Impact of intraperitoneal pressure of a CO2 pneumoperitoneum on the surgical peritoneal environment.

BACKGROUND Animal experiments have suggested that a high intraperitoneal pressure (IPP) might adversely affect the surgical peritoneal environment. The present experimental study investigates the impact of IPP of a CO(2) pneumoperitoneum on human peritoneum. METHODS Patients undergoing laparoscopic surgery were subjected to either low (8 mmHg) or standard (12 mmHg) IPP. Normal peritoneum was collected from the parietal wall at the beginning of surgery and every 60 min thereafter. Expression levels of 168 genes that encode extracellular matrix proteins, adhesion molecules or inflammatory cytokine signaling molecules were measured in peritoneal tissues using real-time polymerase chain reaction (PCR)-based assay panels. Human peritoneal mesothelial cells (HPMCs) and human peritoneal fibroblasts (HPFBs) were incubated in a CO(2) insufflation chamber for 1 h at 12 or 8 mmHg. Hyaluronan (HA) synthesis and mRNA expression levels of hyaluronic acid synthases (HAS) and hyaluronidases (Hyal) in HPMCs and HPFBs were measured at 0, 4, 8, 12, 24 and 48 h after CO(2) gas exposure by ELISA and real-time PCR, respectively. RESULTS Expression levels of connective tissue growth factor (CTGF), matrix metalloproteinase-9, E-selectin, chemokine (C-X-C motif) ligand 2 (CXCL-2), Hyal-1 and Hyal-2 were significantly higher and those of HAS-1, HAS-3, thrombospondin-2 (TSP-2) and interleukin-10 were significantly lower in the 12 mmHg group compared with the 8 mmHg group. HA synthesis was significantly lower in the 12 mmHg group compared with the 8 mmHg group in HPMCs and HPFBs throughout the time course. CONCLUSIONS A low IPP (8 mmHg) may be better than the standard IPP (12 mmHg) to minimize the adverse impact on the surgical peritoneal environment during a CO(2) pneumoperitoneum.

[1]  K. Gurusamy,et al.  Low pressure versus standard pressure pneumoperitoneum in laparoscopic cholecystectomy. , 2014, The Cochrane database of systematic reviews.

[2]  K. Jardon,et al.  Impact of intraperitoneal pressure and duration of surgery on levels of tissue plasminogen activator and plasminogen activator inhibitor-1 mRNA in peritoneal tissues during laparoscopic surgery. , 2011, Human reproduction.

[3]  S. Matsuzaki,et al.  Impaired down-regulation of E-cadherin and beta-catenin protein expression in endometrial epithelial cells in the mid-secretory endometrium of infertile patients with endometriosis. , 2010, The Journal of clinical endocrinology and metabolism.

[4]  K. Jardon,et al.  Carbon dioxide pneumoperitoneum, intraperitoneal pressure, and peritoneal tissue hypoxia: a mouse study with controlled respiratory support , 2010, Surgical Endoscopy.

[5]  J. Windsor,et al.  Systematic review of oxidative stress associated with pneumoperitoneum , 2009, The British journal of surgery.

[6]  J. Bazin,et al.  Molecular mechanisms underlying postoperative peritoneal tumor dissemination may differ between a laparotomy and carbon dioxide pneumoperitoneum: a syngeneic mouse model with controlled respiratory support , 2009, Surgical Endoscopy.

[7]  K. Jardon,et al.  Complete laparoscopic treatment of genital prolapse with meshes including vaginal promontofixation and anterior repair: a series of 138 patients. , 2007, Journal of minimally invasive gynecology.

[8]  T. Chan,et al.  Hyaluronan – Regulator and Initiator of Peritoneal Inflammation and Remodeling , 2007, The International journal of artificial organs.

[9]  J. Bazin,et al.  Peritoneal tissue-oxygen tension during a carbon dioxide pneumoperitoneum in a mouse laparoscopic model with controlled respiratory support. , 2007, Human reproduction.

[10]  M. Pfaffl,et al.  Comparison of relative mRNA quantification models and the impact of RNA integrity in quantitative real-time RT-PCR , 2006, Biotechnology Letters.

[11]  L. Šoltés,et al.  Degradative action of reactive oxygen species on hyaluronan. , 2006, Biomacromolecules.

[12]  Thomas Ragg,et al.  The RIN: an RNA integrity number for assigning integrity values to RNA measurements , 2006, BMC Molecular Biology.

[13]  M. Talamini,et al.  Abdominal insufflation with CO2 causes peritoneal acidosis independent of systemic pH , 2005, Journal of Gastrointestinal Surgery.

[14]  Y. Novitsky,et al.  The net immunologic advantage of laparoscopic surgery , 2004, Surgical Endoscopy And Other Interventional Techniques.

[15]  J. Sleeman,et al.  Hyaluronan-oligosaccharide-induced transcription of metalloproteases , 2004, Journal of Cell Science.

[16]  S. Ziemer,et al.  Influence of the sampling technique on the measurement of peritoneal fibrinolytic activity. , 2002, The European journal of surgery = Acta chirurgica.

[17]  L. Stassen,et al.  Fewer Intraperitoneal Adhesions With Use of Hyaluronic Acid–Carboxymethylcellulose Membrane: A Randomized Clinical Trial , 2002, Annals of surgery.

[18]  D. Remick,et al.  Differential local and systemic regulation of the murine chemokines KC and MIP2. , 2001, Shock.

[19]  M. Canis,et al.  Risk of spread of ovarian cancer after laparoscopic surgery , 2001, Current opinion in obstetrics & gynecology.

[20]  M. Davies,et al.  Induction of hyaluronan metabolism after mechanical injury of human peritoneal mesothelial cells in vitro. , 2000, Kidney international.

[21]  M. Horton,et al.  Regulation of plasminogen activator inhibitor-1 and urokinase by hyaluronan fragments in mouse macrophages. , 2000, American journal of physiology. Lung cellular and molecular physiology.

[22]  E. Steyerberg,et al.  Intraperitoneal tumor growth is influenced by pressure of carbon dioxide pneumoperitoneum , 2000, Surgical Endoscopy.

[23]  I. Stamenkovic,et al.  Cell surface-localized matrix metalloproteinase-9 proteolytically activates TGF-beta and promotes tumor invasion and angiogenesis. , 2000, Genes & development.

[24]  M. Parker,et al.  Adhesion-related hospital readmissions after abdominal and pelvic surgery: a retrospective cohort study , 1999, The Lancet.

[25]  M. Feldmann,et al.  Regulation of monocyte IL-10 synthesis by endogenous IL-1 and TNF-alpha: role of the p38 and p42/44 mitogen-activated protein kinases. , 1998, Journal of immunology.

[26]  E. Kunkel,et al.  Differential effect of E-selectin antibodies on neutrophil rolling and recruitment to inflammatory sites. , 1997, Blood.

[27]  H. Krutzsch,et al.  Regulation of Transforming Growth Factor-β Activation by Discrete Sequences of Thrombospondin 1 (*) , 1995, The Journal of Biological Chemistry.

[28]  E. Stylianou,et al.  Isolation, culture and characterization of human peritoneal mesothelial cells. , 1990, Kidney international.

[29]  P. Noble,et al.  Hyaluronan as an immune regulator in human diseases. , 2011, Physiological reviews.

[30]  D. Jayne,et al.  Molecular biology of peritoneal carcinomatosis. , 2007, Cancer treatment and research.

[31]  A. Jörres,et al.  Peritoneal cell culture: fibroblasts. , 2006, Peritoneal dialysis international : journal of the International Society for Peritoneal Dialysis.

[32]  E. D. De Robertis,et al.  Connective-tissue growth factor (CTGF) modulates cell signalling by BMP and TGF-beta. , 2002, Nature cell biology.

[33]  B. Risberg,et al.  Characterization and fibrinolytic properties of mesothelial cells isolated from peritoneal lavage. , 1998, Scandinavian journal of clinical and laboratory investigation.

[34]  N. Topley,et al.  Human peritoneal fibroblast proliferation in 3-dimensional culture: modulation by cytokines, growth factors and peritoneal dialysis effluent. , 1997, Kidney international.