鈣抑制劑 的英文怎麼說

中文拼音 [gàiyìzhìjì]
鈣抑制劑 英文
calcium inhibitors
  • 鈣 : 名詞[化學] calcium （20號元素, 符號 ca）
  • 抑 : Ⅰ動詞（向下按; 壓制） restrain; repress; curb Ⅱ連詞[書面語]1 （表示抉擇） or 2 （表示轉折） but3 ...
  • 制 : Ⅰ動詞1 （製造） make; manufacture 2 （擬訂; 規定） draw up; establish 3 （用強力約束; 限定; 管束...
  • 劑 : 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...
  • 抑制 : 1 （控制） restrain; control; check; hold up; curb; stop; repress; bridle; choke; prehension; sup...
  1. It is interesting that pma plus calcium ionophore a23187 can inhibit pma - induced pta1 expression, and this effect ca n ' t be reversed by calcmeurin inhibiter fk506. pta1 mabs can inhibit ctl activation and differentiation in mixed lymphocyte culture system when added at the beginning of the culture but can induce platelet activation and aggregation in the fc dependent manner. in 1997, pta1 cdna was cloned from cdna library of tpa activated jurkat cells, which belongs to immunoglobulin superfamily ( igsf ) with two v - like domains of extracelluar region of pta1

    Il - 2 、 tnf - 、 pma可以使t細胞pta1表達上調， tgf -可以下調pta1的表達，而pma加上鈣離子載體a23187可以顯著抑制pma的上調作用，且這種抑制作用不被calcineurin抑制劑fk506所逆轉， 1997年burns教授從pma活化的jurkat細胞cdna文庫中克隆了pta1cdna全長，證實pta1是一個新分子，屬于免疫球蛋白超家族，胞膜外區有兩個v樣結構域。
  2. 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劑、受體阻斷劑、血管緊張素轉換酶抑制劑（ acei ） 、鈣通道阻滯劑（ caa ） 、受體阻斷劑、血管緊張素（ ang ）受體拮抗劑等六大類。
  3. On the other hand, angiotensin converting enzyme inhibitors may be more suitable in a yin deficiency and yang hyperactivity pattern as well as combined liver and kidney yin deficiency pattern

    鈣通道阻滯劑對血脈瘀阻型、痰濕壅型高血壓，受體阻滯劑對于肝陽上亢型高血壓，血管緊張素轉換酶抑制劑對陰虛陽亢型或肝腎陰虛型高血壓療效較好的機制還有待研究。
  4. This is possible because stomach acid is needed to help the body absorb calcium - proton pump inhibitors work by slowing the production of stomach acid

    這項研究結果是可能的因為機體需要胃酸幫助吸收鈣而質子泵抑制劑通過減少胃酸的產生發揮作用。
  5. It was found that plc activity was stimulated by both exogenous purified calmodulin and heterotrimeric g protein agonist cholera toxin. while, the stimulated effect on plc activity caused by exogenous calmodulin was inhibited by heterotrimeric g protein antagonist pertussis toxin, and plc antagonist u - 73122 inhibited the effect caused by cholera toxin. we also measure the free ca ~ ( 2 + ) level in germinating pollen grains, and found that exogenous purified calmodulin was able to increase the free ca ~ ( 2 + ) level, and their effects on ca ~ ( 2 + ) level were inhibited by u - 73122

    實驗中，利用[ ~ 3h ] pip _ 2和花粉原生質體共同孵育的體系，檢測出了百合花粉細胞具有依賴pip _ 2的plc活性；利用該體系還檢測出外源鈣調素可促進plc的活性，其中10 ~ （ - 9 ） m的鈣調素可使plc的活性提高三倍；異三聚體g蛋白的激活劑ctx可以激活plc的活性，而其抑制劑ptx可明顯抑制plc活性；外源鈣調素的這種作用可以被ptx抑制；而plc抑制劑u - 73122抑制ctx對plc的激活效應。
  6. " 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（如鈣離子阻斷劑，內皮素拮抗劑，前列環素，磷酸二酯酶抑制劑等）可能可以干預似乎是繼發發生的纖維化過程。 」
  7. " 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（如鈣離子阻斷劑，內皮素拮抗劑，前列環素，磷酸二酯酶抑制劑等）可能可以干預似乎是繼發發生的纖維化過程。 」
  8. 3. calcitonin gene - related peptide attenuates glutamate - induced inhibition of pulmonary surfactant lipid synthesis ( d cgrp could reverse the decrease of [ 3h ] - choline incorporation induced by glu with dose - dependence ; ( 2 ) cgrp could block the decrease of the content of cct a mrna induced by glu in lung tissue ; ( 3 } cgrp could reduce the impairment of the ultrastructure of at ii cells induced by glu ; ( 4 ) cgrp could reverse the increase of mda content and decrease of sod level induced by glu in cultured lung explants, respectively ; ? grp had no significant effect on nos activity and increase of no production induced by glu

    降鈣素基因相關肽減輕谷氨酸所致肺表面活性物質脂質合成抑制的保護作用降鈣素基因相關肽grp ）可顯著減輕0所致肺組織h一膽堿摻入pc量的降低，並且呈劑量依賴保護效應； cgrp可逆轉gill所致cctqinrna含量的降低； cgrp可減輕o所致肺11上皮細胞超微結構的損傷； cgrp可逆轉o所致肺組織勻漿中mda含量增多、 sod水平降低的效應，並可逆轉q所致肺組織ldh釋放增多的效應； cg販對gill引起的nos活性和no含量的升高均沒有顯著性影響。
  9. Ccbs calcium channel blockers

    鈣通道抑制劑
  10. Among patients with the metabolic syndrome ( 7, 327 black and 15, 750 white patients ), the calcium channel blocker, ace inhibitor and alpha - blocker had higher rates of heart failure compared with the diuretic ; the ace inhibitor and the alpha - blocker also had an increased risk of combined cardiovascular disease

    在合併代謝綜合徵人群（黑種人7327名白種人15750名）中，鈣通道阻滯劑、血管緊張素轉換酶抑制劑-阻滯劑治療組較利尿劑治療組有更高的心衰發病率； -阻滯劑治療組、血管緊張素轉換酶抑制劑治療組也有並發心血管疾病的危險性增高。
  11. The main physiology - biochemistry changes were determined in the two fruits after treating with trifluoperizine, a caimodulin antagnist, and verapamil, a calcium channel blocker. the results showed that trifluoperizine and verapamil weakened the effects of the exogenous ethylene on the the main physiology - biochemistry

    鈣調素拮抗劑tfp和鈣通道阻塞劑ver抑制了外源乙烯促進果實衰老時的乙烯釋放量、 o _ ~ -的積累和膜脂過氧化產物mda的增加。
  12. Randomized, prospective studies of steroid and calcineurin inhibitor minimization and / or avoidance are warranted to clearly confirm the short and long - term safety and efficacy of alternative immunosuppression combinations

    類固醇與鈣調磷酸酶抑制劑的最小化和/或避免應用的前瞻性隨機研究，能夠確保明確替代免疫抑制制劑療法的短期和長期的安全性與有效性。
  13. Calcineurin inhibitor minimization and addition of mycophenolate mofetil ( mmf ) or sirolimus have shown variable improvements in renal function, though suboptimal efficacy and safety with the currently proposed regimes have limited their application

    鈣調磷酸酶抑制劑最小化以及附加麥考酚酸莫酯（ mmf ）或西羅莫司，已經展現出不定的改善腎功能的作用，雖然欠佳的療效和安全性以及當前提出的管理體制限制了它們的應用。
  14. Recent findings : primary interest in antibody induction now falls into four major categories : steroid avoidance ; calcineurin inhibitor reduction as a renal sparing protocol ; minimal immunosuppression protocols ( tolerance ) ; and limiting hepatitis c recurrence

    最近的發現：抗體誘導的主要益處現在可以分成四類：避免類固醇的使用；減少鈣調磷酸酶抑制劑的劑量，作為一種腎保護性方案；獲得最低限度的免疫抑制方案（耐受） ；限制丙型肝炎復發。
  15. Calcineurin inhibitors ( cyclosporine or tacrolimus ) comprised the immunosuppressive therapy in 49 pregnancies ( 94. 2 % )

    49次妊娠（ 94 . 2 % ）是在採用包含鈣調神經抑制劑（環孢素或他克莫司）的免疫抑制方案。
  16. 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型鈣通道特異性阻斷劑nicadipine可以明顯抑制ib 。 ，並且iv曲線分佈在應用nicardipine前後無改受。
  17. Inositol supplied in the medium enhanced both blue - light - induced pigmentation and gene expression. antagonists of cam trifluoperazine ( tfp ) and w7 were used for detecting the role of cam in bl response

    鈣調素kam ）桔抗劑tfo和w7對花色素昔的積累和chs基因表達的作用有抑制也有促進。
  18. We report our experience, the largest to date, of sirolimus - induced pneumonitis following lt. between 1999 and 2006, 186 lier transplant patients receied sirolimus - based immunosuppression, after initial therapy with calcineurin inhibitors ( cnis )

    我們報道了至今為止在肝移植術后西羅莫司誘發性肺炎方面病例數最多的經驗. 1999年至2006年， 186例患者開始給予鈣調抑制劑，後接受基於西羅莫司的免疫抑制治療
  19. 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產生是經由鈣離子介導的，因為它可以被鈣離子通道阻斷劑異搏定（ verapamil ）所抑制。
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