Verbascoside Protects Pancreatic β-Cells against ER-Stress.

ER-stress PERK UPR anti-inflammatory diabetes insulin-producing cells mitochondria oxidative stress polyphenols verbascoside

Journal

Biomedicines
ISSN: 2227-9059
Titre abrégé: Biomedicines
Pays: Switzerland
ID NLM: 101691304

Informations de publication

Date de publication:
08 Dec 2020
Historique:
received: 16 11 2020
revised: 04 12 2020
accepted: 05 12 2020
entrez: 11 12 2020
pubmed: 12 12 2020
medline: 12 12 2020
Statut: epublish

Résumé

Substantial epidemiological evidence indicates that a diet rich in polyphenols protects against developing type 2 diabetes. The phenylethanoid glycoside verbascoside/acteoside, a widespread polyphenolic plant compound, has several biological properties including strong antioxidant, anti-inflammatory and neuroprotective activities. The aim of this research was to test the possible effects of verbascoside on pancreatic β-cells, a target never tested before. Mouse and human β-cells were incubated with verbascoside (0.8-16 µM) for up to five days and a combination of biochemical and imaging techniques were used to assess the β-cell survival and function under normal or endoplasmic reticulum (ER)-stress inducing conditions. We found a dose-dependent protective effect of verbascoside against oxidative stress in clonal and human β-cells. Mechanistic studies revealed that the polyphenol protects β-cells against ER-stress mediated dysfunctions, modulating the activation of the protein kinase RNA-like endoplasmic reticulum kinase (PERK) branch of the unfolded protein response and promoting mitochondrial dynamics. As a result, increased viability, mitochondrial function and insulin content were detected in these cells. These studies provide the evidence that verbascoside boosts the ability of β-cells to cope with ER-stress, an important contributor of β-cell dysfunction and failure in diabetic conditions and support the therapeutic potential of verbascoside in diabetes.

Identifiants

pubmed: 33302345
pii: biomedicines8120582
doi: 10.3390/biomedicines8120582
pmc: PMC7762434
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Alessandra Galli (A)

Department of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, 20134 Milan, Italy.

Paola Marciani (P)

Department of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, 20134 Milan, Italy.

Algerta Marku (A)

Department of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, 20134 Milan, Italy.

Silvia Ghislanzoni (S)

Department of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, 20134 Milan, Italy.

Federico Bertuzzi (F)

Diabetology Unit, Niguarda Hospital, 20162 Milan, Italy.

Raffaella Rossi (R)

Department of Veterinary Medicine, Università degli Studi di Milano, 26900 Lodi, Italy.

Alessia Di Giancamillo (A)

Department of Veterinary Medicine, Università degli Studi di Milano, 26900 Lodi, Italy.

Michela Castagna (M)

Department of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, 20134 Milan, Italy.

Carla Perego (C)

Department of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, 20134 Milan, Italy.

Classifications MeSH