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Fatty Acid-mediated Signaling As a Target for Developing Type 1 Diabetes Therapies

Overview
Publisher Informa Healthcare
Specialty Pharmacology
Date 2023 Sep 14
PMID 37706269
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Abstract

Introduction: Type 1 diabetes (T1D) is an autoimmune disease in which pro-inflammatory and cytotoxic signaling drive the death of the insulin-producing β cells. This complex signaling is regulated in part by fatty acids and their bioproducts, making them excellent therapeutic targets.

Areas Covered: We provide an overview of the fatty acid actions on β cells by discussing how they can cause lipotoxicity or regulate inflammatory response during insulitis. We also discuss how diet can affect the availability of fatty acids and disease development. Finally, we discuss development avenues that need further exploration.

Expert Opinion: Fatty acids, such as hydroxyl fatty acids, ω-3 fatty acids, and their downstream products, are druggable candidates that promote protective signaling. Inhibitors and antagonists of enzymes and receptors of arachidonic acid and free fatty acids, along with their derived metabolites, which cause pro-inflammatory and cytotoxic responses, have the potential to be developed as therapeutic targets also. Further, because diet is the main source of fatty acid intake in humans, balancing protective and pro-inflammatory/cytotoxic fatty acid levels through dietary therapy may have beneficial effects, delaying T1D progression. Therefore, therapeutic interventions targeting fatty acid signaling hold potential as avenues to treat T1D.

Citing Articles

Reduction of Chemokine CXCL9 Expression by Omega-3 Fatty Acids via ADP-Ribosylhydrolase ARH3 in MIN6 Insulin-Producing Cells.

You Y, Sarkar S, Deiter C, Elliott E, Nicora C, Mirmira R Proteomics. 2024; 25(3):e202400053.

PMID: 39648458 PMC: 11794668. DOI: 10.1002/pmic.202400053.


Regulation of β-cell death by ADP-ribosylhydrolase ARH3 via lipid signaling in insulitis.

Sarkar S, Deiter C, Kyle J, Guney M, Sarbaugh D, Yin R Cell Commun Signal. 2024; 22(1):141.

PMID: 38383396 PMC: 10880366. DOI: 10.1186/s12964-023-01437-1.

References
1.
Kaku K, Enya K, Nakaya R, Ohira T, Matsuno R . Efficacy and safety of fasiglifam (TAK-875), a G protein-coupled receptor 40 agonist, in Japanese patients with type 2 diabetes inadequately controlled by diet and exercise: a randomized, double-blind, placebo-controlled, phase III trial. Diabetes Obes Metab. 2015; 17(7):675-81. PMC: 4676912. DOI: 10.1111/dom.12467. View

2.
Serhan C . Pro-resolving lipid mediators are leads for resolution physiology. Nature. 2014; 510(7503):92-101. PMC: 4263681. DOI: 10.1038/nature13479. View

3.
Chiang N, Serhan C . Specialized pro-resolving mediator network: an update on production and actions. Essays Biochem. 2020; 64(3):443-462. PMC: 7682745. DOI: 10.1042/EBC20200018. View

4.
Rahman M, Rodrigues K, Quiel J, Liu Y, Bhargava V, Zhao Y . Restoration of the type I IFN-IL-1 balance through targeted blockade of PTGER4 inhibits autoimmunity in NOD mice. JCI Insight. 2018; 3(3). PMC: 5821190. DOI: 10.1172/jci.insight.97843. View

5.
Serhan C, Chiang N, Dalli J . The resolution code of acute inflammation: Novel pro-resolving lipid mediators in resolution. Semin Immunol. 2015; 27(3):200-15. PMC: 4515371. DOI: 10.1016/j.smim.2015.03.004. View