阻抑劑 的英文怎麼說

中文拼音 []
阻抑劑 英文
inhibitor
  • : 動詞(阻擋; 阻礙) block; hinder; impede; obstruct
  • : 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 ...
  • : 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...
  1. Whereas attractants, repellents, and many incitants are olfactory substances, stimulants, and deterrents are usually gustatory.

    引誘,排斥還是其他的興奮都是嗅覺物質,但刺激阻抑劑常常是味覺物質。
  2. However, the constriction induced by ne was further enhanced when exposure of the aorta to hypotonic solution, which was inhibited by either nfa or nppb

    在此基礎上,陰離子通道nfa 、 nppb舒血管效應減弱;在低滲環境中血管張力進一步增加,並能被nfa 、 nppb所完全制。
  3. On the conventional whole cell patch clamp mode. howevef, under the perforated whole cell patch clamp mode, l00 ll m snp caused a efficient increase in ik (. ) by 20 ' 2 % t4. 5 % at 60mv 4 - ap l0 mm, a kind of selective inhibiter of delayed rectifier potassium current [ ik ( v ) ], can not inhibit the snp - induced increase of ik ( c. )

    應用相同的刺激模式,一在傳統全細胞模式下s pnovm 0卜m于m00vm對ik ( c一尤影啊… o仍)然而在穿孔模式下當細胞膜去極化至均0 v時, 1皿卜m p可明顯增加人0川達zo二士牛5 … 8廠選擇性延遲整流型鉀電流10mm個ap不能制snp對ik ( c 。
  4. 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( acei ) 、鈣通道( caa ) 、受體、血管緊張素( ang )受體拮抗等六大類。
  5. The patch clamp experiment : the cell - attached and inside - out configurations of the patch - clamp techniques were used to investigate single channel properties of nmd a receptors in the actuely dissociated neurons of the marginal division in the rat striatum, recording the current amplitude. long / short term opening / closing times indexes and the effects of incitants and agonists of the nmd a receptors on those parameters. we find that two types of conductance of 42ps and 20ps were recorded, the 42ps was the advantaged conductance

    本研究是在本實驗室以前研究的基礎上,通過膜片鉗( pachclamp )觀測sd ( sprague - dawley , sd )的mrd上nmda受體通道的電生理特性;繼而對青壯年sd大鼠的mrd 、海馬進行毀損並腹腔注射nmda受體ktm ( ketamine , ktm ) ,觀察其對大鼠學習記憶能力的影響:對于學習記憶能力下降的老年鼠進一步做顱內定位注射nmda受體激動,觀察其在特定部位的作用;最後,應用fmri ( functionalmagneticresonanceimaging ; fmri )對注射ktm的志願者做學習記憶與痛覺的對比觀察。
  6. 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

    鈣通道對血脈瘀型、痰濕壅型高血壓,受體對于肝陽上亢型高血壓,血管緊張素轉換酶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。
  7. Intravenous mannitol, high dose methylprednisolone, topical - blocker and oral carbonic anhydrase inhibitor were administered

    立即給予靜脈注射甘露醇、高量的類固醇、局部乙型與口服碳酸酐
  8. " 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,內皮素拮抗,前列環素,磷酸二酯酶等)可能可以干預似乎是繼發發生的纖維化過程。 」
  9. " 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,內皮素拮抗,前列環素,磷酸二酯酶等)可能可以干預似乎是繼發發生的纖維化過程。 」
  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、血管緊張素轉換酶-治療組較利尿治療組有更高的心衰發病率; -治療組、血管緊張素轉換酶治療組也有並發心血管疾病的危險性增高。
  11. A total of 7, 715 men had used bph therapy, and 1, 578 had used both blockers and 5 reductase inhibitors

    共有7 , 715例男性針對前列腺增生進行了治療,其中1 , 578例聯合使用了和5還原酶
  12. 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tfp和鈣通道ver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。
  13. Compared with other flame retardants, it has better function on restraining of the producing of smoke and sulfureted hydrogen, with the advantage of no contaminate, no corrosion and low cost

    氫氧化鎂屬于添加型無機,與同類無機相比,具有更好的制發煙和硫化氧生成的作用,且無毒害、無腐蝕、價格低廉。
  14. Moreover, chloride channel blockers, dids and sits, also significantly prevented sts - induced neuronal cell death. with whole - cell patch - clamp recordings, we found chloride channel currents increased significantly with time when holding potential at 60mv and 80mv after 5min and 10 min of sts exposure. these results indicate that potassium channel, especially bk channels, and chloride channel contribute to sts - induced neuronal apoptosis and apoptotic volume decrease, which is probably one of the mechanisms underlying mediation of neuronal apoptosis by potassium channel

    用斜坡電壓模式記錄的結果顯示, 10min內正常細胞在鉗制電壓下電流未發生明顯變化,氯通道dids可以制所記錄到的電流,加藥10mln就使電流峰值降低到原來的36 % ,向浴槽液中加凋亡誘導stssmin后, + 8伽mv鉗制電壓下電流即增大,為加藥前的131 . 3 % ,加藥后10min電流進一步增大,是加藥前的巧5 . 9 % ,而且電流隨時間延長具有繼續增大的趨勢。
  15. 4. contraction induced by 60 mmol / l kc1 was completely inhibited by nfa and nppb. 5

    陰離子通道nfa 、 nppb都能夠制由60mmol lkci引起的血管收縮。
  16. The anion channel blockers nfa and nppb abolished the kcl - induced contraction of vessels which were pretreated by thapsigargin

    將血管處于含60nunol lkci的高鉀環境中,血管發生收縮。而陰離子通道nfa 、 nppb可以制此收縮。
  17. Then several kinds of selective k + channel blockers were applied to further clarify the specific type of k + channels involved in apoptosis. both bkca channel blockers, ibtx and chtx ( at the concentration of 100 nm ), significantly reduced neuronal death and number of positive tunel - staining cells and inhibited caspase - 3 activation

    通道100nmibtx或100nmchtx均有顯著的神經元保護作用,可減少tunel陽性細胞比例及制caspase上激活;然而, a型鉀通道4apo0qm )或skc 。
  18. It showed that eif - 5a subcellular localizat ion was a dynamic process, and it might be a nucleocytoplasmic shuttle protein. our study is the first to show that the inhibition of hypusine formation altered the subcellular distribution of gfp - eif - 5 a, and made it unable to localize at its proper site of action

    然後利用氨基酸突變、添加等方法,制eif - 5a的hypusine修飾,觀察到eif - 5a始終為全細胞分佈,提示制hypusine的形成可影響eif - 5a的亞細胞定位,進而影響其功能的發揮。
  19. 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nicadipine可以明顯制ib 。 ,並且iv曲線分佈在應用nicardipine前後無改受。
  20. The anion channel blockers niflumic acid ( nfa ) and 5 - nitro - 2 - ( 3 - phenylpropylamino ) - benzoic acid ( nppb ) produced inhibitory effects on ne - evocked contraction in the aorta

    主要研究結果: 1陰離子通道nfa 、 nppb可以制去甲腎上腺素引起的血管收縮。
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