受体阻断剂的英文

• receptor antagonist
• receptor blocker
• receptor blocking agent
• receptor blocking pharmacon

• "剂"英文翻译    a pharmaceutical or other ch ...
• "β-受体阻断剂" 英文翻译 :    beta-blockers; receptor blocking agent
• "多巴胺受体阻断剂" 英文翻译 :    dopamine receptor-blocking agent
• "h1以体阻断剂" 英文翻译 :    h1receptor antagonists
• "受体阻断药" 英文翻译 :    receptor blocking agent
• "h1受体阻断药" 英文翻译 :    h1-blocker histamine h1-receptor blocking drug; histamine h1-receptor blocking drug
• "h2受体阻断药" 英文翻译 :    histamine h2-receptor blocking drug
• "m胆碱受体阻断药" 英文翻译 :    m-cholinergie blocking drug
• "胆硷能受体阻断药" 英文翻译 :    cholinoceptor blocker
• "阻断剂" 英文翻译 :    blockade; blocker; blocking agent
• "β肾上腺素受体阻断药" 英文翻译 :    beta-adrenoceptor blocking drug
• "肾上腺素受体阻断药" 英文翻译 :    adrenoceptor blocking drug; adrenoreceptor blocking drugs
• "封阻剂，阻断剂" 英文翻译 :    blocker
• "钙阻断剂" 英文翻译 :    calcium blockers
• "精神阻断剂" 英文翻译 :    psycholeptics
• "水媒阻断剂" 英文翻译 :    water-borne inhibitor
• "促甲状腺激素受体阻断性抗体" 英文翻译 :    thyrotropin receptor-blocking antibody
• "胆碱能阻断剂" 英文翻译 :    cholinergic blocking agent
• "毒蕈碱阻断剂" 英文翻译 :    muscarinic blocker
• "钙内流阻断剂" 英文翻译 :    calcium influx blockers
• "骨骼骨阻断剂" 英文翻译 :    skeletal muscle blocking agent
• "骨骼肌阻断剂" 英文翻译 :    skeletal muscle blocking agent
• "箭毒样阻断剂" 英文翻译 :    curaremimetic; curarimimetic
• "神经节阻断剂" 英文翻译 :    ganglionic blocker; ganglionic-blocking agent; ganglioplegic
• "受体阻滞剂" 英文翻译 :    aiirbs; arbs; h2ra

• Synthesis and biological study of isopropanol derivatives as - adrenergic blocking agent
  受体阻断剂的合成及生物活性研究
• ( 3 ) yohimbine ( 4 mg / kg ) , a selective a2 - ar antagonist , also partially attenuated the effects of agmatine
  门）预先静注眯哩淋受体门r ）和a厂肾上腺素能受体阻断剂（ a厂ar ） idazoxan （ 2
• The study authors conclude , " these results do not support the use of alpha 2 agonists in eterans with chronic ptsd .
  研究作者推断： “这些结果并不适用于使用2受体阻断剂治疗慢性ptsd的患者。
• ( 4 ) efaroxan ( 2f5 mg / kg ) , a selective antagonist for ii over i2 - imidazoline receptors and a2 - ar , could completely blocked the effects of agmatine
  N ）预先静注眯哩晰受体门； ）禾a 。肾上腺素能受体阻断剂efaroxan （ 2
• The big study to be reported on tuesday compared angioplasty plus optimal heart medications ? aspirin , beta blockers , ace inhibitors and statins to lower cholesterol ? to medications alone
  周二将报道的大型研究比较了血管成形术与最佳心脏病药物（包括阿司匹林，受体阻断剂，血管紧张素转换酶抑制剂和他汀类降脂药）联合使用与单纯药物使用的影响差异。
• 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，世界卫生组织( who )批准用于治疗高血压病的一线药物主要有利尿剂、受体阻断剂、血管紧张素转换酶抑制剂( acei ) 、钙通道阻滞剂( caa ) 、受体阻断剂、血管紧张素( ang )受体拮抗剂等六大类。
• 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天以上的神经元，内向电流之后出现了明显的外向电流，此外向电流可被gaba受体阻断剂荷包牡丹碱（ 50pm ）完全阻断，同时iscs的初始内向电流的幅值和时程均明显增加，并且在阻断gaba受体之后，任一年龄组均未观察到自发性周期性的内向电流。
• Therefore , the purpose of the present study was to determine whether the opioid receptor and its downstream pathway are involved in the cardiovascular effect of il - 2 and whether the effect of il - 2 under physiological or pathological conditions is changed . 1 effect of interieukin - 2 on contraction of enzymatically isolated ventricular myocytes cytokines play significant roles in some cardiovascular disorders , but direct myocardial effects of cytokines remain to be elucidated
  （ 4 ）非选择性阿片受体阻断剂纳洛酮（ nal ） （ 10nmol几）和选择性x阿片受体阻断剂norbni （ 10nmol l ）预处理后，可阻断il 2对心室肌细胞收缩的抑制作用，而选择性5阿片受体阻断剂纳曲呗跺（ nti ）门卜r口）不能阻断此作用。
• The concomitant application of dl - 2 - amino - 5 - phosphonopentanoic acid ( aps , 100 jim ) with bicuculline did not eliminate the polysynaptic second component , but the second component was only elicited in slices in which the ca3 region was kept intact . moreover , the bicuculline - and ap5 - resistant second component was due to the burst activity of ca3 pyramidal neurons , which were antidromically excited by the stimulation of the schaffer collaterals
  在生后1121天，神经元的快兴奋性突触后电流（ fstexcitatorypostsynapticcllntntsfepscs ）出现了典型的多突触第二种成分，同时给予nmda受体阻断剂aps不能消除此多突触第二种成分，但其只有在ca3区保持完整的脑片上才可被引出。