Literature DB >> 11519679

Inhibition of nitric oxide synthase with L-NAME does not increase lactate production at rest or during short-term high-intensity exercise in Thoroughbred horses.

M Manohar1, T E Goetz, A S Hassan, P Rothenbaum, S Humphrey.   

Abstract

The present study was carried out to determine whether inhibition of nitric oxide (NO) synthase promotes anaerobic metabolism in exercising horses, resulting in a significantly increased blood lactate concentration. N(omega)-nitro-L-arginine methyl ester (L-NAME) is a potent inhibitor of NO synthase that has been tested in horses and other species. Two sets of experiments, namely placebo (saline control) and L-NAME (20 mg/kg, i.v.) studies, were carried out on seven healthy, sound, exercise-trained, Thoroughbred horses in random order, 6 to 7 days apart. In both experiments, an incremental exercise protocol was used and data were obtained at rest, during submaximal exercise performed at 8 m/s on a 4.5% uphill grade, and during galloping at 14 m/s on a 4.5% uphill grade--a workload that not only elicited maximal heart rate and induced exercise-induced pulmonary haemorrhage, but also could not be sustained for more than 90 s. Measurements were also made in the recovery period. Mixed-venous blood samples, obtained at matched intervals in the two sets of experiments, were analysed in triplicate for determining the lactate concentration. Following administration of L-NAME, significant bradycardia occurred at rest (27 +/- 1 vs 37 +/- 2 beats/min in the placebo trials; p<0.0001) as well as during submaximal exercise (183 +/- 4 vs 200 +/- 4 beats/min in the placebo trials; p<0.001), but the heart rate increased during galloping at 14 m/s on a 4.5% uphill grade to reach values observed in the placebo trials (215 +/- 2 beats/min) and significant differences were not found. At rest, the mixed-venous blood lactate concentration was similar in the two experiments. With exercise, the mixed-venous blood lactate concentration increased progressively as work intensity increased in both trials, but significant differences were not found between the placebo and the L-NAME experiments during submaximal exercise, near-maximal exercise or recovery. These experiments demonstrated that inhibition of NO synthase in Thoroughbred horses does not promote enhanced anaerobic metabolism at rest or during short-term incremental exercise leading to galloping at maximal heart rate.

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Year:  2001        PMID: 11519679     DOI: 10.1023/a:1010612403902

Source DB:  PubMed          Journal:  Vet Res Commun        ISSN: 0165-7380            Impact factor:   2.459


  14 in total

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Authors:  C R Sweeney
Journal:  Vet Clin North Am Equine Pract       Date:  1991-04       Impact factor: 1.792

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Authors:  D S Bredt; P M Hwang; C E Glatt; C Lowenstein; R R Reed; S H Snyder
Journal:  Nature       Date:  1991-06-27       Impact factor: 49.962

3.  Effect of exogenous and endogenous nitric oxide on mitochondrial respiration of rat hepatocytes.

Authors:  J Stadler; T R Billiar; R D Curran; D J Stuehr; J B Ochoa; R L Simmons
Journal:  Am J Physiol       Date:  1991-05

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Authors:  C A Kindig; L L Gallatin; H H Erickson; M R Fedde; D C Poole
Journal:  Respir Physiol       Date:  2000-04

5.  Metabolic effects of nitric oxide synthase inhibition during exercise in the horse.

Authors:  P C Mills; D J Marlin; C M Scott; N C Smith
Journal:  Res Vet Sci       Date:  1999-04       Impact factor: 2.534

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Authors:  J B Hibbs; R R Taintor; Z Vavrin; E M Rachlin
Journal:  Biochem Biophys Res Commun       Date:  1988-11-30       Impact factor: 3.575

7.  Effect of endogenous nitric oxide on mitochondrial respiration of rat hepatocytes in vitro and in vivo.

Authors:  J Stadler; R D Curran; J B Ochoa; B G Harbrecht; R A Hoffman; R L Simmons; T R Billiar
Journal:  Arch Surg       Date:  1991-02

8.  Effects of glyceryl trinitrate (nitroglycerin) on pulmonary vascular pressures in standing thoroughbred horses.

Authors:  M Manohar
Journal:  Equine Vet J       Date:  1995-07       Impact factor: 2.888

9.  Canine hindlimb blood flow and O2 uptake after inhibition of EDRF/NO synthesis.

Authors:  C E King; M J Melinyshyn; J D Mewburn; S E Curtis; M J Winn; S M Cain; C K Chapler
Journal:  J Appl Physiol (1985)       Date:  1994-03

10.  Sites of inhibition of mitochondrial electron transport in macrophage-injured neoplastic cells.

Authors:  D L Granger; A L Lehninger
Journal:  J Cell Biol       Date:  1982-11       Impact factor: 10.539

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