Surgical stress reduces mortality from endotoxin shock

Langenbecks Arch Surg. 2002 Jan;386(7):512-7. doi: 10.1007/s00423-001-0261-y. Epub 2001 Nov 23.

Abstract

Background and aim: Surgical stress has been considered a preliminary to multiple organ failure through what has been termed a "two-hit" mechanism. Recent evidence, however, suggests that such stress has a beneficial influence in reducing endotoxin [lipopolysaccharide (LPS)]-mediated lethality. This study has been an effort to clarify whether and how LPS-mediated septic shock is prevented by a previous insult with mild (laparotomy) or severe (hepatectomy) surgical stress.

Methods: LPS was injected intraperitoneally into mice after two-thirds hepatectomy or laparotomy only. Survival rates, and protein and messenger RNA (mRNA) levels for tumor necrosis factor-alpha (TNF-alpha) and interleukin-6 (IL-6) were measured.

Results: Most of the unoperated control mice died within 3 days after the LPS challenge. Mortality following LPS injection was reduced after laparotomy only or hepatectomy (P<0.05). A significant reduction in the mortality was observed from 2 days to 7 days after laparotomy only, and from 2 days to 4 weeks after hepatectomy. Correspondingly, the increase in the serum levels of TNF-alpha and IL-6 induced by the LPS injection was partially impaired by either laparotomy only or hepatectomy at an early (2 days) postoperative stage (P<0.05). At a later (7 days) stage, however, the serum level of IL-6 and its mRNA level in the spleen were elevated after the LPS challenge more quickly in the hepatectomy group than in the unoperated control group ( P<0.05).

Conclusion: Surgical stress reduces LPS-induced lethality through biphasically regulating the levels of TNF-alpha and IL-6 production.

MeSH terms

  • Actins / blood
  • Animals
  • Disease Models, Animal
  • Hepatectomy / adverse effects*
  • Interleukin-6 / blood
  • Laparotomy / adverse effects*
  • Lipopolysaccharides / adverse effects
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Shock, Septic / chemically induced
  • Shock, Septic / metabolism*
  • Shock, Septic / mortality*
  • Stress, Physiological / etiology*
  • Stress, Physiological / metabolism*
  • Survival Rate
  • Time Factors
  • Tumor Necrosis Factor-alpha / analysis

Substances

  • Actins
  • Interleukin-6
  • Lipopolysaccharides
  • Tumor Necrosis Factor-alpha