The time window of intermittent hypoxia intervention after middle cerebral artery occlusion

Chinese Journal of Physiology

Volumn 51, Issue 5, 2008, Pages 324-328

  Tsai, Yi Wei ^a   Yang, Yea Ru ^a,b   Chen, Gun Hao ^a   Chang, Huang Chih ^a   Wang, Ray Yau ^a,b  

^a NATIONAL YANG MING UNIVERSITY   (Taiwan)

^b TAIPEI CITY HOSPITAL   (Taiwan)

Author keywords

Cerebral ischemia; Intermittent hypoxia; Time windows

Indexed keywords

ANIMAL; ANOXIA; ARTICLE; BRAIN ISCHEMIA; CEREBRAL ARTERY DISEASE; ISCHEMIC PRECONDITIONING; MALE; METHODOLOGY; MORTALITY; PATHOLOGY; PATHOPHYSIOLOGY; RAT; SPRAGUE DAWLEY RAT; TIME;

ANIMALS; ANOXIA; BRAIN ISCHEMIA; INFARCTION, MIDDLE CEREBRAL ARTERY; ISCHEMIC PRECONDITIONING; MALE; RATS; RATS, SPRAGUE-DAWLEY; TIME FACTORS;

EID: 60849091921     PISSN: 03044920     EISSN: 26660059     Source Type: Journal    
DOI: None     Document Type: Article

References (25)

1. Bernaudin, M., Nedelec, A.S., Divoux, D., MacKenzie, E.T., Petit, E. and Schumann-Bard, P. Normobaric hypoxia induces tolerance to focal permanent cerebral ischemia in association with an increased expression of hypoxia-inducible factor-1 and its target genes, erythropoietin and VEGF, in the adult mouse brain. J. Cereb. Blood Flow Metab. 22: 393-403, 2002.
2. Chien, C., Hwu, C., Liou, T., Huang, Z., Shen, A., Yang, V., Lee, C. and Chien, E. Inducible nitric oxide synthase expression and plasma bilirubin changes in rats under intermittent hypoxia treatment. Chinese J. Physiol. 49: 275-280, 2006.
3. Dirnagl, U., Iadecola, C. and Moskowitz, M. Pathobiology of ischaemic stroke: an integrated view. Trends Neurosci. 22: 391-397, 1999.
4. Gendron, A., Kouassi, E., Nuara, S., Cossette, C., D'Angelo, G., Geadah, D., du Souich, P. and Teitelbaum, J. Transient middle cerebral artery occlusion influence on systemic oxygen homeostasis and erythropoiesis in Wistar rats. Stroke 38: 1979-1984, 2004.
5. Gidday, J., Fitzgibbons, J., Shah, A. and Park, T. Neuroprotection from ischemic brain injury by hypoxic preconditioning in the neonatal rat. Neurosci. Lett. 168: 221-224, 1994.
6. Lee, T.H., Yang, J.T., Kato, H., Wu, J.H. and Chen, S.T. Expression of brain-derived neurotrophic factor immunoreactivity and mRNA in the hippocampal CA1 and cortical areas after chronic ischemia in rats. J. Neurosci. Res. 76: 705-712, 2004.
7. Lin, A.M.Y., Chen, C.F. and Ho, L.T. Neuroprotective effect of intermittent hypoxia on iron-induced oxidative injury in rat brain. Exp. Neurol. 176: 328-335, 2002.
8. Lin, T.N., He, Y.Y., Wu, G., Khan, M. and Hsu, C.Y. Effect of brain edema on infarct volume in a focal cerebral ischemia model in rats. Stroke 24: 117-121, 1993.
9. Mehta, S., Manhas, N. and Raghubir, R. Molecular targets in cerebral ischemia for developing novel therapeutics. Brain Res. Rev. 54: 34-66, 2007.
10. Mies, G., Iijima, T. and Hossmann, K.A. Correlation between periinfarct DC shifts and ischaemic neuronal damage in rat. Neuroreport 4: 709-711, 1993.
11. Muir, K.W., Tyrrella, P., Sattar, N. and Warburton, E. Inflammation and ischaemic stroke. Curr. Opin. Neurol. 20: 334-342, 2007.
12. Neubauer, J.A. Physiological and genomic consequences of intermittent hypoxia: invited review: physiological and pathophysiological responses to intermittent hypoxia. J. Appl. Physiol. 90: 1593-1599, 2001.
13. O'Mahony, D. and Kendall, M.J. Nitric oxide in acute ischaemic stroke: a target for neuroprotection. J. Neurol. Neurosurg. Psychiatr. 67: 1-3, 1999.
14. Prabhakar, N.R. Oxygen sensing during intermittent hypoxia: cellular and molecular mechanisms. J. Appl. Physiol. 90: 1986-1994, 2001.
15. Prabhakar, N.R., Fields, R.D., Baker, T. and Fletcher, E.C. Intermittent hypoxia: cell to system. Am. J. Physiol. 281: 3-8, 2001.
16. Prabhakar, N.R. and Kumar, G.K. Oxidative stress in the systemic and cellular responses to intermittent hypoxia. Biol. Chem. 385: 217-221, 2004.
17. Ran, R., Xu, H., Lu, A., Bernaudin, M. and Sharp, F.R. Hypoxia preconditioning in the brain. Dev. Neurosci. 27: 87-92, 2005.
18. Schabitz, W., Schwab, S., Spranger, M. and Hacke, W. Intravenous BDNF reduces infarct size and counterregulates Bax and Bcl-2 expression after temporary focal cerebral ischemia. Stroke 31: 2212-2217, 2000.
19. Schabitz, W.R., Schwab, S., Spranger, M. and Hacke, W. Intraventricular brain-derived neurotrophic factor size after focal cerebral ischemia in rats. J. Cereb. Blood Flow Metab. 17: 500-506, 1997.
20. Smith, W.S. Pathophysiology of focal cerebral ischemia: a therapeutic perspective. J. Vasc. Interv. Radiol. 15: 3-12, 2004.
21. Stroemer, R.P., Kent, T.A. and Hulsebosch, C.E. Neocortical neural sprouting, synaptogenesis, and behavioral recovery after neocortical infarction in rats. Stroke 26: 2135-2144, 1995.
22. Wang, R.Y., Wang, P.S.G. and Yang, Y.R. The effect of age in rats following middle cerebral artery occlusion. Gerontology 49: 21-26, 2003.
23. Wang, R.Y., Yang, Y.R. and Yu, S.M. Protective effects of treadmill training on infarction in rats. Brain Res. 922: 140-143, 2001.
24. Zhang, J.X., Chen, X.Q., Du, J.Z., Chen, Q, M. and Zhu, C.Y. Neonatal exposure to intermittent hypoxia enhances mice performance in water maze and 8-arm radial maze tasks. J. Neurobiol. 65: 72-84, 2005.
25. Zhao, X., Fu, W., Yuan, W., Wu, Z. and Yang, Z. A study of time window for oxidative stress associated with myocardial ischemia and reperfusion. Chinese Med. J. (Engl). 109: 926-929, 1996.