查询词典 antagonist

The Nicaraguan president, like Ahmadinejad, is also an ally of US antagonist President Hugo Chavez of Venezuela.

尼加拉瓜总统一样，内贾德，也是一个盟友，美国拮抗剂总统乌戈查韦斯的委内瑞拉。

Intravoneous injection of 0.5mg/kgBW jingsongling cause the 60 minutesrelaxation of goat gastric motor.The effects of jingsongling on the gastric motor ofgoat is major of effects of α2 -adrenoceptor agonist,as well as that of α1 -adrenoceptor agonist,the effects of α1 -adrenoceptor agonist concentrate at thecardic and pylorus;the function of α2 -adrenoceptor exit widely at cardic,pylorus,rumen,reticulum,omasum and abomasum,the function at different part is not the same.The lowestdose of jingsonglinginhibiting the amplitude and frequency of the gastricmyoelectric is 0.01mg/kgBW;the influence of jingsonglingto the gastricmotility of goat is dose-dependent,and the amplitude regain after the frequency ofgastric myoelectriv wave.When the goat revived,the gastric motor function is notreach the level of the normal;the major reason ofjingsongling cause the goat gastricrelaxation is the amplitude renew slowly.The intravoneous injection ofjingsonglingfirst,after 5 minutes,intravoneous injection the antagonist,the effect of prazosin and idazoxan mixed is best,which can fast reversal of theinhibition of jingsongling on the gastric motor of goat,the effects of idazoxan isgood,and the prazosin block the effection of jingsongling is better than that ofxylazine,especially at cardia and pylorus.When intravoneous injection of0.5mg/kgBW idazoxan and/or prazosin only,the amplitude of gastric myoelectric ingoat increases at a certain degree,but the frequency is not changed.

静脉注射0.5mk/kgBW的静松灵引起山羊胃蠕动弛缓长达60分钟；静脉注射0.5mg/kgBW的静松灵对山羊胃蠕动机能的影响是以α2肾上腺素受体作用为主的，兼有α1肾上腺素受体的作用，而且静松灵的α1肾上腺素受体的作用主要集中在幽门和贲门；α2肾上腺素受体的作用广泛存在于贲门、瘤胃、网胃、瓣胃、皱胃和幽门中，不同部位间有功能上的差异；静注0.01mg/kgBW的静松灵是对山羊的贲门、瘤胃、网胃、瓣胃、皱胃和幽门的肌电波频率和振幅均产生影响的最低剂量；静注一定剂量的静松灵对山羊胃蠕动的抑制作用与剂量呈相关性；而且山羊胃肌电波振幅的恢复比肌电波频率的恢复慢；苏醒时山羊的胃蠕动机能尚未恢复到正常状态；静松灵引起山羊胃弛缓的主要原因是由于胃肌电波的振幅恢复慢；静注0.5mg/kgBW的静松灵，5分钟后静注0.5mg/kgBW的拮抗剂时，咪唑克生+哌唑嗪的作用最好，能迅速地逆转静松灵对山羊胃蠕动的抑制作用，咪唑克生也有很强的拮抗作用，而哌唑嗪对静松灵的拮抗效果好于对隆朋的拮抗；单独静注0.5mg/kgBW的咪唑克生和/或哌唑嗪时，山羊的瘤胃、网胃、瓣胃、皱胃、贲门和幽门的肌电波振幅有一定程度的增强，而肌电波频率未见变化。

Hence, this GH with partial deletion could function as an antagonist of GH/receptor signaling pathway.

对这些分泌蛋白的开发和利用，对下一世纪民族制药业的发展可能具有重要意义。

AIM To investigate the effect of methyl pentyl 1,4 dihydro 2,6 dimethyl 4 (3 nitrophenyl) 3,5 pyridinedicarboxylate (MN9202),a dihydropyridine calcium antagonist, on cardiac indexes,ultrastructure, superoxide dismatase,glutathione peroxidase activity and malondialdehyde concentration in cardiac hypertrophy induced by L thyroxine in rats.

连续 12 d ip L- Thy0 。5 mg·kg- 1 · d- 1 复制大鼠心肌肥厚模型，实验组 ip MN92 0 2 0 。4mg· kg- 1· d- 1 ，2 mg·kg- 1· d- 1 ，10 mg· kg- 1· d- 1 ，阳性对照组 ip卡托普利 2 5 mg· kg- 1 · d- 1 ，模型组、对照组给予等量溶剂，于给药后的第 13日处死大鼠，检测心脏指数，电镜观察心肌组织的超微结构变化，化学比色法测定心肌匀浆中 SOD、GSH- PX活性和 MDA含量。

We examined the effects and mechanisms of methyl pentyl 1,4-dihydro-2,6-dimethyl-4-(3-notrophenyl)-3,5-pyridinedicarboxylate (Mn9202), a novel DHPs calcium antagonist and lacidipine on the 5-HT2B receptor in cultured rat stomach fundus smooth muscle cells.

本研究以富含5-HT_(2B)受体的大鼠胃底平滑肌细胞为模板，观察了二氢吡啶类钙拮抗剂2，6-二甲基-4-（3-硝基苯基）-1，4-二氢-3，5-吡啶二羧酸-3-甲酯-5-正戊酯（Mn9202）、拉西地平对 5-HT_(2B)受体功能的影响，并对其影响机制进行了较为深入的研究。

The second part of this thesis was concerned with selection of antagonist of FGF from phage display peptide libraries.

本论文的第二部分致力于利用噬菌体肽库技术筛选成纤维细胞生长因子的拮抗剂。

Objective To investigate the changes of thromboxane A 2 receptors and the influence of their antagonist phenol red, and to study in molecular level the mechanism of action of thromboxane A 2 in acute lung injury.

目的研究急性肺损伤肺组织特异性膜受体（TXA2R）的变化及受体拮抗剂酚红对它们的影响，从分子水平阐明血栓素A2（TXA2）在ALI中的作用机制。

The further study showed that flumazenil, the benzodiazepine antagonist, and picrotoxin, the ligand of picrotoxin site on GABA〓 receptor, significantly antagonized hypnotic activity of melatonin by using EEG analysis in rats.

当机体昼夜节律系统功能正常时，在六个昼夜不同时间点给予12小时光照／12小时黑暗下生活的小鼠褪黑素后，延长小鼠睡眠时间的峰值出现在光照期开始，谷值出现在光照末期。

Either picrotoxin, a chloride channel blocker and bicuculline, a 〓 receptor antagonist, enhanced red light responses but reduced the green light responses of L-HCs.

施加氯离子通道阻断剂（印防己毒素，picrotoxin）或〓受体拮抗剂（荷包牡丹碱，bicuculline）均增大LHC对红光的反应，却压抑其对绿光的反应。

Phasic GABA receptorswere selectively blocked using the GABAA antagonist gabazineand tonic responses were blocked using the chloride channelblocker picrotoxin.

使用GABAA拮抗剂gabazine选择性阻断相位性GABA受体，采用氯离子通道阻断剂印防己毒素阻断持续性反应。

Just so you know where we're going...

只要让你知道我们的目标。。。

One of his friends acted as the gobetween in his business.

在这件事中，他的一个朋友充当了中间人。