Protective effects of apocynin on "two-hit" injury induced by hemorrhagic shock and lipopolysaccharide

Acta Pharmacol Sin. 2002 Nov;23(11):1023-8.

Abstract

Aim: To evaluate the protective effects of apocynin on "two-hit" injury in rats.

Methods: "Two-hit" injury model of rat was induced by hemorrhagic shock (40 mmHg for 45 min) followed by iv administration of lipopolysaccharide (LPS, 150 microg/kg). Rats were randomized into seven groups: Sham, LPS, hemorrhage, hemorrhage/LPS, and hemorrhage/LPS+apocynin (2.5, 5.0, and 10.0 mg/kg). Apocynin was dissolved in the resuscitation fluid (normal saline, NS) and administered iv for 2 h. After LPS or NS administration, the survival rates at 8 h, 16 h, 24 h, and 48 h were monitored. The content of malondialdehyde (MDA) was measured in lung at 3 h and 6 h after iv LPS and in serum before hemorrhage, after hemorrhage, and at 0, 0.5, 1, 2, 4, and 6 h after iv LPS. Myeloperoxidase (MPO) activity in lung and liver was examined at 3 h and 6 h after iv LPS/NS.

Results: After "two-hit" injury, the survival rates of rats at 8 h, 16 h, 24 h, and 48 h were 64.3 %, 35.7 %, 28.6 %, and 14.3 % respectively, there were significant differences as compared to sham group (P<0.05 or P<0.01, respectively), the MDA level in lung and serum were significantly enhanced (P<0.01) as compared to sham group, and MPO activity in lung and liver after "two-hit" injury was also significantly increased (P<0.01). Apocynin treatment enhanced the mean arterial pressure (MAP) of hemorrhagic shock rats dose-dependently (P<0.05), increased the survival rate of "two-hit" injury rats, decreased the serum and lung MDA content, and downregulated MPO activity in lung and liver.

Conclusion: Apocynin could preventively ameliorate "two-hit" injury in rats induced by hemorrhagic shock and LPS insult.

MeSH terms

  • Acetophenones / pharmacology
  • Acetophenones / therapeutic use*
  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use*
  • Female
  • Lipopolysaccharides / toxicity*
  • Male
  • Malondialdehyde / metabolism
  • Peroxidase / metabolism
  • Random Allocation
  • Rats
  • Rats, Wistar
  • Shock, Hemorrhagic / complications*
  • Systemic Inflammatory Response Syndrome / chemically induced
  • Systemic Inflammatory Response Syndrome / metabolism
  • Systemic Inflammatory Response Syndrome / prevention & control*

Substances

  • Acetophenones
  • Anti-Inflammatory Agents, Non-Steroidal
  • Lipopolysaccharides
  • Malondialdehyde
  • acetovanillone
  • Peroxidase