Related Experiment Video
Updated: May 3, 2026

A Conditioned Place Preference Protocol for Measuring Incubation of Craving in Rats
Published on: November 6, 2018
Anxiety-like behavior during protracted morphine withdrawal is driven by gut microbial dysbiosis and attenuated with
Abstract:
The development of anxiety during protracted opioid withdrawal heightens the risk of relapse into the cycle of addiction. Understanding the mechanisms driving anxiety during opioid withdrawal could facilitate the development of therapeutics to prevent negative affect and promote continued abstinence. Our lab has previously established the gut microbiome as a driver of various side effects of opioid use, including analgesic tolerance and somatic withdrawal symptoms. We therefore hypothesized that the gut microbiome contributes to the development of anxiety-like behavior during protracted opioid withdrawal. In this study, we first established a mouse model of protracted morphine withdrawal, characterized by anxiety-like behavior and gut microbial dysbiosis. Next, we used fecal microbiota transplantation (FMT) to show that gut dysbiosis alone is sufficient to induce anxiety-like behavior. We further demonstrate that probiotic therapy during morphine withdrawal attenuates the onset of anxiety-like behavior, highlighting its therapeutic potential. Lastly, we examined transcriptional changes in the amygdala of morphine-withdrawn mice treated with probiotics to explore mechanisms by which the gut-brain axis mediates anxiety-like behavior. Our results support the use of probiotics as a promising therapeutic strategy to prevent gut dysbiosis and associated anxiety during opioid withdrawal, with potential implications for improving treatment outcomes in opioid recovery programs.
Insights
The gut microbiome contributes to anxiety during opioid withdrawal. Probiotic therapy can reduce this anxiety, offering a potential treatment to prevent relapse and support recovery.
Area of Science:
- Neuroscience
- Microbiology
- Pharmacology
Background:
- Anxiety during opioid withdrawal increases relapse risk.
- The gut microbiome influences opioid side effects.
- Mechanisms linking gut dysbiosis to withdrawal anxiety are unclear.
Purpose of the Study:
- Investigate the gut microbiome's role in opioid withdrawal anxiety.
- Determine if gut dysbiosis alone causes anxiety.
- Evaluate probiotic therapy for withdrawal-induced anxiety.
Main Methods:
- Established a mouse model of protracted morphine withdrawal.
- Utilized fecal microbiota transplantation (FMT).
- Administered probiotic therapy during withdrawal.
Main Results:
- Morphine withdrawal induced anxiety-like behavior and gut dysbiosis.
- FMT confirmed gut dysbiosis sufficiency for anxiety.
- Probiotics attenuated anxiety onset during withdrawal.
Conclusions:
- Gut dysbiosis contributes to anxiety during opioid withdrawal.
- Probiotic therapy shows therapeutic potential for withdrawal anxiety.
- Findings support gut-brain axis modulation for opioid recovery.
More Related Videos
09:54Combining Laser Capture Microdissection and Microfluidic qPCR to Analyze Transcriptional Profiles of Single Cells: A Systems Biology Approach to Opioid Dependence
Published on: March 8, 2020
07:49Intracerebroventricular Delivery of Gut-Derived Microbial Metabolites in Freely Moving Mice
Published on: June 2, 2022
Related Concept Videos
Drugs Affecting GI Tract Motility: Serotonin Receptor Agonists
Drugs Affecting GI Tract Motility: Opioids as Antidiarrheal Agents
Opioids, widely used antidiarrheal agents, mitigate diarrhea by slowing down...
Drugs for Treatment of Diarrhea-Predominant IBS
Two specific drugs used in the treatment are alosetron (Lotronex) and eluxadoline (Viberzi). Alosetron, a 5-HT3 antagonist, works by slowing the movement of stools in the gut, reducing bowel...
Drugs for Treatment of Constipation-Predominant IBS
Irritable Bowel Syndrome I: Introduction
IBS is a chronic condition that can persist over a long period or recur frequently.
The pathogenesis of IBS involves a complex interplay of the following factors:
Altered...