Search Page
The search found 11 results in 0.026 seconds.
Search results
-
Arrhythmias
The normal heart beats regularly at 60–100 beats per min (bpm), which is controlled by the sinoatrial (SA) node located in the right atrium. Tachycardia describes a heart that beats more rapidly (>100 bpm). Bradycardia describes a situation where the heart beats more slowly (<60 bpm). Electrical signals generated in the SA node travel through a conduction pathway in the wall of the atria (causing atrial contraction) before reaching and depolarising the AV node.
efaccena - 15/03/2022 - 12:40pm
-
Transporters as drug targets, and drug interactions
Monoamine reuptake transporters
efaccena - 21/03/2016 - 1:57pm
-
Anti-arrhythmic drugs
Antiarrhythmic drugs are a group of pharmaceuticals that are used to suppress abnormal rhythms of the heart (cardiac arrhythmias), such as atrial fibrillation, atrial flutter, ventricular tachycardia, and ventricular fibrillation.
Class I antiarrhythmics interfere with sodium channel function, and are subdivided by the effect they have on the action potential (AP)- see figure below

smaxwell - 10/10/2014 - 9:04am
-
Calcium channel blocking drugs
Calcium-channel blockers (CCBs) are prescribed to treat hypertension. These drugs interfere with the inward movement of calcium ions through the slow channels on the membranes of myocardial cells, AV node cells and vascular smooth muscle cells. The overall effect is to reduce myocardial contractility, formation and propagation of electrical impulses within the heart, and vascular tone.
There is a wide variety of CCB medications available to prescribers, including single agent medicines and fixed-dose combination drugs.
smaxwell - 10/10/2014 - 9:08am
-
Ischemic heart disease
Oxygen demand of the heart dynamically changes, and the coronary artery can adjust its blood flow to fulfill the myocardial oxygen demand (coronary blood flow reserve). Normally, the oxygen supply and the oxygen demand are well balanced in healthy subjects. When the oxygen supply to the heart becomes inadequate for the needs of the heart, myocardial ischemia occurs. That is, ischemic heart disease (IHD) is caused by an imbalance between the oxygen supply (coronary blood flow) and the oxygen demand of the heart.
efaccena - 13/02/2018 - 10:14am
-
Voltage-gated ion channels
Voltage-gated ion channels (VGICs) are responsive to changes in the local electrical membrane potential, and are critical for the function of excitable cells, such as neurons and muscle cells. VGICs are ion-selective, with separate channels identified for each of the major physiological ions- Na+, K+, Ca2+, Cl-. Each type of channel is a multimeric complex of subunits encoded by a number of genes. Subunit combinations vary in different tissues, with each combination having distinctive voltage dependence and cellular localization.
efaccena - 24/02/2016 - 3:26pm
-
Beta-adrenoceptor blocking drugs
Beta blockers, also known as beta-adrenoceptor blocking agents, are pharmaceutical agents that act as competitive antagonists of the β-adrenoceptors, which are activated by the endogenous catecholamines epinephrine (adrenaline) and norepinephrine (noradrenaline), of the sympathetic nervous system.
smaxwell - 10/10/2014 - 9:04am
-
Positive inotropic drugs: Cardiac glycosides (digoxin)
-
Drug metabolizing enzymes
Cytochrome P450 enzymes are the main drug metabolising enzymes (xenobiotic inactivators) in humans, and these are the primary contributors to Phase I oxidative metabolism of drugs and other chemicals.
efaccena - 08/03/2016 - 9:21am
-
Other ion channels
Other ion channel families include the aquaporins (which also includes aquaglyceroporins), a family of chloride channels which includes the cystic fibrosis transmembrane conductance regulator (CFTR), the connexins and pannexins
efaccena - 01/03/2016 - 10:15am
