Neuropeptide Y promotes sleep and inhibits ACTH and cortisol release in young men
Anxiolytic and sedative effects of neuropeptide Y (NPY) are thought to involve inhibition of corticotropin-releasing hormone (CRH). Enhanced secretion of CRH plays a critical role in the pathophysiology of major depression, characterized by sleep disturbances, anxiety and loss of appetite. We examin...
Saved in:
Published in: | Neuropharmacology Vol. 39; no. 8; pp. 1474 - 1481 |
---|---|
Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
England
Elsevier Ltd
01-07-2000
|
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Anxiolytic and sedative effects of neuropeptide Y (NPY) are thought to involve inhibition of corticotropin-releasing hormone (CRH). Enhanced secretion of CRH plays a critical role in the pathophysiology of major depression, characterized by sleep disturbances, anxiety and loss of appetite. We examined for the first time in young men effects of intravenous injections of NPY (4×50 or 100 μg,
n=9 and 11, respectively, at 22.00, 23.00, 24.00 and 01.00 compared to saline) on the sleep electroencephalogram (EEG; recorded from 23.00 to 07.00) and nocturnal secretion of adrenocorticotrophic hormone (ACTH), cortisol, growth hormone (GH), prolactin and leptin. Repeated measures MANOVA showed that ACTH secretion during the first half of the night was reduced by the lower dose of NPY only (
F=8.7,
p<0.05), while cortisol secretion during the second half of the night was reduced regardless of the dose (
F=7.9,
p<0.05). Regardless of the dose, NPY enhanced sleep period time and stage 2 sleep (
F=12.8 and 5.4, each
p<0.05), and also reduced sleep latency and time awake (
F=4.9 and 4.4, each
p<0.05) and modulated REM sleep. In summary, NPY promotes sleep and inhibits the hypothalamo–pituitary–adrenocortical (HPA) axis in humans, pointing to a possible role of NPY agonists for the development of novel treatment strategies for affective disorders. |
---|---|
Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-News-3 |
ISSN: | 0028-3908 1873-7064 |
DOI: | 10.1016/S0028-3908(00)00057-5 |