Role of ER stress inhibitors in the management of diabetes

• Published in: European journal of pharmacology 2022-05, Vol.922, p.174893-174893, Article 174893
• Main Authors: Prasad M, Krishna, Mohandas, Sundhar, Ramkumar, Kunka Mohanram
• Format: Article
• Language: English
• Subjects: Chaperones; Diabetes mellitus; Diabetes Mellitus - drug therapy; eIF-2 Kinase - metabolism; Endoplasmic Reticulum Stress; ER stress Inhibitors; Humans; Hyperglycemia; Protein Serine-Threonine Kinases; Therapeutic target; Unfolded Protein Response; UPR
• ISSN: 0014-2999; 1879-0712
• DOI: 10.1016/j.ejphar.2022.174893

Endoplasmic Reticulum (ER) stress has been established to play a key pathophysiological role in developing metabolic diseases such as Diabetes Mellitus (DM). The complications of DM have been closely associated with deregulation of the unfolded protein response (UPR) signaling pathways, which are critically responsible for restoring homeostasis following ER stress. Chronic ER stress in the background of persistent hyperglycemia, as observed in DM, overwhelms the UPR signaling and commits the cells to apoptosis. The factors such as hyperglycemia, increased reactive oxygen species (ROS), disrupted calcium homeostasis, and overt inflammation serve as major UPR signal transduction pathways, including PKR like ER kinase (PERK), Activating transcription factor 6α/β (ATF6), and Inositol requiring enzyme1α/β (IRE1). The constantly developing understanding of these ER stress mediators has also unraveled their potential as therapeutic targets of small molecules termed ER stress inhibitors. A wide range of both naturally occurring and synthetic compounds have been screened and studied for their properties to inhibit ER stress in various experimental models. This review article elucidates the critical signaling pathways associated with response to ER stress. We shed light on the crosstalk between ER stress mediators with oxidative and inflammatory stress mediators in the background of DM. We extensively summarize the pieces of evidence sourced from preclinical and clinical research about the role of ER stress inhibitors and their pharmacological mechanism of action in alleviating ER stress in diabetes. [Display omitted]