Suppression of hERG K+ current and cardiac action potential prolongation by 4-hydroxynonenal via dual mechanismsopen access
- Authors
- Choi, Seong Woo; Choi, Si Won; Jeon, Young Keul; Moon, Sung-Hwan; Zhang, Yin-Hua; Kim, Sung Joon
- Issue Date
- Oct-2018
- Publisher
- ELSEVIER SCIENCE BV
- Keywords
- Lipid peroxidant; 4-hydroxynonenal; hERG channel; Cardiac action potential prolongation
- Citation
- REDOX BIOLOGY, v.19, pp 190 - 199
- Pages
- 10
- Journal Title
- REDOX BIOLOGY
- Volume
- 19
- Start Page
- 190
- End Page
- 199
- URI
- https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/69811
- DOI
- 10.1016/j.redox.2018.08.018
- ISSN
- 2213-2317
- Abstract
- Oxidative stress under pathological conditions, such as ischemia/reperfusion and inflammation, results in the production of various reactive chemicals. Of these chemicals, 4-hydroxynonenal (4-UNE), a peroxidation product of omega 6-polyunsaturated fatty acid, has garnered significant attention. However, the effect of 4-HNE on cardiac electrophysiology has not yet been reported. In the present study, we investigated the effects of 4-HNE on several cardiac ion channels, including human ether-a-go-go-related (hERG) channels, using the whole-cell patch clamp technique. Short-term exposure to 100 mu M 4-FINE (4-HNE100S), which mimics local levels under oxidative stress, decreased the amplitudes of rapidly activating delayed rectifier K+ current (I-Kr) in guinea pig ventricular myocytes (GPVMs) and HEK293T cells overexpressing hERG (I-hERG). MS analysis revealed the formation of 4-HNE-hERG adduct on specific amino acid residues, including C276, K595, H70, and H687. Longterm treatment (1-3 h) with 10 mu NI 4-HNE (4-HNE10L), suppressed I(Kr )and I-hERG, but not I-Ks, and I-ca,(L). Action potential duration (APD) of GPVMs was prolonged by 37% and 64% by 4-HNE100S and 4-HNE10L, respectively. Western blot analysis using surface biotinylation revealed a reduction in mature membrane hERG protein after treatment with 4-HNEio L. Proteasomal degradation inhibitors, such as bortezomib, prevented the 4-HNEloi,induced decrease in mature hERG, suggesting a retrograde degradation of membrane hERG due to 4-HNE. Taken together, 4-HNE100S and 4-HNE10L suppressed I-hERG via functional inhibition and downregulation of membrane expression of hERG, respectively. The exposure of 4-HNE under pathological oxidative stress may increase the risk of proarrhythmic events via APD prolongation.
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