Multiple organ inflammatory response to portosystemic shunt in the rat

Portosystemic shunt surgery is the best procedure to prevent recurrent bleeding of esophageal varices, but carries a high risk of postoperative inflammatory complications, including hepatic encephalopathy. Thus, portosystemic shunting procedures could induce a systemic inflammatory response with multiple organ dysfunction syndrome, including hepatic encephalopathy. To verify this hypothesis we used male Wistar rats at 6 weeks of postoperative evolution: Control (CR; n = 14), Sham-operated (SO; n = 8) and rats with end-to-side portacaval shunt (PCS; n = 15). TNF-alpha, IL-1 beta and IL-10 were assayed by ELISA techniques, the expression of the endothelial constitutive nitric oxide synthase (eNOS), inducible nitric oxide synthase (iNOS), constitutive and inducible heme-oxygenase (HO-1 and HO-2) were assayed by Western-blot. mRNA levels of HO-1, HO-2, TNF-alpha, IL-1 beta and IL-10 were quantified by reverse transcriptase polymerase chain reaction amplification (RT-PCR) in the small bowel, liver, spleen and lungs. Portacaval shunting in the rat produces an interorgan imbalance of pro- and anti-inflammatory mediators. TNF-alpha mRNA expression is decreased in the liver (0.69 +/- 0.28, p < 0.05). The hepatic production of IL-1 beta (204.13 +/- 71.90 pg/100 g; p < 0.001) and IL-10 (4505.47 +/- 337.97 pg/100 g; p < 0.001) is also decreased. However, the intestinal pro-inflammatory (TNF-alpha: 1471.86 +/- 153.62 pg/100 g, p < 0.001; IL-1 beta: 48.35 +/- 9.84 pg/100 g, p < 0.001 and iNOS: 0.59 +/- 0.01, p < 0.01) and anti-inflammatory (IL-10: 1503.39 +/- 53.5 pg/100 g, p < 0.001 and HO-1: 2.23 +/- 0.16, p < 0.001) mediators are increased. Total portacaval shunting in the rat induces impairments of pro- and anti-inflammatory mediators in the splanchnic-lung axis that could be associated with a multiple organ dysfunction syndrome. Therefore, the complications after portosystemic shunts could be integrated into a systemic inflammatory response of possible intestinal origin. (C) 2011 Elsevier Ltd. All rights reserved.