Int J Sports Med 2002; 23(6): 403-407
DOI: 10.1055/s-2002-33743
Physiology & Biochemistry
© Georg Thieme Verlag Stuttgart · New York

L-Arginine Reduces Exercise-Induced Increase in Plasma Lactate and Ammonia

A.  Schaefer1 , F.  Piquard1 , B.  Geny1 , S.  Doutreleau1 , E.  Lampert1 , B.  Mettauer1 , J.  Lonsdorfer1
  • 1Service des Explorations Fonctionnelles Respiratoires et de l’Exercice et EA 3072, Hôpitaux Universitaires et Faculté de Médecine, Strasbourg, France
Further Information

Publication History

Accepted after revision: April 6, 2002

Publication Date:
05 September 2002 (online)

Abstract

To investigate the effect of L-arginine supplementation (L-ARG) on physiological and metabolic changes during exercise, we determined in a double-blind study the cardiorespiratory (heart rate, oxygen consumption (V˙O2) and carbon dioxide production (V˙CO2) and the metabolic (lactate and ammonia) responses to maximal exercise after either an intravenous L-ARG hydrochloride salt or placebo load in 8 healthy subjects.

Exercise-induced increases in heart rate, V˙O2 and V˙CO2 were not significantly different after L-ARG or placebo. By contrast, peak plasma ammonia and lactate were significantly decreased after L-ARG load (60.6 ± 8.2 vs. 73.1 ± 9.1 µmol × l-1, p < 0.01 and 7.1 ± 0.7 vs. 8.2 ± 1.1 mmol × l-1, p < 0.01, for ammonia and lactate, respectively). Plasma L-citrulline increased significantly during exercise only after L-ARG load, despite a concomitant decrease in plasma L-ARG. Furthermore, a significant inverse relationship was observed between changes in lactate and L-citrulline concentrations after L-ARG load (r = -0.84, p = 0.009).

These results demonstrate that intravenous L-ARG reduces significantly exercise-induced increase in plasma lactate and ammonia. Taken together, the specific L-citrulline increase and the inverse relationship observed between L-citrulline and plasma lactate after L-ARG might support that L-ARG supplementation enhances the L-arginine-nitric oxide (NO) pathway during exercise.

References

  • 1 Bangsbo J, Madsen K, Kiens B, Richter E A. Effect of muscle acidity on muscle metabolism and fatigue during intense exercise in man.  J Physiol (Lond). 1996;  495 587-596
  • 2 Barbul A. Arginine: biochemistry, physiology, and therapeutic implications.  J Parent Ent Nutr. 1986;  10 227-238
  • 3 Beaumier L, Castillo L, Ajami A M, Young V R. Urea cycle intermediate kinetics and nitrate excretion at normal and ”therapeutic“ intakes of arginine in humans.  Am J Physiol. 1995;  269 E884-E896
  • 4 Bode-Böger S M, Böger R H, Galland A, Dimitrios T, Frölich JC. L-arginine-induced vasodilatation in healthy humans: pharmacokinetic-pharmacodynamic relationship.  Br J Clin Pharmacol. 1998;  46 487-497
  • 5 Brett S E, Cockcroft J R, Mant T GK, Ritter J M, Chowienczyk P J. Haemodynamic effects of inhibition of nitric oxide synthase and of L-arginine at rest and during exercise.  J Hypertens. 1998;  16 429-435
  • 6 Brouns F, Beckers E, Wagenmakers A J, Saris W H. Ammonia accumulation during highly intensive long lasting cycling: individual observations.  Int J Sports Med. 1990;  11 (suppl 2) S78-84
  • 7 Ceremuzynski L, Chamiec T, Herbaczynska-Cedro T. Effect of supplemental oral L-arginine on exercise capacity in patients with stable Angina Pectoris.  Am J Cardiol. 1990;  80 331-333
  • 8 Denis C, Dormois D, Linossier M T, Eychenne J L, Hauseux P, Lacour J R. Effect of arginine aspartate on the exercise-induced hyperammoniemia in humans: a two period cross-over trial.  Arch Int Physiol Biochim. 1991;  99 123-127
  • 9 Eto B, Peres G, Le Moel G. Effect of an ingested glutamate arginine salt on ammonemia during and after long lasting cycling.  Arch Int Physiol Biochim. 1997;  102 161-162
  • 10 Favero T G, Zable A C, Colter D, Abramson J J. Lactate inhibits Ca(2+)-activated Ca(2+)-channel activity from skeletal muscle sarcoplasmic reticulum.  J Appl Physiol. 1997;  82 447-452
  • 11 Gremion G, Palud P, Gobelet C. Arginine aspartate and muscular activity. Part II.  Schweiz Ztschr Sportmed. 1989;  37 241-246
  • 12 Hargreaves M, Mc Kenna MJ, Jenkins D G, Warmington S A, Li J L, Snow R J, Febbraio M A. Muscle metabolism and performance during high-intensity, intermittent exercise.  J Appl Physiol. 1998;  84 1687-1691
  • 13 Jungersten L, Ambring A, Wall B, Wennmalm A. Both physical fitness and acute exercise regulate nitric oxide formation in healthy humans.  J Appl Physiol. 1997;  82 760-764
  • 14 Kamoun P, Rabier D, Bardet J, Parvy P. Citrulline concentrations in human plasma after arginine load.  Clin Chem. 1991;  37 1287
  • 15 Katz A, Broberg S, Sahlin K, Wahren J. Muscle ammonia and amino acid metabolism during dynamic exercise in man.  Clin Physiol. 1986;  6 365-379
  • 16 Mills P C, Marlin D J, Scott C M, Smith N C. Metabolic effects of nitric oxide synthase inhibition during exercise in the horse.  Res Vet Sci. 1999;  66 135-138
  • 17 Node K, Kitakaze M, Sato H, Koretsune Y, Katsube Y, Karita M, Kosaka H, Hori M. Effect of acute dynamic exercise on circulating plasma nitric oxide level and correlation to norepinephrine release in normal subjects.  Am J Cardiol. 1997;  79 526-528
  • 18 Palmer R MJ, Rees D D, Ashton D S, Moncada S. L-Arginine is the precursor for the formation of nitric oxide in the endothelium-dependent relaxation.  Biochem Biophys Res Commun. 1988;  153 1251-1256
  • 19 Rector T S, Bank A J, Mullen K A, Tschumperlin L K, Sih R, Pillai K, Kubo S H. Randomized, double-blind, placebo-controlled study of supplemental oral L-arginine in patients with heart failure.  Circulation. 1996;  93 2135-2141
  • 20 Reid M B. Role of nitric oxide in skeletal muscle: synthesis, distribution and functional importance.  Acta Physiol Scand. 1997;  162 401-409
  • 21 Roberts C K, Barnard R J, Jasman A, Balon T W. Acute exercise increases nitric oxide synthase activity in skeletal muscle.  Am J Physiol. 1999;  277 E390-E394
  • 22 Salehi A, Carlberg M, Henningson R, Lundquist I. Islet constitutive nitric oxide synthase: biochemical determination and regulatory function.  Am J Physiol. 1996;  270 C1634-C1641
  • 23 Schaefer A, Piquard F, Doutreleau S, Mettauer B, Epailly E, Eisenmann B, Lonsdorfer J, Geny B. Reduced exercise capacity is associated with reduced nitric oxide production after heart transplantation.  J Thorac Cardiovasc Surg. 2001;  122 821-822
  • 24 Sewell D A, Gleeson M, Blannin A K. Hyperammonaemia in relation to high-intensity exercise duration in man.  Eur J Appl Physiol. 1994;  69 350-354
  • 25 Spodaryk K, Szmatlan U, Berger L. The relationship of plasma ammonia and lactate concentrations to perceived exertion in trained and untrained women.  Eur J Appl Physiol. 1990;  61 309-312

A. Schaefer

Institut de Physiologie · Faculté de Médecine

67085 Strasbourg Cedex · France ·

Phone: +33 (390) 24 34 43

Fax: +33 (390) 24 34 44

Email: Adrien.Schaefer@physio-ulp.u-strasbg.fr

    >