Pharmacological inhibition of thioredoxin reductase increases insulin secretion and diminishes beta cell viability.


Journal

Naunyn-Schmiedeberg's archives of pharmacology
ISSN: 1432-1912
Titre abrégé: Naunyn Schmiedebergs Arch Pharmacol
Pays: Germany
ID NLM: 0326264

Informations de publication

Date de publication:
06 2021
Historique:
received: 10 12 2019
accepted: 22 12 2020
pubmed: 20 1 2021
medline: 15 12 2021
entrez: 19 1 2021
Statut: ppublish

Résumé

Apparently, both a decrease in beta cell function and in beta cell mass contribute to the progressive worsening of type 2 diabetes. So, it is of particular interest to define factors which are relevant for the regulation of insulin secretion and at the same time for the maintenance of beta cell mass. The NADPH-thioredoxin system has a candidate role for such a dual function. Here, we have characterized the effects of a highly specific inhibitor of thioredoxin reductase, AM12, on the viability and function of insulin-secreting MIN6 cells and isolated NMRI mouse islets. Viability was checked by MTT testing and the fluorescent live-dead assay. Apoptosis was assessed by annexin V assay. Insulin secretion of perifused islets was measured by ELISA. The cytosolic Ca

Identifiants

pubmed: 33464387
doi: 10.1007/s00210-020-02046-2
pii: 10.1007/s00210-020-02046-2
pmc: PMC8208932
doi:

Substances chimiques

Benzene Derivatives 0
Organogold Compounds 0
thioredoxin reductase inhibitor AM12 0
Thioredoxin-Disulfide Reductase EC 1.8.1.9
Glucose IY9XDZ35W2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1133-1142

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Auteurs

Dennis Brüning (D)

Institute of Pharmacology, Toxicology and Clinical Pharmacy, Technische Universität Braunschweig, D-38106, Braunschweig, Germany.

Kathrin Hatlapatka (K)

Institute of Pharmacology, Toxicology and Clinical Pharmacy, Technische Universität Braunschweig, D-38106, Braunschweig, Germany.

Verena Lier-Glaubitz (V)

Institute of Pharmacology, Toxicology and Clinical Pharmacy, Technische Universität Braunschweig, D-38106, Braunschweig, Germany.

Vincent Andermark (V)

Institute of Medicinal and Pharmaceutical Chemistry, Technische Universität Braunschweig, D-38106, Braunschweig, Germany.

Stephan Scherneck (S)

Institute of Pharmacology, Toxicology and Clinical Pharmacy, Technische Universität Braunschweig, D-38106, Braunschweig, Germany.

Ingo Ott (I)

Institute of Medicinal and Pharmaceutical Chemistry, Technische Universität Braunschweig, D-38106, Braunschweig, Germany.

Ingo Rustenbeck (I)

Institute of Pharmacology, Toxicology and Clinical Pharmacy, Technische Universität Braunschweig, D-38106, Braunschweig, Germany. i.rustenbeck@tu-bs.de.

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Classifications MeSH