Anti-arrhythmic Cardiac Phenotype Elicited by Chronic Intermittent Hypoxia Is Associated With Alterations in Connexin-43 Expression, Phosphorylation, and Distribution

0504257 - FGÚ 2020 RIV CH eng J - Článek v odborném periodiku
Kohutová, J. - Elsnicová, B. - Holzerová, Kristýna - Neckář, Jan - Šebesta, O. - Ježková, J. - Vecka, M. - Vebr, P. - Horníková, D. - Szeiffová Bačová, B. - Egan Beňová, T. - Hlaváčková, Markéta - Tribulová, N. - Kolář, František - Nováková, Olga - Žurmanová, J.M.
Anti-arrhythmic Cardiac Phenotype Elicited by Chronic Intermittent Hypoxia Is Associated With Alterations in Connexin-43 Expression, Phosphorylation, and Distribution.
Frontiers in Endocrinology. Roč. 9, Jan 25 (2019), č. článku 789. ISSN 1664-2392. E-ISSN 1664-2392
Grant CEP: GA ČR GA17-07748S; GA ČR(CZ) GJ16-12420Y; GA MŠMT(CZ) LM2015062
Výzkumná infrastruktura: Czech-BioImaging - 90062
Institucionální podpora: RVO:67985823
Klíčová slova: heart * chronic hypoxia * brief ischemia * arrhythmia * connexin-43 * n-3 PUFA
Obor OECD: Physiology (including cytology)
Impakt faktor: 3.644, rok: 2019
Způsob publikování: Open access
https://doi.org/10.3389/fendo.2018.00789

Remodeling of the cellular distribution of gap junctions formed mainly by connexin-43 (Cx43) can be related to the increased incidence of cardiac arrhythmias. It has been shown that adaptation to chronic intermittent hypobaric hypoxia (IHH) attenuates the incidence and severity of ischemic and reperfusion ventricular arrhythmias and increases the proportion of anti-arrhythmic n-3 polyunsaturated fatty acids (n-3 PUFA) in heart phospholipids. Wistar rats were exposed to simulated IHH (7,000 m, 8-h/day, 35 exposures) and compared with normoxic controls (N). Cx43 expression, phosphorylation, localization and n-3 PUFA proportion were analyzed in left ventricular myocardium. Compared to N, IHH led to higher expression of total Cx43, its variant phosphorylated at Ser368 [p-Cx43(Ser368)], which maintains “end to end” communication, as well as p-Cx43(Ser364/365), which facilitates conductivity. By contrast, expression of non-phosphorylated Cx43 and p-Cx43(Ser278/289), attenuating intercellular communication, was lower in IHH than in N. IHH also resulted in increased expression of protein kinase A and protein kinase G while casein kinase 1 did not change compared to N. In IHH group, which exhibited reduced incidence of ischemic ventricular arrhythmias, Cx43 and p-Cx43(Ser368) were more abundant at “end to end” gap junctions than in N group and this difference was preserved after acute regional ischemia (10 min). We further confirmed higher n-3 PUFA proportion in heart phospholipids after adaptation to IHH, which was even further increased by ischemia. Our results suggest that adaptation to IHH alters expression, phosphorylation and distribution of Cx43 as well as cardioprotective n-3PUFA proportion suggesting that the anti-arrhythmic phenotype elicited by IHH can be at least partly related to the stabilization of the “end to end” conductivity between cardiomyocytes during brief ischemia.
Trvalý link: http://hdl.handle.net/11104/0295928