Kv1.3 channels facilitate the connection between metabolism and blood flow in the heart.

Autor: Ohanyan V; Department of Integrative Medical Sciences, Northeast Ohio Medical University, Rootstown, OH, USA., Yin L; Department of Integrative Medical Sciences, Northeast Ohio Medical University, Rootstown, OH, USA., Bardakjian R; Aultman Hospital, Canton, OH, USA., Kolz C; Department of Integrative Medical Sciences, Northeast Ohio Medical University, Rootstown, OH, USA., Enrick M; Department of Integrative Medical Sciences, Northeast Ohio Medical University, Rootstown, OH, USA., Hakobyan T; Department of Integrative Medical Sciences, Northeast Ohio Medical University, Rootstown, OH, USA., Luli J; Department of Integrative Medical Sciences, Northeast Ohio Medical University, Rootstown, OH, USA., Graham K; Department of Integrative Medical Sciences, Northeast Ohio Medical University, Rootstown, OH, USA., Khayata M; Cleveland Clinic Akron General, Akron, OH, USA., Logan S; Department of Integrative Medical Sciences, Northeast Ohio Medical University, Rootstown, OH, USA., Kmetz J; Department of Integrative Medical Sciences, Northeast Ohio Medical University, Rootstown, OH, USA., Chilian WM; Department of Integrative Medical Sciences, Northeast Ohio Medical University, Rootstown, OH, USA.
Jazyk: angličtina
Zdroj: Microcirculation (New York, N.Y. : 1994) [Microcirculation] 2017 May; Vol. 24 (4).
DOI: 10.1111/micc.12334
Abstrakt: The connection between metabolism and flow in the heart, metabolic dilation, is essential for cardiac function. We recently found redox-sensitive Kv1.5 channels play a role in coronary metabolic dilation; however, more than one ion channel likely plays a role in this process as animals null for these channels still showed limited coronary metabolic dilation. Accordingly, we examined the role of another Kv1 family channel, the energetically linked Kv1.3 channel, in coronary metabolic dilation. We measured myocardial blood flow (contrast echocardiography) during norepinephrine-induced increases in cardiac work (heart rate x mean arterial pressure) in WT, WT mice given correolide (preferential Kv1.3 antagonist), and Kv1.3-null mice (Kv1.3 -/- ). We also measured relaxation of isolated small arteries mounted in a myograph. During increased cardiac work, myocardial blood flow was attenuated in Kv1.3 -/- and in correolide-treated mice. In isolated vessels from Kv1.3 -/- mice, relaxation to H 2 O 2 was impaired (vs WT), but responses to adenosine and acetylcholine were equivalent to WT. Correolide reduced dilation to adenosine and acetylcholine in WT and Kv1.3 -/- , but had no effect on H 2 O 2 -dependent dilation in vessels from Kv1.3 -/- mice. We conclude that Kv1.3 channels participate in the connection between myocardial blood flow and cardiac metabolism.
(© 2016 John Wiley & Sons Ltd.)
Databáze: MEDLINE
Externí odkaz:
Nepřihlášeným uživatelům se plný text nezobrazuje