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1 Department of Internal Medicine, Saga Medical School, Nabeshima, Saga 849, Japan; and 2 Department of Physiology, Louisiana State University Medical Center, Shreveport, Louisiana 71130
Apoptosis after ischemia-reperfusion
(I/R) was characterized in rat small intestine. Under halothane
anesthesia, the superior mesenteric artery in the rat was occluded for
15 or 60 min, followed by reperfusion. Ratios of fragmented DNA to
total DNA, electrophoresis, and immunohistochemical staining were
examined after I/R. Some rats were pretreated with
-difluoromethylornithine (DFMO) to examine the relationship between
intestinal apoptosis and ornithine decarboxylase (ODC) activity. The
percentage of fragmented DNA significantly increased just after
ischemia and peaked at 1 h after reperfusion in the jejunum and
ileum. These increases were significantly higher in the 60-min
ischemia group compared with the 15-min ischemia group.
This increase decreased 6 h after reperfusion. The results were
corroborated by histological evaluations of the intestine under the
same conditions. DFMO completely abolished elevation of ODC activity 6 h after reperfusion but did not change the percentage of fragmented
DNA. Apoptosis in rat small intestine was induced by ischemia
of the gut, and this process was exacerbated by reperfusion. The
changes in apoptosis were independent of ODC activity.
percent fragmented DNA; DNA ladder; terminal deoxynucleotidyl transferase-mediated dUDP-biotin nick end labeling; ornithine decarboxylase
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