Activation of the prostaglandin system in response to sleep loss in healthy humans: potential mediator of increased spontaneous pain

Pain. 2009 Sep;145(1-2):136-41. doi: 10.1016/j.pain.2009.05.029. Epub 2009 Jun 27.


Insufficient duration of sleep is a highly prevalent behavioral pattern in society that has been shown to cause an increase in spontaneous pain and sensitivity to noxious stimuli. Prostaglandins (PGs), in particular PGE2, are key mediators of inflammation and pain, and we investigated whether PGE2 is a potential mediator in sleep-loss-induced changes in nociceptive processing. Twenty-four participants (7 females, age 35.1+/-7.1 years) stayed for 7 days in the Clinical Research Center. After two baseline days, participants were randomly assigned to either 3 days of 88 h of sleep deprivation (TSD, N=15) or 8h of sleep per night (N=9), followed by a night of recovery sleep. Participants rated the intensity of various pain-related symptoms every 2h across waking periods on computerized visual analog scales. PGE2 was measured in 24-h-urine collections during baseline and third sleep deprivation day. Spontaneous pain, including headache, muscle pain, stomach pain, generalized body pain, and physical discomfort significantly increased by 5-14 units on a 100-unit scale during TSD, compared to the sleep condition. Urinary PGE2 metabolite significantly increased by about 30% in TSD over sleep condition. TSD-induced increase in spontaneous pain, in particular headache and muscle pain, was significantly correlated with increase in PGE2 metabolite. Activation of the PGE2 system appears to be a potential mediator of increased spontaneous pain in response to insufficient sleep.

Publication types

  • Randomized Controlled Trial
  • Research Support, N.I.H., Extramural

MeSH terms

  • Adult
  • Affect / physiology
  • Dinoprostone / metabolism*
  • Female
  • Humans
  • Linear Models
  • Male
  • Middle Aged
  • Pain Measurement / methods
  • Pain Threshold / physiology*
  • Polysomnography
  • Prostaglandins / urine
  • Sleep / physiology*
  • Sleep Deprivation / physiopathology*
  • Wakefulness / physiology
  • Young Adult


  • Prostaglandins
  • 7-hydroxy-5,11-dioxotetranorprostane-1,16-dioic acid
  • Dinoprostone