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May 11, 2009Circulation133 citations

Effects of Neuronal Nitric Oxide Synthase on Human Coronary Artery Diameter and Blood Flow In Vivo

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MSMichael D. SeddonNMNarbeh MelikianRDRafał Dworakowski

Key Result

Intracoronary infusion of the nNOS-selective inhibitor SMTC reduced basal coronary blood flow by 34.1% (P<0.01), indicating that nNOS regulates basal coronary vascular tone in vivo.

Structured PICO

Does nNOS-selective inhibition with SMTC reduce basal coronary blood flow and affect flow-mediated dilatation in humans?

P
Population
Patients with angiographically normal coronary arteries and healthy volunteers
I
Intervention
Intracoronary or local infusion of the nNOS-selective inhibitor S-methyl-L-thiocitrulline (SMTC)
C
Comparator
Nonselective NOS inhibitor N(G)-monomethyl-L-arginine
O
Outcome
Basal coronary blood flow, epicardial coronary diameter, and flow-mediated dilatationsurrogate

This study demonstrates that neuronal NO synthase (nNOS) regulates basal blood flow in the human coronary vascular bed, whereas endothelial NOS (eNOS) mediates stimulated vasodilatation.

Main Result

p-value: p=<0.01

Abstract

BACKGROUND: Nitric oxide (NO)-mediated local regulation of vascular tone is considered to involve endothelial NO synthase (eNOS). However, we recently reported that human forearm basal microvascular tone in vivo is tonically regulated by neuronal NO synthase (nNOS), in contrast to an acetylcholine-stimulated reduction in tone, which is eNOS dependent. Here, we investigated the in vivo effects of an nNOS-selective inhibitor, S-methyl-L-thiocitrulline (SMTC), on the human coronary circulation and on flow-mediated dilatation in the forearm. METHODS AND RESULTS: In patients with angiographically normal coronary arteries, intracoronary infusion of SMTC (0.625 micromol/min) reduced basal coronary blood flow by 34.1+/-5.2% (n=10; P<0.01) and epicardial coronary diameter by 3.6+/-1.2% (P=0.02) but had no effect on increases in flow evoked by intracoronary substance P (20 pmol/min). The nonselective NOS inhibitor N(G)-monomethyl-L-arginine (25 micromol/min) also reduced basal coronary flow (by 22.3+/-5.3%; n=8; P<0.01) but, in contrast to SMTC, inhibited substance P-induced increases in flow (P<0.01). In healthy volunteers, local infusion of SMTC (0.2 micromol/min) reduced radial artery blood flow by 36.0+/-6.4% (n=10; P=0.03) but did not affect flow-mediated dilatation (P=0.55). In contrast, N(G)-monomethyl-L-arginine (2 micromol/min) infusion reduced radial blood flow to a similar degree (by 39.7+/-11.8%; P=0.02) but also inhibited flow-mediated dilatation by approximately 80% (P<0.01). CONCLUSIONS: These data indicate that local nNOS-derived NO regulates basal blood flow in the human coronary vascular bed, whereas substance P-stimulated vasodilatation is eNOS mediated. Thus, nNOS and eNOS have distinct local roles in the physiological regulation of human coronary vascular tone in vivo.

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Cite This Study

Seddon et al. (2009) studied Angiographically normal coronary arteries. S-methyl-L-thiocitrulline (SMTC) vs. N(G)-monomethyl-L-arginine (L-NMMA) was evaluated on Reduction in basal coronary blood flow (p=<0.01). Intracoronary infusion of the nNOS-selective inhibitor SMTC reduced basal coronary blood flow by 34.1% (P<0.01), indicating that nNOS regulates basal coronary vascular tone in vivo.

synapsesocial.com/papers/6a12e4fa8793652519a692cfhttps://doi.org/10.1161/circulationaha.108.822205
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