Time-dependent alterations of cerebral proteins following short-term normobaric hyperoxia
- PMID: 20049628
- DOI: 10.1007/s11010-009-0365-1
Time-dependent alterations of cerebral proteins following short-term normobaric hyperoxia
Abstract
Sufficient oxygenation is indispensable for cognitive performance in mammals. In order to assure adequate oxygenation and to prevent hypoxia in medicine or aviation, different approaches of oxygen delivery are realized. With regard to hyperoxia, it is well known that it increases the risk of tissue toxicity and inflammation by generating radical oxygen species. However, this impact of hyperoxia on the expression of specific brain proteins has not been evaluated in detail yet. The present study analyzes time-dependent changes in protein expression in rat brain after a short-term exposure to normobaric hyperoxia. Thirty-six Wistar rats were randomly assigned to six different groups, three normobaric hyperoxia (NH) groups or three normobaric normoxia (NN) groups, each consisting of n = 6 animals. NH animals were exposed to 100% oxygen, NN rats to 21% oxygen, each group for 3 h. One group of NH and one group of NN were killed immediately after the 3 h, one group each after 3 days and one group each after 7 days. Rat brains were removed for analysis and whole brain detergent protein lysates were separated via two-dimensional gel electrophoresis followed by subsequent identification of protein expression alterations by peptide mass fingerprinting using mass spectrometry. Also, a functional network mapping and molecular pathway analysis were carried out. Statistical analysis was performed using analysis of variance (ANOVA) with Bonferroni correction using P < 0.01. Physiological parameters of the animals did not differ significantly between the two groups except for partial oxygen pressure (580 vs. 89 mmHg; P < 0.05). The expression of nine proteins was found to be significantly altered (five up-regulated: GOT1, CCT2, TCP1, G6PD, and ALB; four down-regulated: PEBP1, PRDX2, ENO1, and MDH1). IPA generated a network with eight focus proteins associated with pathways in "cell death, cancer, and signalling". Although hyperoxia was normobaric and induced for only 3 h, significant changes in brain protein expression were detectable immediately after the 3 h, after 3 days, as well as after 7 days. This may indicate effects on brain protein expression take place in the rat brain following a relatively short period of hyperoxia.
Similar articles
-
Hyperoxia-Induced Protein Alterations in Renal Rat Tissue: A Quantitative Proteomic Approach to Identify Hyperoxia-Induced Effects in Cellular Signaling Pathways.Dis Markers. 2015;2015:964263. doi: 10.1155/2015/964263. Epub 2015 May 27. Dis Markers. 2015. PMID: 26106253 Free PMC article.
-
Response of rat lung tissue to short-term hyperoxia: a proteomic approach.Mol Cell Biochem. 2013 Nov;383(1-2):231-42. doi: 10.1007/s11010-013-1771-y. Epub 2013 Aug 11. Mol Cell Biochem. 2013. PMID: 23934118
-
Time Dependent Pathway Activation of Signalling Cascades in Rat Organs after Short-Term Hyperoxia.Int J Mol Sci. 2018 Jul 4;19(7):1960. doi: 10.3390/ijms19071960. Int J Mol Sci. 2018. PMID: 29973540 Free PMC article.
-
Arterial hyperoxia in severe head injury: a useful or harmful option?Curr Pharm Des. 2004;10(18):2163-76. doi: 10.2174/1381612043384187. Curr Pharm Des. 2004. PMID: 15281892 Review.
-
Normobaric hyperoxia therapy for traumatic brain injury and stroke: a review.Br J Neurosurg. 2009 Dec;23(6):576-84. doi: 10.3109/02688690903050352. Br J Neurosurg. 2009. PMID: 19922270 Review.
Cited by
-
Ischemic Neuroprotectant PKCε Restores Mitochondrial Glutamate Oxaloacetate Transaminase in the Neuronal NADH Shuttle after Ischemic Injury.Transl Stroke Res. 2020 Jun;11(3):418-432. doi: 10.1007/s12975-019-00729-4. Epub 2019 Aug 31. Transl Stroke Res. 2020. PMID: 31473978 Free PMC article.
-
Tat-CCT2 Protects the Neurons from Ischemic Damage by Reducing Oxidative Stress and Activating Autophagic Removal of Damaged Protein in the Gerbil Hippocampus.Neurochem Res. 2023 Dec;48(12):3585-3596. doi: 10.1007/s11064-023-03995-9. Epub 2023 Aug 10. Neurochem Res. 2023. PMID: 37561257
-
Hyperoxia-Induced Protein Alterations in Renal Rat Tissue: A Quantitative Proteomic Approach to Identify Hyperoxia-Induced Effects in Cellular Signaling Pathways.Dis Markers. 2015;2015:964263. doi: 10.1155/2015/964263. Epub 2015 May 27. Dis Markers. 2015. PMID: 26106253 Free PMC article.
-
Proteomic analysis of mitochondrial proteins in the guinea pig heart following long-term normobaric hyperoxia.Mol Cell Biochem. 2017 Oct;434(1-2):61-73. doi: 10.1007/s11010-017-3037-6. Epub 2017 Apr 21. Mol Cell Biochem. 2017. PMID: 28432557
-
Response of rat lung tissue to short-term hyperoxia: a proteomic approach.Mol Cell Biochem. 2013 Nov;383(1-2):231-42. doi: 10.1007/s11010-013-1771-y. Epub 2013 Aug 11. Mol Cell Biochem. 2013. PMID: 23934118
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Research Materials
Miscellaneous