可以抑制的

GnRH could markedly suppress progesterone secretion of cultured GCs with or without FSH and LH co-treatments. E〓 could invert the suppression of GnRH completely, also had the additive action on secreting progesterone with GnRH co-treatment. Mel partially released the suppression action of GnRH.

GnRH能强烈地抑制体外培养的颗粒细胞分泌孕酮，其抑制作用几乎不受FSH和LH影响；Mel仅表现部分地缓解了GnRH的抑制效应，但没有逆转。E〓不仅可以完全逆转GnRH的抑制作用，进而与GnRH叠加促进颗粒细胞分泌孕酮。

The inhibitive effect of 1, 2-benzenedicarboxylic acid on the absorption of N, P and K increased with its concentration rising. Low concentration of dibutyl phthalate increased the absorption of N, but decreased the absorption of P and K. Its high concentration restrained the absorption of N, P and K, while the low concentration of diphenylamine could stimulate the absorption of N and K, but restrain the absorption of P.

随着邻苯二甲酸浓度的增加，其对番茄幼苗根系吸收N、P、K的抑制作用增强；低浓度的邻苯二甲酸二丁酯可以促进番茄幼苗根系对N的吸收，抑制对P、K的吸收，高浓度时对N、P、K的吸收均起抑制作用；低浓度的二苯胺可以促进番茄幼苗根系对N、K的吸收，抑制对P的吸收。

Others desynchronized with 5－90 Hz primary depth electrographic after-discharges;(2) primary electrographic after-discharges were driven by primary unit after-discharges in the anterior dorsal HPC;(3) primary unit after-discharges were induced by brief primary electrographic after-discharges; and (4) plasticity of primary electrographic after-discharges and inhibition of single neuron firing were induced by repetitive ATPDH.

非同步性后放电的深部电图癫痫样电活动具有宽频带特征(5－90 Hz)；(2)原发性单位后放-后抑制效应可以引发低频原发性电图后放电，长时程爆发式单位放电可以诱发高频原发性电图后放电；(3)短束原发性电图后放电也可以诱发原发性单位后放电；(4)原发性电图后放电和神经元单位放电的抑制效应具有明显可塑性特征。

These studies indicate the rationality of our molecular design based on the crystal structure of KARI complex. To obtain more KARI inhibitors with high activities, the molecular docking and 3D-QSAR methods were applied to our further studying of these amidine compounds. Two methods AutoDock3. 0.3 and DOCK4. 0 were used in molecular docking, and the calculate results accord with that of herbicidal tests in general. The CoMFA model from 3D-QSAR analysis provided useful guidance for designing highly active compounds prior to their synthesis.

这些分子作为潜在的KARI抑制剂为基于KARI的农药分子设计提供了有利指导；对部分小分子进行了合成，在除草活性初筛的近三十个化合物中，个别化合物表现出较好的除草活性，其中一个化合物wb1596对油菜和稗草具有较高的生长抑制率，并通过E.coli KARI酶活性抑制试验验证了其KARI酶的作用靶标，此化合物可以作为KARI一个有苗头的抑制剂为后续工作奠定了基础；对发现的有苗头的KARI抑制剂进行了结构修饰和优化，合成了一系列脒类化合物并确证了它们的结构，改造后的化合物与原抑制剂相比大多除草活性相当或更佳，从而表明我们基于靶标结构的分子设计的合理可靠性；对所合成一系列脒类化合物进行了分子对接和三维定量构效关系研究。

DCs acquired by our reformed methods express both CD83 and CD 14 molecules highly, and have a higher density than other domestic reports. The higher TNF in DCs culture medium of HC patient suggests DCs in patient still have antigen presenting ability and by optimization the culture medium would improve its presenting ability and have a potential value in design and application individual vaccine. Although antigens pulsed DCs have a decrescent antigen presenting ability but BCG HSP70 could induce its mature and improve its presenting ability. Suggests BCG HSP70 would be a useful mature inducer. Lymphocytes primed by DCs based HC vaccine have the specific cytotoxicity against HCC lines. The CTL after freezing and anabiotic could prophylaxis and therapy HC xenograft on nude mouse. The results also suggests that CD4〓 lymphocytes play a important role in HC with a good differentiation and would be useful in treatment this kind of HC. After being activated by Peptide LLNQHACAV of hAFP and apoptotic HCCs pulsed DCs respectively, the culture medium of activated lymphocytes both contains a high level Th1 cytokines IL-12 and TNF. Primed lymphocytes appeared a characteristic of NK cells. DCs not only inhibited the growth of human HCC and other cancer cells in vitro but also prevented the growth of HC xenograft on nude mouse in vivo. There are at least three kinds of mechanism playing important role in DC based vaccine ,there are inhibition of DCs, HC specific CTL and cytokines pathway.

诱导出的DC共同表达CD83和CD14分子，CD83分子表达明显高于国内报道；肝癌患者DC培养上清中TNF水平高于健康人，提示肝癌患者DC仍具一定的抗原呈递能力，适当调控可使其行使APC功能，以期在肝癌个体化疫苗中发挥作用；DC负载肝癌可溶性抗原后，抗原呈递能力降低，BCG HSP70可促进DC成熟，增加其抗原呈递能力，预示BCG HSP70有可能成为促进DC活化和成熟的另一重要分子；肝癌DC疫苗在体外诱导肝癌特异性淋巴细胞，活化的淋巴细胞在体外对肝癌细胞的杀伤以特异性CTL为主，同时分泌较高水平Th1型细胞因子IL-12和TNF，并抑制4种肝癌细胞生长；冷冻复苏后的肝癌特异性淋巴细胞可以预防和抑制人肝癌裸鼠皮下移植瘤，提示DC负载肝癌可溶性抗原后诱发的MHC-Ⅱ类限制性CD4〓T细胞有可能在分化程度高的肝癌治疗中发挥作用；用DC和HLA-A2〓DC分别负载凋亡肝癌细胞和hAFP218-226位LLNQHACAV HLA-A2限制性九肽，在体外诱导肝癌特异性淋巴细胞，活化后的CTL细胞分泌较高水平的Th1型细胞因子IL-12和TNF，并具较强杀伤活性，此CTL同时具备NK细胞特征；DC对肿瘤细胞的抑制作用可能是通过吞噬实现的，Fas-L在DC抑制中也起一定作用；DC对人肝癌裸鼠皮下移植瘤的抑制率为97％；在肝癌DC疫苗的作用中，至少联合3种以上机制，即通过DC的直接作用、肝癌特异性CTL和细胞因子途径直接或间接地杀伤和抑制肝癌细胞。

Application of EBR induced parthenocarpic growth accompanied with active cell division in Jinchun No.4, a cultivar without parthenocarpic capacity, whereas Brz treatment inhibited fruit set and subsequently fruit growth in Jinchun No.2, a cultivar with natural parthenocarpic capacity, and this inhibitory effect could be rescued by application of EBR.

在非单性结实的津春4号黄瓜栽培品种的子房上添加EBR可以诱导单性结实并且提高细胞分裂能力，而在单性结实的津春2号黄瓜栽培品种的子房上喷施BRs合成抑制剂抑制果实生长，最终导致败育，而这种抑制现象可以通过添加EBR得以恢复。

With its effortless refined turbo diesel engine matched with a dynamic chassis plus a good 6 speed transmission, the S80 brought out superior on road motoring behaviour. It whiskered corners and bends competently, a keen driver will not be disappointed with its ability in excellent body control and mid-corner adjust ability. Not to mention with its excellent fuel economy on highway cruising. The wind and engine sound were minimal, and you can just concentrate on listening to its on board premium sound system.

S80是Volvo车厂精心的为过去，现在及未来的顾客研制的大师级作品，它与福特及越野路华共用一个汽车底盘，而经由Volvo厂方自己再调校，使它比越野车Freelander的底盘更强5个百分比，这个Dynamic Chassis底盘可以不断的监察汽车的反应，以抑制器快速的回应汽车的驾驶情况，并抗衡汽车在强大的加速，极端的制动及快速的转向所造成的俯仰，前潜及翻滚等反应，而它亦配上舒适，运动及先进的选择模式，这些科技帮助驾驶者及乘客取得优良的驾车及乘车经验。

Injection of rhIL-2 (200,100,50,25,12. 5 ku/kg) can inhibit mouse ear swelling, especially when dosage is 25～50 ku/kg. Injection of rhIL-2 (25 ku/kg) can inhibit rat plantar swelling. The function of mononuclear macrophage system was strengthened by hypodermic injection of rhIL-2( 100 ku/kg) once a day for 9 days. The decrease of mouse delayed-type hypersensitivity reaction induced by cyclophosphamide was extenuated by hypodermic injection of rhIL-2(50 ku/kg) once a day for 6 days. IL-2 has anti-inflammatory effects and immunomodulatory effects when administered in certain dosage.

RhIL-2注射液，剂量为20，10，5，2.5，1.25万u/kg时，对小鼠鼠耳肿胀模型有抑制作用，其中剂量为2.5～5万u/kg时，抑制率最大；剂量为2.5万u/kg时，对大鼠足拓肿胀模型有显著的抑制作用；rhIL-2注射液每日sc用药剂量为10万u/kg，连续给药9d后，可以明显增强小鼠单核吞噬细胞功能；rhIL-2注射液每日sc用药剂量为5万u/kg，连续给药6d后，可明显减轻由免疫抑制剂引起的小鼠迟发性变态反应降低的强度。rhIL-2在一定剂量范围内可以起到抗炎和免疫调节作用。

The electric capacity coupling matching and inductance coupling match are two kinds of forms that conducted coupling, passing the analysis to constitute the mechanism and principle to them, putting forward repressing a few of their methods: Match the length that can adopt to let up to lead line and enlarge the line to be apart from to the electric capacity coupling ,.

电容性耦合和电感耦合是传导耦合的两种形式，通过对它们构成机理以及原理的分析，提出了抑制它们的几种方法，如对于电容性耦合可以采用减小导线的长度、增大线间距，平衡法，对干扰源和被干扰源进行屏蔽等方式进行抑制干扰；对于电感耦合可以用减小互感，局部形成耦合环，对干扰源进行屏蔽等方式来对干扰进行抑制。

The depressing ability of the macromolecule organic depressants can be improved by the increase of their D.S.. The high D.S. CPVA and CPEG show strong depressing ability to calcite, while CPEG indicates strong depressing ability to diaspore, and HPAM to pyrite.The depressing mechanism of organic depressants was confirmed by the measurements of zeta potential, contact angles, adsorption capacity and IR spectrum.

利用动电位、接触角、吸附量和红外光谱等测试方法和手段，探讨了抑制剂的作用机理：苯氧乙酸类小分子抑制剂与方解石之间可发生较强的化学作用，可以选择性地吸附在方解石表面，使捕收剂发生解吸或阻止捕收剂在矿物表面的吸附而使矿物受到抑制；大分子抑制剂则主要是依靠亲固基吸附在矿物表面，再利用其长链的强亲水性而使矿物受到抑制。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。