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Sökning: WFRF:(Adler Robert) > (2020-2024) > Effect of selective...

Effect of selective IK,ACh inhibition by XAF-1407 in an equine model of tachypacing-induced persistent atrial fibrillation

Fenner, Merle Friederike (författare)
University of Copenhagen
Carstensen, Helena (författare)
University of Copenhagen
Dalgas Nissen, Sarah (författare)
University of Copenhagen
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Melis Hesselkilde, Eva (författare)
University of Copenhagen
Scott Lunddahl, Christine (författare)
University of Copenhagen
Adler Hess Jensen, Maja (författare)
University of Copenhagen
Loft-Andersen, Ameli Victoria (författare)
University of Copenhagen
Sattler, Stefan Michael (författare)
University Hospital Munich,Copenhagen University Hospital,Ludwig-Maximilian University of Munich
Platonov, Pyotr (författare)
Lund University,Lunds universitet,Electrocardiology Research Group - CIEL,Forskargrupper vid Lunds universitet,Lund University Research Groups,Skåne University Hospital
El-Haou, Said (författare)
Xention Ltd
Jackson, Claire (författare)
Xention Ltd
Tang, Raymond (författare)
Xention Ltd
Kirby, Robert (författare)
Xention Ltd
Ford, John (författare)
Xention Ltd
Schotten, Ulrich (författare)
Maastricht University
Milnes, James (författare)
Xention Ltd
Svane Sørensen, Ulrik (författare)
Acesion Pharma
Jespersen, Thomas (författare)
University of Copenhagen
Buhl, Rikke (författare)
University of Copenhagen
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 (creator_code:org_t)
2020-06-24
2020
Engelska 17 s.
Ingår i: British Journal of Pharmacology. - : Wiley. - 0007-1188 .- 1476-5381. ; 177:16, s. 3778-3794
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Background and Purpose: Inhibition of the G-protein gated ACh-activated inward rectifier potassium current, IK,ACh may be an effective atrial selective treatment strategy for atrial fibrillation (AF). Therefore, the anti-arrhythmic and electrophysiological properties of a novel putatively potent and highly specific IK,ACh inhibitor, XAF-1407 (3-methyl-1-[5-phenyl-4-[4-(2-pyrrolidin-1-ylethoxymethyl)-1-piperidyl]thieno[2,3-d]pyrimidin-6-yl]azetidin-3-ol), were characterised for the first time in vitro and investigated in horses with persistent AF. Experimental Approach: The pharmacological ion channel profile of XAF-1407 was investigated using cell lines expressing relevant ion channels. In addition, eleven horses were implanted with implantable cardioverter defibrillators enabling atrial tachypacing into self-sustained AF. The electrophysiological effects of XAF-1407 were investigated after serial cardioversions over a period of 1 month. Cardioversion success, drug-induced changes of atrial tissue refractoriness, and ventricular electrophysiology were assessed at baseline (day 0) and days 3, 5, 11, 17, and 29 after AF induction. Key Results: XAF-1407 potently and selectively inhibited Kir3.1/3.4 and Kir3.4/3.4, underlying the IK,ACh current. XAF-1407 treatment in horses prolonged atrial effective refractory period as well as decreased atrial fibrillatory rate significantly (~20%) and successfully cardioverted AF, although with a decreasing efficacy over time. XAF-1407 shortened atrioventricular-nodal refractoriness, without effect on QRS duration. QTc prolongation (4%) within 15 min of drug infusion was observed, however, without any evidence of ventricular arrhythmia. Conclusion and Implications: XAF-1407 efficiently cardioverted sustained tachypacing-induced AF of short duration in horses without notable side effects. This supports IK,ACh inhibition as a potentially safe treatment of paroxysmal AF in horses, suggesting potential clinical value for other species including humans.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Farmakologi och toxikologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Pharmacology and Toxicology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kardiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cardiac and Cardiovascular Systems (hsv//eng)

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