Kerman University of Medical Sciences

Document Type : Original Article(s)

Authors

1 Neuroscience Research Center, Aja University of Medical Sciences, Tehran, Iran

2 Trauma Research Center, Aja University of Medical Sciences, Tehran, Iran

3 Department of Oral Medicine, School of Dentistry, Aja University of Medical Sciences, Tehran, Iran

4 Neuroscience Research Center, Institute of Neuropharmacology, Kerman University of Medical Sciences, Kerman, Iran

5 Department of Physiology, School of Medicine AND Neuroscience Research Center, Neuropharmacology Institute, Kerman University of Medical Sciences, Kerman, Iran

Abstract

Background: Empathy is the capability to represent the mental and emotional states of other subjects.
Previous studies have demonstrated a possible correlation between morphine addiction and altered empathy
response in morphine-addicted subjects. This study was performed to evaluate the effect of chronic morphine
exposure as an animal model of morphine addiction on empathic changes in affective and sensory pain.
Methods: Adult male Wistar rats (3 months old) were used for the current study. Animals were grouped in
cages of two (n = 8 for each group) and one animal was selected as the pain observer group. Pain observer
animals received either saline or morphine (10 mg/kg, twice daily for 8 days). At ninth day, formalin [50 µg,
5%, subcutaneous (SC)] was injected into the hindpaw of the cagemate and placed inside the cage. Elevated
plus maze (EPM) and open field test (OFT) were recruited to evaluate anxiety; hot plate and tail flick tests
were used to assay sensory pain. Conditioned place aversion (CPA) was also measured as indicator of
affective pain component.
Findings: Chronic morphine exposure led to a reduced level of anxiety in EPM and OFT assays. An opioidinduced hyperalgesia was observed in the sensory pain assays, while there was a reduced affective pain in the
CPA paradigm in morphine-treated animals.
Conclusion: It might be plausible that chronic morphine exposure might alter empathy for pain through
affective and not sensory pain pathways


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