The goal of this research project is to evaluate the role of the cholinergic system in the mood, behavioral and cognitive symptoms observed in mood disorders in humans, using computerized cognitive testing and functional brain neuroimaging techniques. In addition to pervasive sadness, specific aspects of behavior and cognition are impaired in mood disorders, including selective attention, set-shifting and memory; and there also is evidence that depressed individuals exhibit a mood congruent processing bias whereby they more readily process negatively toned information as compared to positively toned information. This cognitive pattern lends itself to evaluation with functional brain imaging, both in terms of identifying the anatomical correlates of the specific behavioral and cognitive differences as well as characterizing the effects of pharmacological manipulation. Attention and memory functions are closely tied to the cholinergic neurotransmitter system whereby drugs that enhance cholinergic function are found to enhance memory and attention while agents that interfere with normal cholinergic function impair performance on attention and memory tasks. Moreover, the cholinergic system is one of the neurotransmitter systems implicated in the pathophysiology of mood disorders. Evidence suggests that during major depressive episodes, the cholinergic system is hypersensitive to acetylcholine. Agents that enhance muscarinic cholinergic receptor function increase depressive symptoms in depressed subjects, and can produce symptoms of depression in healthy subjects. The preclinical literature more specifically implicates the muscarinic receptors and indicates that the use of muscarinic antagonists, in the context of animal models of depression, results in improvement in the behavioral analogs of depression. The proposed project investigates the role of cholinergic neurotransmission in the mood, behavioral and cognitive symptoms observed in the depressed phase of both major depressive disorder (MDD) and bipolar disorder (BD). The studies proposed here will identify anatomical correlates of the mood congruent processing bias, working memory, attention and set-shifting deficits observed in depressed subjects. Further, these studies will evaluate the effects of the cholinergic antagonist, scopolamine, both on mood in patient populations and on the performance deficits and neural activity in brain regions recruited as subjects perform these tasks. This approach is expected to reveal how neuromodulators influence processing in brain structures recruited to perform these tasks, both in healthy individuals and in major depressive disorders. The combined use of functional brain imaging and pharmacological manipulation to evaluate the role of neurotransmitter dysfunction in depression may direct us to potential therapeutic approaches. These studies also are expected to elucidate the role of cholinergic muscarinic receptors in the mood and cognitive symptoms observed in depression. To date we have found that in healthy individuals, scopolamine modulates performance on attention tasks but does so differentially based on the emotional content of the stimuli with greater effects associated with sad stimuli. This result suggests that manipulation of cholinergic function in healthy individuals modulates the salience of emotional stimuli. We also are beginning to uncover baseline performance differences between the healthy and depressed groups that indicate differential processing of emotional stimuli, which is a potentially important finding as the development of tasks that reliably distinguish between healthy individuals and depressed patients has proven to be extremely difficult. Moreover, we have preliminary data which indicate that scopolamine modulates performance differentially in healthy and depressed individuals based on the emotional content of the stimulus. Brain imagingg studies currently are underway to identify the anatomical correlates of the baseline performance differences between the groups as well as the differential response to drug. Importantly, we also have found extremely promising effects of scopolamine on mood in the patient populations. These results have initiated the pursuit of a treatment study to more thoroughly evaluate the potential of scopolamine for the clinical treatment of depression.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Intramural Research (Z01)
Project #
1Z01MH002813-02
Application #
6982735
Study Section
(DIRP)
Project Start
Project End
Budget Start
Budget End
Support Year
2
Fiscal Year
2004
Total Cost
Indirect Cost
Name
U.S. National Institute of Mental Health
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Ellis, Jessica S; Zarate Jr, Carlos A; Luckenbaugh, David A et al. (2014) Antidepressant treatment history as a predictor of response to scopolamine: clinical implications. J Affect Disord 162:39-42
Rosenbaum, R Shayna; Furey, Maura L; Horwitz, Barry et al. (2010) Altered connectivity among emotion-related brain regions during short-term memory in Alzheimer's disease. Neurobiol Aging 31:780-6
Taylor Tavares, Joana V; Clark, Luke; Furey, Maura L et al. (2008) Neural basis of abnormal response to negative feedback in unmedicated mood disorders. Neuroimage 42:1118-26
Furey, Maura L; Tanskanen, Topi; Beauchamp, Michael S et al. (2006) Dissociation of face-selective cortical responses by attention. Proc Natl Acad Sci U S A 103:1065-70
Furey, Maura L; Drevets, Wayne C (2006) Antidepressant efficacy of the antimuscarinic drug scopolamine: a randomized, placebo-controlled clinical trial. Arch Gen Psychiatry 63:1121-9
Freo, Ulderico; Ricciardi, Emiliano; Pietrini, Pietro et al. (2005) Pharmacological modulation of prefrontal cortical activity during a working memory task in young and older humans: a PET study with physostigmine. Am J Psychiatry 162:2061-70
Ibanez, Vicente; Pietrini, Pietro; Furey, Maura L et al. (2004) Resting state brain glucose metabolism is not reduced in normotensive healthy men during aging, after correction for brain atrophy. Brain Res Bull 63:147-54
Pietrini, Pietro; Furey, Maura L; Ricciardi, Emiliano et al. (2004) Beyond sensory images: Object-based representation in the human ventral pathway. Proc Natl Acad Sci U S A 101:5658-63