Grant: Travel Awards - Institute Community Support
Université de Sherbrooke
$875.00
Impact of family history of type 2 diabetes on substrate oxidation and fatty acid metabolism during submaximal aerobic exercise in aging women
FY 2018-19
Summary
Alterations in fat oxidation (FatOx) are associated with insulin resistance in aging individuals and in first degree relatives (FDR) of diabetics. However, it remains unclear if a family history of diabetes influences FatOx in an aging, yet healthy, population. Our objective was to assess if FatOx is altered during submaximal aerobic exercise in aging FDR women compared with non-FDR women and to verify if circulating substrates influence FatOx. To verify our hypothesis, rates of FatOx, determined by respiratory exchange ratio (RER), were measured during 4 stages of submaximal exercise [1:40-45%, 2:50-55%, 3:60-65% and 4:70-75% of heart rate reserve] in 14 aging women (FDR: n=7; mean age: 61.9 ± 2.6 years; mean BMI: 28.2 ± 3.1 kg/m2). Blood samples were collected after each stage of exercise to measure plasma free fatty acids (FFA), glucose and lactate. We observed that RER and absolute rates of substrate oxidation were similar during exercise in FDR and non-FDR women. Likewise, plasma concentrations of substrates were similar at every stage of exercise between both groups. However, the crossover-point between FFA concentration and absolute rates of FatOx occurred at moderate intensity in non-FDR (stage 3) and at lower intensity in FDR (Stage 1). In conclusion, FDRs seem to display a disconnection between the capacity of oxidizing fat relative to FFA availability at a much lower aerobic workload which could be indicative of lower cardio-respiratory fitness.
Department
Program
Travel Awards - Institute Community Support
Recipient
Location
Quebec, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
387592
Name
Lagace Jean-Christophe
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Aging
Theme2
Clinical
Prcname2
Institute of Aging
Projecttitle
Impact of family history of type 2 diabetes on substrate oxidation and fatty acid metabolism during submaximal aerobic exercise in aging women
Programtype2
Undefined
Orgnameinp2
Université de Sherbrooke
Cihramount2
$875
Cihrequipment2
$0
Programname2
Travel Awards - Institute Community Support
Keyworddelim
Aging; Family History Of Type 2 Diabetes; Submaximal Aerobic Exercise; Substrate Metabolism; Substrate Oxidation
Abstract
Alterations in fat oxidation (FatOx) are associated with insulin resistance in aging individuals and in first degree relatives (FDR) of diabetics. However, it remains unclear if a family history of diabetes influences FatOx in an aging, yet healthy, population. Our objective was to assess if FatOx is altered during submaximal aerobic exercise in aging FDR women compared with non-FDR women and to verify if circulating substrates influence FatOx. To verify our hypothesis, rates of FatOx, determined by respiratory exchange ratio (RER), were measured during 4 stages of submaximal exercise [1:40-45%, 2:50-55%, 3:60-65% and 4:70-75% of heart rate reserve] in 14 aging women (FDR: n=7; mean age: 61.9 ± 2.6 years; mean BMI: 28.2 ± 3.1 kg/m2). Blood samples were collected after each stage of exercise to measure plasma free fatty acids (FFA), glucose and lactate. We observed that RER and absolute rates of substrate oxidation were similar during exercise in FDR and non-FDR women. Likewise, plasma concentrations of substrates were similar at every stage of exercise between both groups. However, the crossover-point between FFA concentration and absolute rates of FatOx occurred at moderate intensity in non-FDR (stage 3) and at lower intensity in FDR (Stage 1). In conclusion, FDRs seem to display a disconnection between the capacity of oxidizing fat relative to FFA availability at a much lower aerobic workload which could be indicative of lower cardio-respiratory fitness.
Competitiondate
201808
Approvedterm2
1 yr 0 mth
Pinamesdelim
Lagace, Jean-Christophe
Approvedterm
1 an 0 mois
Cihrcontribution2
Institute of Aging~ $875~ $0~