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| Content Provider | Royal Society of Chemistry (RSC) |
|---|---|
| Author | Düfer, Martina Krippeit-Drews, Peter Lendeckel, Uwe Drews, Gisela Sahr, Anika Guenther, Elke Kraushaar, Udo Walther, Reinhard Härdtner, Carmen Barthlen, Winfried Schönecker, Sven |
| Copyright Year | 2014 |
| Abstract | Extracellular recording of the glucose-induced electrical activity of mouse islets of Langerhans on microelectrode arrays (MEAs) is an innovative and powerful tool to address beta-cell (patho-)physiology. In a dual approach we tested whether this technique can detect concentration-dependent drug effects as well as characterize alterations in beta-cell activity during prolonged culture. First we established conditions that allow long-term investigation of beta-cell function by recording electrical activity. The results provide the first measurements of beta-cell membrane potential oscillations of individual murine islets during long-term culture. Oscillations were recorded for up to 34 days after islet isolation. Importantly, the glucose dependence of electrical activity did not change over a period of one month. Thus we can follow electrophysiological changes of individual islets induced by alterations in the beta-cell environment over weeks. Second, we used the MEA technique to assay beta-cell damage induced by oxidative stress and to evaluate appropriate protection mechanisms. Oxidative stress plays a key role in the development of type 2 diabetes mellitus (T2DM). Examination of the acute effects of H2O2 on electrical activity showed that the oxidant reduced the electrical activity in a concentration-dependent manner. The superoxide dismutase mimetic, tempol, protected against the detrimental effects of H2O2. In conclusion, we demonstrated that MEA recordings can be used to address disease-related mechanisms and protective interventions in beta-cells. In the future, this fundamental work should enable the monitoring of the electrical activity of islets of Langerhans under controlled ex vivo conditions including long-term exposure to oxidative stress, glucolipotoxicity, and other diabetes-inducing agents. |
| Starting Page | 540 |
| Ending Page | 544 |
| Page Count | 5 |
| File Format | HTM / HTML PDF |
| ISSN | 17579694 |
| Volume Number | 6 |
| Issue Number | 5 |
| Journal | Integrative Biology |
| DOI | 10.1039/c3ib40261d |
| Language | English |
| Publisher | Royal Society of Chemistry |
| Access Restriction | Subscribed |
| Subject Keyword | Langerhans Mouse Microelectrode Physiology Membrane potential Pancreatic islets Glucose Physical dependence Ethanolamine Oxidative stress Protection mechanism Diabetes mellitus type 2 Hydrogen peroxide Superoxide dismutase 4-Hydroxy-TEMPO |
| Content Type | Text |
| Resource Type | Article |
| Subject | Medicine Biochemistry Biophysics |
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