Author Correction: Optical control of L-type Ca2+ channels using a diltiazem photoswitch
Timm Fehrentz1, Florian M E Huber2,3, Nina Hartrampf2
1Institute of Neural and Sensory Physiology, Medical Faculty, University of Düsseldorf, Düsseldorf, Germany. timm.fehrentz@gmail.com.
Nature Chemical Biology
|January 30, 2021
Abstract
No abstract available in PubMed .
Related Concept Videos
Antiarrhythmic Drugs: Class IV Agents as Calcium Channel Blockers
1.3K
Class IV antiarrhythmic drugs, such as verapamil and diltiazem, block calcium channels. They primarily affect the heart, slowing the conduction in calcium-dependent tissues like the SA and AV nodes. These drugs manage reentrant supraventricular tachycardia (SVT) and reduce ventricular rate in atrial flutter/fibrillation.
Verapamil, a calcium channel blocker, inhibits calcium movement across myocardial cell membranes and vascular smooth muscle. This results in the dilation of coronary and...
Verapamil, a calcium channel blocker, inhibits calcium movement across myocardial cell membranes and vascular smooth muscle. This results in the dilation of coronary and...
1.3K
Antihypertensive Drugs: Action of Calcium Channel Blockers
1.2K
Calcium ions are essential to contract smooth muscle cells in blood vessels. They enter these cells through voltage-dependent calcium channels, specifically L-type calcium channels in the cell membrane. These L-type calcium channels are integral to the excitation-contraction coupling process in smooth muscle. When a stimulus is received by smooth muscle cells, their membrane depolarizes. This alteration in membrane potential instigates the opening of L-type calcium channels. As a result,...
1.2K


