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Venous congestion induces mucosal apoptosis via tumor necrosis factor-α-mediated cell death in the rat small intestine

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Abstract

Background

Tissue and organic venous congestion is a common pathophysiologic phenomenon. However, it is unclear whether venous congestion induces small-intestinal mucosal apoptosis. The aim of this study was to investigate whether venous congestion, or congestion followed by re-outflow, induced small-intestinal mucosal apoptosis, and whether tumor necrosis factor-α is involved in this apoptosis.

Methods

Small-intestinal venous congestion was induced in rats by occlusion of the superior mesenteric vein with a micro-bulldog clamp. At the end of the congestive period, the clamp was released to facilitate congestion followed by re-outflow. The rats were injected with a neutral anti-tumor necrosis factor-α antibody (0.15 mg/kg) via the jugular vein for 30 min before venous congestion or congestion followed by re-outflow. Intestinal mucosal apoptosis was evaluated and tumor necrosis factor-α was assayed. The amounts of caspase-8, caspase-3, and cytochrome c were determined by Western blot analysis.

Results

Our results showed that venous congestion and congestion followed by re-outflow significantly increased mucosal apoptosis, the amount of mucosal tumor necrosis factor-α, and the levels of caspase-8 cleavage and caspase-3 activation, but did not induce cytochrome c release from mitochondria to the cytosol. Pretreatment with an anti-tumor necrosis factor-α antibody significantly reduced mucosal apoptosis after intestinal congestion or congestion followed by re-outflow.

Conclusions

The present results support the view that venous congestion and congestion followed by re-outflow induce mucosal apoptosis in the rat small intestine, and show that the apoptosis occurs partly via tumor necrosis factor-α-mediated cell death.

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Wu, B., Fujise, T., Iwakiri, R. et al. Venous congestion induces mucosal apoptosis via tumor necrosis factor-α-mediated cell death in the rat small intestine. J Gastroenterol 39, 1056–1062 (2004). https://doi.org/10.1007/s00535-004-1444-4

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  • DOI: https://doi.org/10.1007/s00535-004-1444-4

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