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Grant: Discovery Grants Program - Individual

Mount Allison University

$29,000.00

Coupling cardiovascular control and energy metabolism in fish: the influence of emerging (nanoparticle) toxicants

EF 2015-16

Résumé
Cardiometabolic coupling is the physiological process linking energy metabolism and cardiovascular function. This is a well-established phenomenon in mammals but it is poorly understood in other vertebrates. The long-term goal of my research program is to identify the cellular mechanisms involved in cardiometabolic coupling using fish as a model. Characterizing these mechanisms will provide insight into core physiological processes and metabolic diseases in mammals. Fish are unique models to study this problem as their natural diet differs within and across species. This leads to large variations in the composition of dietary polyunsaturated fatty acids, which are precursors for compounds that influence cardiovascular function. The dynamic environment inhabited by fish also shapes their metabolism and may influence cardiometabolic coupling. Given the diversity of fish species, it is likely that many have evolved mechanisms to cope with metabolic/physiological disturbances that may not be functional in mammals. The bioactivity of certain toxins is based on changes in reactive oxygen species (ROS) metabolism. For example, inhalation of engineered nanoparticles (NPs) leads to oxidative stress and cardiovascular dysfunction. NPs have unique properties which make it difficult to predict their bioactivity based on information for conventional compounds of similar composition. NPs can be taken up by cells, denature proteins related to energy metabolism and damage lipid membranes. NPs are now being released into aquatic environments and can induce oxidative stress in fish but their cardiovascular effects are unknown. Cardiometabolic coupling is also rooted in changes in ROS metabolism so NPs may therefore have the potential to influence this process via multiple, independent pathways. I will use a multidisciplinary approach to address 2 main research objectives:1) identify cellular mechanisms underlying cardiometabolic coupling in fish under dynamic environmental conditions; 2) characterize the influence of NPs on energy metabolism and cardiovascular function in fish with the aim of identifying mechanisms contributing to cardiometabolic coupling.
Programme
Discovery Grants Program - Individual
Emplacement
New Brunswick, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data

Tel que publié

Application id
418238-2012
Name nom
MacCormack, Tyson
Department département
Chemistry & Biochemistry
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
2015
Competition year année de concours
2012
Award amount
29000
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
1201
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Life sciences (including biotechnology)
Area of application fr
Sciences de la vie (y compris biotechnologie)
Research subject code
5504
Research subject group en
Animal biology
Research subject group fr
Biologie animale
Research subject en
Animal physiology and metabolism
Research subject fr
Physiologie et métabolisme des animaux
Partie
4
Nb partie
5
Application title
Coupling cardiovascular control and energy metabolism in fish: the influence of emerging (nanoparticle) toxicants
Keyword
NSERC
Application summary
Cardiometabolic coupling is the physiological process linking energy metabolism and cardiovascular function. This is a well-established phenomenon in mammals but it is poorly understood in other vertebrates. The long-term goal of my research program is to identify the cellular mechanisms involved in cardiometabolic coupling using fish as a model. Characterizing these mechanisms will provide insight into core physiological processes and metabolic diseases in mammals. Fish are unique models to study this problem as their natural diet differs within and across species. This leads to large variations in the composition of dietary polyunsaturated fatty acids, which are precursors for compounds that influence cardiovascular function. The dynamic environment inhabited by fish also shapes their metabolism and may influence cardiometabolic coupling. Given the diversity of fish species, it is likely that many have evolved mechanisms to cope with metabolic/physiological disturbances that may not be functional in mammals. The bioactivity of certain toxins is based on changes in reactive oxygen species (ROS) metabolism. For example, inhalation of engineered nanoparticles (NPs) leads to oxidative stress and cardiovascular dysfunction. NPs have unique properties which make it difficult to predict their bioactivity based on information for conventional compounds of similar composition. NPs can be taken up by cells, denature proteins related to energy metabolism and damage lipid membranes. NPs are now being released into aquatic environments and can induce oxidative stress in fish but their cardiovascular effects are unknown. Cardiometabolic coupling is also rooted in changes in ROS metabolism so NPs may therefore have the potential to influence this process via multiple, independent pathways. I will use a multidisciplinary approach to address 2 main research objectives:1) identify cellular mechanisms underlying cardiometabolic coupling in fish under dynamic environmental conditions; 2) characterize the influence of NPs on energy metabolism and cardiovascular function in fish with the aim of identifying mechanisms contributing to cardiometabolic coupling.