Cellular Mechanisms of Addictive Processes
Opioid Modulation of the Coeruleo-Cortical Pathway (NIH/NIDA)
Cellular Mechanisms of Addictive Processes
Schematic diagram showing potential ways in which opiates sensitize LC neurons to CRF. Left: LC neurons without morphine. Middle: Chronic morphine may increase second- messenger response to CRF. Right: chronic morphine might reduce internalization of CRF receptors.
Goal: To examine cellular interactions between opioids and the stress-related peptide corticotropin releasing factor in the noradrenergic nucleus locus coeruleus.
The interaction between the stress axis and endogenous opioid systems has gained substantial clinical interest as it is increasingly recognized that stress predisposes to opiate abuse. For example, stress has been implicated as a risk factor in vulnerability to the initiation and maintenance of opiate abuse and is thought to play an important role in relapse in subjects with a history of abuse. However, the impact of stress-opioid interactions extends beyond vulnerability to opiate abuse.
Numerous reports indicating that stress alters individual sensitivity to opiates suggest that prior stress can influence the pharmacodynamics of opiates that are used in clinical settings. Conversely, the effects of opiates on different components of the stress axis can impact on individual responsivity to stressors and potentially predispose individuals to stress-related psychiatric disorders. Because these interactions have potentially widespread clinical consequences, it is important to identify substrates of the stress response and endogenous opioid systems that interact and the specific points at which stress circuits and endogenous opioid systems intersect.