阻斷藥 的英文怎麼說
中文拼音 [zǔduànyào]
阻斷藥
英文
blocking drugs-
Ganglionic blocking drug
神經節阻斷藥Neuromuscular blocking drug
神經肌肉阻斷藥Acting on neuromuscular junction, muscle relaxant can block excitation conduction from nerve to muscle, thus relaxing the muscle
肌松藥作用於神經肌肉接頭,阻斷神經至肌肉的興奮傳遞。Drugs that activate or block these receptors more selectively are detailed in this and the next chapter.
選擇性激活或阻斷這些受體的藥物將于本章和下一章中詳述。The mechanism by which they block the rennin - angiotensin system is different
這種藥物阻斷腎素血管緊張素系統的機制不同於其他藥物。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。Of those, 96 were prescribed tamoxifen, a drug therapy considered one of the best options for blocking the hormones that promote cancerous cell growth
其中, 96名患者正在服用三苯氧胺,這種藥物治療被認為是阻斷促進癌細胞生長的激素的最佳方案之一。Two years ago i spoke to my youngest son ' s fifth - grade class about the work in my lab, explaining about amyloid and how we hoped to block the responsible enzymes to discover new medicines for alzheimer ' s
兩年前,我對我小兒子小學五年級的同學談到我實驗室的研究工作,我向他們介紹類澱粉蛋白,以及我們希望能夠阻斷其切割的酵素,並據此找到新藥物來治療阿茲海默癥。" 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。 」" 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。 」It can be a side effect of drugs, from antihistamines to beta blockers. therefore, diagnosis can be tricky and time - consuming
它可能是藥物的副作用,是抗組織胺類藥或? -受體阻滯藥所引起的。因此,診斷是棘手的,也是耗費時間的。Most of these have been discovered in the last few years, and, as yet, we know of no drugs that enhance or block their effects.
其中多數是近幾年發現的,而且我們還未弄清有哪種藥物可以增強或阻斷它們的功能。More precisely, they block the action of a form of glutamate receptor known as the nmda receptor, which plays a critical role in brain development, learning, memory and neural processing in general
說得更精確些,這些藥物阻斷了一種叫做nmda型的麩胺酸受體,該受體對于大腦的發育、學習、記憶以及一般的神經活動都扮演著舉足輕重的角色。Drugs that block the action of proteases are used to control infection with the aids virus
用於阻斷該酶作用的藥物已用於控制艾滋病毒的感染。Sorafenib, a novel, oral multi - kinase inhibitor, targets on serine / threonine and receptor tyrosine kinases of the tumor cells and vasculature ; blocks the signal transconduction and inhibits tumor growth
摘要索拉非尼是首個口服多激酶抑制藥,靶向作用於腫瘤細胞和腫瘤血管上的絲氨酸和(或)蘇氨酸及受體酪氨酸激酶,阻斷信號傳導,抑制腫瘤生長。Adrenoceptor blocking drug
腎上腺素受體阻斷藥Since both of these two activities might be vulnerable to some kind of pharmaceutical interference or interruption, they present promising new targets for the development of anti - cancer drugs
既然兩種活動都可能是對於一些藥物干擾或者阻斷而易損的,他們呈現為發展抗癌藥物新的目標。These drugs work by reversibly blocking nerve conduction
這些藥物通過可逆性的阻斷神經傳導起作用。2 if doses sufficient to cause paralysis are administered to animals, then anaesthesia and artificial entilation will also be required, which may exert their own effects and so risk obscuring any toxic action
強效神經肌肉阻斷劑的毒性試驗代表了一種平衡,即在物質藥理作用增強的實驗性局限性和毒理學家想要用盡可能大的劑量以發現該物質任何潛在的能引起不合需要的反應之間的平衡。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,氯通道阻斷劑dids可以抑制所記錄到的電流,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劑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。分享友人