抑制...

The results show that as the distance of waveguide to mirror is short, the couple efficiencies for EH11 mode of the cylindrical mirror and the spherical mirror are similar but the cylindrical mirror has stronger restraining function on EH21 and EH12 modes, and as the distance of waveguide to mirror is long, the cylindrical mirror has more restraining function on EH21 mode and less restraining function on EH12 mode.

同时相对球面反射镜，柱面反射镜对EH21模和EH12模具有更强的抑制作用。在d较大时，相对球面反射镜柱面反射镜对EH21模的抑制作用将会变得更强，而对EH12模的抑制作用将会减弱。标签 laser technique reflection coupling diffraction waveguide laser square waveguide cylindrical mirror

The pharmacodynamics action of aspirin besides synthesizing generation to see effect of hot, demulcent He Kangyan through restraining prostate element, delay to stimulate peptide, histamine to wait, still oxidize through checking the link of plaque enzymatic, reduce prostate element generate and have the effect that restrains plaque to gather.

阿司匹林的药理功能除了通过抑制前列腺素、缓激肽、组胺等合成产生解热、镇痛和抗炎功能外，还通过抑制血小板的环氧化酶，减少前列腺素的生成而具有抑制血小板聚集的功能。

They had suppressed the cathodic process of carbon steel electrode. Their inhibition performance was also related with their molecule stereo conformation and electron configuration. Four of bis-(1, 1'-benzotriazoly)-α,β-diamide compounds linked via-CO 〓CO-chain were synthesized and certified by IR and 〓H-NMR. The minimum energy conformations of these compounds were obtained by MM2 forcefield program. The two benzotriazole moiety in BBT1 was more planar than in other compounds. This was beneficial in increasing the inhibition effects of BBT1. In 0.5M H〓SO〓 solution, BBT1 suppressed anodic corrosion reaction. In 3%NaCl solution, BBT1 suppressed both cathodic and anodic corrosion reactions. 1- [ (1'-imidazolly)-methyl] benzotriazole was synthesized by Mannich reaction.

合成了四个通过-CO〓CO-连接的双（1，1'-苯并三唑）-α，ω-二酰胺化合物，采用MM2分子力学程序优化了它们的分子结构，双（1，1'-苯并三唑）-α，ω-二酰胺化合物的缓蚀作用与其分子内两个苯并三唑单元的空间取向有关系，良好的平面性有利于苯并三唑二聚体的吸附和缓蚀作用，苯并三唑二聚体BBT1分子内两个苯并三唑单元近似平行，所以显示出较好的缓蚀效果。0.5M硫酸中BBT1主要抑制铜的阳极溶解的电化学反应；3％NaCl溶液中，BBT1对铜的阳极溶解和氧的阴极还原过程均有抑制作用，相比较而言对阴极过程的抑制作用更大一些。

Based on competition fitting model,the kinetic data including association rate constant,dissociation rate constant were obtained,which provided a new method for inhibitor sensitivity comparison and screening.

选取竞争性拟合模型拟合了抑制剂存在条件下的SPR数据，获得了抑制剂与酶的结合速率常数、解离速率常数及亲合常数等动力学数据，为实现D1蛋白酶抑制剂的生物活性筛选提供了新方法。

Here, we investigated the roles of the PM NADPH oxidase in nickel-induced enhancement in production of ROS and the activity of antioxidant enzymes such as SOD, CAT and GR in roots of wheat Triticum durum D.

而且，镍导致ROS增加以及抑制剂对这些参数抑制的规律与镍和抑制剂对质膜NADPH氧化酶活性影响的规律类似，这些结果证明，镍诱导产生的ROS导致了膜脂过氧化，而这些ROS主要来自质膜NADPH氧化酶。

This distinctive action is not only to the shallow epiphyte but also to the deep epiphyte. The inhibited fungi efficiency of 0.1% acid reaches 90% and the 0.5% clotrimazole is 68%. And they also have inhibition action to grain-negative and gram-positive bacteria.

体积分数为0.1%的白果酸抑制真菌的有效率达90%，而体积分数为0.5%的克霉唑抑制真菌的有效率仅为68%，同时该提取物对各种革兰氏阴性和阳性细菌也均有抑制作用。

The bioactive screening on aldose reductase, nitric oxide synthetase, liver cancer Bel-7402, cavum oris epithelioma KB and colon cancer HCT-8 showed that paeoniflorin inhibited the nitric oxide synthetase by the rate of 83. 4% at the concentration of 5μg/ml, and paeoniflorigenone inhibited the colon cancer HCT-8 cells by the rate of 83. 2% at the concentration of 5μg/ml.

通过醛糖还原酶、NO合酶、肝癌Bel-7402、口腔上皮癌KB以及结肠癌HCT-8五种模型的生物活性筛选表明，在51μg／ml的浓度下，芍药甙对NO合酶的抑制率达83.4％，芍药甙元对结肠癌HCT-8细胞株的抑制率达83.2％，有较好的抑制作用。

The results showed that LRK could significantly inhibit the mammary hyperplasia caused by estrin, reduce the content of serum 〓, raise P level, promote the production of DA in hypothalamus and mammary tissue, decrease the release of 5-HT, inhibit the secretion of serum PRL, reduce the sensitivity of mammary tissue to estrin and progestogen, prevent the expression of mammary tissue on PCNA, the effect was equal to triphenylamine oxide, obviously superior to the control group of Ru Zeng Ning.

通过实验研究，建立了具有肾虚肝郁证侯群的乳腺增生病理模型，利用免疫组化技术、图像分析系统、荧光分光光度法、放射免疫法等现代医学研究方法，从病理形态学、医用体视学、神经内分泌学、阴道细胞学等方面，观察了利乳康口服液对模型动物整体状态、乳腺组织病理形态、血清激素、神经递质以及卵巢功能的影响，结果表明利乳康口服液能明显抑制雌激素引起的乳腺组织增生，降低血清E〓含量，升高P水平，促进下丘脑及乳腺组织中DA的产生，减少5-HT释放，抑制血清PRL分泌，降低乳腺组织对雌、孕激素的敏感性，阻止乳腺组织PCNA的表达，其效应与三苯氧胺相当，明显优于乳增宁对照组；另外，利乳康口服液还能缓解模型动物肾虚肝郁证侯群，增加其体重，调节其整体状况，改善模型动物不规则动情周期，减轻其子宫及卵巢的病变，抑制子宫内膜的过度增长，调节卵巢功能，揭示了中药利乳康口服液对神经内分泌和卵巢功能的整体调控作用，以及对本病发生、发展的预防作用

Rapamycin may extenuate the pathological damage of IgAN rats by inhibiting JAK/STAT signaling pathway, activation of STAT3 and mesangial proliferation.

雷帕霉素可能通过抑制IgA肾病大鼠肾小球JAK/STAT信号途径、直接抑制STAT3的活化以及抑制系膜细胞的增殖而减轻病变程度。

According to the electrochemistry mixed potential theory, the linear sweep voltammagram method is used to study the cathod and anode processes of the stabilizers. The results show that α-α' dipyridyl can decrease the deposition velocity by inhibit the anodic oxidation of formaldehyde, and potassium ferrocyanide can stabilizing the bath by inhibit the deoxidation of Cu~(2+).

根据电化学混合电位理论，用线性伏安法研究表明，α-αˊ联吡啶通过有效地抑制甲醛的阳极氧化来抑制沉铜速率；而亚铁氰化钾主要通过抑制Cu~(2+)的还原峰电流来阻碍Cu~(2+)的还原析出，但宏观的对化学镀铜镀速的影响不大。

The labia have now been sutured together almost completely.The drains and the Foley catheter come out at the top.

此刻阴唇已经几乎完全的缝在一起了，排除多余淤血体液的管子和Foley导管从顶端冒出来。

To get the business done, I suggest we split the difference in price.

为了做成这笔生意，我建议我们在价格上大家各让一半。