A direct negative inotropic effect of acetylcholine on rat ventricular myocytes
S. O. McMorn, S. M. Harrison, W. J. Zang, X. J. Yu and M. R. Boyett Department of Physiology, University of Leeds, United Kingdom. Acetylcholine (ACh) decreased the contraction of rat ventricular cells within 20 s. ACh (3.1 x 10(-8) M) produced a half-maximal effect and 10(-6) M ACh produced a maxim...
Gespeichert in:
Veröffentlicht in: | American journal of physiology. Heart and circulatory physiology 1993-10, Vol.265 (4), p.H1393-H1400 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | S. O. McMorn, S. M. Harrison, W. J. Zang, X. J. Yu and M. R. Boyett
Department of Physiology, University of Leeds, United Kingdom.
Acetylcholine (ACh) decreased the contraction of rat ventricular cells
within 20 s. ACh (3.1 x 10(-8) M) produced a half-maximal effect and 10(-6)
M ACh produced a maximal effect (a 23.8 +/- 5.4% decrease; mean +/- SE, n =
11). During a 3-min exposure to ACh, the inotropic effect faded. Parallel
changes were observed in action potential duration: ACh caused an immediate
shortening of the action potential, but then the effect faded with time.
The changes in action potential duration were the cause of the changes in
contraction, because ACh had no effect on contraction when the contractions
were triggered by voltage-clamp pulses of constant duration. The changes in
action potential duration were the result of the activation of a K+ current
(iK,ACh) by ACh. During an exposure to ACh, this current faded as a result
of desensitization. iK,ACh was 6.3 times smaller in ventricular than in
atrial cells. This may explain why the negative inotropic effect of ACh on
atrial cells was greater: 1.0 x 10(-8) M ACh produced a half-maximal effect
on atrial cells, and 10(-6) M ACh produced a near maximal effect (a 74.5
+/- 9.5% decrease; n = 4). |
---|---|
ISSN: | 0363-6135 0002-9513 1522-1539 |
DOI: | 10.1152/ajpheart.1993.265.4.H1393 |