Long-term objectives: This is a collaborative research effort between the laboratories of Dr. Cecilia Hillard, a basic scientist studying cannabinoid receptor function using animal and cellular models; and Dr. Harriet de Wit, a psychologist studying the effects of gender on stress responsivity and susceptibility to substance abuse in humans. One long term objective of this project is to solidify this collaborative relationship which will enhance both individual research projects through the addition of translational aims that bridge them. We will develop this collaboration through an Exploratory/Developmental project that will begin to test the hypothesis that gender differences in the effects of stress on endocannabinoid (eCB) signaling contribute to the gender differences in susceptibility to psychiatric disorders, including substance abuse. It is well established that depression and anxiety occur more frequently in women than in men, which suggests a gender difference in reactivity to stressful or threatening situations. Therefore, studies of gender differences in response to stress will clarify the differential vulnerability of women and men to these and other stress-related disorders, particularly substance abuse.
The Specific Aims of the project are to determine the effects of gender and estrous stage in mice on: (1) the role of eCB/CB1 receptor signaling in the regulation of basal and stress-induced hypothalamic-pituitary-adrenal axis activation; and (2) expression of CB1 receptors, CB1 receptor function and the expression of eCB synthetic and catabolic proteins in brain regions known to be involved in the stress response. A second goal of this proposal is to explore the relationship between serum eCBs and gender differences in the human stress response. In particular, we will compare the responses to stress and serum eCBs in men and women in both the follicular and luteal phases. We will: (1) measure serum eCB contents in blood collected during two sessions: one that is a control visit to the research area, and the second during and after the administration of the Trier Social Stress Test; and (2) examine the relationships among serum eCB contents, gender/sex hormone status and indicators of the stress response, including ratings of anxiety, heart rate and salivary cortisol levels. These pilot studies will guide the development of hypothesis-driven translational research projects that will further explore the interactions among stress, gender, the risks of developing substance abuse and a novel and important signaling system in the brain, the endocannabinoids and their receptor, CB1. Stress is increasingly recognized as a significant risk factor for the development of many diseases in humans, including cardiovascular disease, depression, anxiety disorders and substance abuse disorders. Men and women differ in their responses to stressful life situations and differ in the stress-related diseases that they develop. Data collected in animals demonstrate that endocannabinoid signaling is """"""""stress-protective"""""""". In addition, limited data suggest that endocannabinoid signaling differs between male and female rodents. The goal of the studies in this proposal are to expand the animal studies and to add human studies to determine whether gender differences in endocannabinoid signaling underlie or contribute to gender differences in stress responses. ? ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21DA022439-01A1
Application #
7305710
Study Section
Biobehavioral Regulation, Learning and Ethology Study Section (BRLE)
Program Officer
Sorensen, Roger
Project Start
2007-09-25
Project End
2009-07-31
Budget Start
2007-09-25
Budget End
2008-07-31
Support Year
1
Fiscal Year
2007
Total Cost
$197,915
Indirect Cost
Name
Medical College of Wisconsin
Department
Pharmacology
Type
Schools of Medicine
DUNS #
937639060
City
Milwaukee
State
WI
Country
United States
Zip Code
53226
Roberts, Christopher J; Stuhr, Kara L; Hutz, Michael J et al. (2014) Endocannabinoid signaling in hypothalamic-pituitary-adrenocortical axis recovery following stress: effects of indirect agonists and comparison of male and female mice. Pharmacol Biochem Behav 117:17-24
Dlugos, Andrea; Childs, Emma; Stuhr, Kara L et al. (2012) Acute stress increases circulating anandamide and other N-acylethanolamines in healthy humans. Neuropsychopharmacology 37:2416-27
Evanson, Nathan K; Tasker, Jeffrey G; Hill, Matthew N et al. (2010) Fast feedback inhibition of the HPA axis by glucocorticoids is mediated by endocannabinoid signaling. Endocrinology 151:4811-9
Hill, Matthew N; Titterness, Andrea K; Morrish, Anna C et al. (2010) Endogenous cannabinoid signaling is required for voluntary exercise-induced enhancement of progenitor cell proliferation in the hippocampus. Hippocampus 20:513-23
Riebe, Caitlin J N; Hill, Matthew N; Lee, Tiffany T Y et al. (2010) Estrogenic regulation of limbic cannabinoid receptor binding. Psychoneuroendocrinology 35:1265-9
Krebs-Kraft, Desiree L; Hill, Matthew N; Hillard, Cecilia J et al. (2010) Sex difference in cell proliferation in developing rat amygdala mediated by endocannabinoids has implications for social behavior. Proc Natl Acad Sci U S A 107:20535-40
Wang, Wei; Sun, Dalong; Pan, Bin et al. (2010) Deficiency in endocannabinoid signaling in the nucleus accumbens induced by chronic unpredictable stress. Neuropsychopharmacology 35:2249-61
Hill, Matthew N; McLaughlin, Ryan J; Bingham, Brenda et al. (2010) Endogenous cannabinoid signaling is essential for stress adaptation. Proc Natl Acad Sci U S A 107:9406-11
Hill, Matthew N; Karatsoreos, Ilia N; Hillard, Cecilia J et al. (2010) Rapid elevations in limbic endocannabinoid content by glucocorticoid hormones in vivo. Psychoneuroendocrinology 35:1333-8
Hill, Matthew N; McLaughlin, Ryan J; Morrish, Anna C et al. (2009) Suppression of amygdalar endocannabinoid signaling by stress contributes to activation of the hypothalamic-pituitary-adrenal axis. Neuropsychopharmacology 34:2733-45

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