Sirtuins (SIRTs) are seven nicotinamide adenine dinucleotide (NAD(+))-dependent protein deacetylases enzymes (SIRT1-7) that play an important role in maintaining cellular homeostasis. Among those, the most studied are SIRT1 and SIRT3, a nuclear SIRT and a mitochondrial SIRT, respectively, which significantly impact with an increase in mammals' lifespan by modulating metabolic cellular processes. Particularly, when activated, both SIRT1 and 3 enhance pancreatic beta-cells' insulin release and reduce inflammation and oxidative stress pancreatic damage, maintaining then glucose homeostasis. Therefore, SIRT1 and 3 activators have been proposed to prevent and counteract metabolic age-related diseases, such as type 2 diabetes mellitus (T2DM). Physical activity (PA) has a well-established beneficial effect on phenotypes of aging like beta-cell dysfunction and diabetes mellitus. Recent experimental and clinical evidence reports that PA increases the expression levels of both SIRT1 and 3, suggesting that PA may exert its healthy contribute even by activating SIRTs. Therefore, in the present article, we discuss the role of SIRT1, SIRT3, and PA on beta-cell function and on diabetes. We also discuss the possible interaction between PA and activation of SIRTs as a possible therapeutic strategy to maintain glucose hemostasis and to prevent T2DM and its complications, especially in the elderly population.

Pacifici, F., Di Cola, D., Pastore, D., Abete, P., Guadagni, F., Donadel, G., et al. (2019). Proposed tandem effect of physical activity and sirtuin 1 and 3 activation in regulating glucose homeostasis. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 20(19), 4748 [10.3390/ijms20194748].

Proposed tandem effect of physical activity and sirtuin 1 and 3 activation in regulating glucose homeostasis

Pacifici F.
Methodology
;
Pastore D.
Data Curation
;
Donadel G.
Supervision
;
Bellia A.
Conceptualization
;
Sinibaldi Salimei P.;Lauro D.
Writing – Review & Editing
;
Della Morte D.
Writing – Review & Editing
2019-01-01

Abstract

Sirtuins (SIRTs) are seven nicotinamide adenine dinucleotide (NAD(+))-dependent protein deacetylases enzymes (SIRT1-7) that play an important role in maintaining cellular homeostasis. Among those, the most studied are SIRT1 and SIRT3, a nuclear SIRT and a mitochondrial SIRT, respectively, which significantly impact with an increase in mammals' lifespan by modulating metabolic cellular processes. Particularly, when activated, both SIRT1 and 3 enhance pancreatic beta-cells' insulin release and reduce inflammation and oxidative stress pancreatic damage, maintaining then glucose homeostasis. Therefore, SIRT1 and 3 activators have been proposed to prevent and counteract metabolic age-related diseases, such as type 2 diabetes mellitus (T2DM). Physical activity (PA) has a well-established beneficial effect on phenotypes of aging like beta-cell dysfunction and diabetes mellitus. Recent experimental and clinical evidence reports that PA increases the expression levels of both SIRT1 and 3, suggesting that PA may exert its healthy contribute even by activating SIRTs. Therefore, in the present article, we discuss the role of SIRT1, SIRT3, and PA on beta-cell function and on diabetes. We also discuss the possible interaction between PA and activation of SIRTs as a possible therapeutic strategy to maintain glucose hemostasis and to prevent T2DM and its complications, especially in the elderly population.
2019
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MED/09 - MEDICINA INTERNA
Settore MED/04 - PATOLOGIA GENERALE
Settore MED/13 - ENDOCRINOLOGIA
Settore MED/05 - PATOLOGIA CLINICA
English
diabetes; glucose homeostasis; inflammation; oxidative stress; physical activity; sirtuins; Animals; Diabetes Mellitus, Type 2; Disease Susceptibility; Exercise; Glucose; Humans; Insulin-Secreting Cells; Metabolic Diseases; Sirtuin 1; Sirtuin 3; Homeostasis
Pacifici, F., Di Cola, D., Pastore, D., Abete, P., Guadagni, F., Donadel, G., et al. (2019). Proposed tandem effect of physical activity and sirtuin 1 and 3 activation in regulating glucose homeostasis. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 20(19), 4748 [10.3390/ijms20194748].
Pacifici, F; Di Cola, D; Pastore, D; Abete, P; Guadagni, F; Donadel, G; Bellia, A; Esposito, E; Salimei, C; Sinibaldi Salimei, P; Ricordi, C; Lauro, D; Della Morte, D
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/233868
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