Abstract

A number of retrospective studies have demonstrated adverse childhood experiences are associated with increased vulnerability to substance use disorders, including opioid use disorders (OUDs). These adverse childhood experiences, also referred to as early life stress (ELS), can be modeled in laboratory animals by various paradigms including limited bedding and nesting (LBN) procedures. Studies using rodent models of ELS have been shown to recapitulate various aspects of OUDs, including relapse propensity and perseverance of drug-seeking behavior. In the current study, we utilized the LBN paradigm to explore potential effects on heroin self-administration, extinction, and relapse-like behaviors in male and female rats. We also utilized in vitro whole-cell electrophysiology to examine the effects of LBN and repeated heroin administration on the excitability of pyramidal neurons in the anterior insular cortex (AIC) projecting to the nucleus accumbens core (NAc), as recent studies suggest that this circuit may mediate various aspects of OUDs and may be compromised as a result of either ELS or OUDs. We observed that compared to control animals, rats exposed to LBN conditions during postnatal days 2–9 showed increased breakpoints for heroin self-administration under a progressive ratio schedule of reinforcement, impaired extinction of heroin-seeking behavior, and increased reinstatement of heroin-seeking behavior induced by heroin-associated cues. No effect of LBN rearing conditions were observed on the acquisition and maintenance of heroin self-administration, and no sex differences in heroin intake were observed. LBN and control reared animals showed no differences in the excitability of AIC-NAc pyramidal neurons, but animals treated with repeated heroin showed decreased excitability of these neurons through a significant increase in rheobase and reduction in action potentials induced by depolarizing currents. Together, these results suggest that ELS exposure produces exacerbations of heroin seeking behavior without parallel effects on AIC-NAc excitability, although heroin itself reduces the excitability of these neurons.

Highlights

  • Opiate abuse and addiction pose a substantial financial economic burden, exceeding over one trillion dollars in the United States in 2017 (Florence et al, 2021)

  • In the current study we aimed to explore how early life stress (ELS), as modeled through the limited bedding and nesting (LBN) paradigm, alters heroin seeking through intravenous self-administration (IVSA), extinction of heroin-seeking, as well as reinstatement elicited by exposure to heroin-paired cues

  • Male and Female Rats Show Similar Acquisition Rates of Heroin Intravenous Self-Administration and Total Heroin Intake First, we examined acquisition of heroin IVSA across male and female animals in both the control and LBN groups

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Summary

Introduction

Opiate abuse and addiction pose a substantial financial economic burden, exceeding over one trillion dollars in the United States in 2017 (Florence et al, 2021). Opioid use disorders (OUDs) are, in large part, perpetuated by negative affect, where continuance and/or resumption of drug intake is driven by the alleviation of severe negative affective states that occur during opiate withdrawal (i.e., dysphoria, depression, and anhedonia) (Koob, 2020; Welsch et al, 2020). Environmental influences on opiate addiction, including early life stress (ELS) and other psychosocial stressors such as discrimination and socioeconomic impoverishment, increase vulnerability toward the development of OUDs (Lupien, 2014; Scarna, 2020). Therapies for patients with OUDs have largely focused on pharmacological maintenance strategies which aide in minimizing opiate withdrawal, yet the existing literature strongly indicates that the use of other strategies such as psychosocial interventions (e.g., counseling, family therapy, community reinforcement), when used in combination of pharmacological approaches, are effective at reducing relapse (Wild et al, 2021)

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