D-Tagatose Feeding Reduces the Risk of Sugar-Induced Exacerbation of Myocardial I/R Injury When Compared to Its Isomer Fructose

Autor: Debora Collotta, Annunziatina Laurino, Emanuela Masini, Laura Lucarini, Silvia Sgambellone, Massimo Collino, Gustavo Provensi, Mariaconcetta Durante, Paola Failli
Jazyk: angličtina
Rok vydání: 2021
Předmět:
0301 basic medicine
medicine.medical_specialty
medicine.medical_treatment
Ischemia
Inflammation
030204 cardiovascular system & hematology
medicine.disease_cause
Biochemistry
Genetics and Molecular Biology (miscellaneous)

Biochemistry
Proinflammatory cytokine
fructose
fructose
myocardial ischemia
inflammation
oxidative stress
D-tagatose

03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
Enos
Internal medicine
Medicine
oxidative stress
Molecular Biosciences
Sugar
D-tagatose
lcsh:QH301-705.5
Molecular Biology
Original Research
biology
business.industry
inflammation
myocardial ischemia
Insulin
Fructose
biology.organism_classification
medicine.disease
030104 developmental biology
Endocrinology
chemistry
lcsh:Biology (General)
medicine.symptom
business
Oxidative stress
Zdroj: Frontiers in Molecular Biosciences
Frontiers in Molecular Biosciences, Vol 8 (2021)
ISSN: 2296-889X
DOI: 10.3389/fmolb.2021.650962
Popis: It is known that fructose may contribute to myocardial vulnerability to ischemia/reperfusion (I/R) injury. D-tagatose is a fructose isomer with less caloric value and used as low-calorie sweetener. Here we compared the metabolic impact of fructose or D-tagatose enriched diets on potential exacerbation of myocardial I/R injury. Wistar rats were randomizedly allocated in the experimental groups and fed with one of the following diets: control (CTRL), 30% fructose-enriched (FRU 30%) or 30% D-tagatose-enriched (TAG 30%). After 24 weeks of dietary manipulation, rats underwent myocardial injury caused by 30 min ligature of the left anterior descending (LAD) coronary artery followed by 24 h′ reperfusion. Fructose consumption resulted in body weight increase (49%) as well as altered glucose, insulin and lipid profiles. These effects were associated with increased I/R-induced myocardial damage, oxidative stress (36.5%) and inflammation marker expression. TAG 30%-fed rats showed lower oxidative stress (21%) and inflammation in comparison with FRU-fed rats. Besides, TAG diet significantly reduced plasmatic inflammatory cytokines and GDF8 expression (50%), while increased myocardial endothelial nitric oxide synthase (eNOS) expression (59%). Overall, we demonstrated that D-tagatose represents an interesting sugar alternative when compared to its isomer fructose with reduced deleterious impact not only on the metabolic profile but also on the related heart susceptibility to I/R injury.
Databáze: OpenAIRE