A decrease in opioid influence could occur in individuals who become opioid tolerant as a result of chronic medical use or abuse. Consistent with this, in rats chronically treated with morphine, LC neurons respond with a greater excitation to hypotensive stress (Xu et al., 2004). This is due in part to sensitization of LC neurons to CRF because the CRF dose-response curve for LC activation is shifted to the left and has a greater maximum response in these animals. Importantly, enhanced LC sensitivity to CRF in rats chronically treated with morphine translated to exaggerated stress-induced

behavioral activation selleck chemical (Xu et al., 2004). For example, morphine-treated rats exposed to swim stress show excessive climbing behavior (Xu et al., 2004), a response that has been linked to brain NE (Detke et al., 1995) and that is similar to the effects of CRF injected locally into the LC (Butler et al., 1990). These basic studies imply that chronic opioid administration by humans can sensitize the LC-NE arousal system to stressors and this can also be a basis for comorbidity of opioid abuse and PTSD. However, in contrast to repeated stress, where the stress leads to adaptive mechanisms that

predispose to opioid abuse, here opioid abuse would be responsible for a predisposition to the hyperarousal symptoms of PTSD. Either case could account for the high comorbidity of opioid abuse and PTSD (Fareed et al., 2013b; Clark et al., 2001). Given the role of opioids in buffering LC-NE activation during stress and the pathological XAV-939 solubility dmso implications unless of excessive or insufficient opioid influence described above, individual differences in either enkephalin expression or MOR sensitivity are potential determinants of stress resilience/vulnerability or the form of pathology that is expressed. For example, whereas decreased MOR function may predispose

to hyperarousal symptoms of stress-related disorders because of a decreased ability to counteract CRF effects, it may protect against substance abuse because the neurons won’t become opioid-dependent. In contrast, individuals with greater MOR sensitivity would be predicted to be protected from hyperarousal symptoms but more prone to substance abuse. Thus, how the balance is tipped will determine how the stress-related pathology is expressed. In this regard MOR density, sensitivity and trafficking, as well as enkephalin expression are affected by sex and hormonal status (Torres-Reveron et al., 2008, Torres-Reveron et al., 2009, Van Kempen et al., 2013, Milner et al., 2013 and Craft, 2008). The relationships are not clear-cut and may be dependent on the species, the endpoint and brain region studied. Nonetheless, studies documenting decreased MOR sensitivity in females (Kepler et al., 1991, Ji et al., 2006 and Wang et al.