鈣阻斷劑 的英文怎麼說

中文拼音 [gàiduàn]
鈣阻斷劑 英文
calcium blockers
  • : 名詞[化學] calcium (20號元素, 符號 ca)
  • : 動詞(阻擋; 阻礙) block; hinder; impede; obstruct
  • : Ⅰ動詞1 (分成段) break; snap 2 (斷絕;隔斷) break off; cut off; stop 3 (戒除) give up; abstai...
  • : Ⅰ名詞1 (藥劑; 制劑) a pharmaceutical or other chemical preparation 2 (某些有化學作用的物品) a...
  • 阻斷劑 : blockade
  • 阻斷 : block out
  1. So far, six kinds of medicines are authorised to be applied to the treatment of hypertension by the world health organization ( who ), including diuretics, - receptor blocking agent, - receptor blocking agent, angiotensin receptor antagon, calcium channal blocking agent and angiotensin converting enzyme inhibitors ( aceis )

    目前,世界衛生組織( who )批準用於治療高血壓病的一線藥物主要有利尿、受體、血管緊張素轉換酶抑制( acei ) 、通道( caa ) 、受體、血管緊張素( ang )受體拮抗等六大類。
  2. " the concept is that systemic sclerosis, which is a severe disease characterized by systemic fibrosis, is at the beginning mainly a vascular disease, and we hypothesize that using major vascular drugs ( calcium channel blockers, endothelin antagonists, prostacyclins, phosphodiesterase inhibitors, etc. ) from the beginning and at appropriate dosage may interfere with the fibrotic process which seems secondary, " dr

    「從概念上講,系統性硬化是一種以系統性的纖維化變性為特徵的嚴重疾病,早期主要表現在血管性的病變,因此我們推測早期、適量地應用主要作用於血管的藥物(如離子,內皮素拮抗,前列環素,磷酸二酯酶抑制等)可能可以干預似乎是繼發發生的纖維化過程。 」
  3. " the concept is that systemic sclerosis, which is a seere disease characterized by systemic fibrosis, is at the beginning mainly a ascular disease, and we hypothesize that using major ascular drugs ( calcium channel blockers, endothelin antagonists, prostacyclins, phosphodiesterase inhibitors, etc. ) from the beginning and at appropriate dosage may interfere with the fibrotic process which seems secondary, " dr

    「從概念上講,系統性硬化是一種以系統性的纖維化變性為特徵的嚴重疾病,早期主要表現在血管性的病變,因此我們推測早期、適量地應用主要作用於血管的藥物(如離子,內皮素拮抗,前列環素,磷酸二酯酶抑制等)可能可以干預似乎是繼發發生的纖維化過程。 」
  4. After pretreated with nifedipine to block the influx of extracellular calcium, the vessels did not contract when they were stimulated by 60 mmol / l kc1 solution ; on the other hand, after pretreated with thapsigargin to deplete the intracellular calcium stores, the vessel remained the ability to contract when stimulated by 60 mmol / l kcl solution

    使用ifedipine預處理血管,細胞外離子內流,將血管置於含60mmol lkci的高鉀環境中,血管不發生收縮。使用細胞內耗竭thapisin呷in預處理血管,耗竭細胞肌漿網內儲存的離子。
  5. With holding potential of - - 80 mv depolarization beyond - - 50 mv elicited an inward current, peaked at + l0mv and reversed between + 40 mv and + 60 mv 5 ll m nicardipine, a potent blocker of l - type calcium channel, markedly blocked the " ib

    開始出現,峰值在去極化刺激至10 20mv出現,翻轉電位為巧0仍0mv 。 l型通道特異性nicadipine可以明顯抑制ib 。 ,並且iv曲線分佈在應用nicardipine前後無改受。
  6. Abstract l : the chinese bird spider, ornithochoctonus huwena, distributed in the hilly areas of yunnan and guangxi in the south of china, was recently identified as a new species and is one of the most venomous spiders in china. in our previous work, we have demonstrated that 0. huwena venom contains a mixture of compounds with different types of biological activities

    它的粗毒中含有多種活性成分,其中研究的比較深入的多為神經毒素,如hwtx - ,這是一種突觸前膜n型離子通道;毒素hwtx - ,它是一種ttx敏感型鈉離子通道;另外,還從虎紋粗毒中純化出一種具有凝集活性毒素成分shl - 。
  7. Lum and co - workers identified h2o2 as an upstream signal that leads to no production. they also found that the h2o2 induced no production was mediated via calcium ion flux, as it was blocked in the presence of a calcium ion channel blocker, verapamil

    Lum和同事發現h _ 2o _ 2作為上游信號誘導no的產生,他們還發現aba誘導的no產生是經由離子介導的,因為它可以被離子通道異搏定( verapamil )所抑制。
  8. Furthermore, the combinations of cts with exogenous ca2 + and the factors elevating [ ca2 + ] i could raise the activities of gdh and gs, whereas cts declined the activity levels of gdh and gs after calcium messenger system having been blocked by calcium chelator ( egta ), plasma membrane calcium channel inhibitors ( verapamil and lacl3 ) and cam repel reagent ( chloropromaize )

    Cam拮抗氛丙漆在信使系統后,也降低了gdh和gs的活性。同時, cts可以與外源ca 』 『及有利於胞質內ca 』 『濃度上升的因子(如dtt和atp )互作促進gdh和gs活性;而在egta 、異博定、 laci ,和氛丙漆分別存在下,則引起gdh和gs活性的減弱。
分享友人