The consequences of
sleep deprivation on memory, cognition, nociception, stress, and endocrine function are related to the balance of
neuropeptides, with
peptidases being particularly essential.
Thimet oligopeptidase (THOP1) is a
metallopeptidase implicated in the metabolism of many sleep-related
peptides, including
angiotensin I,
gonadotropin releasing hormone (
GnRH),
neurotensin, and
opioid peptides. In the present study, we evaluated the effect of
sleep deprivation and sleep recovery in male rats on THOP1 expression and specific activity in the central nervous system. In the striatum and hypothalamus, THOP1 activity decreased following
sleep deprivation and a recovery period. Meanwhile, THOP1 activity and immunoexpression increased in the hippocampal dentate gyrus during the sleep recovery period. Changes in THOP1 expression after
sleep deprivation and during sleep recovery can potentially alter the processing of
neuropeptides. In particular, processing of
opioid peptides may be related to the known increase in
pain sensitivity in this model. These results suggest that THOP1 may be an important player in the effects of
sleep deprivation.