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Rationale and objective <p>Buprenorphine is an FDA-approved medication for opioid addiction, but the brain regions underlying its therapeutic effects remain unknown. We previously found that chronic buprenorphine treatment decreases several relapse-related behaviors in rats. Here, we tested whether chronic buprenorphine decreases the time-dependent increase (incubation) in heroin seeking during abstinence. We also used the activity marker Fos to test whether buprenorphine’s inhibition of incubation of heroin seeking is associated with decreased activation of cortical and striatal regions.</p> Methods <p>We trained <i>Oprm1-Cre</i> rats and their wild-type littermates to self-administer heroin for 12 days (6&#xa0;h/day). On abstinence Day 1, we tested for heroin seeking under extinction conditions. On Day 14, we implanted osmotic minipumps containing saline or buprenorphine (6&#xa0;mg/kg/day). On abstinence Days 21–22, we tested the rats (or not tested, baseline condition) for incubation of heroin seeking, after which brains were collected for Fos immunohistochemistry.</p> Results <p><i>Oprm1-Cre</i> rats did not differ from wild-type littermates in heroin self-administration or ‘non-incubated’ heroin seeking on abstinence Day 1. In both genotypes, chronic buprenorphine decreased incubated heroin seeking on Days 21–22. Buprenorphine also decreased incubation-related neuronal activation in several cortical areas (cingulate cortex 1 and dorsal peduncular, but not prelimbic, infralimbic, or orbitofrontal cortex) and striatal areas (dorsolateral and dorsomedial striosomes and nucleus accumbens core, but not shell).</p> Conclusions <p>Chronic buprenorphine decreased incubation of heroin seeking, supporting the predictive validity of the rat model. This effect was associated with decreased neuronal activity in specific subregions of the medial prefrontal cortex and striatum.</p>

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Chronic delivery of buprenorphine during abstinence decreases incubation of heroin seeking and neuronal activation in medial prefrontal cortex and striatum in male and female rats

  • 期刊论文

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  • 发表日期：

    2025年12月9日

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  • Jennifer M. Bossert,
  • Kiera E. Caldwell,
  • Hannah Bonbrest,
  • Rohan Patil,
  • Mona S. Pishgar,
  • Rajtarun Madangopal,
  • Huiling Wang,
  • Yavin Shaham

摘要

Rationale and objective

Buprenorphine is an FDA-approved medication for opioid addiction, but the brain regions underlying its therapeutic effects remain unknown. We previously found that chronic buprenorphine treatment decreases several relapse-related behaviors in rats. Here, we tested whether chronic buprenorphine decreases the time-dependent increase (incubation) in heroin seeking during abstinence. We also used the activity marker Fos to test whether buprenorphine’s inhibition of incubation of heroin seeking is associated with decreased activation of cortical and striatal regions.

Methods

We trained Oprm1-Cre rats and their wild-type littermates to self-administer heroin for 12 days (6 h/day). On abstinence Day 1, we tested for heroin seeking under extinction conditions. On Day 14, we implanted osmotic minipumps containing saline or buprenorphine (6 mg/kg/day). On abstinence Days 21–22, we tested the rats (or not tested, baseline condition) for incubation of heroin seeking, after which brains were collected for Fos immunohistochemistry.

Results

Oprm1-Cre rats did not differ from wild-type littermates in heroin self-administration or ‘non-incubated’ heroin seeking on abstinence Day 1. In both genotypes, chronic buprenorphine decreased incubated heroin seeking on Days 21–22. Buprenorphine also decreased incubation-related neuronal activation in several cortical areas (cingulate cortex 1 and dorsal peduncular, but not prelimbic, infralimbic, or orbitofrontal cortex) and striatal areas (dorsolateral and dorsomedial striosomes and nucleus accumbens core, but not shell).

Conclusions

Chronic buprenorphine decreased incubation of heroin seeking, supporting the predictive validity of the rat model. This effect was associated with decreased neuronal activity in specific subregions of the medial prefrontal cortex and striatum.