Childhood and adolescent adversity is associated with a wide range of psychiatric disorders, including an increased risk for substance abuse. Despite this, the molecular mechanisms underlying how chronic stress during adolescence alters reward signaling remains largely unexplored. Understanding how adolescent stress increases addictionlike phenotypes could inform the development of targeted interventions both before and after drug use. The current study examined how adolescent-onset isolation stress affected behavioral, molecular, and physiological responses to cocaine in male and female mice. Adolescent-onset social isolation did not alter the ability of mice to learn an operant response for food, nor influence food self-administration or motivation for food on a progressive ratio schedule. However, male and female socially stressed mice exhibited an increase in motivation for cocaine and cocaine seeking during a cueinduced reinstatement session. Additionally, we demonstrated that adolescent-onset social isolation increased cocaine-induced neuronal activation, as assessed by Fos expression, within the nucleus accumbens core and shell, ventral pallidum, dorsal bed nucleus of the stria terminalis, lateral septum and basolateral amygdala. Taken together, the present studies demonstrate that social stress during adolescence augments the behavioral responses to cocaine during adulthood and alters the responsiveness of reward-related brain circuitry.