WordNet
- the 3rd letter of the Roman alphabet (同)c
- (music) the keynote of the scale of C major
- a general-purpose programing language closely associated with the UNIX operating system
PrepTutorEJDIC
- carbonの化学記号
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2015/01/02 17:01:15」(JST)
[Wiki ja表示]
化学受容器引き金帯(かがくじゅようきひきがねたい、英:chemoreceptor trigger zone, CTZ)とは第4脳室に接する脳幹領域に存在する受容器。血中のある種の薬物や毒物に反応して嘔吐中枢に刺激を送り、嘔吐を誘発する。ドパミンD2受容体、5-HT3受容体、ムスカリンM1受容体などがある。
関連項目
参考文献
- 高橋迪雄監訳 『獣医生理学 第2版』 文永堂出版 2000年 ISBN 4830031824
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この項目は、生物学に関連した書きかけの項目です。この項目を加筆・訂正などしてくださる協力者を求めています(プロジェクト:生命科学/Portal:生物学)。 |
[Wiki en表示]
CTZ may refer to:
- Chemoreceptor trigger zone in neuroscience
- CTZ is the ICAO airline designator for CATA Línea Aérea, Argentina
- CTZ is the IATA airport code for Sampson County Airport, United States
- CTZ is the United States Federal Aviation Administration location identifier for Sampson County Airport
- Chelyabinsk Tractor Plant, Russia
- cyclothiazide, a positive allosteric modulator of the AMPA receptor
- Combat Tactical Zone
- Central Time Zone
- Count trailing zeros, a bit operation
UpToDate Contents
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English Journal
- Bioavailability of the imidazole antifungal agent clotrimazole and its effects on key biotransformation genes in the common carp (Cyprinus carpio).
- Corcoran J1, Lange A2, Cumming RI3, Owen SF3, Ball JS3, Tyler CR2, Winter MJ3.Author information 1University of Exeter, Biosciences, College of Life & Environmental Sciences, Exeter, UK. Electronic address: j.f.corcoran@exeter.ac.uk.2University of Exeter, Biosciences, College of Life & Environmental Sciences, Exeter, UK.3AstraZeneca Safety, Health and Environment, Brixham Environmental Laboratory, Freshwater Quarry, Brixham, UK.AbstractClotrimazole (CTZ) is a persistent imidazole antifungal agent which is frequently detected in the aquatic environment and predicted to bio-concentrate in fish. Common carp (Cyprinus carpio) were exposed to mean measured concentrations of either 1.02 or 14.63μgl-1 CTZ for 4 and 10 days, followed by a depuration period of 4 days in a further group of animals. Following each exposure regimen, plasma and liver CTZ concentrations were measured. Mean measured plasma concentrations of CTZ in animals exposed to the lower concentration of CTZ were 30 and 44μgl-1 on days 4 and 10, respectively, and in the higher concentration were 318 and 336μgl-1. Mean measured liver levels in the same animals were 514, 1725, 2111 and 7017μgl-1 suggesting progressive hepatic accumulation. Measurement of CTZ in plasma after depuration suggested efficient elimination within 4 days, but appreciable levels of CTZ remained in the liver after depuration suggesting a degree of persistence in this tissue. In addition we measured responses of a number of key hepatic detoxification gene targets in the liver associated with the transcription factor pregnane X receptor (PXR); namely cyp450s 2k and 3a, glutathione-S-transferases a and p (gsta and p), and drug transporters multidrug resistance protein1 (mdr1), and MDR-related protein2 (mrp2). CTZ is a potent ligand of the PXR in humans and there is some evidence of PXR activation following exposure to CTZ in fish. The highest concentration of CTZ was adopted to explore the potential for alterations to detoxification gene expression in fish at a pharmacologically relevant dose level, and the lower concentration is within the range reported in effluents from waste water treatment works (WWTW). The genes for all biotransformation enzymes were up-regulated after exposure to the higher concentration of CTZ for 10 days, and alterations in expression occurred for the drug transporter genes mdr1 and mrp2 following exposure to the lower concentration of 1.02μgl-1 CTZ (mean measured concentration). These data support the potential for CTZ to induce alterations in biotransformation and drug transporter genes associated with PXR in fish at concentrations measured in some WWTW effluents.
- Aquatic toxicology (Amsterdam, Netherlands).Aquat Toxicol.2014 Mar 29;152C:57-65. doi: 10.1016/j.aquatox.2014.03.016. [Epub ahead of print]
- Clotrimazole (CTZ) is a persistent imidazole antifungal agent which is frequently detected in the aquatic environment and predicted to bio-concentrate in fish. Common carp (Cyprinus carpio) were exposed to mean measured concentrations of either 1.02 or 14.63μgl-1 CTZ for 4 and 10 days, followed by
- PMID 24727216
- Analysis of the cytotoxic effects of ruthenium-ketoconazole and ruthenium-clotrimazole complexes on cancer cells.
- Robles-Escajeda E1, Martínez A, Varela-Ramirez A, Sánchez-Delgado RA, Aguilera RJ.Author information 1Border Biomedical Research Center and Department of Biological Sciences, The University of Texas at El Paso, El Paso, TX, 79968, USA.AbstractRuthenium-based compounds have intriguing anti-cancer properties, and some of these novel compounds are currently in clinical trials. To continue the development of new metal-based drug combinations, we coupled ruthenium (Ru) with the azole compounds ketoconazole (KTZ) and clotrimazole (CTZ), which are well-known antifungal agents that also display anticancer properties. We report the activity of a series of 12 Ru-KTZ and Ru-CTZ compounds against three prostate tumor cell lines with different androgen sensitivity, as well as cervical cancer and lymphoblastic lymphoma cell lines. In addition, human cell lines were used to evaluate the toxicity against non-transformed cells and to establish selectivity indexes. Our results indicate that the combination of ruthenium and KTZ/CTZ in a single molecule results in complexes that are more cytotoxic than the individual components alone, displaying in some cases low micromolar CC50 values and high selectivity indexes. Additionally, all compounds are more cytotoxic against prostate cell lines with lower cytotoxicity against non-transformed epidermal cell lines. Some of the compounds were found to primarily induce cell death via apoptosis yet weakly interact with DNA. Our studies also demonstrate that the cytotoxicity induced by our Ru-based compounds is not directly related to their ability to interact with DNA.
- Cell biology and toxicology.Cell Biol Toxicol.2013 Dec;29(6):431-43. doi: 10.1007/s10565-013-9264-z. Epub 2013 Nov 24.
- Ruthenium-based compounds have intriguing anti-cancer properties, and some of these novel compounds are currently in clinical trials. To continue the development of new metal-based drug combinations, we coupled ruthenium (Ru) with the azole compounds ketoconazole (KTZ) and clotrimazole (CTZ), which
- PMID 24272524
- Evaluation of dispersive liquid-liquid microextraction in the stereoselective determination of cetirizine following the fungal biotransformation of hydroxyzine and analysis by capillary electrophoresis.
- Fortes SS1, Barth T, Furtado NA, Pupo MT, de Gaitani CM, de Oliveira AR.Author information 1Departamento de Química, Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto, Universidade de São Paulo, 14040-901 Ribeirão Preto,-SP, Brazil.AbstractWe developed a capillary electrophoresis (CE) and dispersive liquid-liquid microextraction (DLLME) method to stereoselectively analyze hydroxyzine (HZ) and cetirizine (CTZ) in liquid culture media. The CE analyses were performed on an uncoated fused-silica capillary; 50mmolL(-1) sodium borate buffer (pH 9.0) containing 0.8% (w/v) S-β-CD was used as the background electrolyte. The applied voltage and temperature were +6 kV and 15 °C, respectively, and the UV detector was set to 214 nm. Chloroform (300 µL) and ethanol (400 µL) were used as the extraction and disperser solvents, respectively, for the DLLME. Following the formation of a cloudy solution, the samples were subjected to vortex agitation at 2000 rpm for 30s and to centrifugation at 3000 rpm for 5 min. The recoveries ranged from 87.4 to 91.7%. The method was linear over a concentration range of 250-12,500 ng mL(-1) for each HZ enantiomer (r>0.998) and 125-6250 ng mL(-1) for each CTZ enantiomer (r>0.998). The limits of quantification were 125 and 250 ng mL(-1) for CTZ and HZ, respectively. Among the six fungi studied, three species were able to convert HZ to CTZ enantioselectively, particularly the fungus Cunninghamella elegans ATCC 10028B, which converted 19% of (S)-HZ to (S)-CTZ with 65% enantiomeric excess.
- Talanta.Talanta.2013 Nov 15;116:743-52. doi: 10.1016/j.talanta.2013.07.062. Epub 2013 Aug 1.
- We developed a capillary electrophoresis (CE) and dispersive liquid-liquid microextraction (DLLME) method to stereoselectively analyze hydroxyzine (HZ) and cetirizine (CTZ) in liquid culture media. The CE analyses were performed on an uncoated fused-silica capillary; 50mmolL(-1) sodium borate buffer
- PMID 24148469
Japanese Journal
- Functional roles of YPT31 and YPT32 in clotrimazole resistance of Saccharomyces cerevisiae through effects on vacuoles and ATP-binding cassette transporter(s)(GENETICS, MOLECULAR BIOLOGY, AND GENE ENGINEERING)
- Tsujimoto Yoshiyuki,Takase Daisuke,Okano Hajime [他],Tomari Naohiro,Watanabe Kunihiko,Matsui Hiroshi
- Journal of bioscience and bioengineering 115(1), 4-11, 2013-01
- … We identified YPT31, which is involved in Golgi traffic, as a clotrimazole (CTZ)-resistance gene in a multicopy library screen. … Multicopies of the YPT31 homolog YPT32 also conferred resistance to CTZ, and single disruption of YPT31 or YPT32 resulted in sensitivity to CTZ. …
- NAID 110009578180
- 意識障害を伴う嘔吐 (特集 気道確保法の選択とその実際) -- (気道確保を要する徴候への対応)
- 吐き気・嘔吐 (特集 症状緩和のための治療とケア)
Related Links
- Copyright(C) ARAI HELMET LTD., 2012
- キャスター付きフラッピングテーブル CTZ|愛知株式会社/axona AICHIは講義室・教室・会議室などのイス・テーブルを製造・販売する家具メーカーです。 ... クールモダンデザイン 直線的な美しさを持つ、キャスター付フラッピング ...
Related Pictures
★リンクテーブル★
[★]
- 英
- vomiting, emesis
- ラ
- vomitus
- 関
- 悪心、嘔気 nausea、悪心・嘔吐 nausea and vomiting
概念
- 胃の内容物をはき出す現象。
- 胃または腸内容が食道を経て口腔より吐出される現象。
嘔吐中枢
嘔吐中枢の近傍に存在するもの
- 呼吸中枢、血管運動中枢、消化管運動中枢、唾液分泌中枢、前庭神経核
随伴症状
- 発汗、唾液分泌、顔面蒼白、脈拍微弱、徐脈、頻脈、血圧の動揺、めまいなど
症状の出現形式と原因の所在
噴水状、噴射状嘔吐
- projectile vomiting is where stomach contents 'shoot out' (like a fountain) to a distance sometimes many feet away.
嘔吐に関わる経路
- IMD.351
- 1. 嘔吐中枢(延髄網様体背側神経背側核近傍)への直接刺激(脳圧亢進、循環障害)
- 2. 化学受容体誘発帯(CTZ; 第四脳室底)への刺激(代謝異常や中毒による化学物質の作用) → 1.
- 3. 大脳皮質(中枢神経など高位中枢)からの入力 → 1.
- 4. 求心性迷走神経や交感神経を介する入力 → 1.
原因
小児科で遭遇する嘔吐の原因
[★]
- 英
- chemoreceptor trigger zone, CTZ
- 関
- 嘔吐、嘔吐中枢、催吐薬、鎮吐薬
[show details]
化学受容器引き金帯 : 約 11,900 件
化学受容器引金帯 : 約 11,100 件
化学受容器誘発帯 : 1 件
化学受容器引き金領域 : 0 件
化学受容器引金領域 : 2 件
化学受容器誘発領域 : 0 件
化学受容体引き金帯 : 約 11,900 件
化学受容体引金帯 : 約 42 件
化学受容体誘発帯 : 約 21 件
化学受容体引き金領域 :
化学受容体引金領域 : 2 件
化学受容体誘発領域 : 2 件
化学受容器引き金帯 CTZ : 91 件
化学受容器引金帯 CTZ : 99 件
化学受容器誘発帯 CTZ : 1 件
化学受容器引き金領域 CTZ : 0 件
化学受容器引金領域 CTZ : 2 件
化学受容器誘発領域 CTZ : 0 件
化学受容体引き金帯 CTZ : 28 件
化学受容体引金帯 CTZ : 41 件
化学受容体誘発帯 CTZ : 約 15 件
化学受容体引き金領域 CTZ :
化学受容体引金領域 CTZ : 2 件
化学受容体誘発領域 CTZ : 1 件
概念
- 化学物質による刺激の入力を受け、延髄の外側網様体に存在する嘔吐中枢を興奮させる
- 血液脳関門が存在しないので、血液中の化学物質(薬物、重金属、代謝産物)をモニターして化学受容器引金帯が興奮する。
- ドパミン受容体を持ち、受容体刺激により嘔吐が引き起こされる。
- apomorphine, ergotalkaloide, morphine
- 中枢性鎮吐薬はドパミン受容体を遮断する。
解剖
[★]
- 英
- ceftezole CTZ
- ラ
- ceftezolum
- 化
- セフテゾールナトリウム ceftezole sodium
- 関
- 抗菌薬、セファロスポリン系抗生物質
[★]
- 英
- chemoreceptor trigger zone CTZ
- 関
- 化学受容器
[★]
化学受容器引金帯 CTZ
[★]
[★]