Cw. Chen et al., Effects of N-omega-nitro-L-arginine (L-NOARG) on blood flow and vasomotionin rat diaphragm microcirculation during hemorrhagic hypotension, SHOCK, 12(1), 1999, pp. 69-74
The role of N-omega-nitro-L-arginine (L-NOARG), a nitric oxide (NO) synthas
e inhibitor, in the control of blood flow and vasomotion in rat diaphragm m
icrocirculation during hemorrhagic hypotension was investigated by means of
laser Doppler flowmetry (LDF). Fifty-six Sprague-Dawley rats were divided
into seven groups. Ten minutes after one-stage hemorrhage to 40-60% of init
ial blood pressure, the rats received 15 min topical superfusion of saline
(group 1, time control), 0.1 mM L-NOARG (group 2), 10 mM L-arginine (group
3), or vehicle (0.1% DMSO and 0.9 mN NaOH, group 4). For groups 5 and 6, L-
NOARG or its vehicle was superfused for 15 min without hemorrhage. In group
7, the vasodilator responses to the endothelium-dependent vasorelaxant ace
tylcholine (ACH) and the endothelium-independent vasorelaxant sodium nitrop
russide (SNP) were assessed at rest and after 25 min of hemorrhagic hypoten
sion. The results showed no significant differences in blood flow, fundamen
tal frequency, or relative amplitude of the rat diaphragm microcirculation
before or after administration of the test agents among the first four grou
ps during hemorrhagic hypotension or in groups 5 and 6 during sham operatio
n without hypoperfusion. Hemorrhagic hypotension significantly decreased th
e vasodilator response to ACH (p = 0.003), but not to SNP. We conclude that
NO did not play an important role in the regulation of blood flow or vasom
otion in rat diaphragm microcirculation during acute hemorrhagic hypotensio
n.