sham, the SNP, and the L-carnitine groups ( P > .05). SNP used as an NO donor produced a significant decrease in MDA levels. There was a significant difference between the MDA levels of the SNP and the I/R groups ( P < .05). Also, the difference between this group and the I/R group was significant ( P < .05). Conclusion SNP helped to both prevent and reduce mucosal damage in terms of histological and tissue MDA levels. Since the results of the L-carnitine group and the SNP group were similar, L-carnitine was as effective as exogenous NO. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0041-1345 1873-2623 |
DOI: | 10.1016/j.transproceed.2007.03.112 |