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Am J Physiol Gastrointest Liver Physiol 274: G270-G276, 1998;
0193-1857/98 $5.00
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Vol. 274, Issue 2, G270-G276, February 1998

Programmed cell death induced by ischemia-reperfusion in rat intestinal mucosa

Takahiro Noda1, Ryuichi Iwakiri1, Kazuma Fujimoto1, Shuzo Matsuo1, and Tak Yee Aw2

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 alpha -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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