You are not currently logged in.
Access your personal account or get JSTOR access through your library or other institution:
If You Use a Screen ReaderThis content is available through Read Online (Free) program, which relies on page scans. Since scans are not currently available to screen readers, please contact JSTOR User Support for access. We'll provide a PDF copy for your screen reader.
Evidence for a Role of Delta Sleep-Inducing Peptide in Slow-Wave Sleep and Sleep-Related Growth Hormone Release in the Rat
Kanak S. Iyer, G. A. Marks, A. J. Kastin and S. M. McCann
Proceedings of the National Academy of Sciences of the United States of America
Vol. 85, No. 10 (May 15, 1988), pp. 3653-3656
Published by: National Academy of Sciences
Stable URL: http://www.jstor.org/stable/31723
Page Count: 4
Since scans are not currently available to screen readers, please contact JSTOR User Support for access. We'll provide a PDF copy for your screen reader.
Preview not available
To examine the role of delta sleep-inducing peptide (DSIP) in sleep-related growth hormone (GH) release, male rats were deprived of sleep for 4 hr by placing them on a slowly rotating wheel. Sleep deprivating by this method caused a significant increase in GH release, as indicated by the increase in plasma GH concentrations (P < 0.01), and also in the amount of slow-wave sleep (SWS) (P < 0.001) above initial values after removal of the animals from the rotating wheel. These increases were blocked by microinjection into the third cerebral ventricle of highly specific antiserum to DSIP. In control rats receiving an equal volume of normal rabbit serum, the significant increase in plasma GH as well as SWS remained after removal of the rats from the wheel. The increased release of endogenous DSIP in the sleep-deprived animals may have caused an increase in SWS as well as plasma GH. Since DSIP increases plasma GH after its injection into the third cerebral ventricle and since passive immunization against DSIP blocks the increase in SWS and GH release that follows the 4 hr of sleep deprivation, the results suggest that DSIP can be a physiological stimulus for sleep-related GH release as well as for the induction of SWS.
Proceedings of the National Academy of Sciences of the United States of America © 1988 National Academy of Sciences