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Pharmacological Modulators of Endoplasmic Reticulum Stress in Metabolic Diseases

Authors
Jung, Tae WooChoi, Kyung Mook
Issue Date
Feb-2016
Publisher
MDPI
Keywords
endoplasmic reticulum stress; unfolded protein response; AMPK-activated protein kinase; glucagon-like peptide-1; peroxisome proliferator-activated receptors; angiotensin II type 1 receptor blockers
Citation
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, v.17, no.2
Indexed
SCIE
SCOPUS
Journal Title
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
Volume
17
Number
2
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/89624
DOI
10.3390/ijms17020192
ISSN
1661-6596
Abstract
The endoplasmic reticulum (ER) is the principal organelle responsible for correct protein folding, a step in protein synthesis that is critical for the functional conformation of proteins. ER stress is a primary feature of secretory cells and is involved in the pathogenesis of numerous human diseases, such as certain neurodegenerative and cardiometabolic disorders. The unfolded protein response (UPR) is a defense mechanism to attenuate ER stress and maintain the homeostasis of the organism. Two major degradation systems, including the proteasome and autophagy, are involved in this defense system. If ER stress overwhelms the capacity of the cell's defense mechanisms, apoptotic death may result. This review is focused on the various pharmacological modulators that can protect cells from damage induced by ER stress. The possible mechanisms for cytoprotection are also discussed.
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