Article ; Online: β-Cell Insulin Resistance Plays a Causal Role in Fat-Induced β-Cell Dysfunction In Vitro and In Vivo.
2024 Volume 165, Issue 5
Abstract: In the classical insulin target tissues of liver, muscle, and adipose tissue, chronically elevated levels of free fatty acids (FFA) impair insulin signaling. Insulin signaling molecules are also present in β-cells where they play a role in β-cell ... ...
| Abstract | In the classical insulin target tissues of liver, muscle, and adipose tissue, chronically elevated levels of free fatty acids (FFA) impair insulin signaling. Insulin signaling molecules are also present in β-cells where they play a role in β-cell function. Therefore, inhibition of the insulin/insulin-like growth factor 1 pathway may be involved in fat-induced β-cell dysfunction. To address the role of β-cell insulin resistance in FFA-induced β-cell dysfunction we co-infused bisperoxovanadate (BPV) with oleate or olive oil for 48 hours in rats. BPV, a tyrosine phosphatase inhibitor, acts as an insulin mimetic and is devoid of any antioxidant effect that could prevent β-cell dysfunction, unlike most insulin sensitizers. Following fat infusion, rats either underwent hyperglycemic clamps for assessment of β-cell function in vivo or islets were isolated for ex vivo assessment of glucose-stimulated insulin secretion (GSIS). We also incubated islets with oleate or palmitate and BPV for in vitro assessment of GSIS and Akt (protein kinase B) phosphorylation. Next, mice with β-cell specific deletion of PTEN (phosphatase and tensin homolog; negative regulator of insulin signaling) and littermate controls were infused with oleate for 48 hours, followed by hyperglycemic clamps or ex vivo evaluation of GSIS. In rat experiments, BPV protected against fat-induced impairment of β-cell function in vivo, ex vivo, and in vitro. In mice, β-cell specific deletion of PTEN protected against oleate-induced β-cell dysfunction in vivo and ex vivo. These data support the hypothesis that β-cell insulin resistance plays a causal role in FFA-induced β-cell dysfunction. |
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| MeSH term(s) | Animals ; Insulin Resistance/physiology ; Insulin-Secreting Cells/drug effects ; Insulin-Secreting Cells/metabolism ; Rats ; Mice ; Male ; PTEN Phosphohydrolase/metabolism ; Oleic Acid/pharmacology ; Insulin/metabolism ; Mice, Inbred C57BL ; Insulin Secretion/drug effects ; Fatty Acids, Nonesterified/metabolism ; Rats, Sprague-Dawley | |||||
| Chemical Substances | PTEN Phosphohydrolase (EC 3.1.3.67) ; Oleic Acid (2UMI9U37CP) ; Insulin ; Fatty Acids, Nonesterified | |||||
| Language | English | |||||
| Publishing date | 2024-04-04 | |||||
| Publishing country | United States | |||||
| Document type | Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, N.I.H., Extramural | |||||
| ZDB-ID | 427856-2 | |||||
| ISSN | 1945-7170 ; 0013-7227 | |||||
| ISSN (online) | 1945-7170 | |||||
| ISSN | 0013-7227 | |||||
| DOI | 10.1210/endocr/bqae044 | |||||
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| Database | MEDical Literature Analysis and Retrieval System OnLINE |
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