|
|
||||||||
Department of Medicine, University of Calgary, Calgary, Alberta, Canada T2N 4N1
Developmental changes in electrocardiogram (ECG) and
response to selective K+ channel
blockers were assessed in conscious, unsedated neonatal (days 1, 7, 14) and adult male mice
(>60 days of age). Mean sinus R-R interval decreased from 120 ± 3 ms in day 1 to 110 ± 3 ms in
day 7, 97 ± 3 ms in
day 14, and 81 ± 1 ms in adult
mice (P < 0.001 by ANOVA; all 3 groups different from day 1). In
parallel, the mean P-R interval progressively decreased during
development. Similarly, the mean Q-T interval decreased from 62 ± 2 ms in day 1 to 50 ± 2 ms in
day 7, 47 ± 8 ms in
day 14 neonatal mice, and 46 ± 2 ms in adult mice (P < 0.001 by
ANOVA; all 3 groups are significantly different from
day 1).
Q-Tc was calculated as
Q-
interval.
Q-Tc significantly shortened from
179 ± 4 ms in day 1 to 149 ± 5 ms in day 7 mice
(P < 0.001). In addition, the J junction-S-T segment elevation observed in day
1 neonatal mice resolved by day
14. Dofetilide (0.5 mg/kg), the selective blocker of
the rapid component of the delayed rectifier
(IKr) abolished S-T segment elevation and prolonged Q-T and
Q-Tc intervals in day 1 neonates but not in adult mice.
In contrast, 4-aminopyridine (4-AP, 2.5 mg/kg) had no effect on
day 1 neonates but in adults prolonged
Q-T and Q-Tc intervals and
specifically decreased the amplitude of a transiently repolarizing
wave, which appears as an r' wave at the end of the apparent QRS
in adult mice. In conclusion, ECG intervals and configuration change
during normal postnatal development in the mouse.
K+ channel blockers affect the
mouse ECG differently depending on age. These data are consistent with
the previous findings that the dofetilide-sensitive
IKr is dominant
in day 1 mice, whereas 4-AP-sensitive
currents, the transiently repolarizing
K+ current, and the rapidly
activating, slowly inactivating K+
current are the dominant K+
currents in adult mice. This study provides background information useful for assessing abnormal development in transgenic mice.
mouse heart; development
This article has been cited by other articles:
![]() |
J. Guo, S. Zhan, J. Somers, R. E. Westenbroek, W. A. Catterall, D. E. Roach, R. S. Sheldon, J. P. Lees-Miller, P. Li, Y. Shimoni, et al. Decrease in density of INa is in the common final pathway to heart block in murine hearts overexpressing calcineurin Am J Physiol Heart Circ Physiol, December 1, 2006; 291(6): H2669 - H2679. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. Kim, K. M. Boyle, and J. L. Carroll Postnatal development of E-4031-sensitive potassium current in rat carotid chemoreceptor cells J Appl Physiol, April 1, 2005; 98(4): 1469 - 1477. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. M. Gillis, K. M. Kavanagh, H. J. Mathison, J. R. Somers, S. Zhan, and H. J. Duff Heart block in mice overexpressing calcineurin but not NF-AT3 Cardiovasc Res, December 1, 2004; 64(3): 488 - 495. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. C. Knollmann, M. C. Casimiro, A. N. Katchman, S. G. Sirenko, T. Schober, Q. Rong, K. Pfeifer, and S. N. Ebert Isoproterenol Exacerbates a Long QT Phenotype in Kcnq1-Deficient Neonatal Mice: Possible Roles for Human-Like Kcnq1 Isoform 1 and Slow Delayed Rectifier K+ Current J. Pharmacol. Exp. Ther., July 1, 2004; 310(1): 311 - 318. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Liu, J. B. Iden, K. Kovithavongs, R. Gulamhusein, H. J. Duff, and K. M. Kavanagh In vivo temporal and spatial distribution of depolarization and repolarization and the illusive murine T wave J. Physiol., February 15, 2004; 555(1): 267 - 279. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Tiemann, D. Weyer, P. C. Djoufack, A. Ghanem, T. Lewalter, U. Dreiner, R. Meyer, C. Grohe, and K. B. Fink Increasing myocardial contraction and blood pressure in C57BL/6 mice during early postnatal development Am J Physiol Heart Circ Physiol, February 1, 2003; 284(2): H464 - H474. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Lande, S. Demolombe, A. Bammert, A. Moorman, F. Charpentier, and D. Escande Transgenic mice overexpressing human KvLQT1 dominant-negative isoform Part II: Pharmacological profile Cardiovasc Res, May 1, 2001; 50(2): 328 - 334. [Abstract] [Full Text] [PDF] |
||||
![]() |
W. Guo, H. Li, B. London, and J. M. Nerbonne Functional Consequences of Elimination of Ito, f and Ito, s : Early Afterdepolarizations, Atrioventricular Block, and Ventricular Arrhythmias in Mice Lacking Kv1.4 and Expressing a Dominant-Negative Kv4 {alpha} Subunit Circ. Res., July 7, 2000; 87(1): 73 - 79. [Abstract] [Full Text] [PDF] |
||||
![]() |
D. Vaidya, H. S. Tamaddon, C. W. Lo, S. M. Taffet, M. Delmar, G. E. Morley, and J. Jalife Null Mutation of Connexin43 Causes Slow Propagation of Ventricular Activation in the Late Stages of Mouse Embryonic Development Circ. Res., June 8, 2001; 88(11): 1196 - 1202. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |