CO sub(2) pneumoperitoneum impact on early liver and lung cytokine expression in a rat model of abdominal sepsis
Background: Experimental evidence suggests that laparoscopy could have reduced inflammatory sequelae compared with laparotomy following abdominal surgery for peritonitis. The aim of the present study is to investigate the possible beneficial effects of CO sub(2) insufflation on liver and lung expres...
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Veröffentlicht in: | Surgical endoscopy 2012-04, Vol.26 (4), p.984-989 |
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Sprache: | eng |
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Zusammenfassung: | Background: Experimental evidence suggests that laparoscopy could have reduced inflammatory sequelae compared with laparotomy following abdominal surgery for peritonitis. The aim of the present study is to investigate the possible beneficial effects of CO sub(2) insufflation on liver and lung expression of proinflammatory cytokines during sepsis. Methods: Cecal ligation and puncture (CLP) was induced in Sprague-Dawley rats, and 6 h later rats were randomly subjected to CO sub(2) pneumoperitoneum (5-7 mmHg) or to laparotomy for 1 h. At the end of the CO sub(2) pneumoperitoneum or laparotomy procedures, animals were sacrificed, and liver and lung were removed and stored for molecular and histological analysis. Results: Liver and lung expression of proinflammatory cytokines was significantly reduced in animals subjected to CO sub(2) pneumoperitoneum compared with laparotomy. In particular, tumor necrosis factor-alpha (TNF- alpha ) protein expression was significantly reduced (p < 0.05) following CO sub(2) pneumoperitoneum compared with laparotomy procedures. Interleukin (IL)-6 protein expression was accordingly, markedly reduced (p < 0.05) following CO sub(2) pneumoperitoneum. Histological analysis showed a reduced inflammatory infiltrate in liver and lung from animals subjected to CO sub(2) pneumoperitoneum compared with laparotomy. Conclusions: Our results support the hypothesis that laparoscopic procedures reduce the inflammatory cascade, following peritoneal sepsis, via reduced expression of proinflammatory cytokines. |
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ISSN: | 0930-2794 1432-2218 |
DOI: | 10.1007/s00464-011-1982-9 |