Subscribe to RSS
DOI: 10.1055/s-2005-870846
© Georg Thieme Verlag Stuttgart · New York
Ivabradin - Ein neues Prinzip zur Herzfrequenzsenkung
Ivabradine - A novel approach for heart rate loweringPublication History
eingereicht: 18.2.2005
akzeptiert: 19.5.2005
Publication Date:
08 June 2005 (online)

Zahlreiche epidemiologische Studien zeigen eine inverse Assoziation zwischen dem Überleben und der Herzfrequenz [5] [6] [7] [11]. Die Herzfrequenz ist maßgeblich am Herz-Minuten-Volumen und dem myokardialen Sauerstoff-Verbrauch beteiligt. Aus diesem Grund stellt die Kontrolle und Modulation der Herzfrequenz eine wichtige Anpassung an sich ändernde physiologische Bedingungen dar. Patienten mit chronischer Herzinsuffizienz entwickeln als Kompensationsmechanismus typischerweise eine Tachykardie. Bei Patienten mit stenosierender koronarer Herzerkrankung kommt es regelmäßig zu einem Missverhältnis zwischen Sauerstoff-Verbrauch und -Angebot. Diese koronare Insuffizienz führt zu Angina pectoris. Neben der interventionellen Behandlung stehen bei diesen Patienten zahlreiche medikamentöse Therapie-Möglichkeiten zur Verfügung.
Literatur
- 1
Bois P, Bescond J, Renaudon B, Lenfant J.
Mode of action of bradycardic agent, S 16257, on ionic currents of rabbit sinoatrial
node cells.
Br J Pharmacol.
1996;
118
1051-1057
MissingFormLabel
- 2
Borer J S, Fox K, Jaillon P, Lerebours G.
Antianginal and antiischemic effects of ivabradine, an I(f) inhibitor, in stable angina:
a randomized, double-blind, multicentered, placebo-controlled trial.
Circulation.
2003;
107
817-823
MissingFormLabel
- 3
Brown H F, DiFrancesco D, Noble S J.
How does adrenaline accelerate the heart?.
Nature.
1979;
280
235-236
MissingFormLabel
- 4
Er F, Larbig R, Ludwig A, Biel M, Hofmann F, Beuckelmann D J, Hoppe U C.
Dominant-negative suppression of HCN channels markedly reduces the native pacemaker
current I(f) and undermines spontaneous beating of neonatal cardiomyocytes.
Circulation.
2003;
107
485-489
MissingFormLabel
- 5
Gillum R F.
The epidemiology of resting heart rate in a national sample of men and women: associations
with hypertension, coronary heart disease, blood pressure, and other cardiovascular
risk factors.
Am Heart J.
1988;
116
163-174
MissingFormLabel
- 6
Goldberg R J, Larson M, Levy D.
Factors associated with survival to 75 years of age in middle-aged men and women.
The Framingham Study.
Arch Intern Med.
1996;
156
505-509
MissingFormLabel
- 7
Hjalmarson A, Gilpin E A, Kjekshus J, Schieman G, Nicod P, Henning H, Ross J, Jr.
Influence of heart rate on mortality after acute myocardial infarction.
Am J Cardiol.
1990;
65
547-553
MissingFormLabel
- 8
Hoppe U C, Beuckelmann D J.
Characterization of the hyperpolarization-activated inward current in isolated human
atrial myocytes.
Cardiovasc Res.
1998;
38
788-801
MissingFormLabel
- 9
Hoppe U C, Beuckelmann D J.
Modulation of the hyperpolarization-activated inward current (If) by antiarrhythmic
agents in isolated human atrial myocytes.
Naunyn Schmiedebergs Arch Pharmacol.
1998;
358
635-640
MissingFormLabel
- 10
Hoppe U C, Jansen E, Sudkamp M, Beuckelmann D J.
Hyperpolarization-activated inward current in ventricular myocytes from normal and
failing human hearts.
Circulation.
1998;
97
55-65
MissingFormLabel
- 11
Kjekshus J K.
Importance of heart rate in determining beta-blocker efficacy in acute and long-term
acute myocardial infarction intervention trials.
Am J Cardiol.
1986;
57
43F-49F
MissingFormLabel
- 12
Ludwig A, Zong X, Jeglitsch M, Hofmann F, Biel M.
A family of hyperpolarization-activated mammalian cation channels.
Nature.
1998;
393
587-591
MissingFormLabel
- 13
Manz M, Reuter M, Lauck G, Omran H, Jung W.
A single intravenous dose of ivabradine, a novel I(f) inhibitor, lowers heart rate
but does not depress left ventricular function in patients with left ventricular dysfunction.
Cardiology.
2003;
100
149-155
MissingFormLabel
- 14
Michels G, Er F, Khan I, Sudkamp M, Herzig S, Hoppe U C.
Single-channel properties support a potential contribution of hyperpolarization-activated
cyclic nucleotide-gated channels and If to cardiac arrhythmias.
Circulation.
2005;
111
399-404
MissingFormLabel
- 15
Monnet X, Ghaleh B, Colin P, de Curzon O P, Giudicelli J F, Berdeaux A.
Effects of heart rate reduction with ivabradine on exercise-induced myocardial ischemia
and stunning.
J Pharmacol Exp Ther.
2001;
299
1133-1139
MissingFormLabel
- 16
Mulder P, Barbier S, Chagraoui A, Richard V, Henry J P, Lallemand F, Renet S, Lerebours G, Mahlberg-Gaudin F, Thuillez C.
Long-term heart rate reduction induced by the selective I(f) current inhibitor ivabradine
improves left ventricular function and intrinsic myocardial structure in congestive
heart failure.
Circulation.
2004;
109
1674-1679
MissingFormLabel
- 17
Tardif J C FI, Tendera M, Fox K F.
Anti-anginal and anti-ischemic effects of the If current inhibitor ivabradine versus
atenolol in stable angina. A 4-month randomised, double-blind, multicenter trial.
Eur Heart J.
2003;
24
20
MissingFormLabel
- 18
Vilaine J P, Bidouard J P, Lesage L, Reure H, Peglion J L.
Anti-ischemic effects of ivabradine, a selective heart rate-reducing agent, in exercise-induced
myocardial ischemia in pigs.
J Cardiovasc Pharmacol.
2003;
42
688-696
MissingFormLabel
Priv.-Doz. Dr. med. Uta C. Hoppe
Klinik III für Innere Medizin der Universität zu Köln
Kerpener Straße 62
50937 Köln
Phone: 0221/4785059
Fax: 0221/4787929
Email: Uta.Hoppe@uni-koeln.de