Advertising Disclaimer
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow E-mail this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My File Cabinet
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Van Bel, F.
Right arrow Articles by Berger, H. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Van Bel, F.
Right arrow Articles by Berger, H. M.
Related Collections
Right arrow Premature & Newborn
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Facebook   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

PEDIATRICS Vol. 101 No. 2 February 1998, pp. 185-193

Effect of Allopurinol on Postasphyxial Free Radical Formation, Cerebral Hemodynamics, and Electrical Brain Activity

Received Feb 2, 1997; accepted Oct 10, 1997.

Frank Van Bel*, Dagger , Majidah Shadid*, Ralf M. W. Moison*, Caroline A. Dorrepaal*, Jehudith Fontijn*, Louisa Monteiro*, Margot Van De Bor*, and Howard M. Berger*

From the * Department of Pediatrics, Leiden University Hospital, Leiden, The Netherlands, and the Dagger  Department of Neonatology, Wilhelmina Children's Hospital, Utrecht, The Netherlands.

Objective.  Free radical-induced postasphyxial reperfusion injury has been recognized as an important cause of brain tissue damage. We investigated the effect of high-dose allopurinol (ALLO; 40 mg/kg), a xanthine-oxidase inhibitor and free radical scavenger, on free radical status in severely asphyxiated newborns and on postasphyxial cerebral perfusion and electrical brain activity.

Methods.  Free radical status was assessed by serial plasma determination of nonprotein-bound iron (µM), antioxidative capacity, and malondialdehyde (MDA; µM). Cerebral perfusion was investigated by monitoring changes in cerebral blood volume (Delta CBV; mL/100 g brain tissue) with near infrared spectroscopy; electrocortical brain activity (ECBA) was assessed in microvolts by cerebral function monitor. Eleven infants received 40 mg/kg ALLO intravenously, and 11 infants served as controls (CONT). Plasma nonprotein-bound iron, antioxidative capacity, and MDA were measured before 4 hours, between 16 and 20 hours, and at the second and third days of age. Changes in CBV and ECBA were monitored between 4 and 8, 16 and 20, 58 and 62, and 104 and 110 hours of age.

Results.  Six CONT and two ALLO infants died after neurologic deterioration. No toxic side effects of ALLO were detected. Nonprotein-bound iron (mean ± SEM) in the CONT group showed an initial rise (18.7 ± 4.6 µM to 21.3 ± 3.4 µM) but dropped to 7.4 ± 3.5 µM at day 3; in the ALLO group it dropped from 15.5 ± 4.6 µM to 0 µM at day 3. Uric acid was significantly lower in ALLO-treated infants from 16 hours of life on. MDA remained stable in the ALLO group, but increased in the CONT group at 8 to 16 hours versus <4 hours (mean ± SEM; 0.83 ± 0.31 µM vs 0.50 ± 0.14 µM). During 4 to 8 hours, Delta CBV-CONT showed a larger drop than Delta CBV-ALLO from baseline. During the subsequent registrations CBV remained stable in both groups. ECBA-CONT decreased, but ECBA-ALLO remained stable during 4 to 8 hours of age. Neonates who died had the largest drops in CBV and ECBA.

Conclusion.  This study suggests a beneficial effect of ALLO treatment on free radical formation, CBV, and electrical brain activity, without toxic side effects.

Key words: birth asphyxia, allopurinol, side effects, free radicals, brain perfusion, electrical brain activity.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Facebook Facebook   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?


This article has been cited by other articles:


Home page
PediatricsHome page
H. L. Torrance, M. J. Benders, J. B. Derks, C. M. A. Rademaker, A. F. Bos, P. Van Den Berg, M. Longini, G. Buonocore, M. Venegas, H. Baquero, et al.
Maternal Allopurinol During Fetal Hypoxia Lowers Cord Blood Levels of the Brain Injury Marker S-100B
Pediatrics, July 1, 2009; 124(1): 350 - 357.
[Abstract] [Full Text] [PDF]


Home page
Arch. Dis. Child. Fetal Neonatal Ed.Home page
M J N L Benders, A F Bos, C M A Rademaker, M Rijken, H L Torrance, F Groenendaal, and F van Bel
Early postnatal allopurinol does not improve short term outcome after severe birth asphyxia
Arch. Dis. Child. Fetal Neonatal Ed., May 1, 2006; 91(3): F163 - F165.
[Abstract] [Full Text] [PDF]


Home page
Pharmacol. Rev.Home page
P. Pacher, A. Nivorozhkin, and C. Szabo
Therapeutic effects of xanthine oxidase inhibitors: renaissance half a century after the discovery of allopurinol.
Pharmacol. Rev., March 1, 2006; 58(1): 87 - 114.
[Abstract] [Full Text] [PDF]


Home page
PediatricsHome page
J. M. Perlman
Summary proceedings from the neurology group on hypoxic-ischemic encephalopathy.
Pediatrics, March 1, 2006; 117(3 Pt 2): S28 - S33.
[Abstract] [Full Text] [PDF]


Home page
PediatricsHome page
M. C. Toet, P. M.A. Lemmers, L. J. van Schelven, and F. van Bel
Cerebral Oxygenation and Electrical Activity After Birth Asphyxia: Their Relation to Outcome
Pediatrics, February 1, 2006; 117(2): 333 - 339.
[Abstract] [Full Text] [PDF]


Home page
J. Exp. Biol.Home page
D. S. Warner, H. Sheng, and I. Batinic-Haberle
Oxidants, antioxidants and the ischemic brain
J. Exp. Biol., August 15, 2004; 207(18): 3221 - 3231.
[Abstract] [Full Text] [PDF]


Home page
PediatricsHome page
R. R. Clancy, S. A. McGaurn, J. E. Goin, D. G. Hirtz, W. I. Norwood, J. W. Gaynor, M. L. Jacobs, G. Wernovsky, W. T. Mahle, J. D. Murphy, et al.
Allopurinol Neurocardiac Protection Trial in Infants Undergoing Heart Surgery Using Deep Hypothermic Circulatory Arrest
Pediatrics, July 1, 2001; 108(1): 61 - 70.
[Abstract] [Full Text] [PDF]


Home page
Arch. Dis. Child. Fetal Neonatal Ed.Home page
K Hirano, T Morinobu, H Kim, M Hiroi, R Ban, S Ogawa, H Ogihara, H Tamai, and T Ogihara
Blood transfusion increases radical promoting non-transferrin bound iron in preterm infants
Arch. Dis. Child. Fetal Neonatal Ed., May 1, 2001; 84(3): 188F - 193.
[Abstract] [Full Text]


Home page
PediatricsHome page
V. Fellman and L. von Bonsdorff
Exogenous Apotransferrin and Exchange Transfusions in Hereditary Iron Overload Disease
Pediatrics, February 1, 2000; 105(2): 398 - 401.
[Abstract] [Full Text]


Home page
Arch. Dis. Child. Fetal Neonatal Ed.Home page
M C Toet, L Hellström-Westas, F Groenendaal, P Eken, and L S de Vries
Amplitude integrated EEG 3 and 6 hours after birth in full term neonates with hypoxic-ischaemic encephalopathy
Arch. Dis. Child. Fetal Neonatal Ed., July 1, 1999; 81(1): 19F - 23.
[Abstract] [Full Text]