Oxygen delivery enhancers: past, present, and future.

Oxygen delivery enhancers: past, present, and future / P. Borrione, A. Mastrone, R.A. Salvo, A. Spaccamiglio, L. Grasso, A. Angeli. - (Journal of Endocrinological Investigation 31 ( (2008) 2 (February); p. 185-192)

  • PMID: 18362513
  • DOI: 10.1007/BF03345588


Abstract

In endurance sport the delivery of oxygen to muscles plays a critical role. Indeed, muscle performance declines during prolonged and intense activity as a consequence of the shift from the aerobic to the anaerobic metabolism with an increase of lactate. To enhance the aerobic capacity 2 alternatives may be used: increasing either the transport or the delivery of oxygen. In this setting, blood doping is the practice of illicitly using a drug or blood product to improve athletic performance. Based on this definition, blood doping techniques may include: 1) blood transfusion (autologous or omologous); 2) erythropoiesis-stimulating substances [recombinant human erythropoietin (alpha, beta, omega), darbepoietin-alpha, continuous erythropoiesis receptor activator, hematide]; 3) blood substitutes (hemoglobin-based oxygen carriers, perfluorocarbon emulsions); 4) allosteric modulators of hemoglobin (RSR-13 and RSR-4); 5) gene doping (human erythropoietin gene transfection); 6) gene regulation (hypoxia-inducible transcription factors pathway). In the present overview we will briefly describe the above-mentioned techniques with the aim of underlining potential hematological alternatives to gene doping for increasing aerobic capacity in sport.

Original document

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Science
Review
Date
1 February 2008
People
Borrione, Paolo
Grasso, L.
Mastrone, R.A.
Salvo, R.A.
Spaccamiglio, A.
Country
Italy
Language
English
Other organisations
Università degli Studi di Torino (UNITO) - University of Turin
Doping classes
M1. Manipulation Of Blood And Blood Components
M3. Gene And Cell Doping
S2. Peptide Hormones, Growth Factors
Substances
Darbepoetin (dEPO)
Erythropoietin (EPO)
Methoxy polyethylene glycol-epoetin beta (CERA)
RSR-13
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Date generated
29 February 2012
Date of last modification
24 January 2022
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