阻斷劑 的英文怎麼說
中文拼音 [zǔduànjì]
阻斷劑
英文
blockade-
Adrenergic blocking agent
類腎上腺素阻斷劑Synthesis and biological study of isopropanol derivatives as - adrenergic blocking agent
受體阻斷劑的合成及生物活性研究Its action site is located on the postsynaptic membrane and the biological activity of hwtx - i is located in the fifth p - turn containing lys25 and lys 27. to - conotoxin mviia is a neurotoxin belonging to one of n - type ca2 + channels inhibitors, purified from the venom of the conus marine snails, contains 25 amino acid residues with three disulfide binds. it adopts the pattern of ick and its linkage of the disulfide binds and space conformation are highly similar to hwtx - i
-芋螺毒素mviia （ - conotoxinmviia ）是從芋螺屬（ conus ）海底蝸牛毒液中分離提純的一種活性多肽，屬于n -型ca ~ （ 2 + ）通道阻斷劑中一種，含25個氨基酸殘基，三對二硫鍵，其二硫鍵連接方式、分子的空間構象與hwtx -很相似，採取ick結構模體。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，陰離子通道阻斷劑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所完全抑制。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阻斷劑10mm個ap不能抑制snp對ik （ c 。In many cases, a neuromuscular - blocking agent and a potent sedative are needed to facilitate intubation
在許多病例中，需要使用神經肌肉阻斷劑和有效的鎮靜劑。The study authors conclude, " these results do not support the use of alpha 2 agonists in eterans with chronic ptsd.
研究作者推斷： 「這些結果並不適用於使用2受體阻斷劑治療慢性ptsd的患者。Use of renin - angiotensin system blockers improved minimally, as did blood pressure control
運用腎素-血管緊張素系統阻斷劑組改善最小，和血壓對照組一樣。( 3 ) yohimbine ( 4 mg / kg ), a selective a2 - ar antagonist, also partially attenuated the effects of agmatine
門）預先靜注瞇哩淋受體門r ）和a廠腎上腺素能受體阻斷劑（ a廠ar ） idazoxan （ 2So 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。However, a - type channel blocker 4 - ap and channel blocker apamin displayed no effect on cell death and percentage of tunel positive cells and caspase - 3 activation
通道阻斷劑叩amin門卜m ）對缺氧復氧后神經元死亡、 tunel陽性細胞比例以及caspascs激活均無顯著影響，表明bkc 。Distinct outward fpsc following the inward fpsc emerged in neurons ^ pll and was abolished by bicuculline ( 50 um ). bicuculline increased the amplitude and duration of the initial inward fpsc in all age groups and characteristically recruited the polysynaptic second component of fepscs in neurons p11 - p21. no spontaneous periodic inward current was detected in any age groups after blocking gabaa receptors
在生后11天以上的神經元，內向電流之後出現了明顯的外向電流，此外向電流可被gaba受體阻斷劑荷包牡丹堿（ 50pm ）完全阻斷，同時iscs的初始內向電流的幅值和時程均明顯增加，並且在阻斷gaba受體之後，任一年齡組均未觀察到自發性周期性的內向電流。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、高劑量的類固醇、局部乙型阻斷劑與口服碳酸酐抑制劑。" 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。 」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。We injected carbennoxolone, a gap junction blocker, into the lateral ventricle, which was followed by hyperosmotic stimulation, the immunohistochemical staining of neurons and astrocytes and vp content in plasm were studied. western blot was performed to detect the content of cx43 and cx32 in son following hyperosmotic stimulation
側腦室注射縫隙連接阻斷劑甘珀酸（ carbenoxolone ， cbx ）后，再給予高第四軍醫大學博士學位論文滲刺激，觀察視上核膠質細胞和神經元免疫組化反應的改變，並檢測血漿vp含量的變化。The first parts studied the time course and response strength of mapks activation by gc, as well as the actions of distinct blockers of receptors and signal transduction
第一部分是gc激活mapks的時間過程和mapks激活的強度，以及在gc受體和信號傳導通路的阻斷劑的作用下， mapks的激活水平的變化。Nogo receptor and antagoist associated with spinal cord injury
受體和阻斷劑與脊髓損傷分享友人