نتایج جستجو برای: stress induced analgesia

تعداد نتایج: 1353498  

2016

The current study addressed two important concerns, one pertinent to the impact of PDE-5 inhibitor (tadalafil) on morphine-induced analgesia and the second relevant to its influence on morphine-induced oxidative stress in two different pain models, the the tail-flick test (representing an acute thermal phasic pain model ) and the formalin test (representing an inflammatory tonic pain model ). T...

Journal: :Pain physician 2017
Jessica Van Oosterwijck Uros Marusic Inge De Wandele Lorna Paul Mira Meeus Greta Moorkens Luc Lambrecht Lieven Danneels Jo Nijs

BACKGROUND Patients with myalgic encephalomyelitis / chronic fatigue syndrome (ME/CFS) are unable to activate brain-orchestrated endogenous analgesia (or descending inhibition) in response to exercise. This physiological impairment is currently regarded as one factor explaining post-exertional malaise in these patients. Autonomic dysfunction is also a feature of ME/CFS. OBJECTIVES This study ...

Journal: :Brain research 1987
J W Lewis G Baldrighi H Akil

Opioid peptides appear to be important neurochemical mediators in central nervous system mechanisms of analgesia, cardiovascular control, and many endocrinological responses to stress. The nucleus tractus solitarius (NTS), a brain region expressing all 3 opioid peptide families, is also associated with regulation of autonomic and endocrine functions. We now report that electrical stimulation of...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 1988
Y O Taiwo J D Levine

Spinal intrathecal injections of the nonsteroidal antiinflammatory analgesics (NSAIAs) indomethacin and acetylsalicylic acid, which inhibit prostaglandin synthesis, cause dose-dependent hypoalgesia in the rat. Intrathecal injections of prostaglandin-E2 (PGE2) produce dose-dependent hyperalgesia. To determine whether this action of prostaglandins on the central nervous system is mediated through...

Journal: :Physiology & behavior 1986
M B Kristal A C Thompson S B Heller B R Komisaruk

Ingestion of placenta has previously been shown to enhance opiate-mediated analgesia (measured as tail-flick latency) induced either by morphine injection or by footshock. The present study was designed to test whether placenta ingestion would enhance the partly opiate-mediated analgesia produced by vaginal/cervical stimulation. Nulliparous Sprague-Dawley rats were tested for analgesia, using t...

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