http://www.cnr.it/ontology/cnr/individuo/prodotto/ID300066
Peroxiredoxin 6, a Novel Player in the Pathogenesis of Diabetes (Articolo in rivista)
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- Label
- Peroxiredoxin 6, a Novel Player in the Pathogenesis of Diabetes (Articolo in rivista) (literal)
- Anno
- 2014-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.2337/db14-0144 (literal)
- Alternative label
Pacifici, Francesca; Arriga, Roberto; Sorice, Gian Pio; Capuani, Barbara; Scioli, Maria Giovanna; Pastore, Donatella; Donadel, Giulia; Bellia, Alfonso; Caratelli, Sara; Coppola, Andrea; Ferrelli, Francesca; Federici, Massimo; Sconocchia, Giuseppe; Tesauro, Manfredi; Sbraccia, Paolo; Della-Morte, David; Giaccari, Andrea; Orlandi, Augusto; Lauro, Davide (2014)
Peroxiredoxin 6, a Novel Player in the Pathogenesis of Diabetes
in Diabetes (N.Y.N.Y.)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Pacifici, Francesca; Arriga, Roberto; Sorice, Gian Pio; Capuani, Barbara; Scioli, Maria Giovanna; Pastore, Donatella; Donadel, Giulia; Bellia, Alfonso; Caratelli, Sara; Coppola, Andrea; Ferrelli, Francesca; Federici, Massimo; Sconocchia, Giuseppe; Tesauro, Manfredi; Sbraccia, Paolo; Della-Morte, David; Giaccari, Andrea; Orlandi, Augusto; Lauro, Davide (literal)
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- ISI Web of Science (WOS) (literal)
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- University of Rome Tor Vergata; Catholic University of the Sacred Heart; Assoc Cavalieri Italiani Sovrano Mil Ordine; University of Rome Tor Vergata; Consiglio Nazionale delle Ricerche (CNR); Ist Ricovero & Cura Carattere Sci San Raffaele Pi (literal)
- Titolo
- Peroxiredoxin 6, a Novel Player in the Pathogenesis of Diabetes (literal)
- Abstract
- Enhanced oxidative stress contributes to the pathogenesis of diabetes and its complications. Peroxiredoxin 6 (PRDX6) is a key regulator of cellular redox balance, with the peculiar ability to neutralize peroxides, peroxynitrite, and phospholipid hydroperoxides. In the current study, we aimed to define the role of PRDX6 in the pathophysiology of type 2 diabetes (T2D) using PRDX6 knockout (-/-) mice. Glucose and insulin responses were evaluated respectively by intraperitoneal glucose and insulin tolerance tests. Peripheral insulin sensitivity was analyzed by euglycemic-hyperinsulinemic clamp, and molecular tools were used to investigate insulin signaling. Moreover, inflammatory and lipid parameters were evaluated. We demonstrated that PRDX6(-/-) mice developed a phenotype similar to early-stage T2D caused by both reduced glucose-dependent insulin secretion and increased insulin resistance. Impaired insulin signaling was present in PRDX6(-1-) mice, leading to reduction of muscle glucose uptake. Morphological and ultrastructural changes were observed in islets of Langerhans and livers of mutant animals, as well as altered plasma lipid profiles and inflammatory parameters. In conclusion, we demonstrated that PRDX6 is a key mediator of overt hyperglycemia in T2D glucose metabolism, opening new perspectives for targeted therapeutic strategies in diabetes care. (literal)
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- Autore CNR
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