receptor inhibitor 中文意思是什麼
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The toxin can reversible block the neuromuscular transmission in an isolated mouse phrenic nerve - diaphragm preparation and also is a neurotoxin ( n - type ca2 + channels inhibitor ) which binds to the postsynaptic nicotinic acetylcholine receptor ( nachr )
溶液構象研究表明，它採取自然界中其它蛋白質多肽普遍採用的一種緊湊、緻密的抑制劑胱氨酸結模體（ ick ） 。 -
Mechanism of glutamate - induced inhibition of pulmonary surfactant lipid synthesis ? mda receptor ( nmdar ) antagonist mk - 801 could reverse glutamate - induced inhibition of [ 3h ] - choline incorporation in lung explants ; ? he expression of nmdar1 subtype existed in alveolar type ii epithelial cells ; ? he effect of glu on pc synthesis required l - arginine in cultured lung explants, nos activity and no production were increased significantly in lung explants with glu treatment ; and mk - 801 and nos inhibitor l - nna could block the increase of nos activity and no production induced by glu ; l - nna also could reverse the inhibition of [ 3h ] - choline incorporation induced by glu ; ( 4 ) mda content increased and sod level decreased in cultured lung explants of glu treament groups, mk - 801 and l - nna could reverse these effects ; ( 3 ) mk - 801, l - nna could block the release of ldh induced by glu
谷氨酸對肺表面活性物質脂質合成抑制的機制研究nmda受體拮抗劑mk - 801能逆轉glu所致肺組織[ ~ 3h ] -膽堿摻入減少的效應；肺泡上皮細胞有nmda受體nmdar1亞單位的表達； glu對ps脂質合成的影響依賴l -精氨酸的存在， glu可使肺組織勻漿中nos活性、 no合成量升高； mk - 801 、 nos的抑制劑l - nna均可阻斷glu所致的這些效應； l - nna可逆轉glu所致肺組織[ ~ 3h ] -膽堿摻入減少的效應； glu可使肺組織勻漿中mda碩士學位論文中文摘要含量增高、 sod水平下降。 mk七0 、 l nna能阻斷q所致的這些效應； mk80 、 l nna還能阻斷gill誘導的ldh釋放增多的效應。 -
Gefitinib ( iressa, zd1839 ), a specific tyrosine kinase inhibitor that targets the epidermal growth factor receptor ( egfr ), is a novel molecular - targeting antineoplastic agent
摘要吉非替尼是一種新型的分子靶向抗癌藥物，它選擇性抑製表皮生長因子受體酪氨酸激酶而發揮作用。 -
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。 -
Pretreatment with the phospholipase c inhibitor u73122 ( 5 umol / l ) significantly inhibited the il - 2 - induced depression of contraction. conclusion : it is concluded that the effect of il - 2 on contraction of ventricular myocytes is mediated via the cardiac k opioid receptor, and the post - receptor signal transduction pathway includes a ptx sensitive g protein and phospholipase c. 2 effect of interieukin - 2 on intracellular calcium tran
5 200u ffil ）濃度依賴性地降低單個心室肌細胞電刺激誘導的鈣瞬變幅度，使舒張末鈣水平升高； （ 2 ） il 2 （ 200u ml ）使咖啡因誘導的肌漿網內貯鈣的釋放降低： （ 3 ） 50偷i熱失活！
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