Nitric oxide-dependent factors (serotonin, activated platelets, acetylcholine) cause vasodilation in normal coronary arteries but vasoconstrict atherosclerotic vessels. This experiment tested the hypothesis that intravenous systemic infusions of L-arginine, a precursor for nitric oxide production, dilate the coronary vascular bed of patients undergoing coronary artery bypass graft surgery.


Twenty patients scheduled for coronary artery bypass graft surgery surgery were studied in a prospective, blinded, randomized clinical trial. Saphenous vein graft blood flow was measured with a transit time flow probe, and coronary vascular resistance was calculated. After weaning from bypass, patients were given a venous infusion (placebo or 10% arginine hydrochloride [30 g]) over 15 min. Arterial blood samples for the determination of L-arginine and L-citrulline levels were drawn before, 10 min after starting infusion, and 10 min after end of infusion.


The placebo group experienced an increase in mean arterial pressure and coronary vascular resistance and a decrease in graft blood flow. Patients in the L-arginine group maintained their baseline values. Mean arterial pressure (L-arginine, 88+/-17 to 92+/-13 mmHg vs. placebo, 80+/-12 to 92+/-9 mmHg, P = 0.021), coronary vascular resistance (L-arginine, 97,000+/-60,000 to 99,600+/-51,000 dynes x s x cm(-5) vs. placebo, 81,000+/-69,000 to 117,000+/-64,000 dynes x s x cm(-5), P = 0.05), and graft blood flow (L-arginine, 55+/-25 to 50+/-19 ml/min vs. placebo, 60+/-34 to 46+/-18, P = 0.05) remained more stable in the L-arginine-treated patients.


Systemic L-arginine infusion reduced postbypass coronary vasoconstriction. There were no adverse events associated with the drug infusion.

Key words: CABG; clinical trial; nitric oxide; vascular resistance.

IN patients with atherosclerotic coronary arteries, the basal secretion of nitric oxide (NO) is reduced, [1]and NO-mediated endothelium-dependent relaxations fail to occur. [1-3]As a consequence, NO-dependent factors that cause vasodilation in normal coronary arteries may cause vasoconstriction in atherosclerotic vessels. [3]This paradoxic effect is endothelium-dependent and is thought to be caused by the inability of the endothelium to synthesize adequate amounts of NO, thus leaving unopposed vasoconstriction. Moreover, after ischemic reperfusion, coronary arteries lose the ability to dilate in response to NO-dependent factors (prostaglandin F2 [Greek small letter alpha] and platelets). [4] 

L-arginine (L-ARG), the precursor for NO, [5-7]increases the levels of NO and causes vasodilation. [8-11]Although L-ARG infusions have been shown to improve endothelial function in patients with coronary atherosclerosis, [12-18]it is unknown if L-ARG vasodilates coronary arteries in patients with postbypass reperfusion injury. After coronary artery bypass graft (CABG), patients have severely injured coronary endothelium and may not respond to L-ARG infusions.

This experiment tested the hypothesis that post-cardiopulmonary bypass infusions of L-ARG improve coronary blood flow and decrease coronary vascular resistance. This experiment measured the ability of L-ARG to increase NO-dependent vasodilation in patients who have just undergone cardioplegic arrest and myocardial revascularization.


With informed consent and institutional review board approval, 20 patients aged more than 40 yr undergoing elective CABG surgery at the San Francisco Veterans Administration Medical Center were studied in this prospective, randomized, blinded clinical trial. Patients with aortic or mitral valvular disease requiring valve repair or replacement, left bundle branch block, previous coronary surgery, or esophageal disease were excluded from the study.

Anesthetic Care

History was taken and physical examination performed preoperatively, with specific attention to cardiac disease, myocardial infarction, current angina, congestive heart failure, arrhythmias, and cardiac catheterization data. Patients were premedicated with diazepam (0.15 mg/kg orally) and morphine (0.15 mg/kg intramuscularly) 60 min before arrival at the operating room. Before induction of anesthesia, five-lead electrocardiography equipment, a peripheral intravenous line, a 20-gauge radial arterial line, and a right internal jugular pulmonary artery catheter with thermodilution cardiac output were placed. Baseline measurements of cardiac output, pulmonary artery pressure, pulmonary artery wedge pressure, and arterial blood gas values were obtained. A standard anesthetic of fentanyl (25-125 [micro sign]g/kg intravenously) and midazolam (0.1-0.5 mg/kg intravenously) was administered, with muscle relaxation achieved by vecuronium (0.1 mg/kg). Controlled ventilation with 100% oxygen was used to maintain a PaO(2) greater than 80 mmHg and a PaCO(2) between 35 and 45 mmHg, as determined by arterial blood gas sampling. Inadequate anesthesia was treated with boluses of fentanyl (1-5 [micro sign]g/kg intravenously).

Experimental Period

The patients underwent standard bypass surgery and were subsequently weaned from bypass in routine fashion. Changes in the infusion rates of vasoconstrictors, vasodilators, or inotropic agents or the administration of anesthetics could result in systemic and coronary vascular changes. We therefore did not start the experimental period until the patient was stable after bypass. Stability was defined as (1) completion of the protamine infusion, (2) no change in anesthetic management for preceding 10 min, (3) systolic blood pressure greater than 100 mmHg, and (4) cardiac index greater than 2.0 1 [middle dot] min-1[middle dot] m-2. Once the experimental period began, no changes in the infusion rate or administration of any drugs were allowed. Constant infusions (neosynephrine or dopamine) were allowed if necessary for weaning from bypass. No NO donors (nitroprusside or nitroglycerine) or vasodilators (inhaled agents) were used during the experimental period. The only change during the experimental period was the administration (initiation, infusion, and termination) of the study drug (placebo or L-ARG).

Once patients met criteria for stability after bypass, the experiment began. Baseline hemodynamic levels were recorded. A transit time flow probe (H4SB Transonics Systems, Ithaca, NY) was placed on one of the saphenous grafts. Grafts were chosen that perfused beds with severe (greater than 80% stenosis) proximal disease. The saphenous grafts served as convenient locations to measure blood flow and provide a method of measuring the resistance in the myocardial beds fed by the graft. A decrease in resistance of the vascular bed would result in a subsequent increase in saphenous graft blood flow.

Patients were given an infusion into the right internal jugular cordis (placebo [300 ml of saline solution] or 10% arginine hydrochloride [30 g/300 ml; R-Gene 10 Kabi Pharmacia, Piscataway, NJ]) provided by the pharmacy in a double-blind fashion. The dosage was chosen to achieve a predicted concentration of approximately 10-2M, the maximal level demonstrated to improve endothelial function. [13]In patients randomized to receive the active drug, 30 g of L-ARG was infused over 15 min. The placebo group received an equal volume (300 ml) of normal saline solution, with all other procedures identical between the two test groups.

Systolic, diastolic, and mean arterial pressures; central venous pressure; heart rate; O2saturation (Propaq 106EL, Protocol Systems, Beaverton, OR); and saphenous bypass-graft blood flow (Transonics HT207, Transonics Systems, Ithaca, NY) were recorded by computer (Compaq Contura 400C, Houston, TX) using custom software (MCMS, IREF, San Francisco, CA) every 10 s from 10 min preinfusion to 15 min after termination of infusion and stored for later analysis.

Laboratory Studies

Three arterial blood samples were drawn, one before sample infusion, one 10 min after starting the infusion, and one 10 min after the end of the infusion for the measurement of serum levels of L-ARG and L-citrulline (L-CIT; amino acid assays were performed by Quest Diagnostics, Teterboro, NJ, with an ion-exchange chromatographer, the Beckman 6300 amino acid analyzer, Beckman, Fullerton, CA). Creatine phosphokinase (CPK) (Kodak Ektachem technique, Kodak, Rochester, NY) and creatinine phosphokinase myocardial band (CPK-MB) analysis (Abbott IMX immunoassay; Abbott, Abbott Park, IL) were performed at the hospital laboratory on the first postoperative day as an indicator of myocardial infarction. A CPK-MB isoenzyme concentration of greater than 100 ng/ml in any postoperative sample was chosen as the threshold for biochemical evidence of myocardial infarction. [19]Serum osmolality was measured using a freezing-point osmometer at the hospital laboratory.

Holter Electrocardiography

Ambulatory Holter electrocardiographic monitoring using a three-channel AM Holter electrocardiogram recorder (with ST-segment detection; Series 8500, Marquette Electronics, Milwaukee, WI) began 12 h before anesthetic induction and was continued for 36 h postoperatively. Holter analysis technique was identical to that used in previous work. [20]Electrocardiographic ischemic episodes were defined as reversible ST-segment changes lasting at least 1 min and involving either a shift from baseline (adjusted for positional changes) of >or= to 0.1 mV of ST depression (with slope <or= to 0), or a shift from baseline of >or= to 0.2 mV of ST elevation at the J-point.

Twelve-lead Electrocardiography

Twelve-lead electrocardiograms were obtained preoperatively, immediately postoperatively, and on postoperative days 1 and 2. All electrocardiographic data were subsequently analyzed by two investigators unaware of clinical data. Minnesota codes I1 or I2 were used to identify new Q waves. Persistent changes in the ST-T waves were identified by Minnesota codes IV or V. [21] 

Time-dependent hemodynamic data were divided into three time segments: preinfusion (5 min), during the infusion (15 min), and postinfusion (10 min). For each patient, hemodynamic parameters (cardiac output, mean arterial pressure, central venous pressure, graft blood flow, coronary vascular resistance, and systemic vascular resistance) were averaged over each of the time segments. Because the time course of the response was not know before study initiation, the decision was made to average the entire time segment. Coronary vascular and systemic vascular resistances were calculated using: Equation 1

Two-way repeated measures analysis of variance with one-factor repetition (SigmaStat 2.03S, SPSS, Chicago, IL) was used to test for the difference between the two study groups as hemodynamic values (mean arterial pressure, central venous pressure, systemic vascular resistance, cardiac output, graft flow, and coronary vascular resistance) varied with time. Dunnett method of multiple comparisons versus a control group was used if the P values were significant for the two-way repeated-measures analysis of variance. The Fisher exact test was used for categorical data. A P value less than 0.05 was taken as statistically significant. Values in text are listed as mean +/- SD.

Of the 20 patients that were randomized for the study, a computer malfunction resulted in the loss of the hemodynamic data of three patients (two in the placebo group and one patient in the L-ARG group). All 20 patients were included in summary results, but only the 17 subjects with hemodynamic data were included in hemodynamic analysis. Table 1shows the baseline demographic data for the two groups. There was an increased number of preoperative myocardial infarctions in the placebo group. The two groups show no other significant differences.

Table 1. Presurgery Demographic Data

Table 1. Presurgery Demographic Data
Table 1. Presurgery Demographic Data

There were no statistically significant differences in perioperative adverse events between the two groups (Table 2). There were no deaths in the study. Five patients developed new Q waves on electrocardiography consistent with a diagnosis of myocardial infarction. Only one of these patients developed a CPK-MB concentration greater than 100 ng/ml. This patient also had postbypass ischemic episodes as assessed by Holter analysis.

Table 2. Postsurgery Data

Table 2. Postsurgery Data
Table 2. Postsurgery Data

L-arginine had minimal effects on the peripheral vasculature in patients after cardiopulmonary bypass (Figure 1, Table 3). Mean arterial pressure increased in the control patients compared with the patients receiving L-ARG (L-ARG, 88 +/- 17 to 92 +/- 13 mmHg, vs. placebo, 80 +/- 12 to 92 +/- 9 mmHg; P = 0.021). This difference was between preinfusion and postinfusion periods (P < 0.050). There was no significant change in cardiac output (P = 0.945), systemic vascular resistance (P = 0.284), or central venous pressure (P = 0.655) with drug infusion.

Figure 1. Results for each individual patient as well as the mean +/- standard deviation are plotted versus time. (Top) The mean arterial pressure response to L-arginine or placebo infusion. Mean arterial pressure decreased compared with placebo, in response to the L-arginine infusion (P < 0.050). (Upper middle) The central venous pressure response. (Lower middle) The systemic vascular resistance. (Bottom) The cardiac output response. Significance indicated with asterisk.

Figure 1. Results for each individual patient as well as the mean +/- standard deviation are plotted versus time. (Top) The mean arterial pressure response to L-arginine or placebo infusion. Mean arterial pressure decreased compared with placebo, in response to the L-arginine infusion (P < 0.050). (Upper middle) The central venous pressure response. (Lower middle) The systemic vascular resistance. (Bottom) The cardiac output response. Significance indicated with asterisk.

Close modal

Table 3. Hemodynamics Data

Table 3. Hemodynamics Data
Table 3. Hemodynamics Data

The coronary vasculature of placebo-treated patients constricted during the experimental period (81,000 +/- 69,000 to 117,000 +/- 64,000 dynes [middle dot] s [middle dot] cm-5, P = 0.05; Table 3); in the L-ARG group the resistance remained constant (97,000 +/- 60,000 to 99,600 +/- 51,000 dynes [middle dot] s [middle dot] cm-5; P = 0.05). Saphenous graft blood flow decreased in the control patients (60 +/- 34 to 46 +/- 18 ml/min); it remained more stable in the L-ARG-treated patients (55 +/- 25 to 50 +/- 19 ml/min; P = 0.05). The initial response to the L-ARG infusion is an increase in graft flow and a decrease in coronary vascular resistance. The top panel of Figure 2shows a representative example of the increase in saphenous graft flow with L-ARG infusion in one patient and compares it with the recording of graft flow in a placebo-treated patients. The bottom panel of Figure 2shows the calculated coronary vascular resistance in the same two patients. The typical response is an increase in graft blood flow immediately following L-ARG infusion initiation, with a peak approximately 2.5 min later. The increase in graft blood flow tapers off following the initial maximum, but the graft blood flow remains markedly higher than the control group. Coronary vascular resistance decreases immediately following L-ARG infusion initiation and reaches a minimum approximately 2.5 min after infusion initiation. It then returns to baseline after termination of the infusion. In summary, saphenous graft blood flow normally decreases after cardiopulmonary bypass. L-ARG infusions prevent the decrease. Coronary vascular resistance increases after cardiopulmonary bypass-L-ARG infusions prevent that increase (Figure 3).

Figure 2. Plots of saphenous graft flow and coronary vascular resistance versus time from two patients. Data are plotted from before the start of the infusion, during the infusion, and after completion of the infusion. Dark diamonds = L-ARG patient; hollow squares = placebo patient. (Top) The saphenous graft blood flow. (Bottom) The coronary vascular resistance.

Figure 2. Plots of saphenous graft flow and coronary vascular resistance versus time from two patients. Data are plotted from before the start of the infusion, during the infusion, and after completion of the infusion. Dark diamonds = L-ARG patient; hollow squares = placebo patient. (Top) The saphenous graft blood flow. (Bottom) The coronary vascular resistance.

Close modal

Figure 3. Results for each individual patient as well as the mean +/- standard deviation are plotted versus time. (Top) Saphenous graft blood flow increased compared with placebo, in response to L-arginine infusion (P < 0.05). (Bottom) Coronary vascular resistance decreased compared with placebo n response to L-arginine infusion (P < 0.05). Significance indicated with asterisk.

Figure 3. Results for each individual patient as well as the mean +/- standard deviation are plotted versus time. (Top) Saphenous graft blood flow increased compared with placebo, in response to L-arginine infusion (P < 0.05). (Bottom) Coronary vascular resistance decreased compared with placebo n response to L-arginine infusion (P < 0.05). Significance indicated with asterisk.

Close modal

Before the infusion, serum concentrations of L-ARG and L-CIT in patients receiving placebo and L-ARG are not significantly different (Table 4). Ten minutes after the start of the infusion, serum concentrations of L-ARG in patients receiving L-ARG are two orders of magnitude higher than those of placebo patients (L-ARG, 6,900 +/- 600 [micro sign]mol, vs. placebo, 81 +/- 8 [micro sign]mol; P < 0.05). Ten minutes after termination of the infusion, the serum concentration of L-CIT in L-ARG patients is statistically significantly higher than in the placebo patients (L-CIT, 38 +/- 3.9 [micro sign]mol, vs. placebo, 25 +/- 1.3 [micro sign]mol; P < 0.05).

Table 4. Amino Acid Levels

Table 4. Amino Acid Levels
Table 4. Amino Acid Levels

The L-ARG infusion increased serum osmolality (272 +/- 36.7 to 299 +/- 7.2 mOsm/kg) compared with the placebo group (291 +/- 9 to 291 +/- 140 mOsm/kg; P = 0.05).

This study demonstrated that systemic L-ARG infusions dilated coronary vasculature in patients after cardiopulmonary bypass without significant systemic vascular effects. Infusions of L-ARG significantly increased the serum L-ARG concentration and had a small effect on serum L-CIT concentrations. There was no statistically significant difference in postsurgical adverse events.

This study was a small, prospective, randomized clinical trial designed to test the hypothesis that L-ARG infusions would improve coronary blood flow. It was not designed with significant power to identify changes in prevalence of myocardial ischemia, myocardial infarction, or death. These data were collected as safety monitors, with no expectation of statistically significant outcomes.

This study used transit time flow probes, which provide an accurate measure of absolute flow in the saphenous graft. There are, however, several problems with this technique. First, flow can only be measured after placement of the saphenous graft; no prebypass data can be acquired. Second, the flow probes must be removed prior to chest closure; no data can be obtained postoperatively. Finally, the probes only measure flow in the saphenous grafts; they do not measure total flow to the vascular bed. We chose grafts that went to vascular beds with high-grade proximal stenosis, but some of the flow to these beds came from the proximal native vessel and was not measured. The saphenous grafts are large in relationship to the distal native vessel, so the changes in flow and resistance primarily reflect changes in downstream coronary resistance, not changes in saphenous graft resistance. Despite the limitations of the transit time flow probes, we were clearly able to measure changes in graft flow in response to L-ARG infusion.

The placebo used in this study was normal saline solution. The L-ARG infusion (R-Gene [registered sign] 10, 10% arginine hydrochloride) is hypertonic (950 mOsm/l). The osmolality of the patients receiving L-ARG infusion increased by 10% (272 +/- 36.7 to 299 +/- 7.2 mOsm/kg); that of the placebo group remained constant (291 +/- 9 to 291 +/- 140 mOsm/kg; P = 0.05). This increase in osmolality would be predicted to decrease coronary vascular resistance by about 15%. [22,23]Coronary vascular resistance decreased by 20% (97,008 +/- 59,962 to 77,447 +/- 38,019 dynes [middle dot] s [middle dot] cm-5) in the L-ARG group. Changes in serum osmolality may be partially responsible for the observed coronary vasodilation associated with L-ARG infusion.

We measured L-ARG and L-CIT concentrations from samples drawn from a radial artery. L-ARG is converted by NO synthase (NOS) into L-CIT and NO, making L-CIT a marker of the production of NO. The small increase in L-CIT levels in the L-ARG group suggests that L-ARG was converted into L-CIT with production of NO. We did not measure coronary sinus L-CIT or NO levels, which may have provided a more accurate representation of the conversion of L-ARG to L-CIT with production of NO. The small but significant change in L-CIT levels indicates that only a fraction of the delivered L-ARG was converted to L-CIT with production of NO, which is consistent with previous reports. [24,25]The small changes in mean arterial pressure with no significant change in systemic vascular resistance is consistent with the conclusion that little L-ARG was converted to L-CIT by NOS in the peripheral vasculature. Although the increase in serum L-CIT occurred simultaneously with the reduction in serum L-ARG concentration, L-ARG and L-CIT did not change in stoichiometric proportions. This discrepancy may simply be due to other metabolic pathways for L-ARG. [26,27]Although direct measurement of NO production by the coronary vasculature was not attempted, we propose that NO is the likely mediator responsible for the observed coronary vasodilation. Patients in the L-ARG group had a significant increase in serum concentration of L-CIT, the physiologic byproduct in the production of NO from L-ARG by NOS.

There is some controversy concerning the systemic vascular effects of L-ARG infusions. Although most studies find that L-ARG infusions have minimal effects on blood pressure or cardiac output, [28-30]most demonstrate an improved endothelial function in patients with atherosclerosis. [12-14]L-ARG has been shown to considerably improve postischemic recovery of cardiac mechanical function after cardioplegic arrest and ischemia if given in the reperfusate (animal model of cardiac transplantation). [31-35]It also has been shown to improve coronary endothelial response to acetylcholine after cardiac transplant. [36]Intracoronary L-ARG infusions have been shown to improve endothelium-dependent coronary vascular function in patients with coronary artery disease. [15-18]Two studies [37,38]have demonstrated an improvement in clinical symptoms of coronary artery disease with oral administration of L-ARG. Long-term (6 months) oral L-ARG administration (3 g orally, three times a day) in patients with angiographically significant coronary artery disease improved coronary small-vessel endothelial function, decreased plasma endothelin concentrations, and significantly improved clinical symptoms. [38]Oral supplementation with L-ARG increased exercise capacity in patients with stable angina after healed myocardial infarction. [37] 

This study found a slight decrease in systemic arterial pressure compared with control with L-ARG infusion, and no other effects on the peripheral vasculature, which is consistent with previous reports. [13,14,28]In contrast to previous reports [14]we found an increase in coronary blood flow and concomitant decrease in coronary vascular resistance when compared to control.

There are several possible explanations for this discrepancy. The conversion of L-ARG into L-CIT and NO by NOS is regulated. NO production is a significant regulator of the response to inadequate blood flow. [39-44]In normal patients with adequate blood flow, increasing the substrate for NOS may have little effect. In vascular beds experiencing ischemia or relative ischemia, increases in substrate may have a profound effect. [45]In patients undergoing extracorporeal bypass for CABG surgery, the peripheral vasculature is frequently profoundly vasodilated. If the peripheral vasculature is fully dilated after bypass, additional NO produced by increased substrate may have minimal effect on the peripheral vascular resistance. Alternatively, the coronary vasculature of patients with atherosclerosis may be unable to produce enough NO. [1]Increases in substrate may then have a profound effect and result in vasodilation. It is not that the systemic vasculature is unresponsive and the coronary circulation is responsive to L-ARG infusions but rather where that vascular bed lies on the dose-response curve to L-ARG-NO. The change in coronary vascular resistance associated with L-ARG infusion was greatest in grafts that had low initial blood flow, suggesting that these beds may have been vasoconstricted and be on a steep portion of the L-ARG-NO dose-response curve.

The placebo group showed an increase in coronary vascular resistance with time. In the L-ARG group, however, this effect was offset by infusions of L-ARG. L-ARG infusion prevented an increase in coronary vascular resistance. The corollary is that if the resistance had been stable, L-ARG infusion would resulted in a net dilation of the vessel. Similar assessment can be made about the graft blood flow. It should be noted that graft blood flow in the placebo group steadily decreased with time. Graft flow increased initially with L-ARG infusion and then remained higher than in the control group.

This study was too small to demonstrate any effects on clinical outcomes (myocardial infarction, death, or myocardial ischemia). Larger trials designed with sufficient power to determine clinical outcomes are required before any conclusions.

This study clearly demonstrates that infusions of L-ARG in patients undergoing CABG surgery have minimal effects on the systemic vasculature and improve coronary blood flow. Further trials are required to determine if infusions of L-ARG are able to reduce the incidence of postbypass myocardial ischemia and infarction by improving endothelial function. L-ARG infusion has potential as an anti-ischemic therapy for post-CABG surgery patients.

Chester AH, O'Neil GS, Moncada S, Tadjkarimi S, Yacoub MH: Low basal and stimulated release of nitric oxide in atherosclerotic epicardial coronary arteries (see comments). Lancet 1990; 336:897-900
Bossaller C, Habib GB, Yamomoto H, Williams C, Wells S, Henry PD: Impaired muscarinic endothelium-dependent relaxation and cyclic guanosine 5'-monophosphate formation in atherosclerotic human coronary artery and rabbit aorta. J Clin Invest 1987; 79:170-4
Golino P, Piscione F, Willerson JT, Cappelli-Bigazzi M, Focaccio A, Villari B, Indolfi C, Russolillo E, Condorelli M, Chiariello M: Divergent effects of serotonin on coronary-artery dimensions and blood flow in patients with coronary atherosclerosis and control patients (see comments). N Engl J Med 1991; 324:641-8
Pearson PJ, Schaff HV, Vanhoutte PM: Acute impairment of endothelium-dependent relaxations to aggregating platelets following reperfusion injury in canine coronary arteries. Circ Res 1990; 67:385-93
Moncada S Palmer RM, Higgs EA: The biological significance of nitric oxide formation form L-arginine. Biochem Soc Trans 1989; 17:642-4
Moncada S, Palmer RM, Higgs EA: Biosynthesis of nitric oxide from L-arginine. A pathway for the regulation of cell function and communication. Biochem Pharmacol 1989; 38:1709-15
Palmer RM, Rees DD, Ashton DS, Moncada S: L-arginine is the physiological precursor for the formation of nitric oxide in endothelium-dependent relaxation. Biochem Biophys Res Commun 1988; 153:1251-6
Vallance P, Collier J, Moncada S: Effects of endothelium-derived nitric oxide on peripheral arteriolar tone in man (see comments). Lancet 1989; 2:997-1000
Vallance P, Collier J, Moncada S: Nitric oxide synthesised from L-arginine mediates endothelium dependent dilatation in human veins in vivo. Cardiovasc Res 1989; 23:1053-7
Vallance P: The interplay between platelet and vessel-wall mediators in coronary artery occlusion. Biomed Pharmacother 1989; 43:113-9
Richard V, Tanner FC, Tschudi M, Luscher TF: Different activation of L-arginine pathway by bradykinin, serotonin, and clonidine in coronary arteries. Am J Physiol 1990; 259:H1433-9
Clarkson P, Adams MR, Powe AJ, Donald AE, McCredie R, Robinson J, McCarthy SN, Keech A, Celermajer DS, Deanfield JE: Oral L-arginine improves endothelium-dependent dilation in hypercholesterolemic young adults. J Clin Invest 1995; 97:1989-94
Creager MA, Gallagher SJ, Girerd XJ, Coleman SM, Dzau VJ, Cooke JP: L-arginine improves endothelium-dependent vasodilation in hypercholesterolemic humans. J Clin Invest 1992; 90:1248-53
Drexler H, Zeiher AM, Meinzer K, Just H: Correction of endothelial dysfunction in coronary microcirculation of hypercholesterolaemic patients by L-arginine. Lancet 1991; 338:1546-50
Hirooka Y, Egashira K, Imaizumi T, Tagawa T, Kai H, Sugimachi M, Takeshita A: Effect of L-arginine on acetylcholine-induced endothelium-dependent vasodilation differs between the coronary and forearm vasculatures in humans. J Am Coll Cardiol 1993; 24:948-55
Quyyumi AA, Dakak N, Diodati JG, Gilligan DM, Panza JA, Cannon RO III: Effect of L-arginine on human coronary endothelium-dependent and physiologic vasodilation. J Am Coll Cardiol 1997; 30:1220-7
Quyyumi AA: Does acute improvement of endothelial dysfunction in coronary artery disease improve myocardial ischemia? A double-blind comparison of parenteral D- and L-arginine. J Am Coll Cardiol 1998: 32:904-11
Egashira K, Hirooka Y, Kuga T, Mohri M, Takeshita A: Effects of L-arginine supplementation on endothelium-dependent coronary vasodilation in patients with angina pectoris and normal coronary arteriograms (see comments). Circulation 1996; 94:130-4
Jain U, Laflamme CJ, Aggarwal A, Ramsay JG, Comunale ME, Ghoshal S, Ngo L, Ziola K, Hollenberg M, Mangano DT: Electrocardiographic and hemodynamic changes and their association with myocardial infarction during coronary artery bypass surgery: A multicenter study. Multicenter Study of Perioperative Ischemia (McSPI) Research Group. Anesthesiology 1997; 86:576-91
Wallace A, Layug B, Tateo I, Li J, Hollenberg M, Browner W, Miller D, Mangano D, Group MR: Prophylactic atenolol reduces post-operative myocardial ischemia. Anesthesiology 1998; 88:7-17
Blackburn H, Keys A, Simonson E, Rautaharju P, Punsar S: The electrocardiogram in population studies: A classification system. Circulation 1960; 21:1160-75
Brace RA, Scott JB, Chen WT, Anderson DK, Haddy FJ: Direct effects of hypoosmolality on vascular resistance and myocardial contractile force (38587). Proce Soc Exp Biol Med 1975; 148:578-83
Stainsby WN, Fregly MJ: Effect of plasma osmolality on resistance to blood flow through skeletal muscle. Proc Soc Exp Biol Med 1968; 128:284-7
Rhodes P, Leone AM, Francis PL, Struthers AD, Moncada S, Rhodes PM: The L-arginine:nitric oxide pathway is the major source of plasma nitrite in fasted humans (published erratum appears in Biochem Biophys Res Commun 1995; 211:705). Biochem Biophys Commun 1995; 190:590-6
Castillo L, deRojas TC, Chapman TE, Vogt J, Burke JF, Tannenbaum SR, Young VR: Splanchnic metabolism of dietary arginine in relation to nitric oxide synthesis in normal adult man. Proc Natl Acad Sci U S A 1993; 90:193-7
Hecker M, Sessa WC, Harris HJ, Anggard EE, Vane JR: The metabolism of L-arginine and its significance for the biosynthesis of endothelium-derived relaxing factor: Cultured endothelial cells recycle L-citrulline to L-arginine. Proc Natl Acad Sci U S A 1990; 87:8612-6
Hecker M, Mitchell JA, Swierkosz TA, Sess WC, Vane JR: Inhibition by L-glutamine of the release of endothelium-derived relaxing factor from cultured endothelial cells. Br J Pharmacol 1990; 101:237-9
Baudouin SV, Bath P, Martin JF, Du Bois R, Evans TW: L-arginine infusion has no effect on systemic haemodynamics in normal volunteers, or systemic and pulmonary haemodynamics in patients with elevated pulmonary vascular resistance. Br J Clin Pharmacol 1993; 36:45-9
Bode-Boger SM, Boger RH, Creutzig A, Tsikas D, Gutzki FM, Alexander K, Frolich JC: L-arginine infusion decreases peripheral arterial resistance and inhibits platelet aggregation in healthy subjects. Clin Sci (Colch) 1994; 87:303-10
Boger RH, Mugge A, Bode-Boger SM, Heinzel D, Hoper MM, Frolich JC: Differential systemic and pulmonary hemodynamic effects of L-arginine in patients with coronary artery disease or primary pulmonary hypertension. Int J Clin Pharmacol Ther 1996; 34:323-8
Amrani M, Gray CC, Smolenski RT, Goodwin AT, london A, Yacoub MH: The effect of L-arginine on myocardial recovery after cardioplegic arrest and ischemia under moderate and deep hypothermia. Circulation 1997; 96:II-274-9
Lee R, Nitta T, Schmid RA, Schuessler RB, Harris KM, Say WA Jr. Retrograde infusion of lidocaine or L-arginine before reperfusion reduces myocardial infarct size. Ann Thorac Surg 1998; 65:1353-9
Mizuno T, Watanabe M, Sakamoto T, Sunamori M: L-arginine, a nitric oxide precursor, attenuates ischemia-reperfusion injury by inhibiting inositol-1,4,5-triphosphate. J Thorac Cardiovasc Surg 1998; 115:931-6
Szabo G, Bahrle S, Batkai S, Stumpf N, Dengler TJ, Zimmerman R, Vahl CF, Hagl S: L-arginine: Effect on reperfusion injury after heart transplantation. World J Surg 1998; 22:791-7; discussion 797-8
Szabo G, Batkai S, Bahrle S, Dengler TJ, Vahl CF, Zimmermann R, Hagl S: Effects of nitric oxide synthesis on reperfusion injury and catecholamine responsiveness in a heterotopic rat heart-transplantation model. J Cardiovasc Pharmacol 1998; 31:221-30
Drexler H, Fischell TA, Pinto FJ, Chenzbraun A, Botas J, Cooke JP, Alderman EL: Effect of L-arginine on coronary endothelial function in cardiac transplant recipients: Relation to vessel wall morphology. Circulation 1993; 89:1615-23
Ceremuzynski L, Chamiec T, Herbaczynska-Cedro K: Effect of supplemental oral L-arginine on exercise capacity in patients with stable angina pectoris. Am J Cardiol 1997; 80:331-3
Lerman A, Burnett JC Jr, Higano ST, McKinley LJ, Holmes DR Jr: Long-term L-arginine supplementation improves small-vessel coronary endothelial function in humans (in process citation). Circulation 1998; 97:2123-8
Otomo J, Nozaki N, Tomoike H: Roles of nitric oxide and adenosine in the regulation of coronary conductance in the basal state and during reactive hyperemia. Jpn Circ J 1997; 61:441-9
Gryglewski RJ, Chlopicki S, Niezabitowski P: Myocardial reactive hyperaemia in perfused guinea pig heart. Pol J Pharmacol 1997; 47:479-83
Gryglewski RJ, Chlopicki S, Niezabitowski P, Jakubowski A, Lomnicka M: Ischaemic cardiac hyperaemia: Role of nitric oxide and other mediators. Physiol Res 1996; 45:255-60
Macho P, Domenech R, Penna M: Relative participation of adenosine and endothelium derived mediators in coronary reactive hyperemia in the dog. Biol Res 1997; 28:165-71
Sagach VF, Tkachenko MN: Role of nitric oxide in myocardial reactive hyperemia in a dog. Pol J Pharmacol 1994; 46:609-14
Huckstorf C, Zanzinger J, Fink B, Bassenge E: Reduced nitric oxide formation causes coronary vasoconstriction and impaired dilator responses to endogenous agonists and hypoxia in dogs. Naunyn Schmiedebergs Arch Pharmacol 1994; 349:367-73
Bode-Boger SM, Boger RH, Alfke H, Heinzel D, Tsikas D, Creutzig A, Alexander K, Frolich JC: L-arginine induces nitric oxide-dependent vasodilation in patients with critical limb ischemia: A randomized, controlled study. Circulation 1996; 93:85-90