| 영문 | receptor | 한글 | 수용체 |
|---|---|---|---|
| 설명 | 세포질내 또는 세포표면에 존재하는 분자구조로서 특이물질과 선택적으로 결합하며 결합에 의해 특이한 생리적 작용을 나타낸다. 펩티드호르몬, 신경전달물질, 항원, 보체, 면역글로불린에 대한 세포표면 수용체와 스테로이드에 대한 세포질내 수용체가 있다. |
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| 영문 | antihypertensive drug | 한글 | 고혈압약, 항고혈압제 |
|---|---|---|---|
| 설명 | 고혈압의 치료에 사용하며 높은 혈압을 낮추는 약물을 말한다. 고혈압약에는 혈관평활근에 직접 작용하여 이완시키는 혈관확장제(히드라라진), 교감신경의 활동을 어디선가 차단하는 약물(레세르핀, 메틸도파, 프로프라노롤), 이뇨제(프로세미드, 에타크린산)이 사용된다. |
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| 영문 | antimalarial drug | 한글 | 말라리아약, 항말라리아제 |
|---|---|---|---|
| 설명 | 말라리아 치료에 쓰는 약. 키니네, 클로로퀸, 프리마퀸 따위가 있다. 말라리아 원충의 발육주기에 대응해서 약물이 있으나 대부분은 병용요법에 따라서 말라리아 치료를 한다. 모기에 의한 포자체감염에 대한 항포자체 약은 독성 등의 문제가 있어서 아직 없다. 적혈구내에서의 환상체, 번식체에만 작용하는 것(항번식체 약은 클로로퀸, 피리메타민, 클로로구아나이드, 키니네)은 적혈구 외의 발육은 억제하지 않으므로 감염을 완전히 저지되지 않는다. 적혈구내외의 원충에 작용해 완전히 감염을 억제하는 것(파마킨, 펜타킨, 프리마킨), 혈중의 생식체를 죽이는 것(대부분의 항말라리아제)은 모기에 의한 타인으로의 전염원은 끊기는데 환자자신의 증상은 변화하지 않는다. |
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| 영문 | drug | 한글 | 약, 약물, 약제 |
|---|---|---|---|
| 설명 | 1. 병, 기타 병적 상태의 진단, 치료, 예방이나 고통의 경감, 또는 생리적, 병리적 상태를 호전시키는 것을 목적으로 사람 또는 동물에 투여되는 화합물. 약리학에서는 치료약만이 아니라, 생체에 주어졌을 때 어떠한 반응을 나타내는 화학물질 모두를 약물이라고 한다. 작용이 강하고 안전성이 낮은 순서로 독약-극약-보통약으로 구분하고 있다. 약물치료에 영향을 미치는 인자로서, 생체쪽 인자로는 개체차, 연령, 체중 등이 있고, 약물쪽 인자로서는 투여방법, 투여량, 병용되고 있는 다른 약물 등이 있다. 2. 약의 재료가 되는 물질. 3. 여러 가지 약재를 섞어 조제한 약. |
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| 영문 | drug resistance | 한글 | 약물내성 |
|---|---|---|---|
| 설명 | 1. 화학요법제나 항생물질의 어떤 일정 농도로 세균을 죽이거나 증식저해를 받는 것을 이 화학요법제나 항생물질에 감수성이 있다고 하는데, 이 감수성이 없게 된 생태를 저항성이라든가 내성이라고 말한다. 따라서 변이미생물의 약제에 대한 자항성이라든가 내성이라고 말한다. 2. 의약품을 계속 복용하면 점차 증량하지 않으면 효력이 나타나지 않는 성질. 이러한 때를 약제내성이 생겼다고 한다. 모든 미생물은 감수성을 가지는 약물에 의하여 사멸되지만, 소수의 것은 살아남아 그것이 진화됨으로써 사멸하지 않는 수가 있다. 또, 최초에는 감수성을 가지고 있던 균이 차차 내성균으로 되기도 한다. 많은 병원균은 감수성이 있는 의약품에 대하여 내성이 생긴다. 가장 고도의 내성균이 생기기 쉬운 것은 스트렙토마이신인데 결핵균과 그람음성균에 대하여 쉽게 내성이 생긴다. 페니실린이나 테트라시클린(아크로마이신) 등의 항생물질도 내성이 생기기 쉬우므로, 사용할 때는 적응을 잘 확인하여 필요량을 정하고 연용을 피한다. 같은 효과가 있는 다른 종류의 약제를 소량씩 2, 3종 병용하면 내성의 발생이 크게 억제된다는 것이 알려져 있다. 결핵약으로서 스트렙토마이신과 파스, 또는 이소니아지드를 병용하는 것 등이 그 예이다. |
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| DA | dark adaptation; dark agouti [rat]; daunomycin; degenerative arthritis; delayed action; Dental Assis... |
|---|---|
| DR | degeneration reaction; delivery room; deoxyribose; diabetic retinopathy; diagnostic radiology; digit... |
| ER | efficiency ratio; epigastric region; ejection rate; electroresection; emergency room; endoplasmic re... |
| RAR | rapidly adapting receptor; rat insulin receptor; retinoic acid receptor; right arm reclining; right ... |
| CD | cadaver donor; canine distemper; canine dose; carbohydrate dehydratase; carbon dioxide; cardiac dise... |
| ADAP | AIDS Drug Assistance Program |
|---|---|
| ADE | Adverse Drug Event |
| ADR | Adverse Drug Reaction |
| ADAMHA | Alcohol, Drug Abuse, and Mental Health Administration |
| AED | Antiepileptic drug |
| drug-drug interaction | The effects that occur when two or more drugs are used together. Such effects include changes of absorption in the digestive tract, changes in rate of the drugs' breakdown in the liver, new or enhanced side effects and changes in the drugs' activity. (09 Oct 1997) |
|---|---|
| acetylcholine receptor antibodies | <neurology, investigation> A test used to measure the amount of antibodies to acetylcholine receptors on nerve endings. This is a diagnostic test for myasthenia gravis. A normal value is no antibodies in the bloodstream. Acetylcholine receptor (AChR) binding autoantibodies (i.e. Antibodies reactive with several epitopes other than the binding site for acetylcholine or alpha-bungarotoxin) are present in approximately 88% of patients with generalised myasthenia gravis, 70% of ocular myasthenia and in approximately 80% of myasthenia gravis in remission. Although serum concentrations of AChR binding autoantibodies do not in general correlate well with severity of weakness, there is typical decrease in concentration as weakness improves with immunosuppressive therapy. AChR blocking autoantibodies (i.e., antibodies reactive with the AChR binding site) are present in about 50% of patients with myasthenia gravis, 30% with ocular myasthenia gravis and 20% of myasthenia gravis in remission, AChR blocking autoantibodies are the only AChR autoantibodies present in about 1% of myasthenia gravis. AChR modulating autoantibodies (i.e., autoantibodies which cross-link AChRs and cause their removal from muscle membrane surfaces) are present in more than 90% of myasthenia gravis and occasionally are the only AchR autoantibodies detectable in mild, recent onset or ocular-restricted myasthenia gravis. Results for AChR modulating autoantibodies can be transiently false-positive due to curare-like drugs used during general anesthesia. AChR autoantibodies of one or more types are found in at least 80% of ocular myasthenia gravis. Although generally absent in neurological conditions other than myasthenia gravis(and consequently unlikely to cause confusion in neurodiagnosis), false-positive results for AChR autoantibodies occasionally occur in primary biliary cirrhosis, tardive dyskinesia, autoimmune thyroiditis, the elderly, amyotrophic lateral sclerosis patients treated with cobra venom and patients with thymoma in the absence of myasthenia gravis. Approximately 1% of patients with rheumatoid arthritis treated with D-penicillamine develop AChR autoantibodies and myasthenia gravis, both of which disappear when the drug is discontinued. Babies born to ~10% of myasthenia gravis mothers have a transient neonatal form of myasthenia gravis that responds well to anticholinesterase therapy and usually remits within 1 month as maternal IgG disappears. (29 Dec 1997) |
| amino acid receptor | <biochemistry> Ligand gated ion channels with specific receptors for amino acid transmitters. An extended protein superfamily that also includes subunits of the nicotinic acetylcholine receptor. (18 Nov 1997) |
| AMPA receptor | <cell biology> Glutamate operated ion channel. See: excitatory amino acid receptor channels. (05 Feb 1998) |
| ANP receptor | <molecular biology> Family of 3 receptors for atrial natriuretic peptide. ANP A and ANP B have intracellular guanylate cyclase and protein kinase like domains. ANP C, shares the extracellular ligand binding and transmembrane domains, but lacks the functional intracellular domains and is not thought to be involved in signal transduction. (18 Nov 1997) |
| asialoglycoprotein receptor | A surface receptor found in hepatocytes that binds galactose-terminal glycoproteins; thus, this receptor removes those proteins from circulation and they are in turn acted upon by hepatocyte lysosomes. (05 Mar 2000) |
| auditory receptor cells | Columnar cell's in the epithelium of the organ of Corti, having hairs (stereocilia) on their apical ends. See: Corti's cells. (05 Mar 2000) |
| beta-adrenergic receptor blocking agent | 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) |
| beta-adrenergic receptor kinase | <enzyme> Cyclic-AMP protein kinase which specifically phosphorylates the agonist-occupied form of beta-adrenergic receptor Registry number: EC 2.7.1.- Synonym: beta-ar kinase, beta-adrenergic receptor kinase 1, g-protein-coupled receptor kinase 2, grk2 (kinase), beta-adrenergic receptor kinase 2, beta-ar kinase 2 (26 Jun 1999) |
| cAMP receptor protein | catabolite (gene) activator protein |
| GABA receptor | <physiology> Ligand gated chloride ion channel forming receptor opened by gamma aminobutyric acid. Two distinct types: A and B. A receptor: One of a family of neurotransmitter receptors with fast intrinsic ion channels that includes the glycine receptor and the nicotinic acetylcholine receptor. Distinct from another major receptor family, the muscarininc acetylcholine receptor and rhodopsin, with no intrinsic ion channel. The A receptor is specifically blocked by bicuculline. It consists of two pairs of protein chains forming an A2B2 complex, the A chains bind benzodiazepine and the B chains bind GABA. The 4 subunits are thought to form a tight group with the chloride channel in the middle. There is considerable similarity between the amino acid sequences of the receptor subunits and those of the nicotinic acetylcholine receptor suggesting that both receptors are derived from some evolutionary ancestor. See: amino acid receptor superfamily. B receptor: Brain receptor (80 kD) for the inhibitory neurotransmitter gamma amino butyric acid. Differs from the A receptor both in agonist specificity (baclofen is a specific agonist) and its effects on cells. It modulates intracellular calcium levels through a Go mediated effect on N type calcium channels and also lowers intracellular cAMP levels by an effect on adenylyl cyclase, thereby reducing the secretion of catecholamines. (05 Jan 1998) |
| p60 tumour necrosis factor receptor-associated kinase | <enzyme> Interacts with and causes phosphorylation of the cytoplasmic domain of the tnf receptor Registry number: EC 2.7.10.- Synonym: p60 tnf receptor-associated kinase, p60-trak (26 Jun 1999) |
| gamma aminobutyric acid receptor | <physiology> Ligand gated chloride ion channel forming receptor opened by gamma aminobutyric acid. Two distinct types: A and B. A receptor: One of a family of neurotransmitter receptors with fast intrinsic ion channels that includes the glycine receptor and the nicotinic acetylcholine receptor. Distinct from another major receptor family, the muscarininc acetylcholine receptor and rhodopsin, with no intrinsic ion channel. The A receptor is specifically blocked by bicuculline. It consists of two pairs of protein chains forming an A2B2 complex, the A chains bind benzodiazepine and the B chains bind GABA. The 4 subunits are thought to form a tight group with the chloride channel in the middle. There is considerable similarity between the amino acid sequences of the receptor subunits and those of the nicotinic acetylcholine receptor suggesting that both receptors are derived from some evolutionary ancestor. See: amino acid receptor superfamily. B receptor: Brain receptor (80 kD) for the inhibitory neurotransmitter gamma amino butyric acid. Differs from the A receptor both in agonist specificity (baclofen is a specific agonist) and its effects on cells. It modulates intracellular calcium levels through a Go mediated effect on N type calcium channels and also lowers intracellular cAMP levels by an effect on adenylyl cyclase, thereby reducing the secretion of catecholamines. (05 Jan 1998) |
| GAP-1 receptor tyrosine kinase | <enzyme> Similar to rasGTPase-activating proteins; inhibits signaling activity of let-60; amino acid sequence given in first source Registry number: EC 2.7.1.- Synonym: gap-1 gene product, gap-1 protein (26 Jun 1999) |
| gene rearrangement, alpha-chain T-cell antigen receptor | Ordered rearrangement of T-cell variable gene regions coding for the alpha-chain of antigen receptors. (12 Dec 1998) |
| drug receptor |
A protein-containing complex on a cell membrane that is capable of being stimulated by drugs in the extracellular fluid and translating that stimulation into an intracellular response. There may be thousands of such receptors on th
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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제품명 |
판매사 |
보험코드 | 성분/함량 | 구분/보험급여 |
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