Antithrombin acts as a negative acute phase protein as established with studies on HepG2 cells and in baboons

Thromb Haemost. 1997 Sep;78(3):1088-92.

Abstract

Patients with sepsis or after major surgery have decreased plasma levels of the anticoagulant protein antithrombin. In such patients elevated levels of interleukin-6 (IL-6) are present and this interleukin is known to induce positive and negative acute phase responses. To investigate the possibility that antithrombin acts as a negative acute phase response-protein we performed studies on the human hepatoma cell line HepG2 in vitro and baboons in vivo. HepG2 cells were treated with recombinant human IL-6, IL-1beta, or combinations of the latter two, and tested for production of antithrombin, fibrinogen and prealbumin (transthyretin). This treatment resulted in a dose dependent increase in fibrinogen concentration (with a maximum effect of 2.8-2.9-fold) and a dose dependent decrease in prealbumin (with a maximum effect of 0.6-0.7-fold) and antithrombin concentrations (with a maximum effect of 0.6-0.8-fold). Simultaneous treatment of the HepG2 cells with IL-6 (1,000 pg/ml or 2,500 pg/ml) and IL-1beta (25 pg/ml), provided more extensively decreased prealbumin (0.8 and 0.6-fold, respectively) and antithrombin concentration (0.7 and 0.6-fold, respectively) compared to the single interleukin treatment at these concentrations. Baboons treated with 2 microg IL-6 x kg body-weight(-1) x day(-1) showed increased plasma CRP levels (59-fold, p <0.05) and decreased prealbumin (0.9-fold, p <0.05) and antithrombin (0.8-fold, p <0.05) plasma levels, without evidence for coagulation activation. Our results indicate that antithrombin acts as a negative acute phase protein, which may contribute to the decreased antithrombin plasma levels observed after major surgery or in sepsis.

MeSH terms

  • Acute-Phase Reaction*
  • Animals
  • Antithrombin III / biosynthesis*
  • C-Reactive Protein / biosynthesis
  • Carcinoma, Hepatocellular
  • Humans
  • Interleukin-1 / pharmacology
  • Interleukin-6 / pharmacology
  • Liver / drug effects
  • Liver / metabolism*
  • Papio
  • Prealbumin / biosynthesis
  • Recombinant Proteins / pharmacology
  • Tumor Cells, Cultured
  • Urinary Bladder Neoplasms / metabolism

Substances

  • Interleukin-1
  • Interleukin-6
  • Prealbumin
  • Recombinant Proteins
  • Antithrombin III
  • C-Reactive Protein