Oxytocin Reduces Noradrenergic-Induced Opioid-Like Withdrawal Symptoms in Individuals on Opioid Agonist Therapy

Intranasal administration of the neuropeptide oxytocin has been explored as a potential therapeutic agent for substance use disorder including opioid use disorder (OUD). This phase 1, crossover, randomized, double-blind, placebo-controlled trial tested the safety, tolerability, and efficacy of intra...

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Veröffentlicht in:Biological psychiatry global open science 2025-01, Vol.5 (1), p.100395, Article 100395
Hauptverfasser: Gully, Brian J., Brown, Zoe E., Hornbacher, Rivkah, Brown, Joshua C., Back, Sudie E., McCance-Katz, Elinore F., Swift, Robert M., Haass-Koffler, Carolina L.
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Sprache:eng
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Zusammenfassung:Intranasal administration of the neuropeptide oxytocin has been explored as a potential therapeutic agent for substance use disorder including opioid use disorder (OUD). This phase 1, crossover, randomized, double-blind, placebo-controlled trial tested the safety, tolerability, and efficacy of intranasal oxytocin (80 IU) twice a day for 7 days in participants (N = 20) with OUD who were taking an opioid agonist therapy. In the laboratory, participants underwent opioid cue exposure paired with noradrenergic activation produced by yohimbine (32.4 mg) or placebo. Assessments included, 1) subjective response: craving, withdrawal, anxiety, and stress; 2) biomedical markers: hypothalamic-pituitary-adrenal axis response (cortisol) and noradrenergic activation (α-amylase); and 3) safety measures: hemodynamics and adverse event evaluation. Generalized linear model with model-based estimator in the covariance matrix was used, with medication (oxytocin/placebo) and noradrenergic activation (yohimbine/placebo) as within-subject factors. Oxytocin significantly reduced opioid-like withdrawal, anxiety symptoms, and cortisol levels elicited by cue exposure under noradrenergic activation produced by yohimbine. This effect was specific because oxytocin did not reduce craving, hemodynamics, or α-amylase levels increased by yohimbine administration. A single dose of yohimbine elicited the noradrenergic stimulation, and 7-day oxytocin administration was safe and well tolerated among individuals diagnosed with OUD and taking opioid agonist therapy. The findings of this study suggest that oxytocin alleviates opioid-like withdrawal symptoms and anxiety by modulating the hypothalamic-pituitary-adrenal axis. Oxytocin was administered intranasally to 20 participants with opioid use disorder (OUD) to determine whether it reduced cravings for opioids and helped to improve symptoms of the disorder in general. The study sample included individuals with OUD who were currently abstinent from opioids and were receiving medication treatment to help maintain abstinence. Results indicated that after a stress-induced procedure, oxytocin was not effective in reducing opioid cravings, but it was able to reduce opioid-like withdrawal symptoms, and other markers of anxiety.
ISSN:2667-1743
2667-1743
DOI:10.1016/j.bpsgos.2024.100395