Abstract
Drug addiction is a neuropsychiatric disorder with grave personal consequences that has an extraordinary global economic impact. Despite decades of research, the options available to treat addiction are often ineffective because our rudimentary understanding of drug-induced pathology in brain circuits and synaptic physiology inhibits the rational design of successful therapies. This understanding will arise first from animal models of addiction where experimentation at the level of circuits and molecular biology is possible. We will review the most common preclinical models of addictive behavior and discuss the advantages and disadvantages of each. This includes non-contingent models in which animals are passively exposed to rewarding substances, as well as widely used contingent models such as drug self-administration and relapse. For the latter, we elaborate on the different ways of mimicking craving and relapse, which include using acute stress, drug administration or exposure to cues and contexts previously paired with drug self-administration. We further describe paradigms where drug-taking is challenged by alternative rewards, such as appetitive foods or social interaction. In an attempt to better model the individual vulnerability to drug abuse that characterizes human addiction, the field has also established preclinical paradigms in which drug-induced behaviors are ranked by various criteria of drug use in the presence of negative consequences. Separation of more vulnerable animals according to these criteria, along with other innate predispositions including goal- or sign-tracking, sensation-seeking behavior or impulsivity, has established individual genetic susceptibilities to developing drug addiction and relapse vulnerability. We further examine current models of behavioral addictions such as gambling, a disorder included in the DSM-5, and exercise, mentioned in the DSM-5 but not included yet due to insufficient peer-reviewed evidence. Finally, after reviewing the face validity of the aforementioned models, we consider the most common standardized tests used by pharmaceutical companies to assess the addictive potential of a drug during clinical trials.
Highlights
Using receptor-specific agonists and antagonists, many studies have established a necessary role of the usual suspects within reward circuitry in the induction and maintenance of Conditioned Place Preference (CPP). Consistent with this idea of shared rewardrelated mechanisms, inducing CPP often potentiates the behavior observed in other models of addiction as seen in a study where expression of cocaine behavioral sensitization is only observed in the compartment paired with the drug during CPP, and not in a novel compartment (Duvauchelle et al, 2000)
Intermittent Access (IntA) results in greater dopamine concentrations within the nucleus accumbens (NAc) core following a single infusion of cocaine compared to Long Access (LgA) training, and dopamine levels correlated with several measures of motivation for cocaine (Kawa et al, 2019)
It is apparent that while Short Access (ShA), LgA and IntA all produce drug-taking and drug-seeking behavior, the behavioral paradigms differ in several other measures of motivation for a drug and resultant neurobiological effects, both of which are factors that should be taken into consideration during experimental design
Summary
Department of Neuroscience, Medical University of South Carolina, Charleston, SC, United States Reviewed by: Marco Venniro, National Institute on Drug Abuse (NIDA), United States Santiago Monleón, University of Valencia, Spain Specialty section: This article was submitted to Motivation and Reward, a section of the journal
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