British Journal of Anaesthesia, Vol 77, Issue 3 413-418, Copyright © 1996 by The Board of Management and Trustees of the British Journal of Anaesthesia
F. Freden, J. E. Berglund, A. Reber, M. Hogman and G. Hedenstierna
I.v. administration of the nitric oxide synthase inhibitor, nitro-L-
arginine methyl ester (L-NAME), not only reduces blood flow in a hypoxic
lung region but also causes systemic vasoconstriction and a decrease in
cardiac output. In this study, we delivered nebulized L- NAME 0.2-1 mg kg-1
to the left lower lobe of 10 anaesthetized pigs. The left lower lobe was
made hypoxic by selective inhalation of 5% oxygen or collapsed by
interrupted ventilation, or both. Inhalation of L-NAME reduced fractional
blood flow to the left lower lobe from 5.3 (SD 3.1)% to 1.7 (1.4)% (P <
0.05) in lobar hypoxia and from 6.0 (3.3) to 2.7 (2.7)% (P < 0.05) in
lobar collapse. These reductions were accompanied by a significant increase
in PaO2. There were no significant changes in arterial pressure, cardiac
output or heart rate. We have shown that selective inhalation of L-NAME
reduced blood flow to a hypoxic or collapsed lung region without systemic
effects. The possible role for nitric oxide synthase inhibition in reducing
shunt during one-lung ventilation, however, requires further study.
LABORATORY INVESTIGATIONS
Inhalation of a nitric oxide synthase inhibitor to a hypoxic or collapsed lung lobe in anaesthetized pigs: effects on pulmonary blood flow distribution
Department of Anaesthesiology and Intensive Care, Uppsala University Hospital, S-752 31 Uppsala, Sweden; Department of Clinical Physiology, Uppsala University Hospital, S-752 31 Uppsala, Sweden
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