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Vascular response to hypoxic preconditioning in the immature brain

Gustavsson, Malin, 1975 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för fysiologi,Institute of Neuroscience and Physiology, Department of Physiology
Mallard, Carina, 1963 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för fysiologi,Institute of Neuroscience and Physiology, Department of Physiology
Vannucci, Susan J. (författare)
visa fler...
Wilson, Mary Ann (författare)
Johnston, Michael. V. (författare)
Hagberg, Henrik, 1955 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för kliniska vetenskaper,Institute of Clinical Sciences
visa färre...
 (creator_code:org_t)
2007
2007
Engelska.
Ingår i: J Cereb Blood Flow Metab. ; 27:5, s. 928-38
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • We hypothesized that hypoxic preconditioning (PC) modifies the microvasculature in the immature brain and thereby affects the cerebral blood flow (CBF) during a subsequent hypoxic-ischemic (HI) insult. On postnatal day 6 rats were exposed to hypoxia (36 degrees C, 8.0% O2) or normoxia for 3 h. Unilateral HI (unilateral carotid ligation and 8% hypoxia) was induced 24 h later. Cortical CBF was measured with the 14C-iodoantipyrine technique (at the end of HI) or with laser Doppler flowmetry (Perimed PF5001) before and during HI. At 0, 2, 8, and 24 h cerebral cortex was sampled and analyzed with gene arrays (Affymetrix 230 2.0). L-nitroarginine or vehicle was administrated before hypoxic PC or 30 mins before HI followed by CBF measurement (laser Doppler) during subsequent HI. Twenty-four hours after PC animals were perfusion-fixed and brains immunolabeled for von Willebrand factor and vascular density was determined by stereological quantification. The decrease in CBF during HI was attenuated significantly in PC versus control animals (P<0.01), as detected by both techniques. Several vascular genes (Angpt2, Adm, Apln, Vegf, Flt1, Kdr, Pdgfra, Agtrap, Adora2a, Ednra, serpine1, caveolin, Id1, Prrx1, Ero1l, Acvrl1, Egfl7, Nudt6, Angptl4, Anxa2, and NOS3) were upregulated and a few (Csrp2, Adora2b) were downregulated after PC. A significant increase in vascular density (P<0.05) was seen after PC. Nitric oxide synthase inhibition did not affect CBF during HI after PC. In conclusion, hypoxic PC upregulates vascular genes, increases vascular density and attenuates the decrease of CBF during a subsequent HI, which could contribute to tolerance.

Nyckelord

Animals
Brain/*growth & development/pathology
Cerebrovascular Circulation/*physiology
Enzyme Inhibitors/pharmacology
Flow Cytometry
Gene Expression/physiology
Hypoxia
Brain/genetics/pathology/*physiopathology
Microcirculation/physiology
Nitric Oxide/biosynthesis/physiology
Nitric Oxide Synthase Type I/antagonists & inhibitors
Oligonucleotide Array Sequence Analysis
Rats
Rats
Sprague-Dawley
Reverse Transcriptase Polymerase Chain Reaction
von Willebrand Factor/physiology

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