| 영문 | iodine uptake | 한글 | 요오드 섭취 |
|---|---|---|---|
| 설명 | 소량의 131I를 경구 투여 후 2, 6, 12, 24시간 등 일정한 시간 경과 후 갑상샘에서의 섭취율을 측정하는 것으로 전반적 갑상샘 기능 상태를 측정하는 검사법이다. |
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| MAOI | MonoAmine Oxidase Inhibitors |
|---|---|
| ADRA1C | alpha-1C-adrenergic receptor |
| ADRBK | beta-1-adrenergic receptor kinase |
| ADRBR | adrenergic beta-receptor |
| ARB | adrenergic receptor binder |
| SSRI | Specific serotonin re-uptake inhibitors |
|---|---|
| Uptake-1 | uptake |
| AChE-I | acetylcholine esterase inhibitors |
| ChEI | Cholinesterase inhibitors |
| IAPs | Inhibitors of apoptosis |
| adrenergic uptake inhibitors | Drugs that block the transport of adrenergic transmitters into axon terminals or into storage vesicles within terminals. The tricyclic antidepressants (antidepressive agents, tricyclic) and amphetamines are among the therapeutically important drugs that may act via inhibition of adrenergic transport. Many of these drugs also block transport of serotonin. (12 Dec 1998) |
|---|
| serotonin uptake inhibitors | Compounds that specifically inhibit the reuptake of serotonin in the brain. This increases the serotonin concentration in the synaptic cleft which then activates serotonin receptors to a greater extent. These agents have been used in treatment of depression, panic disorder, obsessive-compulsive behaviour, and alcoholism, as analgesics, and to treat obesity and bulimia. Many of the adrenergic uptake inhibitors also inhibit serotonin uptake; they are not included here. (12 Dec 1998) |
|---|---|
| neurotransmitter uptake inhibitors | Drugs that inhibit the transport of neurotransmitters into axon terminals or into storage vesicles within terminals. For many transmitters, uptake determines the time course of transmitter action so inhibiting uptake prolongs the activity of the transmitter. Blocking uptake may also deplete available transmitter stores. Many clinically important drugs are uptake inhibitors although the indirect reactions of the brain rather than the acute block of uptake itself is often responsible for the therapeutic effects. (12 Dec 1998) |
| dopamine uptake inhibitors | Drugs that block the transport of dopamine into axon terminals or into storage vesicles within terminals. most of the adrenergic uptake inhibitors also inhibit dopamine uptake. (12 Dec 1998) |
| Amine Precursor Uptake and Decarboxylation | <pharmacology, physiology> Paracrine cells of which argentaffin cells are an example. Usage of the term APUD is neither helpful nor memorable. Acronym: APUD (11 Nov 1997) |
| gallium uptake with normal chest film | <radiology> Pulmonary drug toxicity, tumour infiltration, sarcoidosis, pneumocystis carinii see: lung: gallium imaging (12 Dec 1998) |
| radioactive iodide uptake test | A test of thyroid function in which 131I-iodide is given orally; after 24 hours, the amount present in the thyroid gland is measured and compared with normal values. Synonym: radioactive iodide uptake test, RAI test. (05 Mar 2000) |
| iodine uptake test | A test of thyroid function in which 131I-iodide is given orally; after 24 hours, the amount present in the thyroid gland is measured and compared with normal values. Synonym: radioactive iodide uptake test, RAI test. (05 Mar 2000) |
| T3 uptake test | A test of thyroid function in which triiodothyronine (T3) is added to a patient's serum in vitro to measure the relative affinities of serum proteins and of an added competitive substance for T3; higher T3 uptakes are associated with hyperthyroidism. Synonym: T3 uptake test. (05 Mar 2000) |
| triiodothyronine uptake test | A test of thyroid function in which triiodothyronine (T3) is added to a patient's serum in vitro to measure the relative affinities of serum proteins and of an added competitive substance for T3; higher T3 uptakes are associated with hyperthyroidism. Synonym: T3 uptake test. (05 Mar 2000) |
| uptake | The absorption by a tissue of some substance, food material, mineral, etc. And its permanent or temporary retention. (05 Mar 2000) |
| uptake hydrogenase | <enzyme> Isolated from heterocysts of aerobically grown anabena filaments; also from rhodobacter capsulatus; belongs to the class of nife hydrogenases; allows the cell to grow autographically with h(2) as the electron source; isolated as a heterodimer comprising a small and large subunit; has been sequenced Registry number: EC 1.12.- Synonym: h2-oxidizing(uptake) hydrogenase, hydrogenase II, h2-uptake hydrogenase (26 Jun 1999) |
| blood coagulation factor inhibitors | Substances, usually endogenous, that act as inhibitors of blood coagulation. They may affect one or multiple enzymes throughout the process. As a group, they also inhibit enzymes involved in processes other than blood coagulation, such as those from the complement system, fibrinolytic enzyme system, blood cells, and bacteria. (12 Dec 1998) |
| Bowman Birk protease inhibitors | <pharmacology> Family of serine protease inhibitors found in seeds of leguminous plants and cereals. (18 Nov 1997) |
| carbonic anhydrase inhibitors | A class of compounds that reduces the secretion of h+ ions by the proximal kidney tubule through inhibition of carbonic anhydrase (carbonate dehydratase). Although their therapeutic use as diuretics is not frequent, they are used in clinical conditions where alkalinization of the urine is beneficial. Their most frequent application is in the reduction of intra-ocular pressure in the treatment of glaucoma. (12 Dec 1998) |
| reverse transcriptase inhibitors | Inhibitors of reverse transcriptase (RNA-directed DNA polymerase), an enzyme that synthesises DNA on an RNA template. (12 Dec 1998) |
Synonyms : Inhibitors, Adrenergic Reuptake, Inhibitors, Adrenergic Uptake, Reuptake Inhibitors, Adrenergic, Uptake Inhibitors, Adrenergic
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|
제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
|---|