The effect of high- to low-altitude adaptation on the multifocal electroretinogram.

PURPOSE To examine variations in retinal electrophysiology assessed by multifocal electroretinogram (mfERG) during acclimatization of native highlanders to normobaric normoxia at sea level. METHODS Eight healthy residents of the greater La Paz area in Bolivia (3600 m above sea level) were examined over 72 days after arriving in Copenhagen, Denmark (sea level). A control group of eight healthy lowlanders was used for comparison. RESULTS During the period of observation, hemoglobin decreased from 16.7 to 15.0 g/dL (P = 0.0031), erythrocytes decreased from 5.3 to 4.6 trillion cells/L (P = 0.0006), and hematocrit decreased from 49.4% to 42.2% (P = 0.0008). At baseline, day 2 after arrival, the amplitudes (N1, P1, and N2) of the mfERG were 43.1% to 59.9% higher in the highlanders than in the lowlanders (P < 0.017). During acclimatization, the mfERG amplitudes increased 16.9% to 20.4% (P < 0.028) to a level of 73.2% to 87.0% higher in the highlanders than in the lowlanders (P < 0.0008). The increase in numerical amplitudes was proportional to the decrease in erythrocyte concentration (P = 0.023, 0.053, and 0.12 for N1, P1, and N2, respectively). CONCLUSIONS On arrival at sea level, the highlanders had markedly supernormal multifocal electroretinographic amplitudes that continued to increase during the 72-day period of observation where the highlanders' hematocrit normalized. The results suggest that acclimatization after a change in altitude and hence in ambient oxygen tension involves intrinsic retinal mechanisms and that acclimatization was not complete by the end of the study.

[1]  M. Larsen,et al.  Lens autofluorescence is not increased at high altitude , 2010, Acta ophthalmologica.

[2]  M. Larsen,et al.  Retinal vessel diameters in relation to hematocrit variation during acclimatization of highlanders to sea level altitude. , 2009, Investigative ophthalmology & visual science.

[3]  Donald C. Hood,et al.  ISCEV guidelines for clinical multifocal electroretinography (2007 edition) , 2007, Documenta Ophthalmologica.

[4]  K. Kirsch,et al.  Erythropoietin regulations in humans under different environmental and experimental conditions , 2007, Respiratory Physiology & Neurobiology.

[5]  M. Larsen,et al.  The effect of acute hypoxia and hyperoxia on the slow multifocal electroretinogram in healthy subjects. , 2007, Investigative ophthalmology & visual science.

[6]  C. Beall Two routes to functional adaptation: Tibetan and Andean high-altitude natives , 2007, Proceedings of the National Academy of Sciences.

[7]  G. Benedek,et al.  Hypobaric hypoxia reduces the amplitude of oscillatory potentials in the human ERG , 2007, Documenta Ophthalmologica.

[8]  C. Kuo,et al.  The role of dehydroepiandrosterone levels on physiologic acclimatization to chronic mountaineering activity. , 2006, High altitude medicine & biology.

[9]  Kristian Klemp,et al.  The multifocal ERG in diabetic patients without retinopathy during euglycemic clamping. , 2005, Investigative ophthalmology & visual science.

[10]  A. Vaag,et al.  Effect of short-term hyperglycemia on multifocal electroretinogram in diabetic patients without retinopathy. , 2004, Investigative ophthalmology & visual science.

[11]  J. Bittel,et al.  Pre-adaptation, adaptation and de-adaptation to high altitude in humans: cardio-ventilatory and haematological changes , 2004, European Journal of Applied Physiology and Occupational Physiology.

[12]  N. D. Wangsa-Wirawan,et al.  Retinal Oxygen Fundamental and Clinical Aspects , 2003 .

[13]  J. Lovasik,et al.  Neuroretinal function during mild systemic hypoxia. , 2002, Aviation, space, and environmental medicine.

[14]  J. Gamboa,et al.  Energetic metabolism in mouse cerebral cortex during chronic hypoxia , 2001, Neuroscience Letters.

[15]  R. Linsenmeier,et al.  Effects of hypoxemia on the a- and b-waves of the electroretinogram in the cat retina. , 2000, Investigative ophthalmology & visual science.

[16]  C. Beall Tibetan and Andean contrasts in adaptation to high-altitude hypoxia. , 2000, Advances in experimental medicine and biology.

[17]  S. Easter,et al.  An assessment of rat photoreceptor sensitivity to mitochondrial blockade. , 1997, Investigative ophthalmology & visual science.

[18]  W Seiple,et al.  A comparison of the components of the multifocal and full-field ERGs , 1997, Visual Neuroscience.

[19]  A. Bill,et al.  Glucose metabolism in pig outer retina in light and darkness. , 1997, Acta physiologica Scandinavica.

[20]  E. Schmeisser,et al.  Visual system effects of exercise on Mauna Kea at 2,200 and 4,200 meters altitude. , 1997, Military medicine.

[21]  J. Boero,et al.  Reduced mitochondrial respiration in mouse cerebral cortex during chronic hypoxia , 1995, Neuroscience Letters.

[22]  R. Hoffman,et al.  Hematology: Basic Principles and Practice , 1995 .

[23]  A. Ames,et al.  Energy requirements of CNS cells as related to their function and to their vulnerability to ischemia: a commentary based on studies on retina. , 1992, Canadian journal of physiology and pharmacology.

[24]  W. L. Weller,et al.  How thick should a retina be? A comparative study of mammalian species with and without intraretinal vasculature , 1991, Vision Research.

[25]  J. Chase,et al.  The evolution of retinal vascularization in mammals. A comparison of vascular and avascular retinae. , 1982, Ophthalmology.

[26]  J. J. Meyer,et al.  Attenuation curves and averaged ERG in the normal rat. , 1971, Vision research.

[27]  M. Carapancea ERG scotopic manifestation and their determinism, in experimental conditions of high altitude. , 1971, Vision research.

[28]  J. Hill,et al.  The effect of hypoxia on the human electroretinogram. , 1957, American journal of ophthalmology.