Pain-induced impulsivity in rats and its mechanisms - Pain is a complex subjective process consisting of sensory, affective and cognitive components. Although much
effort has been made in developing rodent models for sensory and affective pain components, less is known
about models that represent the cognitive component of pain. The importance of studying the cognitive
component of pain is 2-fold: 1- certain features of the cognitive component, such as impulsivity, contribute to
psychiatric comorbidities that result from chronic pain conditions; and 2- impulsivity is a significant contributing
factor for the development of substance use disorders. It is critical to examine pain models that shed light on
the mechanisms and etiology of psychiatric and substance abuse comorbidities stemming from chronic pain and
opioid analgesics. Moreover, inclusion of females in examining pain-induced impulsivity is particularly important
as females are more prone in to develop various comorbidities during chronic pain states. This application
introduces the delay discounting task (DDT) as a rodent model of the cognitive component of pain. The DDT has
been used to demonstrate deficits in decision-making and impulsivity in models of psychiatric and substance use
conditions in rodents and in humans. Our preliminary findings suggest that male and female rats treated with
hind paw complete freund’s adjuvant (CFA)-induced inflammatory pain exhibit delay discounting (i.e. impulsivity)
that is blocked by morphine. The pain-induced impulsivity is sexually dimorphic as females show stronger
discounting than males. Over three aims, this proposal will examine the role of gonadal hormones, VTA mu-opioid receptors, and nucleus accumbens D2 receptor on CFA-induced impulsivity. This study is the first step
in examining a rodent model of pain-induced impulsivity and its underlying mechanisms. Findings from the
proposed studies will advance our understanding of the multifactorial nature of pain perception, as well as the
mechanisms that contribute to complications and comorbidities often associated with chronic pain conditions.