Abstract

Multiphoton microscopy is one of several new technologies providing unprecedented insight into the activity dynamics and function of neural circuits. Unfortunately, some of these technologies require experimentation in head-restrained animals, limiting the behavioral repertoire that can be integrated and studied. This issue is especially evident in drug addiction research, as no laboratories have coupled multiphoton microscopy with simultaneous intravenous drug self-administration, a behavioral paradigm that has predictive validity for treatment outcomes and abuse liability. Here, we describe a new experimental assay wherein head-restrained mice will press an active lever, but not inactive lever, for intravenous delivery of heroin or cocaine. Similar to freely moving animals, we find that lever pressing is suppressed through daily extinction training and subsequently reinstated through the presentation of relapse-provoking triggers (drug-associative cues, the drug itself, and stressors). Finally, we show that head-restrained mice will show similar patterns of behavior for oral delivery of a sucrose reward, a common control used for drug self-administration experiments. Overall, these data demonstrate the feasibility of combining drug self-administration experiments with technologies that require head-restraint, such as multiphoton imaging. The assay described could be replicated by interested labs with readily available materials to aid in identifying the neural underpinnings of substance use disorder.

Highlights

  • Multiphoton microscopy is a powerful tool used to help dissect the neurobiological substrates that coordinate behavior

  • Head-Restrained Drug Self-Administration cell morphology in awake, behaving animals. Such technology could be transformative for studying substance use disorder (SUD), which is rooted in plasticity in the neural circuits that govern motivated behavior (Russo and Nestler, 2013)

  • We find that omission of the cue and drug results in extinction learning, wherein active lever pressing is suppressed across days

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Summary

Introduction

Multiphoton microscopy is a powerful tool used to help dissect the neurobiological substrates that coordinate behavior. Head-Restrained Drug Self-Administration cell morphology (e.g., dendritic spine plasticity; Muñoz-Cuevas et al, 2013; Moda-Sava et al, 2019) in awake, behaving animals Such technology could be transformative for studying substance use disorder (SUD), which is rooted in plasticity in the neural circuits that govern motivated behavior (Russo and Nestler, 2013). By pairing self-administration with bench approaches, critical factors underlying drug-seeking behavior have been identified at the cellular, molecular, and circuit levels (Koob and Le Moal, 1997; Kalivas and Volkow, 2005; Deadwyler, 2010; Russo et al, 2010) Despite these advances, our ability to precisely observe, longitudinally track, and manipulate these implicated factors in live, behaving animals has been limited

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