Irritable bowel syndrome patients show altered sensitivity to exogenous opioids

Alterations in activation of pain modulation systems may play a role in the pathophysiology of irritable bowel syndrome (IBS). However, little is known about the effects of exogenous opioids on the perceptual and autonomic responses to aversive visceral stimulation. The aim of the study was to evalu...

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Published in:Pain (Amsterdam) Vol. 87; no. 2; pp. 137 - 147
Main Authors: Lembo, Tony, Naliboff, Bruce D, Matin, Kamran, Munakata, Julie, Parker, Robert A, Gracely, Richard H, Mayer, Emeran A
Format: Journal Article
Language:English
Published: Amsterdam Elsevier B.V 01-08-2000
Lippincott Williams & Wilkins, Inc
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Abstract Alterations in activation of pain modulation systems may play a role in the pathophysiology of irritable bowel syndrome (IBS). However, little is known about the effects of exogenous opioids on the perceptual and autonomic responses to aversive visceral stimulation. The aim of the study was to evaluate the effect of the mu opioid-preferring analgesic fentanyl (FEN), given intravenously, on perceptual and autonomic responses to rectal distension. Ten IBS patients and ten normal subjects received, on separate days, either high dose (HD) fentanyl (112 μg bolus followed by 0.04 μg/kg per min infusion), low dose (LD) fentanyl (56 μg bolus followed by 0.02 μg/kg per min) or normal saline (SAL) (50 cc bolus followed by 45 cc/h infusion). Perception thresholds for discomfort and pain during rectal distension were assessed using a tracking paradigm. Intensity and unpleasantness ratings of the distensions, and cardiac autonomic parameters were assessed during randomly delivered rectal stimuli. Effects of FEN on rectal compliance and tone as well as mental status were also assessed. IBS patients had lower perceptual thresholds for discomfort and pain under control conditions. FEN dose-dependently increased the perception thresholds in both healthy control subjects and in IBS patients with a greater relative efficacy in IBS patients than in normal subjects. IBS patients used significantly higher unpleasantness ratings of rectal stimuli compared to healthy controls, but showed no difference in the sensory intensity rating of the stimulus. FEN decreased both intensity and unpleasantness ratings for IBS and normals. FEN lowered cardiosympathetic tone in normal subjects but had no effect on IBS patients. FEN had no effect on rectal tone or compliance. FEN dose-dependently attenuates the perception of phasic rectal distension and affects unpleasantness ratings during random fixed rectal distension, with a greater relative efficacy for this antinociceptive effect in IBS patients. These findings support the hypothesis that IBS patients may have an altered central release of endogenous opioids in response to visceral stimulation.
AbstractList Alterations in activation of pain modulation systems may play a role in the pathophysiology of irritable bowel syndrome (IBS). However, little is known about the effects of exogenous opioids on the perceptual and autonomic responses to aversive visceral stimulation. The aim of the study was to evaluate the effect of the mu opioid-preferring analgesic fentanyl (FEN), given intravenously, on perceptual and autonomic responses to rectal distension. Ten IBS patients and ten normal subjects received, on separate days, either high dose (HD) fentanyl (112 μg bolus followed by 0.04 μg/kg per min infusion), low dose (LD) fentanyl (56 μg bolus followed by 0.02 μg/kg per min) or normal saline (SAL) (50 cc bolus followed by 45 cc/h infusion). Perception thresholds for discomfort and pain during rectal distension were assessed using a tracking paradigm. Intensity and unpleasantness ratings of the distensions, and cardiac autonomic parameters were assessed during randomly delivered rectal stimuli. Effects of FEN on rectal compliance and tone as well as mental status were also assessed. IBS patients had lower perceptual thresholds for discomfort and pain under control conditions. FEN dose-dependently increased the perception thresholds in both healthy control subjects and in IBS patients with a greater relative efficacy in IBS patients than in normal subjects. IBS patients used significantly higher unpleasantness ratings of rectal stimuli compared to healthy controls, but showed no difference in the sensory intensity rating of the stimulus. FEN decreased both intensity and unpleasantness ratings for IBS and normals. FEN lowered cardiosympathetic tone in normal subjects but had no effect on IBS patients. FEN had no effect on rectal tone or compliance. FEN dose-dependently attenuates the perception of phasic rectal distension and affects unpleasantness ratings during random fixed rectal distension, with a greater relative efficacy for this antinociceptive effect in IBS patients. These findings support the hypothesis that IBS patients may have an altered central release of endogenous opioids in response to visceral stimulation.
Alterations in activation of pain modulation systems may play a role in the pathophysiology of irritable bowel syndrome (IBS). However, little is known about the effects of exogenous opioids on the perceptual and autonomic responses to aversive visceral stimulation. The aim of the study was to evaluate the effect of the mu opioid-preferring analgesic fentanyl (FEN), given intravenously, on perceptual and autonomic responses to rectal distension. Ten IBS patients and ten normal subjects received, on separate days, either high dose (HD) fentanyl (112 microg bolus followed by 0.04 microg/kg per min infusion), low dose (LD) fentanyl (56 microg bolus followed by 0.02 microg/kg per min) or normal saline (SAL) (50 cc bolus followed by 45 cc/h infusion). Perception thresholds for discomfort and pain during rectal distension were assessed using a tracking paradigm. Intensity and unpleasantness ratings of the distensions, and cardiac autonomic parameters were assessed during randomly delivered rectal stimuli. Effects of FEN on rectal compliance and tone as well as mental status were also assessed. IBS patients had lower perceptual thresholds for discomfort and pain under control conditions. FEN dose-dependently increased the perception thresholds in both healthy control subjects and in IBS patients with a greater relative efficacy in IBS patients than in normal subjects. IBS patients used significantly higher unpleasantness ratings of rectal stimuli compared to healthy controls, but showed no difference in the sensory intensity rating of the stimulus. FEN decreased both intensity and unpleasantness ratings for IBS and normals. FEN lowered cardiosympathetic tone in normal subjects but had no effect on IBS patients. FEN had no effect on rectal tone or compliance. FEN dose-dependently attenuates the perception of phasic rectal distension and affects unpleasantness ratings during random fixed rectal distension, with a greater relative efficacy for this antinociceptive effect in IBS patients. These findings support the hypothesis that IBS patients may have an altered central release of endogenous opioids in response to visceral stimulation.
Author Matin, Kamran
Parker, Robert A
Lembo, Tony
Munakata, Julie
Naliboff, Bruce D
Mayer, Emeran A
Gracely, Richard H
AuthorAffiliation Department of Medicine, Beth Israel Deaconess Hospital, Boston, MA, USA Department of Psychology and Biobehavioral Sciences, UCLA/West Los Angeles VA Healthcare Center, Los Angeles, CA, USA CURE Digestive Diseases Research Center/Neuroenteric Disease Program, Department of Medicine, UCLA School of Medicine, Los Angeles, CA, USA CMMU, PNMB, NIDCR, NIH, Bethesda, MD, USA Department of Physiology, UCLA School of Medicine, Los Angeles, CA, USA
AuthorAffiliation_xml – name: Department of Medicine, Beth Israel Deaconess Hospital, Boston, MA, USA Department of Psychology and Biobehavioral Sciences, UCLA/West Los Angeles VA Healthcare Center, Los Angeles, CA, USA CURE Digestive Diseases Research Center/Neuroenteric Disease Program, Department of Medicine, UCLA School of Medicine, Los Angeles, CA, USA CMMU, PNMB, NIDCR, NIH, Bethesda, MD, USA Department of Physiology, UCLA School of Medicine, Los Angeles, CA, USA
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  givenname: Tony
  surname: Lembo
  fullname: Lembo, Tony
  organization: Department of Medicine, Beth Israel Deaconess Hospital, Boston, MA, USA
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  givenname: Bruce D
  surname: Naliboff
  fullname: Naliboff, Bruce D
  organization: Department of Psychology and Biobehavioral Sciences, UCLA/West Los Angeles VA Healthcare Center, Los Angeles, CA, USA
– sequence: 3
  givenname: Kamran
  surname: Matin
  fullname: Matin, Kamran
  organization: CURE Digestive Diseases Research Center/Neuroenteric Disease Program, Department of Medicine, UCLA School of Medicine, Los Angeles, CA, USA
– sequence: 4
  givenname: Julie
  surname: Munakata
  fullname: Munakata, Julie
  organization: CURE Digestive Diseases Research Center/Neuroenteric Disease Program, Department of Medicine, UCLA School of Medicine, Los Angeles, CA, USA
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  givenname: Robert A
  surname: Parker
  fullname: Parker, Robert A
  organization: Department of Medicine, Beth Israel Deaconess Hospital, Boston, MA, USA
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– sequence: 7
  givenname: Emeran A
  surname: Mayer
  fullname: Mayer, Emeran A
  email: emayer@ucla.edu
  organization: CURE Digestive Diseases Research Center/Neuroenteric Disease Program, Department of Medicine, UCLA School of Medicine, Los Angeles, CA, USA
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IsPeerReviewed true
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Issue 2
Keywords Fentanyl
Antinociception
Visceral pain
Human
Pathophysiology
μ Opioid receptor
Opiates
Narcotic analgesic
Opioid peptide
Analgesia
Sensitivity
Analgesic
Pain
Modulation
Irritable bowel syndrome
Digestive diseases
Intestinal disease
Language English
License CC BY 4.0
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Lippincott Williams & Wilkins, Inc
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Snippet Alterations in activation of pain modulation systems may play a role in the pathophysiology of irritable bowel syndrome (IBS). However, little is known about...
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StartPage 137
SubjectTerms Adult
Analgesics, Opioid - pharmacology
Analysis of Variance
Antinociception
Biological and medical sciences
Case-Control Studies
Colonic Diseases, Functional - physiopathology
Female
Fentanyl
Fentanyl - pharmacology
Gastroenterology. Liver. Pancreas. Abdomen
Humans
Male
Medical sciences
Middle Aged
Other diseases. Semiology
Pain Measurement - drug effects
Pain Measurement - psychology
Pain Threshold - drug effects
Pain Threshold - psychology
Receptors, Opioid, mu - drug effects
Rectum - drug effects
Stomach. Duodenum. Small intestine. Colon. Rectum. Anus
Visceral pain
Title Irritable bowel syndrome patients show altered sensitivity to exogenous opioids
URI https://dx.doi.org/10.1016/S0304-3959(00)00282-7
http://ovidsp.ovid.com/ovidweb.cgi?T=JS&NEWS=n&CSC=Y&PAGE=fulltext&D=ovft&AN=00006396-200008010-00004
https://www.ncbi.nlm.nih.gov/pubmed/10924807
https://search.proquest.com/docview/71264320
Volume 87
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