4.4 Article

Stress-Induced Hypertension and Increased Sympathetic Activity in Mice Overexpressing Neuropeptide Y in Noradrenergic Neurons

期刊

NEUROENDOCRINOLOGY
卷 89, 期 3, 页码 351-360

出版社

KARGER
DOI: 10.1159/000188602

关键词

Transgenic mouse model; Sympathetic nervous system; Adrenal gland; Corticosterone

资金

  1. Academy of Finland
  2. Finnish Funding Agency for Technology and Innovation
  3. Turku University Foundation
  4. Finnish Cultural Foundation
  5. Emil Aaltonen Foundation
  6. Portuguese Foundation for Science and Technology
  7. FEDER [POCI/SAU-FCF/60399/2004]

向作者/读者索取更多资源

Background and Aims: Neuropeptide Y (NPY) is a sympathetic neurotransmitter co-stored and co-released with noradrenaline and adrenaline. We have constructed a novel NPY transgenic mouse model (OE-NPYDBH mouse) where targeted overexpression results in increased levels of NPY in the brainstem and adrenal glands. The present study was aimed to understand the role of NPY released from sympathetic nerves and brain noradrenergic neurons in regulation of blood pressure, and behavioral responses to stress. Methods: Blood pressure was measured by radiotelemetry in conscious male OE-NPYDBH and wild-type mice during surgical stress and in baseline conditions. Plasma and adrenal gland catecholamine levels were measured at baseline. Acute immobilization and cold exposure were used to study the plasma levels of NPY and corticosterone in stress, and brown adipose tissue thermogenic activity was measured with [H-3] GDP binding after cold. Results: Here, we demonstrate that sympathoadrenal activity is enhanced in the OE-NPYDBH mice. Blood pressure during surgical stress was significantly increased in comparison with wild-type controls. Furthermore, OE-NPYDBH mice showed sexually dimorphic NPY responses to stress, and an anxiolytic-like behavior in elevated plus-maze and light-dark tests. Conclusion: This study shows that the overactive noradrenergic NPY system plays a role in regulation of blood pressure and adaptive responses to stress, and may be a link between chronic stress and adiposity-associated disturbances in metabolism. Copyright (C) 2008 S. Karger AG, Basel

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