In:
Clinical and Experimental Pharmacology and Physiology, Wiley, Vol. 35, No. 12 ( 2008-12), p. 1465-1470
Abstract:
Ketamine is widely used for the induction of anaesthesia in high‐risk patients with cardiovascular instability or severe hypovolaemia. However, the ionic mechanisms involved in the effects of ketamine at therapeutically relevant concentrations in human cardiac myocytes are unclear. The present study was designed to investigate the effects of ketamine on L‐type Ca 2+ (I Ca ), transient outward K + (I to ), ultra‐rapid delayed rectifier K + (I Kur ) and inward rectifier potassium (I K1 ) currents, as well as on action potentials, in human isolated atrial myocytes. Atrial myocytes were isolated enzymatically from specimens of human atrial appendage obtained from patients undergoing coronary artery bypass grafting. The action potential and membrane currents were recorded in both current‐ and voltage‐clamp modes using the patch‐clamp technique. Ketamine inhibited I Ca with an IC 50 of 1.8 µmol/L. In addition, 10 µmol/L ketamine decreased the I Ca peak current at +10 mV from 5.1 ± 0.3 to 2.1 ± 0.4 pA/pF ( P 〈 0.01), but did not change the threshold potential, peak current potential and reverse potential. Ketamine had no effect on I to , I Kur or I K1 , but it reversibly shortened the duration of the action potential in human atrial myocytes. In conclusion, ketamine, at a clinically relevant concentration, shortens the action potential duration of the human atrial myocytes, probably by inhibiting I Ca .
Type of Medium:
Online Resource
ISSN:
0305-1870
,
1440-1681
DOI:
10.1111/cep.2008.35.issue-12
DOI:
10.1111/j.1440-1681.2008.05012.x
Language:
English
Publisher:
Wiley
Publication Date:
2008
detail.hit.zdb_id:
2020033-X
SSG:
15,3
