Literature DB >> 10573504

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

R R Chaturvedi1, V E Hjortdal, E V Stenbog, H B Ravn, P White, T D Christensen, A B Thomsen, J Pedersen, K E Sorensen, A N Redington.   

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.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10573504      PMCID: PMC1729213          DOI: 10.1136/hrt.82.6.740

Source DB:  PubMed          Journal:  Heart        ISSN: 1355-6037            Impact factor:   5.994


  26 in total

1.  Acute myocardial dysfunction and recovery: a common occurrence after coronary bypass surgery.

Authors:  W M Breisblatt; K L Stein; C J Wolfe; W P Follansbee; J Capozzi; J M Armitage; R L Hardesty
Journal:  J Am Coll Cardiol       Date:  1990-05       Impact factor: 24.094

2.  Left ventricular dysfunction after open repair of simple congenital heart defects in infants and children: quantitation with the use of a conductance catheter immediately after bypass.

Authors:  R R Chaturvedi; C Lincoln; J W Gothard; M H Scallan; P A White; A N Redington; D F Shore
Journal:  J Thorac Cardiovasc Surg       Date:  1998-01       Impact factor: 5.209

3.  Comparison of measures of left ventricular contractile performance derived from pressure-volume loops in conscious dogs.

Authors:  W C Little; C P Cheng; M Mumma; Y Igarashi; J Vinten-Johansen; W E Johnston
Journal:  Circulation       Date:  1989-11       Impact factor: 29.690

4.  Continuous measurement of left ventricular volume in animals and humans by conductance catheter.

Authors:  J Baan; E T van der Velde; H G de Bruin; G J Smeenk; J Koops; A D van Dijk; D Temmerman; J Senden; B Buis
Journal:  Circulation       Date:  1984-11       Impact factor: 29.690

5.  Role of controlled cardiac reoxygenation in reducing nitric oxide production and cardiac oxidant damage in cyanotic infantile hearts.

Authors:  K Morita; K Ihnken; G D Buckberg; M P Sherman; H H Young; L J Ignarro
Journal:  J Clin Invest       Date:  1994-06       Impact factor: 14.808

6.  Myocardial performance after repair of congenital cardiac defects in infants and children. Response to volume loading.

Authors:  F A Burrows; W G Williams; K H Teoh; A E Wood; J Burns; J Edmonds; G A Barker; G A Trusler; R D Weisel
Journal:  J Thorac Cardiovasc Surg       Date:  1988-10       Impact factor: 5.209

7.  Physiological concentrations of nitric oxide do not elicit an acute negative inotropic effect in unstimulated cardiac muscle.

Authors:  A S Weyrich; X L Ma; M Buerke; T Murohara; V E Armstead; A M Lefer; J M Nicolas; A P Thomas; D J Lefer; J Vinten-Johansen
Journal:  Circ Res       Date:  1994-10       Impact factor: 17.367

8.  Time-dependent enhancement or inhibition of endotoxin-induced vascular injury in rat intestine by nitric oxide synthase inhibitors.

Authors:  F Laszlo; B J Whittle; S Moncada
Journal:  Br J Pharmacol       Date:  1994-04       Impact factor: 8.739

9.  The role of L-arginine in ameliorating reperfusion injury after myocardial ischemia in the cat.

Authors:  A S Weyrich; X L Ma; A M Lefer
Journal:  Circulation       Date:  1992-07       Impact factor: 29.690

10.  Effects of L-arginine and L-nitro-arginine methyl ester on recovery of neonatal lamb hearts after cold ischemia. Evidence for an important role of endothelial production of nitric oxide.

Authors:  T Hiramatsu; J M Forbess; T Miura; J E Mayer
Journal:  J Thorac Cardiovasc Surg       Date:  1995-01       Impact factor: 5.209

View more
  1 in total

1.  Remote ischaemic preconditioning protects against cardiopulmonary bypass-induced tissue injury: a preclinical study.

Authors:  R K Kharbanda; J Li; I E Konstantinov; M M H Cheung; P A White; H Frndova; J Stokoe; P Cox; M Vogel; G Van Arsdell; R MacAllister; A N Redington
Journal:  Heart       Date:  2006-07-03       Impact factor: 5.994

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.