JHSM

Journal of Health Sciences and Medicine (JHSM) is an unbiased, peer-reviewed, and open access international medical journal. The Journal publishes interesting clinical and experimental research conducted in all fields of medicine, interesting case reports, and clinical images, invited reviews, editorials, letters, comments, and related knowledge.

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Original Article
The role of carbondioxide insufflation in preventing postoperative peritoneal adhesions in rats
Aims: Adhesion is the pathological connections that occur during the healing with scar formation of peritoneal surface defects. CO2 is used the most frequently in laparoscopic operations for insufflation. It is believed that it causes to changes in the inflammatory reply of the pneumo-peritoneum, defects in acid-base balance and decrease in peritoneal macrophage functions. CO2 is the only gas whose immunologic effects have been shown. It has been proven in experimental studies that the CO2 insufflation causes to local peritoneal acidosis without affecting the systemic status. Moreover, it has also been shown that it decreases the pneumo-peritoneum TNF-? and IL-6 production; however, increases the IL-10 production which is an anti-inflammatory cytokine. In the literature, the relation between the laparoscopy and the postoperative adhesions has always been explained by taking the suggestion of its causing to less tissue trauma as a basis when compared with the open surgery. The inflammatory reply of the CO2 has been less dealt with. In this study, we wanted to find the answer to the question whether the capno-peritoneum has a role in preventing the postoperative adhesion formation only by using CO2 without a a laparoscopic operation.
Methods: 30 female Wistar Albino type rats whose weights varied between 250±20 were used in the study. The rats were divided into 5 groups. Each group had 6 rats. Rats were placed in standard polycarbon cages in groups of 6. The room temperature was kept in 21°C. The rats were fed with standard pellet food during the study and tap water was provided to them. The operational anesthesia was performed by injecting intramuscular Ketamine Hydrochloride (Ketalar, Parke Davis and Eczacıbaşı, İstanbul) 50 mg/kg and Xylazine hydrochloride (Rompun, Bayer HealthCare) 5 mg/kg.
Results: A meaningful difference (p<0.05) was determined between the inflammation results of the groups. The inflammation findings become lighter as moved from Group 1 to Group 5. A meaningful difference (p<0.05) was determined between the fibrosis results. The fibrosis findings become lower as moved from Group 1 to Group 5. A meaningful difference (p<0.05) was determined between the adhesion results of the groups. The adhesion findings become lower as moved from Group 1 to Group 5. A statistically meaningful difference was not determined (p>0.05) between the PAI values of the groups. A statistically meaningful difference was not determined (p<0.05) between the MDA values of the groups. The difference stems from Group 1 and Group 5. The MDA values of Group 1 is relatively higher than those of other groups; while the MDA values of Group 5 is found to be lower when compared with the other groups
Conclusion: Our results suggest that CO2 pneumo-peritoneum has positive effects in postoperative intraperitoneal adhesion development. Since we formed a scraping model in our study, we cannot suggest that the adhesion formation is decreased with mechanical effect. The patho-physiological and molecular bases of the postoperative adhesion formation have been documented and described well. However, we consider that the capno-peritoneum and postoperative adhesion formation is prevented with anti-inflammatory effect. We need to conduct more studies to examine this mechanism.


1. Menzies D. Postoperative adhesions: their treatment and relevancein clinical practice. Ann R Coll Surg Engl. 1993;75(3):147-153.
2. ten Broek RP, Issa Y, van Santbrink EJ, et al. Burden of adhesionsin abdominal and pelvic surgery: systematic review and met-analysis. BMJ. 2013;347:f5588.
3. Hellebrekers BW, Trimbos-Kemper TC, Trimbos JB, EmeisJJ, Kooistra T. Use of fibrinolytic agents in the prevention ofpostoperative adhesion formation. Fertil Steril. 2000;74(2):203-212. doi:10.1016/s0015-0282(00)00656-7
4. G&uuml;nay C, Sağlıyan A, Yaman İ. Ratlarda deneysel olarakoluşturulan intraabdominal adezyonların &ouml;nlenmesindeaprotinin ile metilen mavisinin etkinliğinin karşılaştırılması. F&Uuml;Sağlık Bil Derg. 2005;19(1):51-55.
5. Reed KL, Stucchi AF, Becker JM. The peritoneal fibrinolyticresponse to conventional and prolonged surgery is similar. J SurgRes. 2009;152(2):175-177. doi:10.1016/j.jss.2008.04.042
6. Rahimi VB, Shirazinia R, Fereydouni N, et al. Comparisonof honey and dextrose solution on post-operative peritonealadhesion in rat model. Biomed Pharmacother. 2017;92:849-855.doi:10.1016/j.biopha.2017.05.114
7. Holmdahl L, Eriksson E, Eriksson BI, Risberg B. Depression ofperitoneal fibrinolysis during operation is a local response totrauma. Surgery. 1998;123(5):539-544. doi:10.1067/msy.1998.86984
8. Raftery AT. Effect of peritoneal trauma on peritonealfibrinolytic activity and intraperitoneal adhesion formation. Anexperimental study in the rat. Eur Surg Res. 1981;13(6):397-401.doi:10.1159/000128208
9. Schn&uuml;riger B, Barmparas G, Branco BC, Lustenberger T, Inaba K,Demetriades D. Prevention of postoperative peritoneal adhesions:a review of the literature. Am J Surg. 2011;201(1):111-121.doi:10.1016/j.amjsurg.2010.02.008
10. Raisi A, Dezfoulian O, Davoodi F, Taheri S, Ghahremani SA.Salvia miltiorrhiza hydroalcoholic extract inhibits postoperativeperitoneal adhesions in rats. BMC Complement Med Ther.2021;21(1):126. doi:10.1186/s12906-021-03300-7
11. Scott-Coombes D, Whawell S, Vipond MN, Thompson J. Humanintraperitoneal fibrinolytic response to elective surgery. Br J Surg.1995;82(3):414-417. doi:10.1002/bjs.1800820346
12. Poerwosusanta H, Gunadi, Noor Z, et al. The effect of laparoscopyon mast cell degranulation and mesothelium thickness in rats.BMC Surg. 2020;20(1):111. doi:10.1186/s12893-020-00775-y
13. Lau WY, Leow CK, Li AK. History of endoscopic and laparoscopicsurgery. World J Surg. 1997;21(4):444-453. doi:10.1007/pl00012268
14. Valdivieso E, Saenz R, Claudio N. Natural orifice transluminalendoscopic surgery: putting together minimally invasivetechniques for a new era. Gastrointest Endosc. 2007;66(2):340-342.doi:10.1016/j.gie.2007.03.1039
15. Are C, Talamini MA, Murata K, De Maio A. Carbon dioxidepneumoperitoneum alters acute-phase response inducedby lipopolysaccharide. Surg Endosc. 2002;16(10):1464-1467.doi:10.1007/s00464-001-8305-5
16. Ellis H, Moran BJ, Thompson JN, et al. Adhesion-related hospitalreadmissions after abdominal and pelvic surgery: a retrospectivecohort study. Lancet. 1999;353(9163):1476-1480. doi:10.1016/S0140-6736(98)09337-4
17. Nagelschmidt M, Gerbecks D, Minor T. The impact of gaslaparoscopy on abdominal plasminogen activator activity. SurgEndosc. 2001;15(6):585-588. doi:10.1007/s004640010282
18. Brokelman WJ, Lensvelt M, Borel Rinkes IH, Klinkenbijl JH,Reijnen MM. Peritoneal changes due to laparoscopic surgery. SurgEndosc. 2011;25(1):1-9. doi:10.1007/s00464-010-1139-2
19. Orhurhu VJ, Gao CC, Ku C. Carbon Dioxide Embolism. In:StatPearls. Treasure Island (FL): StatPearls Publishing; November28, 2022.
20. Fuentes JM, Hanly EJ, Aurora AR, et al. CO2 abdominal insufflationpretreatment increases survival after a lipopolysaccharide-contaminated laparotomy. J Gastrointest Surg. 2006;10(1):32-38.doi:10.1016/j.gassur.2005.07.031
21. Hanly EJ, Mendoza-Sagaon M, Murata K, Hardacre JM, DeMaio A, Talamini MA. CO2 Pneumoperitoneum modifies theinflammatory response to sepsis. Ann Surg. 2003;237(3):343-350.doi:10.1097/01.SLA.0000055271.58945.E2
22. Hanly EJ, Aurora AR, Fuentes JM, et al. Abdominal insufflationwith CO2 causes peritoneal acidosis independent of systemicpH. J Gastrointest Surg. 2005;9(9):1245-1252. doi:10.1016/j.gassur.2005.09.007
23. O&#39;Boyle CJ, deBeaux AC, Watson DI, et al. Helium vs carbon dioxidegas insufflation with or without saline lavage during laparoscopy.Surg Endosc. 2002;16(4):620-625. doi:10.1007/s00464-001-8218-3
24. West MA, Hackam DJ, Baker J, Rodriguez JL, BellinghamJ, Rotstein OD. Mechanism of decreased in vitro murinemacrophage cytokine release after exposure to carbon dioxide:relevance to laparoscopic surgery. Ann Surg. 1997;226(2):179-190.doi:10.1097/00000658-199708000-00010
25. Kopernik G, Avinoach E, Grossman Y, et al. The effect of a highpartial pressure of carbon dioxide environment on metabolismand immune functions of human peritoneal cells-relevanceto carbon dioxide pneumoperitoneum. Am J Obstet Gynecol.1998;179(6 Pt 1):1503-1510. doi:10.1016/s0002-9378(98)70016-x
26. Douvdevani A, Rapoport J, Konforty A, Yulzari R, Moran A,Chaimovitz C. Intracellular acidification mediates the inhibitoryeffect of peritoneal dialysate on peritoneal macrophages. J Am SocNephrol. 1995;6(2):207-213. doi:10.1681/ASN.V62207
27. Guzm&aacute;n-Valdivia G&oacute;mez G, Tena-Betancourt E, Angulo Trejo M.Different doses of enoxaparin in the prevention of postoperativeabdominal adhesions. experimental study. Ann Med Surg (Lond).2021;73:103132. doi:10.1016/j.amsu.2021.103132
28. Menger MD, Vollmar B. Surgical trauma: hyperinflammationversus immunosuppression?. Langenbecks Arch Surg. 2004;389(6):475-484. doi:10.1007/s00423-004-0472-0
29. Romeo C, Cruccetti A, Turiaco A, et al. Monocyte and neutrophilactivity after minor surgical stress. J Pediatr Surg. 2002;37(5):741-744. doi:10.1053/jpsu.2002.32268
30. Miyano G, Yamataka A, Doi T, et al. Carbon dioxidepneumoperitoneum prevents intraperitoneal adhesions afterlaparotomy in rats. J Pediatr Surg. 2006;41(5):1025-1028.doi:10.1016/j.jpedsurg.2005.12.048
31. Soltany S. Postoperative peritoneal adhesion: an update onphysiopathology and novel traditional herbal and modernmedical therapeutics. Naunyn Schmiedebergs Arch Pharmacol.2021;394(2):317-336. doi:10.1007/s00210-020-01961-8
32. Cheong YC, Laird SM, Li TC, Shelton JB, Ledger WL, Cooke ID.Peritoneal healing and adhesion formation/reformation. HumReprod Update. 2001;7(6):556-566. doi:10.1093/humupd/7.6.556
33. Bryant LR. an evaluation of the effect of fibrinolysin onintraperitoneal adhesion formation. Am J Surg. 1963;106:892-897.doi:10.1016/0002-9610(63)90152-1
34. Moris D, Chakedis J, Rahnemai-Azar AA, et al. Postoperativeabdominal adhesions: clinical significance and advances inprevention and management. J Gastrointest Surg. 2017;21(10):1713-1722. doi:10.1007/s11605-017-3488-9
35. Corona R, Verguts J, Schonman R, Binda MM, Mailova K, KoninckxPR. Postoperative inflammation in the abdominal cavity increasesadhesion formation in a laparoscopic mouse model. Fertil Steril.2011;95(4):1224-1228. doi:10.1016/j.fertnstert.2011.01.004
36. Dixon CT, Rixford EL. Cytologic response to peritoneal irritation inman: a protective mechanism. Am J Surg. 1934;25(3):504-505.
Volume 6, Issue 5, 2023
Page : 1080-1086
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