May Nesfatin-1 be a Biomarker in Acute Mesenteric Ischemia?
To investigate the diagnostic value of nesfatin-1 in cases of intestinal ischemia and ischemia/reperfusion. An experimental study. The Experimental Animals Laboratory of Bezmialem University, in June 2018. Twenty-one healthy male Sprague Dawley rats were randomly divided into three groups of 7 rats...
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Published in | Journal of the College of Physicians and Surgeons--Pakistan Vol. 29; no. 10; pp. 928 - 931 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Pakistan
College of Physicians and Surgeons Pakistan
01.10.2019
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Subjects | |
Online Access | Get full text |
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Summary: | To investigate the diagnostic value of nesfatin-1 in cases of intestinal ischemia and ischemia/reperfusion.
An experimental study.
The Experimental Animals Laboratory of Bezmialem University, in June 2018.
Twenty-one healthy male Sprague Dawley rats were randomly divided into three groups of 7 rats each. In group 1: 1-hour intestinal ischemia followed by 5-hour reperfusion was performed. In group 2: rats were subjected to 6-hour intestinal ischemia. In group 3: rats underwent laparotomy and closure without performing any further procedure. Changes in leukocyte count, amylase, blood sugar, LDH, SGOT, CRP, and nesfatin-1 levels were determined. For histopathological examination, a small intestinal sample was taken and preserved in 10% formaldehyde.
Nesfatin-1 value in group 2 was significantly higher than that in group 1 and group 3 (p=0.005, and p <0.001 respectively). Nesfatin-1 value in group 1 was significantly higher than that in group 3. A significant (r = 0.864/p <0.001) positive correlation was observed between nesfatin-1 value and pathology score. The pathology score of group 2 was significantly higher than that of group 1 and group 3 (p <0.001).
Serum nesfatin-1 can be a biomarker in acute mesenteric ischemia. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1022-386X 1681-7168 |
DOI: | 10.29271/jcpsp.2019.10.928 |