Regulation of Catecholamines by Sustained and Intermittent Hypoxia in Neuroendocrine Cells and Sympathetic Neurons
Open Access
- 1 December 2003
- journal article
- research article
- Published by Wolters Kluwer Health in Hypertension
- Vol. 42 (6) , 1130-1136
- https://doi.org/10.1161/01.hyp.0000101691.12358.26
Abstract
Chronic intermittent hypoxia, a characteristic feature of sleep-disordered breathing, induces hypertension through augmented sympathetic nerve activity and requires the presence of functional carotid body arterial chemoreceptors. In contrast, chronic sustained hypoxia does not alter blood pressure. We therefore analyzed the biosynthetic pathways of catecholamines in peripheral nervous system structures involved in the pathogenesis of intermittent hypoxia-induced hypertension, namely, carotid bodies, superior cervical ganglia, and adrenal glands. Rats were exposed to either intermittent hypoxia (90 seconds of room air alternating with 90 seconds of 10% O 2 ) or to sustained hypoxia (10% O 2 ) for 1 to 30 days. Dopamine, norepinephrine, epinephrine, dihydroxyphenylacetic acid, and 5-hydroxytyptamine contents were measured by high-performance liquid chromatography. Expression of tyrosine hydroxylase and its phosphorylated forms, dopamine β-hydroxylase, phenylethanolamine N -methyltransferase, and GTP cyclohydrolase-1 were determined by Western blot analyses. Both sustained and intermittent hypoxia significantly increased dopamine and norepinephrine content in carotid bodies but not in sympathetic ganglia or adrenal glands. In carotid bodies, both types of hypoxia augmented total levels of tyrosine hydroxylase protein and its phosphorylation on serines 19, 31, 40, as well as levels of GTP cyclohydrolase-1. However, the effects of intermittent hypoxia on catecholaminergic pathways were significantly smaller and delayed than those induced by sustained hypoxia. Thus, attenuated induction of catecholaminergic phenotype by intermittent hypoxia in carotid body may play a role in development of hypertension associated with sleep-disordered breathing. The effects of both types of hypoxia on expression of catecholaminergic enzymes in superior cervical neurons and adrenal glands were transient and small.Keywords
This publication has 45 references indexed in Scilit:
- Effects of Substitution at Serine 40 of Tyrosine Hydroxylase on Catecholamine BindingBiochemistry, 2001
- Stoichiometry of Tyrosine Hydroxylase Phosphorylation in the Nigrostriatal and Mesolimbic Systems In VivoJournal of Neurochemistry, 2000
- The sympathetic nervous system and obstructive sleep apneaJournal Of Hypertension, 1997
- Hypertension caused by chronic intermittent hypoxia – influence of chemoreceptors and sympathetic nervous systemJournal Of Hypertension, 1997
- Phosphorylation and activation of human tyrosine hydroxylase in vitro by mitogen‐activated protein (MAP) kinase and MAP‐kinase‐activated kinases 1 and 2European Journal of Biochemistry, 1993
- Long-term hypoxia increases the number of norepinephrine-containing glomus cells in the rat carotid body: A correlative immunocytochemical and biochemical studyJournal of the Autonomic Nervous System, 1993
- Sympathetic denervation blocks blood pressure elevation in episodic hypoxia.Hypertension, 1992
- Influence of long-term hypoxia on tyrosine hydroxylase in the rat carotid body and adrenal glandJournal of the Autonomic Nervous System, 1992
- Feedback Inhibition of Ca2+ Currents by Dopamine in Glomus Cells of the Carotid BodyEuropean Journal of Neuroscience, 1990
- Depression of Ventilation by Dopamine in ManJournal of Clinical Investigation, 1978