Abstract
We tested whether reoxygenation with 100% O2 for 5 min after experimental asphyxia in newborn piglets was as efficient as 100% O2 for 20 min compared with room air. Forty-one anesthetized piglets, 1–3 d old, were randomized to cerebral hypoxemia-ischemia-hypercapnia (HIH) or control (n = 5). HIH was achieved by ventilation with 8% O2, temporary occlusion of the common carotid arteries, and adding of CO2. After 25 min, reoxygenation-reperfusion was started with 100% O2 for 20 min (group 1, n = 12), or 21% 12), 100% O2 for 5 min (group 2, n = 12). All piglets were observed for 2 h. During O2 (group 3, n = reoxygenation-reperfusion, significantly higher blood pressure and more complete restoration of microcirculation (laser Doppler flow) in the cerebral cortex was found in both groups reoxygenated with 100% O2 compared with 21% O2 (regional cerebral blood flow ≥ 100%versus 70% of baseline, p = 0.04). Reoxygenation with 100% O2 for 5 min was as efficient as 20 min. Oxygen delivery in cortex was significantly higher in groups 1 and 2 compared with group 3 (p = 0.03), but there were no significant differences in cerebral metabolic rate for oxygen. In the striatum, no significant differences in flow or extracellular glutamate, glycerol, and lactate/pyruvate ratio were found between the groups. In conclusion, after experimental asphyxia, newborn piglets can be reoxygenated as efficiently with 100% O2 for only 5 min as 100% O2 for 20 min compared with room air.
Similar content being viewed by others
Log in or create a free account to read this content
Gain free access to this article, as well as selected content from this journal and more on nature.com
or
Abbreviations
- BE:
-
base excess
- CaO2:
-
arterial O2 content
- CvssO2:
-
sagittal sinus O2 content
- CBF:
-
cerebral blood flow
- CMRO2:
-
metabolic rate for oxygen
- DO2:
-
oxygen delivery
- HIH:
-
hypoxemia-ischemia-hypercapnia
- MABP:
-
mean arterial blood pressure
- OER:
-
oxygen extraction ratio
- PaCO2:
-
arterial CO2 tension
- PaO2:
-
arterial O2 tension
- ROS:
-
reactive oxygen species
References
Vento M, Asensi M, Sastre J, Garcia-Sala F, Pallardo FV, Vina J 2001 Resuscitation with room air instead of 100% oxygen prevents oxidative stress in moderately asphyxiated term neonates. Pediatrics 107: 642–647.
Rootwelt T, Loberg EM, Moen A, Oyasaeter S, Saugstad OD 1992 Hypoxemia and reoxygenation with 21% or 100% oxygen in newborn pigs: changes in blood pressure, base deficit, and hypoxanthine and brain morphology. Pediatr Res 32: 107–113.
Rootwelt T, Odden JP, Hall C, Ganes T, Saugstad OD 1993 Cerebral blood flow and evoked potentials during reoxygenation with 21 or 100% O2 in newborn pigs. J Appl Physiol 75: 2054–2060.
Feet BA, Gilland E, Groenendaal F, Brun NC, Hellstrom-Westas L, Hagberg H, Saugstad OD 1998 Cerebral excitatory amino acids and Na+, K+-ATPase activity during resuscitation of severely hypoxic newborn piglets. Acta Paediatr 87: 889–895.
Feet BA, Yu XQ, Rootwelt T, Oyasaeter S, Saugstad OD 1997 Effects of hypoxemia and reoxygenation with 21% or 100% oxygen in newborn piglets: extracellular hypoxanthine in cerebral cortex and femoral muscle. Crit Care Med 25: 1384–1391.
Ramji S, Ahuja S, Thirupuram S, Rootwelt T, Rooth G, Saugstad OD 1993 Resuscitation of asphyxic newborn infants with room air or 100% oxygen. Pediatr Res 34: 809–812.
Saugstad OD, Rootwelt T, Aalen O 1998 Resuscitation of asphyxiated newborn infants with room air or oxygen: an international controlled trial: the Resair 2 study. Pediatrics 102: e1.
Solas AB, Kutzsche S, Vinje M, Saugstad OD 2001 Cerebral hypoxemia-ischemia and reoxygenation with 21% or 100% oxygen in newborn piglets: effects on extra-cellular levels of excitatory amino acids and microcirculation. Pediatr Crit Care Med 2: 340–345.
Feet BA, Brun NC, Hellstrom-Westas L, Svenningsen NW, Greisen G, Saugstad OD 1998 Early cerebral metabolic and electrophysiological recovery during controlled hypoxemic resuscitation in piglets. J Appl Physiol 84: 1208–1216.
Nilsson GE, Tenland T, Oberg PA 1980 Evaluation of a laser Doppler flowmeter for measurement of tissue blood flow. IEEE Trans Biomed Eng 27: 597–604.
Brown DW, Hadway J, Lee TY 2003 Near-infrared spectroscopy measurement of oxygen extraction fraction and cerebral metabolic rate of oxygen in newborn piglets. Pediatr Res 54: 861–867.
Leenders KL, Perani D, Lammertsma AA, Heather JD, Buckingham P, Healy MJ, Gibbs JM, Wise RJ, Hatazawa J, Herold S et al. 1990 Cerebral blood flow, blood volume and oxygen utilization. Normal values and effect of age. Brain 113: 27–47.
Takahashi T, Shirane R, Sato S, Yoshimoto T 1999 Developmental changes of cerebral blood flow and oxygen metabolism in children. AJNR Am J Neuroradiol 20: 917–922.
Hutchinson PJ, Gupta AK, Fryer TF, Al-Rawi PG, Chatfield DA, Coles JP, O'Connell MT, Kett-White R, Minhas PS, Aigbirhio FI, Clark JC, Kirkpatrick PJ, Menon DK, Pickard JD 2002 Correlation between cerebral blood flow, substrate delivery, and metabolism in head injury: a combined microdialysis and triple oxygen positron emission tomography study. J Cereb Blood Flow Metab 22: 735–745.
Frykholm P, Andersson JL, Valtysson J, Silander HC, Hillered L, Persson L, Olsson Y, Yu WR, Westerberg G, Watanabe Y, Langstrom B, Enblad P 2000 A metabolic threshold of irreversible ischemia demonstrated by PET in a middle cerebral artery occlusion-reperfusion primate model. Acta Neurol Scand 102: 18–26.
Niijima S, Shortland DB, Levene MI, Evans DH 1988 Transient hyperoxia and cerebral blood flow velocity in infants born prematurely and at full term. Arch Dis Child 63: 1126–1130.
Menzel M, Doppenberg EM, Zauner A, Soukup J, Reinert MM, Clausen T, Brockenbrough PB, Bullock R 1999 Cerebral oxygenation in patients after severe head injury: monitoring and effects of arterial hyperoxia on cerebral blood flow, metabolism and intracranial pressure. J Neurosurg Anesthesiol 11: 240–251.
Wei EP, Christman CW, Kontos HA, Povlishock JT 1985 Effects of oxygen radicals on cerebral arterioles. Am J Physiol 248: H157–H162.
Iida Y, Katusic ZS 2000 Mechanisms of cerebral arterial relaxations to hydrogen peroxide. Stroke 31: 2224–2230.
Kutzsche S, Kirkeby OJ, Rise IR, Saugstad OD 1999 Effects of hypoxia and reoxygenation with 21% and 100%-oxygen on cerebral nitric oxide concentration and microcirculation in newborn piglets. Biol Neonate 76: 153–167.
Low JA, Robertson DM, Simpson LL 1989 Temporal relationships of neuropathologic conditions caused by perinatal asphyxia. Am J Obstet Gynecol 160: 608–614.
Rorke LB 1992 Perinatal brain damage. In: Adams JH, Duchen LW (eds) Greenfield's Neuropathology. Oxford University Press, New York, pp 639–708.
Martin LJ, Brambrink A, Koehler RC, Traystman RJ 1997 Primary sensory and forebrain motor systems in the newborn brain are preferentially damaged by hypoxia-ischemia. J Comp Neurol 377: 262–285.
Ashwal S, Dale PS, Longo LD 1984 Regional cerebral blood flow: studies in the fetal lamb during hypoxia, hypercapnia, acidosis, and hypotension. Pediatr Res 18: 1309–1316.
Lou HC, Tweed WA, Davies JM 1985 Preferential blood flow increase to the brain stem in moderate neonatal hypoxia: reversal by naloxone. Eur J Pediatr 144: 225–227.
Goplerud JM, Wagerle LC, Delivoria-Papadopoulos M 1989 Regional cerebral blood flow response during and after acute asphyxia in newborn piglets. J Appl Physiol 66: 2827–2832.
Berger R, Lehmann T, Karcher J, Schachenmayr W, Jensen A 1996 Relation between cerebral oxygen delivery and neuronal cell damage in fetal sheep near term. Reprod Fertil Dev 8: 317–321.
Huang CC, Yonetani M, Lajevardi N, Delivoria-Papadopoulos M, Wilson DF, Pastuszko A 1995 Comparison of postasphyxial resuscitation with 100% and 21% oxygen on cortical oxygen pressure and striatal dopamine metabolism in newborn piglets. J Neurochem 64: 292–298.
Goplerud JM, Wagerle LC, Delivoria-Papadopoulos M 1991 Sympathetic nerve modulation of regional cerebral blood flow during asphyxia in newborn piglets. Am J Physiol 260: H1575–H1580.
Rosenberg AA 1986 Cerebral blood flow and O2 metabolism after asphyxia in neonatal lambs. Pediatr Res 20: 778–782.
Marchal G, Young AR, Baron JC 1999 Early postischemic hyperperfusion: pathophysiologic insights from positron emission tomography. J Cereb Blood Flow Metab 19: 467–482.
Hillered, L, Persson, L. 1999 Neurochemical monitoring of the acutely injured human brain. Scand J Clin Lab Invest Suppl 229: 9–18
Lodato RF 1989 Decreased O2 consumption and cardiac output during normobaric hyperoxia in conscious dogs. J Appl Physiol 67: 1551–1559.
Reinhart K, Bloos F, Konig F, Bredle D, Hannemann L 1991 Reversible decrease of oxygen consumption by hyperoxia. Chest 99: 690–694.
Acknowledgements
The authors thank the staff at the Institute for Experimental Medical Research, Ullevaal University Hospital, for their skilled technical assistance, enthusiasm, and support.
Author information
Authors and Affiliations
Corresponding author
Additional information
Supported in part by grants from the Medical Faculty, University of Oslo; the Norwegian Society of Anaesthesiology; and Rolf Geir Gjertsen's Foundation. A.B.S. is a research fellow with the Norwegian Council on Cardiovascular Diseases.
Rights and permissions
About this article
Cite this article
Solås, AB., Munkeby, B. & Saugstad, O. Comparison of Short- and Long-Duration Oxygen Treatment after Cerebral Asphyxia in Newborn Piglets. Pediatr Res 56, 125–131 (2004). https://doi.org/10.1203/01.PDR.0000128978.90201.1D
Received:
Accepted:
Issue date:
DOI: https://doi.org/10.1203/01.PDR.0000128978.90201.1D
This article is cited by
-
Erstversorgung von Neugeborenen
Monatsschrift Kinderheilkunde (2010)
-
Avoiding hyperoxia in infants ⩽1250?g is associated with improved short- and long-term outcomes
Journal of Perinatology (2006)
-
Lebensrettende Maßnahmen bei Kindern (Paediatric Life Support, PLS)
Notfall + Rettungsmedizin (2006)


