Book contents
- Pharmacology for Anaesthesia and Intensive Care
- Pharmacology for Anaesthesia and Intensive Care
- Copyright page
- Contents
- Preface
- Foreword
- Section I Basic Principles
- Section II Core Drugs in Anaesthetic Practice
- Section III Cardiovascular Drugs
- Chapter 13 Sympathomimetics
- Chapter 14 Adrenoceptor Antagonists
- Chapter 15 Anti-Arrhythmics
- Chapter 16 Vasodilators
- Chapter 17 Antihypertensives
- Section IV Other Important Drugs
- Index
Chapter 15 - Anti-Arrhythmics
from Section III - Cardiovascular Drugs
Published online by Cambridge University Press: 26 February 2021
- Pharmacology for Anaesthesia and Intensive Care
- Pharmacology for Anaesthesia and Intensive Care
- Copyright page
- Contents
- Preface
- Foreword
- Section I Basic Principles
- Section II Core Drugs in Anaesthetic Practice
- Section III Cardiovascular Drugs
- Chapter 13 Sympathomimetics
- Chapter 14 Adrenoceptor Antagonists
- Chapter 15 Anti-Arrhythmics
- Chapter 16 Vasodilators
- Chapter 17 Antihypertensives
- Section IV Other Important Drugs
- Index
Summary
The heart is composed of pacemaker, conducting and contractile tissue. Each has a different action potential morphology allowing the heart to function as a coordinated unit.
The sino-atrial (SA) node is in the right atrium, and of all cardiac tissue it has the fastest rate of spontaneous depolarisation so that it sets the heart rate. The slow spontaneous depolarisation (pre-potential or pacemaker potential) of the membrane potential is due to increased Ca2+ conductance (directed inward). At −40 mV, slow voltage-gated Ca2+ channels (L channels) open, resulting in membrane depolarisation. Na+ conductance changes very little. Repolarisation is due to increased K+ conductance while Ca2+ channels close (see Figure 15.1a).
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- Information
- Pharmacology for Anaesthesia and Intensive Care , pp. 217 - 232Publisher: Cambridge University PressPrint publication year: 2021