Mesenteric lymph duct ligation provides long term protection against hemorrhagic shock-induced lung injury
- PMID: 11028566
Mesenteric lymph duct ligation provides long term protection against hemorrhagic shock-induced lung injury
Abstract
Recently we have shown that ligation of the main mesenteric lymph (MLN) duct prior to an episode of hemorrhagic shock (HS) prevents shock-induced lung injury. Yet, ligation or diversion of intestinal lymph immediately prior to injury is not clinically feasible. Diversion of intestinally derived lymph after injury to protect against secondary insults is possible, but it is not known how long the protective effects of lymph ligation would last. Thus, we tested whether ligation of the MLN duct seven days prior to HS would still be protective. Male Sprague-Dawley rats were subjected to laparotomy with or without MLN duct ligation. Seven days later, half of the sham and actual MLN duct ligated animals randomly were selected to undergo HS (30 mmHG for 90 min). The other half of the animals was subjected to sham shock. Lung permeability, pulmonary myeloperoxidase (MPO) activity, and bronchoalveolar fluid (BALF) protein content were used to determine lung injury. Lymphatic division 7 days prior to HS continued to prevent shock induced lung injury as assessed by a lower Evans Blue dye concentration, BALF protein and MPO activity. In addition, there was no evidence of Patent Blue dye in the previously ligated MLN duct. Since ligation of the main mesenteric lymphatic duct continues to protect against shock-induced lung injury 1 week after duct ligation, it is feasible that lymphatic ligation performed after an injury remains protective against certain secondary insults for at least 1 week.
Similar articles
-
Amiloride moderates increased gut permeability and diminishes mesenteric lymph-mediated priming of neutrophils in trauma/hemorrhagic shock.Surgery. 2006 Nov;140(5):810-7. doi: 10.1016/j.surg.2006.03.003. Epub 2006 Aug 28. Surgery. 2006. PMID: 17084725
-
Pancreatic duct ligation abrogates the trauma hemorrhage-induced gut barrier failure and the subsequent production of biologically active intestinal lymph.Shock. 2007 Oct;28(4):441-6. doi: 10.1097/shk.0b013e31804858f2. Shock. 2007. PMID: 17558354
-
[Effect of mesenteric lymph duct ligation on lung injury in hemorrhagic shock rats].Zhongguo Wei Zhong Bing Ji Jiu Yi Xue. 2007 May;19(5):274-8. Zhongguo Wei Zhong Bing Ji Jiu Yi Xue. 2007. PMID: 17490565 Chinese.
-
Role of the gut lymphatic system in multiple organ failure.Curr Opin Crit Care. 2001 Apr;7(2):92-8. doi: 10.1097/00075198-200104000-00007. Curr Opin Crit Care. 2001. PMID: 11373517 Review.
-
Treatment or prevention of pulmonary cellular damage with pharmacologic doses of corticosteroid.Surg Gynecol Obstet. 1972 Apr;134(4):675-81. Surg Gynecol Obstet. 1972. PMID: 4552525 Review. No abstract available.
Cited by
-
Role of gut-lymph factors in the induction of burn-induced and trauma-shock-induced acute heart failure.Int J Clin Exp Med. 2008;1(2):171-80. Epub 2008 Mar 31. Int J Clin Exp Med. 2008. PMID: 19079671 Free PMC article.
-
Ketamine suppresses intestinal NF-kappa B activation and proinflammatory cytokine in endotoxic rats.World J Gastroenterol. 2004 Apr 1;10(7):1028-31. doi: 10.3748/wjg.v10.i7.1028. World J Gastroenterol. 2004. PMID: 15052687 Free PMC article.
-
Ketamine suppresses intestinal TLR4 expression and NF-kappaB activity in lipopolysaccharide-treated rats.Croat Med J. 2006 Dec;47(6):825-31. Croat Med J. 2006. PMID: 17167854 Free PMC article.
-
Intravenous injection of post-hemorrhagic shock mesenteric lymph induces multiple organ injury in rats.Exp Ther Med. 2019 Feb;17(2):1449-1455. doi: 10.3892/etm.2018.7048. Epub 2018 Dec 5. Exp Ther Med. 2019. PMID: 30680027 Free PMC article.
-
Effects of intestinal lymph on expression of neutrophil adhesion factors and lung injury after trauma-induced shock.World J Gastroenterol. 2004 Nov 1;10(21):3221-4. doi: 10.3748/wjg.v10.i21.3221. World J Gastroenterol. 2004. PMID: 15457581 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Research Materials
Miscellaneous