Effects of N-omega-nitro-L-arginine (L-NOARG) on blood flow and vasomotionin rat diaphragm microcirculation during hemorrhagic hypotension

Citation
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
Citations number
35
Categorie Soggetti
Cardiovascular & Hematology Research
Journal title
SHOCK
ISSN journal
10732322 → ACNP
Volume
12
Issue
1
Year of publication
1999
Pages
69 - 74
Database
ISI
SICI code
1073-2322(199907)12:1<69:EON(OB>2.0.ZU;2-L
Abstract
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.