Background and Study Objective: Posttraumatic stress disorder (PTSD) affects as many as 15% of service members and Veterans following deployment. Current treatments are insufficient: most medications for PTSD decrease symptom intensity only moderately, and often appear to be less effective in Veterans than civilians. Prazosin, an antagonist of one of the major receptors for noradrenaline, has demonstrated significant efficacy for particularly hyperarousal symptoms and trauma nightmares in Veterans and service members with PTSD, but is still not effective for approximately 1/3 of the population. Recently, in a post hoc analysis, it was found that a simple, clinically-accessible measurement of the strength of noradrenergic signaling (standing blood pressure) was able to predict who would respond to prazosin. If this result is validated in a prospective study, it would provide a rapidly useful clinical tool. In addition, preliminary data from an observational study of Veterans suggests that exposure to life-threatening or similarly severe trauma (with or without diagnoseable PTSD) may change the way post-synaptic neurons adjust the strength of their reaction to noradrenaline. If this observation is supported by further data, it could lead to new treatment approaches. Study Design and Methods: We will test several new and emerging biomarkers of noradrenergic signaling in Veterans with PTSD, in Veterans with a history of combat trauma but without PTSD, and in Veterans who have been deployed but without a history of trauma exposure. These biomarkers will include systolic blood pressure two minutes after standing; the average dilation velocity of the pupil following the completion of a brief pulse of light; and the maximal dilation of the pupil in response to phenylephrine eye drops. We will also measure levels of noradrenaline in plasma and in cerebrospinal fluid. Using these measures, we will test the hypothesis that exposure to trauma results in a failure to downregulate the post-synaptic response to noradrenaline when the amount of noradrenaline released increases, and that it is the combination of increased noradrenaline release and a lack of postsynaptic downregulation that leads to PTSD symptom expression. For those with current PTSD, we will also administer the anti-adrenergic drug prazosin, using a modified crossover trial design that integrates concepts from N-of-1 trial methodology, in order to test the hypothesis that baseline measures of overall noradrenaline signaling are able to predict who will respond to prazosin and who will not. Career Goals: The research proposal and training plan are designed to prepare the applicant for a long-term translational VA research career studying the role of noradrenergic dysregulation in the pathophysiology of PTSD, and using this knowledge to develop improved treatments. Particular emphasis will be placed on the impact of noradrenergic dysregulation in the alteration of sleep structure and function, and...