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Mitochondrial ion channels in pancreatic β-cells: Novel pharmacological targets for the treatment of Type 2 diabetes. | LitMetric

AI Article Synopsis

  • Pancreatic beta-cells play a vital role in regulating blood sugar levels by sensing nutrients and adjusting insulin secretion accordingly, and their dysfunction can lead to Type 2 diabetes.
  • Mitochondria are essential in beta-cells, linking glucose metabolism to insulin signaling, and are involved in energy production and regulation of cellular processes.
  • The article highlights mitochondrial ion channels in beta-cells and discusses potential therapeutic targets for treating Type 2 diabetes, supported by evidence from clinical studies.

Article Abstract

Pancreatic beta-cells are central regulators of glucose homeostasis. By tightly coupling nutrient sensing and granule exocytosis, beta-cells adjust the secretion of insulin to the circulating blood glucose levels. Failure of beta-cells to augment insulin secretion in insulin-resistant individuals leads progressively to impaired glucose tolerance, Type 2 diabetes, and diabetes-related diseases. Mitochondria play a crucial role in β-cells during nutrient stimulation, linking the metabolism of glucose and other secretagogues to the generation of signals that promote insulin secretion. Mitochondria are double-membrane organelles containing numerous channels allowing the transport of ions across both membranes. These channels regulate mitochondrial energy production, signalling, and cell death. The mitochondria of β-cells express ion channels whose physio/pathological role is underappreciated. Here, we describe the mitochondrial ion channels identified in pancreatic β-cells, we further discuss the possibility of targeting specific β-cell mitochondrial channels for the treatment of Type 2 diabetes, and we finally highlight the evidence from clinical studies. LINKED ARTICLES: This article is part of a themed issue on Cellular metabolism and diseases. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v178.10/issuetoc.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8246559PMC
http://dx.doi.org/10.1111/bph.15018DOI Listing

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