Calcium Channel Blockers
β Scribed by ThΓ©ophile Godfraind (auth.)
- Publisher
- BirkhΓ€user Basel
- Year
- 2004
- Tongue
- English
- Leaves
- 268
- Series
- Milestones in Drug Therapy
- Edition
- 1
- Category
- Library
No coin nor oath required. For personal study only.
β¦ Synopsis
The drugs named calcium channel blockers (CCBs) were initially termed calΒ cium antagonists (see Chapter 1). They are also designated as calcium entry blockers (CEBs), calcium blockers, calcium channel antagonists, calcium channel inhibitors (and in French anticalciques). As this is reported in several chapters of this book, their main effect is a blockade of calcium entry into cells through voltage operated calcium channels (VOCCs). Chemically related drugs, such as Bay K 8644, exert the opposite effect by increasing the probaΒ bility of calcium channel opening. One of the subcommittees of the Nomenclature Committee (NC-IUPAR) of the International Union of Pharmacology has been devoted to the classification of calcium channels and the site of action of drugs modifying channel function. The members of this Committee are noted for their significant contribution to the field (Tab. 1). A report has been published in 1992 in Pharmacological Reviews [3]. A list of criteria was approved for the identification of distinct drug binding 2 sites on Ca + channels. It included: (a) the demonstration of a stereoselective binding site supported by drug interaction studies (competition with other drugs, non-competitive interactions with other sites, reversal of inhibitory effects by channel activators); (b) demonstration of the electrophysiologieal effects of the drug and selectivity of action compared to other sites; (c) deterΒ mination of the affinity for the type and subtype of ion channel. These criteria have identified different classes of Ca antagonists (see Chapter 2).
β¦ Table of Contents
Front Matter....Pages I-XIV
Historical perspective: from early steps on calcium research to the identification of calcium antagonist prototypes and of the signaling functions of Ca 2+ ....Pages 1-9
Calcium channel blockers and calcium channels....Pages 11-80
The action of calcium antagonists on Ca 2+ movements in isolated vessels....Pages 81-112
The tissue selectivity of calcium antagonists....Pages 113-129
Acute haemodynamic effects of calcium channel blockers....Pages 131-149
Calcium channels and regulation of vascular tone in hypertension....Pages 151-159
Long-term effects of calcium antagonists....Pages 161-179
Blood pressure-independent effects of calcium antagonists....Pages 181-197
From early clinical studies to randomized controlled clinical trials....Pages 199-236
Beyond the cardiovascular system....Pages 237-254
Back Matter....Pages 255-262
β¦ Subjects
Pharmacology/Toxicology; Cardiology
π SIMILAR VOLUMES
In March 2001, the National Institutes of Health issued the following warning: ''The number of Web sites offering health-related resources grows every day. Many sites provide valuable information, while others may have information that is unreliable or misleading.'' Furthermore, because of the rapi
Potassium channels are the most widely distributed type of ion channel and are found in virtually all living organisms. They form potassium-selective pores that span cell membranes, and are found in most cell types and control a wide variety of cell functions. This book presents current research in
<p>Voltage-gated calcium channels are critical regulators of cytoplasmic levels of calcium, the universal signaling ion. As such, calcium channels trigger a wide range of cellular functions, from muscle contraction to neurotransmitter secretion, and are important players in human disease. Prominent
<p>oltage-gated calcium channels are essential mediators of a range of physiological functions, including the communication between nerve Vcells, the regulation of heart beat, muscle contraction, and secretion of hormones such as insulin. Consequently, these channels are critical pharΒ macological t