Inhibition of nitric oxide synthesis improves left ventricular contractility in neonatal pigs late after cardiopulmonary bypass

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Inhibition of nitric oxide synthesis improves left ventricular contractility in neonatal pigs late after cardiopulmonary bypass. / Chaturvedi, R R; Hjortdal, V E; Stenbog, E V; Ravn, H B; White, P; Christensen, T D; Thomsen, A B; Pedersen, J; Sorensen, K E; Redington, A N.

In: Heart (British Cardiac Society), Vol. 82, No. 6, 12.1999, p. 740-4.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Chaturvedi, RR, Hjortdal, VE, Stenbog, EV, Ravn, HB, White, P, Christensen, TD, Thomsen, AB, Pedersen, J, Sorensen, KE & Redington, AN 1999, 'Inhibition of nitric oxide synthesis improves left ventricular contractility in neonatal pigs late after cardiopulmonary bypass', Heart (British Cardiac Society), vol. 82, no. 6, pp. 740-4. https://doi.org/10.1136/hrt.82.6.740

APA

Chaturvedi, R. R., Hjortdal, V. E., Stenbog, E. V., Ravn, H. B., White, P., Christensen, T. D., Thomsen, A. B., Pedersen, J., Sorensen, K. E., & Redington, A. N. (1999). Inhibition of nitric oxide synthesis improves left ventricular contractility in neonatal pigs late after cardiopulmonary bypass. Heart (British Cardiac Society), 82(6), 740-4. https://doi.org/10.1136/hrt.82.6.740

Vancouver

Chaturvedi RR, Hjortdal VE, Stenbog EV, Ravn HB, White P, Christensen TD et al. Inhibition of nitric oxide synthesis improves left ventricular contractility in neonatal pigs late after cardiopulmonary bypass. Heart (British Cardiac Society). 1999 Dec;82(6):740-4. https://doi.org/10.1136/hrt.82.6.740

Author

Chaturvedi, R R ; Hjortdal, V E ; Stenbog, E V ; Ravn, H B ; White, P ; Christensen, T D ; Thomsen, A B ; Pedersen, J ; Sorensen, K E ; Redington, A N. / Inhibition of nitric oxide synthesis improves left ventricular contractility in neonatal pigs late after cardiopulmonary bypass. In: Heart (British Cardiac Society). 1999 ; Vol. 82, No. 6. pp. 740-4.

Bibtex

@article{d793ed52af97446b9f7d999f4ee4e5e8,
title = "Inhibition of nitric oxide synthesis improves left ventricular contractility in neonatal pigs late after cardiopulmonary bypass",
abstract = "BACKGROUND: Following neonatal open heart surgery a nadir occurs in left ventricular function six to 12 hours after cardiopulmonary bypass. Although initiated by intraoperative events, little is known about the mechanisms involved.OBJECTIVE: To evaluate the involvement of nitric oxide in this late phase dysfunction in piglets.DESIGN: Piglets aged 2 to 3 weeks (4-5 kg) underwent cardiopulmonary bypass (1 h) and cardioplegic arrest (0.5 h) and then remained ventilated with inotropic support. Twelve hours after bypass, while receiving dobutamine (5 microg/kg/min), the left ventricular response to non-selective nitric oxide synthase inhibition (l-N(G)-monomethylarginine (l-NMMA)) was evaluated using load dependent and load independent indices (E(es), the slope of the end systolic pressure-volume relation; M(w), the slope of the stroke work-end diastolic volume relation; [dP/dt(max)](edv), the slope of the dP/dt(max)-end diastolic volume relation), derived from left ventricular pressure-volume loops generated by conductance and microtip pressure catheters.RESULTS: 10 pigs received 7.5 mg l-NMMA intravenously and six of these received two additional doses (37.5 mg and 75 mg). E(es) (mean (SD)) increased with all three doses, from 54.9 (40.1) mm Hg/ml (control) to 86.3 (69.5) at 7.5 mg, 117.9 (65.1) at 37.5 mg, and 119 (80.4) at 75 mg (p < 0.05). At the two highest doses, [dP/dt(max)](edv) increased from 260.8 (209.3) (control) to 470.5 (22.8) at 37.5 mg and 474.1 (296.6) at 75 mg (p < 0.05); and end diastolic pressure decreased from 16.5 (5.6) mm Hg (control) to 11.3 (5.0) at 37.5 mg and 11.4 (4.9) at 75 mg (p < 0. 05).CONCLUSIONS: In neonatal pigs 12 hours after cardiopulmonary bypass with ischaemic arrest, low dose l-NMMA improved left ventricular function, implying that there is a net deleterious cardiac action of nitric oxide at this time.",
keywords = "Animals, Animals, Newborn, Cardiopulmonary Bypass, Dose-Response Relationship, Drug, Enzyme Inhibitors/therapeutic use, Heart Arrest, Induced, Nitric Oxide Synthase/antagonists & inhibitors, Swine, Time Factors, Ventricular Function, Left/drug effects, omega-N-Methylarginine/therapeutic use",
author = "Chaturvedi, {R R} and Hjortdal, {V E} and Stenbog, {E V} and Ravn, {H B} and P White and Christensen, {T D} and Thomsen, {A B} and J Pedersen and Sorensen, {K E} and Redington, {A N}",
year = "1999",
month = dec,
doi = "10.1136/hrt.82.6.740",
language = "English",
volume = "82",
pages = "740--4",
journal = "Heart",
issn = "1355-6037",
publisher = "B M J Group",
number = "6",

}

RIS

TY - JOUR

T1 - Inhibition of nitric oxide synthesis improves left ventricular contractility in neonatal pigs late after cardiopulmonary bypass

AU - Chaturvedi, R R

AU - Hjortdal, V E

AU - Stenbog, E V

AU - Ravn, H B

AU - White, P

AU - Christensen, T D

AU - Thomsen, A B

AU - Pedersen, J

AU - Sorensen, K E

AU - Redington, A N

PY - 1999/12

Y1 - 1999/12

N2 - BACKGROUND: Following neonatal open heart surgery a nadir occurs in left ventricular function six to 12 hours after cardiopulmonary bypass. Although initiated by intraoperative events, little is known about the mechanisms involved.OBJECTIVE: To evaluate the involvement of nitric oxide in this late phase dysfunction in piglets.DESIGN: Piglets aged 2 to 3 weeks (4-5 kg) underwent cardiopulmonary bypass (1 h) and cardioplegic arrest (0.5 h) and then remained ventilated with inotropic support. Twelve hours after bypass, while receiving dobutamine (5 microg/kg/min), the left ventricular response to non-selective nitric oxide synthase inhibition (l-N(G)-monomethylarginine (l-NMMA)) was evaluated using load dependent and load independent indices (E(es), the slope of the end systolic pressure-volume relation; M(w), the slope of the stroke work-end diastolic volume relation; [dP/dt(max)](edv), the slope of the dP/dt(max)-end diastolic volume relation), derived from left ventricular pressure-volume loops generated by conductance and microtip pressure catheters.RESULTS: 10 pigs received 7.5 mg l-NMMA intravenously and six of these received two additional doses (37.5 mg and 75 mg). E(es) (mean (SD)) increased with all three doses, from 54.9 (40.1) mm Hg/ml (control) to 86.3 (69.5) at 7.5 mg, 117.9 (65.1) at 37.5 mg, and 119 (80.4) at 75 mg (p < 0.05). At the two highest doses, [dP/dt(max)](edv) increased from 260.8 (209.3) (control) to 470.5 (22.8) at 37.5 mg and 474.1 (296.6) at 75 mg (p < 0.05); and end diastolic pressure decreased from 16.5 (5.6) mm Hg (control) to 11.3 (5.0) at 37.5 mg and 11.4 (4.9) at 75 mg (p < 0. 05).CONCLUSIONS: In neonatal pigs 12 hours after cardiopulmonary bypass with ischaemic arrest, low dose l-NMMA improved left ventricular function, implying that there is a net deleterious cardiac action of nitric oxide at this time.

AB - BACKGROUND: Following neonatal open heart surgery a nadir occurs in left ventricular function six to 12 hours after cardiopulmonary bypass. Although initiated by intraoperative events, little is known about the mechanisms involved.OBJECTIVE: To evaluate the involvement of nitric oxide in this late phase dysfunction in piglets.DESIGN: Piglets aged 2 to 3 weeks (4-5 kg) underwent cardiopulmonary bypass (1 h) and cardioplegic arrest (0.5 h) and then remained ventilated with inotropic support. Twelve hours after bypass, while receiving dobutamine (5 microg/kg/min), the left ventricular response to non-selective nitric oxide synthase inhibition (l-N(G)-monomethylarginine (l-NMMA)) was evaluated using load dependent and load independent indices (E(es), the slope of the end systolic pressure-volume relation; M(w), the slope of the stroke work-end diastolic volume relation; [dP/dt(max)](edv), the slope of the dP/dt(max)-end diastolic volume relation), derived from left ventricular pressure-volume loops generated by conductance and microtip pressure catheters.RESULTS: 10 pigs received 7.5 mg l-NMMA intravenously and six of these received two additional doses (37.5 mg and 75 mg). E(es) (mean (SD)) increased with all three doses, from 54.9 (40.1) mm Hg/ml (control) to 86.3 (69.5) at 7.5 mg, 117.9 (65.1) at 37.5 mg, and 119 (80.4) at 75 mg (p < 0.05). At the two highest doses, [dP/dt(max)](edv) increased from 260.8 (209.3) (control) to 470.5 (22.8) at 37.5 mg and 474.1 (296.6) at 75 mg (p < 0.05); and end diastolic pressure decreased from 16.5 (5.6) mm Hg (control) to 11.3 (5.0) at 37.5 mg and 11.4 (4.9) at 75 mg (p < 0. 05).CONCLUSIONS: In neonatal pigs 12 hours after cardiopulmonary bypass with ischaemic arrest, low dose l-NMMA improved left ventricular function, implying that there is a net deleterious cardiac action of nitric oxide at this time.

KW - Animals

KW - Animals, Newborn

KW - Cardiopulmonary Bypass

KW - Dose-Response Relationship, Drug

KW - Enzyme Inhibitors/therapeutic use

KW - Heart Arrest, Induced

KW - Nitric Oxide Synthase/antagonists & inhibitors

KW - Swine

KW - Time Factors

KW - Ventricular Function, Left/drug effects

KW - omega-N-Methylarginine/therapeutic use

U2 - 10.1136/hrt.82.6.740

DO - 10.1136/hrt.82.6.740

M3 - Journal article

C2 - 10573504

VL - 82

SP - 740

EP - 744

JO - Heart

JF - Heart

SN - 1355-6037

IS - 6

ER -

ID: 243520938