This research will use behavioral, autonomic, and neuroendocrine approaches to investigate the hypothesis that neural mechanisms involving oxytocin underlie the documented association between depression and heart disease. Disorders relating to negative affect, such as depression and anxiety, are recognized risk factors for cardiovascular disease; this relationship is especially important for individuals with specific vulnerabilities (such as persons with a family history of heart disease or aging populations). Psychological and physiological responses to stressors, and in particular reactions in the social context, play an important role in the development of affective symptoms and behaviors, and have been linked directly to cardiovascular dysfunction. Furthermore, evidence indicates that oxytocin mediates behavioral and physiological processes associated with stress and social experiences, and therefore this neuropeptide may have a mechanistic role in the link between mood and cardiovascular disorders. The current research project will use a rodent model, the socially monogamous prairie vole, to study the behavioral, neuroendocrine, and autonomic responses to a social stressor (social isolation), and the potential oxytocinergic mechanisms that underlie these responses. Converging evidence suggests that the prairie vole provides a unique model system for studying responsiveness to social experiences, and that this species has utility for studying autonomic mechanisms related to mood and cardiac function. Experiment 1 will employ (a) behavioral tests relevant to depression, (b) continuous recording of autonomic and cardiac parameters, and (c) measures of circulating and central nervous system hormones and peptides, to test the hypothesis that social isolation induces behavioral and physiological responses relevant to depression and cardiovascular disease (Specific Aim 1). Experiment 2 will employ (a) chronic administration of oxytocin and (b) administration of an oxytocin antagonist, to test the hypothesis that oxytocinergic mechanisms underlie specifically the behavioral, autonomic, and neuroendocrine responses to social isolation (Specific Aim 2). This research proposes a novel mechanism by which the social environment impacts behavior, physiology, and brain function, which can promote the development of more comprehensive treatments for patients with depression and cardiovascular disease. There are important interactions among behavior, brain function, and the cardiovascular system; one such example of these interactions is the association between depression and heart disease. The current research project will investigate directly the link between these conditions by studying in an animal model the behavioral, endocrine (hormones), autonomic (control of cardiovascular function), and brain processes involved in mediating mood and cardiovascular function. This research can lead to the development of more effective treatments for patients with depression and heart disease. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Exploratory/Developmental Grants (R21)
Project #
7R21MH077581-02
Application #
7737659
Study Section
Biobehavioral Mechanisms of Emotion, Stress and Health Study Section (MESH)
Program Officer
Meinecke, Douglas L
Project Start
2008-02-01
Project End
2010-01-31
Budget Start
2008-10-16
Budget End
2009-01-31
Support Year
2
Fiscal Year
2008
Total Cost
$74,069
Indirect Cost
Name
Northern Illinois University
Department
Psychology
Type
Schools of Arts and Sciences
DUNS #
001745512
City
De Kalb
State
IL
Country
United States
Zip Code
60115
Grippo, Angela J; Scotti, Melissa-Ann L; Wardwell, Joshua et al. (2018) Cardiac and behavioral effects of social isolation and experimental manipulation of autonomic balance. Auton Neurosci 214:1-8
McNeal, Neal; Appleton, Katherine M; Johnson, Alan Kim et al. (2017) The protective effects of social bonding on behavioral and pituitary-adrenal axis reactivity to chronic mild stress in prairie voles. Stress 20:175-182
Scotti, Melissa-Ann L; Carlton, Elizabeth D; Demas, Gregory E et al. (2015) Social isolation disrupts innate immune responses in both male and female prairie voles and enhances agonistic behavior in female prairie voles (Microtus ochrogaster). Horm Behav 70:7-13
Grippo, Angela J; Moffitt, Julia A; Henry, Matthew K et al. (2015) Altered Connexin 43 and Connexin 45 protein expression in the heart as a function of social and environmental stress in the prairie vole. Stress 18:107-14
McNeal, Neal; Scotti, Melissa-Ann L; Wardwell, Joshua et al. (2014) Disruption of social bonds induces behavioral and physiological dysregulation in male and female prairie voles. Auton Neurosci 180:9-16
Grippo, Angela J; Ihm, Elliott; Wardwell, Joshua et al. (2014) The effects of environmental enrichment on depressive and anxiety-relevant behaviors in socially isolated prairie voles. Psychosom Med 76:277-84
Grippo, Angela J; Moffitt, Julia A; Sgoifo, Andrea et al. (2012) The integration of depressive behaviors and cardiac dysfunction during an operational measure of depression: investigating the role of negative social experiences in an animal model. Psychosom Med 74:612-9
Peuler, Jacob D; Scotti, Melissa-Ann L; Phelps, Laura E et al. (2012) Chronic social isolation in the prairie vole induces endothelial dysfunction: implications for depression and cardiovascular disease. Physiol Behav 106:476-84
Grippo, Angela J; Pournajafi-Nazarloo, Hossein; Sanzenbacher, Lisa et al. (2012) Peripheral oxytocin administration buffers autonomic but not behavioral responses to environmental stressors in isolated prairie voles. Stress 15:149-61
Grippo, Angela J (2011) The Utility of Animal Models in Understanding Links between Psychosocial Processes and Cardiovascular Health. Soc Personal Psychol Compass 5:164-179

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