Grant: Discovery Grants Program - Individual
Mount Allison University
$28,000.00
Cellular and Synaptic Physiology of the Dorsomedial Hypothalamus
FY 2017-18
Summary
Stressful stimuli trigger rapid and requisite changes that allow organisms to effectively cope with stress and restore homeostasis. While this response can be beneficial in the short term, prolonged exposure to stress can result in the disruption of numerous important physiological processes, including appetite regulation. The mechanisms underlying the link between stress and appetite; however, are poorly understood. The long term goal of my research program is to characterize the cellular, molecular, and synaptic mechanisms that underlie stress-induced alterations in food intake and metabolism. Numerous feeding circuits in the brain play an important role in regulating appetite and body weight, but no region is as fundamentally linked to stress and appetite as the dorsomedial nucleus of the hypothalamus (DMH). The DMH processes neural signals related to stress and satiety and I have recently demonstrated that stress triggers a functional rewiring of inhibitory synapses in the DMH such that presumed satiety neurons are inhibited. This is accomplished by alterations of two key signals that regulate neuronal communication in the DMH: endocannabinoids and nitric oxide. Much remains unknown, however, regarding the mechanisms by which stress influences synaptic function and endocannabinoid and nitric oxide signaling/interactions in the DMH. The behavioral consequences with respect to appetite regulation are also unknown. Thus, our short term objectives are threefold. First, we will use whole cell patch clamp electrophysiology to determine the effect of various stressors on synaptic transmission and changes in synaptic strength mediated by endocannabinoids and nitric oxide (Objective 1). Second, because endocannabinoids and nitric oxide interact to regulate neuronal communication in the DMH, we will study the mechanisms of these interactions and the effect of stress using electrophysiological and molecular (immunohistochemistry) techniques (Objective 2). Third, we will address the physiological consequences of endocannabinoid and nitric oxide administration in the DMH. Specifically, we will determine the effect of endocannabinoids and nitric oxide, and their interactions, in the DMH on food intake and body weight in nave and stressed animals. (Objective 3). Together, these studies will provide important insight into the effect of stress on appetite regulation.
Program
Discovery Grants Program - Individual
Recipient
Location
New Brunswick, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data
As published
Application id
RGPIN-2016-06257
Name nom
Crosby, Karen
Department département
Biology - Biology
Organization id
74
Institution établissement
Mount Allison University
Province en
New Brunswick
Province fr
Nouveau-Brunswick
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2017
Competition year année de concours
2016
Award amount
28000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
1502
Committee name en
Biological Systems and Functions
Committee name fr
Systèmes et fonctions biologiques
Area of application code
1101
Area of application group en
Health, education and social services
Area of application group fr
Santé publique, éducation et services sociaux
Area of application en
Human health (including medically-related psychological research)
Area of application fr
Santé publique (y compris recherche psychologique liée à la médecine)
Research subject code
5112
Research subject group en
Cell biology
Research subject group fr
Biologie cellulaire
Research subject en
Electrophysiology
Research subject fr
Électrophysiologie
Partie
2
Nb partie
5
Application title
Cellular and Synaptic Physiology of the Dorsomedial Hypothalamus
Keyword
NSERC
Application summary
Stressful stimuli trigger rapid and requisite changes that allow organisms to effectively cope with stress and restore homeostasis. While this response can be beneficial in the short term, prolonged exposure to stress can result in the disruption of numerous important physiological processes, including appetite regulation. The mechanisms underlying the link between stress and appetite; however, are poorly understood. The long term goal of my research program is to characterize the cellular, molecular, and synaptic mechanisms that underlie stress-induced alterations in food intake and metabolism. Numerous feeding circuits in the brain play an important role in regulating appetite and body weight, but no region is as fundamentally linked to stress and appetite as the dorsomedial nucleus of the hypothalamus (DMH). The DMH processes neural signals related to stress and satiety and I have recently demonstrated that stress triggers a functional rewiring of inhibitory synapses in the DMH such that presumed satiety neurons are inhibited. This is accomplished by alterations of two key signals that regulate neuronal communication in the DMH: endocannabinoids and nitric oxide. Much remains unknown, however, regarding the mechanisms by which stress influences synaptic function and endocannabinoid and nitric oxide signaling/interactions in the DMH. The behavioral consequences with respect to appetite regulation are also unknown. Thus, our short term objectives are threefold. First, we will use whole cell patch clamp electrophysiology to determine the effect of various stressors on synaptic transmission and changes in synaptic strength mediated by endocannabinoids and nitric oxide (Objective 1). Second, because endocannabinoids and nitric oxide interact to regulate neuronal communication in the DMH, we will study the mechanisms of these interactions and the effect of stress using electrophysiological and molecular (immunohistochemistry) techniques (Objective 2). Third, we will address the physiological consequences of endocannabinoid and nitric oxide administration in the DMH. Specifically, we will determine the effect of endocannabinoids and nitric oxide, and their interactions, in the DMH on food intake and body weight in nave and stressed animals. (Objective 3). Together, these studies will provide important insight into the effect of stress on appetite regulation.