Tyrosine hydroxylase expression and activity in the rat brain: differential regulation after long-term intermittent or sustained hypoxia

• Published in: Journal of applied physiology (1985) 2005-08, Vol.99 (2), p.642-649
• Main Authors: Gozal, Evelyne, Shah, Zahoor A, Pequignot, Jean-Marc, Pequignot, Jacqueline, Sachleben, Leroy R, Czyzyk-Krzeska, Maria F, Li, Richard C, Guo, Shang-Z, Gozal, David
• Format: Article
• Language: English
• Subjects: Acute Disease; Adaptation; Adaptation, Physiological; Animals; Biochemistry and metabolism; Biological and medical sciences; Brain; Brain - enzymology; Central nervous system; Chronic Disease; Enzyme Activation; Fundamental and applied biological sciences. Psychology; Gene expression; Gene Expression Regulation, Enzymologic; Hypoxia - classification; Hypoxia - metabolism; Life Sciences; Male; Other; Rats; Rats, Sprague-Dawley; Time Factors; Tissue Distribution; Tissues; Tyrosine 3-Monooxygenase - metabolism; Vertebrates: nervous system and sense organs
• ISSN: 8750-7587; 1522-1601
• DOI: 10.1152/japplphysiol.00880.2004

1 Department of Pediatrics, Kosair Children’s Hospital Research Institute, and 2 Department of Pharmacology and Toxicology, University of Louisville, Louisville, Kentucky; 3 Department of Genome Science, Genome Research Institute, University of Cincinati, Cincinnati, Ohio; and 4 Physiologie Integrative Cellulaire et Moleculaire, Unité Mixte de Recherche 5123, Centre National de la Recherche Scientifique, University of Lyon, Lyon, France Submitted 13 August 2004 ; accepted in final form 2 April 2005 Tyrosine hydroxylase, a hypoxia-regulated gene, may be involved in tissue adaptation to hypoxia. Intermittent hypoxia, a characteristic feature of sleep apnea, leads to significant memory deficits, as well as to cortex and hippocampal apoptosis that are absent after sustained hypoxia. To examine the hypothesis that sustained and intermittent hypoxia induce different catecholaminergic responses, changes in tyrosine hydroxylase mRNA, protein expression, and activity were compared in various brain regions of male rats exposed for 6 h, 1 day, 3 days, and 7 days to sustained hypoxia (10% O 2 ), intermittent hypoxia (alternating room air and 10% O 2 ), or normoxia. Tyrosine hydroxylase activity, measured at 7 days, increased in the cortex as follows: sustained > intermittent > normoxia. Furthermore, activity decreased in the brain stem and was unchanged in other brain regions of sustained hypoxia-exposed rats, as well as in all regions from animals exposed to intermittent hypoxia, suggesting stimulus-specific and heterotopic catecholamine regulation. In the cortex, tyrosine hydroxylase mRNA expression was increased, whereas protein expression remained unchanged. In addition, significant differences in the time course of cortical Ser 40 tyrosine hydroxylase phosphorylation were present in the cortex, suggesting that intermittent and sustained hypoxia-induced enzymatic activity differences are related to different phosphorylation patterns. We conclude that long-term hypoxia induces site-specific changes in tyrosine hydroxylase activity and that intermittent hypoxia elicits reduced tyrosine hydroxylase recruitment and phosphorylation compared with sustained hypoxia. Such changes may not only account for differences in enzyme activity but also suggest that, with differential regional brain susceptibility to hypoxia, recruitment of different mechanisms in response to hypoxia will elicit region-specific modulation of catecholamine response. sleep apnea; high altitude; neuro