| Literature DB >> 30073505 |
Eugenio Barone1,2, Antonella Tramutola1, Francesca Triani1, Silvio Calcagnini3, Fabio Di Domenico1, Cristian Ripoli4,5, Silvana Gaetani3, Claudio Grassi4,5, D Allan Butterfield6, Tommaso Cassano7, Marzia Perluigi8.
Abstract
Impairment of biliverdin reductase-A (BVR-A) is an early event leading to brain insulin resistance in AD. Intranasal insulin (INI) administration is under evaluation as a strategy to alleviate brain insulin resistance; however, the molecular mechanisms underlying INI beneficial effects are still unclear. We show that INI improves insulin signaling activation in the hippocampus and cortex of adult and aged 3×Tg-AD mice by ameliorating BVR-A activation. These changes were associated with a reduction of nitrosative stress, Tau phosphorylation, and Aβ oligomers in brain, along with improved cognitive functions. The role of BVR-A was strengthened by showing that cells lacking BVR-A: (i) develop insulin resistance if treated with insulin and (ii) can be recovered from insulin resistance only if treated with a BVR-A-mimetic peptide. These novel findings shed light on the mechanisms underlying INI treatment effects and suggest BVR-A as potential therapeutic target to prevent brain insulin resistance in AD.Entities:
Keywords: Alzheimer disease; Biliverdin reductase-A; Insulin resistance; Intranasal; Neuroprotection
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Year: 2018 PMID: 30073505 DOI: 10.1007/s12035-018-1231-5
Source DB: PubMed Journal: Mol Neurobiol ISSN: 0893-7648 Impact factor: 5.590