| ECG | Electro-Cardio-Graphy(-Gram); ½ÉÀüµµ = EKG 1. Conducting System Structu... |
|---|---|
| ILR | interleukin receptor; irreversible loss rate |
| antag | antagonist |
| CA | anterior commissure [Lat. commissura anterior]; calcium antagonist; California [rabbit]; cancer; Can... |
| FAA | folic acid antagonist; formaldehyde, acetic acid, alcohol |
| ILR | irreversible loss rate |
|---|---|
| Ant | Antagonist |
| CA | calcium antagonist |
| GnRH-A | GnRH antagonist |
| H2-RA | Histamine-2 receptor antagonist |
| irreversible | Incapable of being reversed. (18 Nov 1997) |
|---|---|
| irreversible colloid | A colloid that is not again soluble in water after having been dried at ordinary temperature. Synonym: unstable colloid. (05 Mar 2000) |
| irreversible hydrocolloid | A hydrocolloid whose physical state is changed by an irreversible chemical reaction when water is added to a powder and an insoluble substance is formed. (05 Mar 2000) |
| irreversible process | <chemistry> Any real process, when a system undergoes the changes State 1 - greater than State 2 - greater than State 1 by any real pathway, the universe is different that before the cyclic process took place in the system. (09 Jan 1998) |
| irreversible reaction | A reaction or response by the tissues to a pathogenic agent characterised by a permanent pathologic change. (05 Mar 2000) |
| irreversible shock | Shock that has progressed beyond the stage when it will respond to transfusion or other form of treatment, and recovery is impossible. (05 Mar 2000) |
| aldosterone antagonist | An agent that opposes the action of the adrenal hormone aldosterone on renal tubular mineralocorticoid retention; these agents, e.g., spironolactone, are useful in treating the hypertension of primary hyperaldosteronism, or the sodium retention of secondary hyperaldosteronism. (05 Mar 2000) |
| antagonist | <pharmacology> A substance that tends to nullify the action of another, as a drug that binds to a cell receptor without eliciting a biological response. Origin: Gr. Antagonistes = an opponent (18 Nov 1997) |
| associated antagonist | One of two muscles or groups of muscles which pull in nearly opposite directions, but which, when acting together, move the part in a path between their diverging lines of action. (05 Mar 2000) |
| beta-adrenoreceptor antagonist | A class of drugs that compete with beta-adrenergic agonists for available receptor sites; some compete for both b1 and b2 receptors (e.g., propranolol) while others are primarily either b1 (e.g., metoprolol) or b2 blockers; used in the treatment of a variety of cardiovascular diseases where beta-adrenergic blockade is desirable. Synonym: beta-adrenergic receptor blocking agent, beta-adrenoreceptor antagonist, beta-blocker. (05 Mar 2000) |
| calcium antagonist | calcium channel-blocking agent |
| calcium channel antagonist | <pharmacology> A class of drugs that act by selective inhibition of calcium ion influx through or across cell membranes or on the release and binding of calcium in intracellular pools. Calcium channel blockers are used primarily in the treatment of certain heart conditions and stroke. As they are inducers of vascular and other smooth muscle relaxation, they are also used in the treatment of hypertension and cerebrovascular spasms, as myocardial protective agents, and in the relaxation of uterine spasms. Synonym: calcium antagonist, calcium channel-blocker, slow channel-blocking agent. (12 May 2002) |
| mixed opioid agonist-antagonist | <pharmacology> A compound that has an affinity for two or more types of opioid receptors and blocks opioid effects on one receptor type while producing opioid effects on a second receptor type. (13 Nov 1997) |
| competitive antagonist | An antimetabolite. (05 Mar 2000) |
| muscarinic antagonist | Drugs which bind with muscarinic cholinergic receptors but do not activate them, thus preventing access to acetylcholine; examples include atropine, scopolamine, propantheline, and pirenzepine. (05 Mar 2000) |
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