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[The change of polymorphonuclear elastase releasing from ischemic skeleton muscles after reperfusion]

K Inazawa1

  • 1Second Department of Surgery, Yamagata University, School of Medicine, Japan.

Insights

Polymorphonuclear Elastase (PMNE) significantly increases after skeletal muscle reperfusion during aortic aneurysm surgery. Ulinastatin (U) effectively inhibits this PMNE increase, potentially preventing post-operative organ damage.

Area of Science:

  • Vascular Surgery
  • Biochemistry
  • Pharmacology

Background:

  • Abdominal aortic aneurysm surgery involves muscle reperfusion, leading to potential complications.
  • Polymorphonuclear Elastase (PMNE) is implicated in post-reperfusion injury.
  • Alpha 1-antitrypsin (alpha 1-AT) is a known inhibitor of PMNE.

Purpose of the Study:

  • To evaluate the activity of PMNE after skeletal muscle reperfusion in infra-renal abdominal aortic aneurysm surgery.
  • To investigate the effect of Ulinastatin (U), a PMNE inhibitor, on PMNE levels and post-operative complications.

Main Methods:

  • A study involving 20 patients undergoing abdominal aortic aneurysm surgery.
  • Patients were divided into two groups: Group I (non-Ulinastatin treated) and Group II (Ulinastatin treated).
  • Measurements of PMNE levels were taken before and 2 hours after reperfusion, with correlation analysis to clamping time.

Main Results:

  • PMNE levels significantly increased from pre-clamping to post-reperfusion in Group I (233.7 to 848.0 µg/l, p < 0.001).
  • Group II showed a significantly lower increase in PMNE post-reperfusion (204.8 to 416.7 µg/l) compared to Group I.
  • A positive correlation was observed between clamping duration and PMNE levels in Group I.

Conclusions:

  • Skeletal muscle reperfusion during aortic surgery leads to a statistically significant increase in PMNE.
  • Ulinastatin demonstrates significant inhibition of PMNE activity.
  • Ulinastatin may serve as a protective agent against visceral organ damage following acute arterial occlusion surgery.

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