Abstract
Relative hyperoxia is a condition frequently encountered in premature infants, either spontaneously or during treatment in the Neonatal Intensive Care Unit. The effects of high inspiratory oxygen concentrations on immature brain cells and their signaling cascades are largely unknown. The aim of the study was to investigate the effect of hyperoxia on the amount and topographic distribution of iNOS-expression (inducible nitric oxide synthase) in the immature rat brain, and to localize hyperoxia-induced formation of peroxynitrite as a potential marker of cellular damage to immature cerebral structures. Seven-day-old Wistar rat pups were exposed to >80% oxygen for 24 h and were then transcardially perfused. Following paraformaldehyde fixation, brains were paraffin-embedded and immunohistochemically stained for iNOS and nitrotyrosine. iNOS protein was quantified by Western blot; iNOS mRNA expression was studied by RT-PCR. Total brain iNOS mRNA was up-regulated, demonstrating a peak at 6 h following the onset of hyperoxia. Immunohistochemical staining was predominantly observed in microglial cells of hippocampus and frontal cortex with some iNOS reactivity in endothelial and perivascular cells. Nitrotyrosine staining was positive in apical dendrites of neurons in the frontal cortex. There was no positive staining for iNOS or nitrotyrosine in control animals. Hyperoxia causes iNOS mRNA and protein up-regulation in microglial cells of the immature rat brain. Positive neuronal nitrotyrosine staining indicates formation of peroxynitrite with potential deleterious effects for immature cellular structures in the neonatal brain.
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
- CFR:
-
frontal cortex
- eNOS:
-
endothelial NO synthase
- HIP:
-
hippocampus
- iNOS:
-
inducible NO synthase
- MOP:
-
primary motor cortex
- MOS:
-
secondary motor cortex
- MSN:
-
medial septal nucleus
- nNOS:
-
neuronal NO synthase
- NO:
-
nitric oxide
- RSC:
-
retrosplenial cortex
- THA:
-
thalamus
References
Cunha FQ, Assreuy J, Xu D, Charles I, Liew FY, Moncada S 1993 Repeated induction of nitric oxide synthase and leishmanicidal activity in murine macrophages. Eur J Immunol 23: 1385–1388
Hoehn T, Huebner J, Paboura E, Krause M, Leititis JU 1998 Effect of therapeutic concentrations of nitric oxide on bacterial growth in vitro. Crit Care Med 26: 1857–1862
Änggard E 1994 Nitric oxide: mediator, murderer, and medicine. Lancet 343: 1199–1206
Kröncke KD, Fehsel K, Suschek C, Kolb-Bachofen V 2001 Inducible nitric oxide synthase-derived nitric oxide in gene regulation, cell death and cell survival. Int Immunopharmacol 1: 1407–1420
Weisz A, Cicatiello L 1996 Regulation of the mouse inducible-type nitric oxide synthase gene promoter by interferon-gamma, bacterial lipopolysaccharide and NG-monomethyl-L-arginine. Biochem J 316: 209–215
Weinberger B, Weiss K, Heck DE, Laskin DL, Laskin JD 2001 Pharmacologic therapy of persistent pulmonary hypertension of the newborn. Pharmacol Ther 89: 67–79
Liaudet L, Soriano FG, Szabo C 2000 Biology of nitric oxide signaling. Crit Care Med 28( 4 Suppl): N37–52
Wink DA, Mitchell JB 1998 Chemical biology of nitric oxide: Insights into regulatory, cytotoxic, and cytoprotective mechanisms of NO. Free Radic Biol Med 25: 434–456
Heneka MT, Feinstein DL 2001 Expression and function of inducible nitric oxide synthase in neurons. J Neuroimmunol 114: 8–18
Murphy S, Simmons ML, Agullo L, Garcia A, Feinstein DL, Galea E, Reis DJ, Minc-Golomb D, Schwartz JP 1993 Synthesis of nitric oxide in CNS glial cells. Trends Neurosci 16: 323
Brosnan CF, Lee SC, Liu J 1997 Regulation of inducible nitric oxide synthase expression in human glia: implications for inflammatory central nervous system diseases. Biochem Soc Trans 25: 679
Minghetti L, Levi G 1998 Microglia as effector cells in brain damage and repair: focus on prostanoids and nitric oxide. Prog Neurobiol 54: 99
Raghuram N, Fortenberry JD, Owens ML, Brown LA 1999 Effects of exogenous nitric oxide and hyperoxia on lung fibroblast viability and DNA fragmentation. Biochem Biophys Res Commun 262: 685–691
Koppenol WH, Moreno JJ, Pryor WA, Ischiropoulos H, Beckman JS 1992 Peroxynitrite, a cloaked oxidant formed by nitric oxide and superoxide. Chem Res Toxicol 5: 834–842
Lee C, Miura K, Liu X, Zweier JL 2000 Biphasic regulation of leukocyte superoxide generation by nitric oxide and peroxynitrite. J Biol Chem 275: 38965–38972
Demiryurek AT, Karamsetty MR, McPhaden AR, Wadsworth RM, Kane KA, MacLean MR 2000 Accumulation of nitrotyrosine correlates with endothelial NO synthase in pulmonary resistance arteries during chronic hypoxia in the rat. Pulm Pharmacol Ther 13: 157–165
Cross AR, Jones OTG 1991 Enzyme mechanisms of superoxide production. Biochim Biophys Acta 1057: 281–298
Ischiropoulos H, Zhu L, Chen J, Tsai M, Martin JC, Smith CD, Beckman JS 1992 Peroxynitrite-mediated tyrosine nitration catalyzed by superoxide dismutase. Arch Biochem Biophys 298: 431–437
Zhang H, Squadrito GL, Pryor WA 1997 The mechanism of the peroxynitrite-carbon dioxide reaction probed using tyrosine. Nitric Oxide 1: 301–307
Bland RD 1980 Special considerations in oxygen therapy of infants and children. Am Rev Respir Dis 122: 45–54
Chen Y, Whitney PL, Frank L 1994 Comparative responses of premature versus full-term newborn rats to prolonged hyperoxia. Pediatr Res 35: 233–237
O'Donovan DJ, Fernandes CJ 2000 Mitochondrial glutathione and oxidative stress: implications for pulmonary oxygen toxicity in premature infants. Mol Genet Metab 71: 352–358
Appleby CJ, Towner RA 2001 Magnetic resonance imaging of pulmonary damage in the term and premature rat neonate exposed to hyperoxia. Pediatr Res 50: 502–507
Ahdab-Barmada M, Moossy J, Nemoto EM, Lin MR 1986 Hyperoxia produces neuronal necrosis in the rat. J Neuropathol Exp Neurol 45: 233–246
Golde S, Chandran S, Brown GC, Compston A 2002 Different pathways for iNOS-mediated toxicity in vitro dependent on neuronal maturation and NMDA receptor expression. J Neurochem 82: 269–282
Ikonomidou C, Bosch F, Miksa M, Bittigau P, Vockler J, Dikranian K, Tenkova TI, Stefovska V, Turski L, Olney JW 1999 Blockade of NMDA receptors and apoptotic neurodegeneration in the developing brain. Science 283: 70–74
Bucher JR, Roberts RJ 1981 The development of the newborn rat lung in hyperoxia: a dose-response study of lung growth, maturation, and changes in antioxidant enzyme activities. Pediatr Res 15: 999–1008
Manji JS, O'Kelly CJ, Leung WI, Olson DM 2001 Timing of hyperoxic exposure during alveolarization influences damage mediated by leukotrienes. Am J Physiol Lung Cell Mol Physiol 281: L799–806
Kobayashi H, Hataishi R, Mitsufuji H, Tanaka M, Jacobson M, Tomita T, Zapol WM, Jones RC 2001 Antiinflammatory properties of inducible nitric oxide synthase in acute hyperoxic lung injury. Am J Respir Cell Mol Biol 24: 390–397
Radomski A, Sawicki G, Olson DM, Radomski MW 1998 The role of nitric oxide and metalloproteinases in the pathogenesis of hyperoxia-induced lung injury in newborn rats. Br J Pharmacol 125: 1455–1462
Sjoberg F, Gustafsson U, Eintrei C 1999 Specific blood flow reducing effects of hyperoxaemia on high flow capillaries in the pig brain. Acta Physiol Scand 165: 33–38
Taglialatela G, Perez-Polo JR, Rassin DK 1998 Induction of apoptosis in the CNS during development by the combination of hyperoxia and inhibition of glutathione synthesis. Free Radic Biol Med 25: 936–942
Miralles C, Busquets X, Santos C, Togores B, Hussain S, Rahman I, MacNee W, Agusti AG 2000 Regulation of iNOS expression and glutathione levels in rat liver by oxygen tension. FEBS Lett 476: 253–257
Coeroli L, Renolleau S, Arnaud S, Plotkine D, Cachin N, Plotkine M, Ben-Ari Y, Charriaut-Marlangue C 1998 Nitric oxide production and perivascular tyrosine nitration following focal ischemia in neonatal rat. J Neurochem 70: 2516–2525
Ikeno S, Nagata N, Yoshida S, Takahashi H, Kigawa J, Terakawa N 2000 Immature brain injury via peroxynitrite production induced by inducible nitric oxide synthase after hypoxia-ischemia in rats. J Obstet Gynaecol Res 26: 227–234
Dobbing J, Sands J 1979 Comparative aspects of the brain growth spurt. Early Hum Dev 3: 79–83
Noack H, Possel H, Rethfeldt C, Keilhoff G, Wolf G 1999 Peroxynitrite mediated damage and lowered superoxide tolerance in primary cortical glial cultures after induction of the inducible isoform of NOS. Glia 28: 13–24
Heneka MT, Dumitrescu L, Loschmann PA, Wullner U, Klockgether T 2000 Temporal, regional, and cell-specific changes of iNOS expression after intrastriatal microinjection of interferon gamma and bacterial lipopolysaccharide. J Chem Neuroanat 18: 167–179
Possel H, Noack H, Putzke J, Wolf G, Sies H 2000 Selective upregulation of inducible nitric oxide synthase (iNOS) by lipopolysaccharide (LPS) and cytokines in microglia: in vitro and in vivo studies. Glia 32: 51–59
Clark RS, Kochanek PM, Schwarz MA, Schiding JK, Turner DS, Chen M, Carlos TM, Watkins SC 1996 Inducible nitric oxide synthase expression in cerebrovascular smooth muscle and neutrophils after traumatic brain injury in immature rats. Pediatr Res 39: 784–790
Sinz EH, Kochanek PM, Dixon CE, Clark RS, Carcillo JA, Schiding JK, Chen M, Wisniewski SR, Carlos TM, Williams D, DeKosky ST, Watkins SC, Marion DW, Billiar TR 1999 Inducible nitric oxide synthase is an endogenous neuroprotectant after traumatic brain injury in rats and mice. J Clin Invest 104: 647–656
Petrov T, Page AB, Owen CR, Rafols JA 2000 Expression of the inducible nitric oxide synthase in distinct cellular types after traumatic brain injury: an in situ hybridization and immunocytochemical study. Acta Neuropathol Berl 100: 196–204
Gahm C, Holmin S, Mathiesen T 2000 Temporal profiles and cellular sources of three nitric oxide synthase isoforms in the brain after experimental contusion. Neurosurgery 46: 169–177
Javeshghani D, Magder S 2001 Presence of nitrotyrosine with minimal inducible nitric oxide synthase induction in lipopolysaccharide-treated pigs. Shock 16: 304–311
Brovkovych V, Patton S, Brovkovych S, Kiechle F, Huk I, Malinski T 1997 In situ measurement of nitric oxide, superoxide and peroxynitrite during endotoxemia. J Physiol Pharmacol 48: 633–644
Halliwell B 1997 What nitrates tyrosine? Is nitrotyrosine specific as a biomarker of peroxynitrite formation in vivo?. FEBS Lett 411( 2–3): 157–160
Kirsch M, Lehnig M, Korth HG, Sustmann R, de Groot H 2001 Inhibition of peroxynitrite-induced nitration of tyrosine by glutathione in the presence of carbon dioxide through both radical repair and peroxynitrate formation. Chemistry 7: 3313–3320
Acknowledgements
The authors thank Evy Strauss, Wolfgang Brück, Anthony Preston, and Roger Wadsworth for their practical and intellectual help with immunohistochemical methods.
Author information
Authors and Affiliations
Corresponding author
Additional information
This study was supported by a grant from the Federal Department of Research and Technology (BMBF #01 ZZ 0101), by intramural research aid from the Charité Faculty of Medicine (#89522104), and by the Sonnenfeld-Stiftung.
Rights and permissions
About this article
Cite this article
Hoehn, T., Felderhoff-Mueser, U., Maschewski, K. et al. Hyperoxia Causes Inducible Nitric Oxide Synthase-Mediated Cellular Damage to the Immature Rat Brain. Pediatr Res 54, 179–184 (2003). https://doi.org/10.1203/01.PDR.0000075220.17631.F1
Received:
Accepted:
Issue date:
DOI: https://doi.org/10.1203/01.PDR.0000075220.17631.F1
This article is cited by
-
Can Excessive Oxygen Cause Hyperactive Behavior Disorder in Preterm Children? Cognitive Effects of Hyperoxia in the Preterm Brain of Rats
Neurophysiology (2019)
-
Zonisamide attenuates hyperoxia-induced apoptosis in the developing rat brain
Neurological Sciences (2014)
-
Perspectives on Neonatal Hypoxia/Ischemia-Induced Edema Formation
Neurochemical Research (2010)
-
Effect of Hyperoxia on Serine Phosphorylation of Apoptotic Proteins in Mitochondrial Membranes of the Cerebral Cortex of Newborn Piglets
Neurochemical Research (2009)
-
Acute and long-term proteome changes induced by oxidative stress in the developing brain
Cell Death & Differentiation (2006)