L-Arginine administration during reperfusion improves pulmonary function

Yuji Shiraishi, Jeong Ryul Lee, Hillel Laks, Paul F. Waters, Avedis Meneshian, Arie Blitz, Keith Johnson, Lydia Lam, Paul A. Chang

Research output: Contribution to journalArticlepeer-review

24 Scopus citations


Background. Nitric oxide is crucial to the maintenance of vascular homeostasis. Because nitric oxide levels decline upon lung reperfusion, infusion of L-arginine, a nitric oxide precursor, during reperfusion might prove effective at ameliorating reperfusion injury. Methods. Neonatal piglet heart-lung blocks were preserved with Euro-Collins solution for 12 hours, rewarmed at room temperature for 1 hour, and reperfused for 10 minutes with either whole blood (n = 5), whole blood containing L-arginine (10 mmol/L; n = 6), or leukocyte-depleted blood (n = 6) on an isolated, blood-perfused, working heart-lung circuit. After the initial 10 minutes, all blocks received whole blood for 4 hours. Control blocks were continuously perfused on the circuit without intervening ischemia (n = 6). Results. The partial pressure of oxygen in the whole blood group (113.8 ± 33.1 mm Hg) was significantly less than in controls (417.3 ± 6.2 mm Hg; p < 0.01). Lung compliance was significantly less in the whole blood group (0.8 ± 0.2 mL/cm H2O) than in controls (2.9 ± 0.4 mL/cm H2O; p < 0.01). The L-arginine and leukocyte-depleted blood groups showed no significant difference from controls. Conclusions. L-Arginine infusion during reperfusion improves pulmonary function, making it a simple alternative to leukocyte depletion.

Original languageEnglish (US)
Pages (from-to)1580-1587
Number of pages8
JournalAnnals of Thoracic Surgery
Issue number6
StatePublished - Dec 1996
Externally publishedYes

ASJC Scopus subject areas

  • Surgery
  • Pulmonary and Respiratory Medicine
  • Cardiology and Cardiovascular Medicine


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