Influence of Intestinal Lymphatic Ligation on Pulmonary Injury in Rats with Severe Acute Pancreatitis

Curr Med Sci. 2022 Aug;42(4):711-719. doi: 10.1007/s11596-022-2594-4. Epub 2022 Aug 13.

Abstract

Objective: The present study explored the mechanisms involved in intestinal lymphatic ligation in rats with severe acute pancreatitis (SAP).

Methods: Male Sprague Dawley rats were randomly divided into 4 groups: saline group, saline+ligation group, SAP group, and SAP+ligation group. Rats in the SAP group were administered sodium taurocholate solution. Isolated mesenteric lymph duct ligation was administered to the saline+ligation and SAP+ligation groups. Endotoxin (ET), nitric oxide (NO), tumor necrosis factor-α (TNF-α), interleukin-1 (IL-1), myeloperoxidase (MPO), and superoxide dismutase (SOD) were detected. Nuclear factor-κB (NF-κB) and intercellular cell adhesion molecule-1 (ICAM-1) proteins were observed. The mRNA of inducible nitric oxide synthase(iNOS) and Toll-like receptor 4 (TLR4) was detected by PCR.

Results: Pathomorphological analysis showed that necrosis was present in the lung of rats in the SAP group, but only mild lesions in the SAP+ligation group. ET, NO, TNF-α, and IL-1 in the serum and lung tissue were significantly decreased and MPO was increased in the SAP+ligation group as compared with the SAP group. However, MPO was increased. The expression of NF-κB and ICAM-1, either iNOS or TLR4, was upregulated in the SAP group, but downregulated in the SAP+ligation group. Intestinal lymph duct ligation prevented ET translocation, the release of inflammation factors, and inflammation injury.

Conclusion: The intestinal lymph duct ligation could alleviate SAP-induced pulmonary injury by suppressing NF-κB activation in rats.

Keywords: intestinal bacterial translocation; intestinal lymphatic ligation; lung injury; severe acute pancreatitis.

MeSH terms

  • Acute Disease
  • Acute Lung Injury* / prevention & control
  • Animals
  • Inflammation
  • Intercellular Adhesion Molecule-1 / genetics
  • Interleukin-1
  • Male
  • NF-kappa B / metabolism
  • Pancreatitis* / pathology
  • Rats
  • Rats, Sprague-Dawley
  • Toll-Like Receptor 4
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Interleukin-1
  • NF-kappa B
  • Toll-Like Receptor 4
  • Tumor Necrosis Factor-alpha
  • Intercellular Adhesion Molecule-1