抑制...

The volume of stimulant amino acid in the hypothalamic tuberal part of rat is dcreased,the volume of rejective amimo acid increased,the volume of Catecholamines drceased,the volume of the stimulant amino acid in spinal cord intermediolateralis,the rate of stimulant amino acid and rejective amimo acid,and the volume of Catechomamones dcreased,the volume of NE in spleen tissue dcreased,all of which means the irritability of sympathetic nervous circulus in spleen is restrained.

运动组大鼠下丘脑结节部兴奋性氨基酸含量下降，抑制性氨基酸含量上升，儿茶酚胺含量下降，脊髓中间外侧柱兴奋性氨基酸含量下降、兴奋性氨基酸/抑制性氨基酸下降、儿茶酚胺含量降低，脾组织内NE含量降低，提示有氧运动组大鼠的脾脏交感神经调节通路的兴奋性受到抑制。

For normal adult male rat,calcitonin depresses the osteoclastic resorption obviously through reducing the number of active resorptive surface and depressing osteoclastic activity;on the other hand,calcitonin depresses the osteoid producing activity of osteoblasts by indirectly affecting the coupling process between resorption and formation.Calcitonin administered in short did not affect the bone volume.

降钙素对正常成年雄性大鼠松质骨而言，可以明显抑制破骨吸收，这种作用可能是通过减少活性吸收表面数量和降低破骨细胞的吸收功能来完成的；可以抑制成骨细胞形成类骨质的活性，这种作用可能不是直接的，而是通过降钙素对骨吸收的抑制作用进而影响了骨吸收与骨形成的之间的偶联而完成的；短期应用降钙素骨量无变化。

All of HCC cell linesexpressed Hh pathway to different extent,with predominance in SMMC-7721,which wereregarded as poorly differentiated.Blockade Hh pathway by KAAD-cyclopaminesignificantly inhibited the DNA synthesis and resultantly inhibited proliferation inSMMC-7721 cells.

利用KAAD-cyclopamine特异性阻断SMMC-7721细胞中Hh通路后，可明显抑制细胞DNA合成，进而抑制肝癌细胞生长增殖能力，其机制可能与促进p21的表达，抑制CyclinD1的表达有关。

Our results indicate that 1 NSC606985, at nanomolar level, can effectively induce apoptosis in AML cells NB4 and U937 and significantly inhibit the proliferation without cell death in breakpoint cluster region–Abelson murine leukemia kinase-carrying leukemic K562 cells; 2 At such low concentrations, this agent also significantly inhibits the clonogenic activity of hematopoietic progenitors from patients with AML; 3 For apoptosis induction, NSC606985 rapidly induces the proteolytic activation of protein kinase Cδ with loss of mitochondrial transmembrane potential and caspase-3 activation; 4 Co-treatment with rottlerin, a PKCδ-specific inhibitor, completely blocks NSC606985-induced mitochondrial m loss and caspase-3 activation, while the

结果显示：(1)纳摩尔浓度的NSC606985即可有效诱导AML细胞系NB4和U937细胞凋亡并显著抑制含有bcr-abl融合蛋白激酶的K562细胞的增殖；(2)低浓度的NSC606985也显著抑制来自AML病人骨髓的新鲜白血病细胞的克隆形成能力；(3)除了迅速诱导线粒体跨膜电位的崩塌及Caspase-3的活化外，NSC60698也导致蛋白激酶Cδ的水解激活；(4)PKCδ特异的抑制剂rottlerin能够完全抑制NSC606985诱导的线粒体跨膜电位的崩塌和Caspase-3的活化，而Caspase-3特异的抑制剂z-DEVD-fmk仅能部分削弱PKCδ的活化及细胞的凋亡；(5)以移植PML-RARα转基因小鼠产生的白血病细胞建立的模型研究了该化合物对白血病可能的治疗作用。

Inhibition of SAHH has been known to result in accumulation of intracellular levels of AdoHcy, which is a potent inhibitor of all S-adenosyl-L-methionine-dependent transmethylation reactions.

抑制SAHH将导致细胞内甲基化抑制物AdoHcy的堆积，从而时转甲基反应产生反馈性抑制作用。而甲基化对于维持细胞的活性是必需的。

Inhibition of SAHH has been known to result in accumulation of intracellular levels of AdoHcy, which is a potent inhibitor of all S -adenosyl- L -methionine-dependent transmethylation reactions.

抑制SAHH将导致细胞内甲基化抑制物AdoHcy的堆积，从而对转甲基反应产生反馈性抑制作用。而甲基化对于维持细胞的活性是必需的。

Second, residues in the reactive site of the inhibitor were replaced by the consensus substrate recognition sequence of furin, namely, Arg at P_1, Lys at P_2, Arg at P_4 and Arg at P_6. In addition, the P_7 residue Asp was substituted with Ala to avoid possible electrostatic interference with furin inhibition. Finally, the extra N and C terminal residues beyond the doubly conjugated disulfide loops were further truncated. However, all resultant synthetic peptides were found to be temporary inhibitors of furin and kexin during a prolonged incubation, with the scissile peptide bond between P1 and P'1 cleaved to different extents by the enzymes.

高活性、低分子量的furin酶抑制剂有可能发展成为新型的抗细菌内毒素和抗病毒感染的药物，我们以绿豆胰蛋白酶抑制剂Lys片段长链22肽为模板，设计了一系列能抑制furin和kexin活性的突变体，采用如下三种方法逐步优化：一、去除Lys片段长链三对二硫键中的一对，用Ser替换Cys，减少可能存在的二硫键错误配对；二、抑制剂的活性中心根据furin底物的专一性逐步改变，即P1、P2、P4和P6位分别变为Arg、Lys、Arg和Arg，同时为了避免P7 Asp和P6 Arg之间可能存在的相互作用，将P7位Asp替换为Ala；三、将两对二硫键形成的双环的外面5个氨基酸残基去除。

Deduced by the proportion of typical sterile plants and normal fertile plants in segregative generations derived from WA zhenqiuA/6078 that:I gene could inhibit the expression of Rf gene completely by the heterozygosity of 1 pair of Rf in genotype;and only reduce the expression of Rf genes with two heterozygous Rf genes in genotype ;but it would never inhibit the expression of Rf genes if the genotype included 3 pairs of heterozygous Rf genes. When Rf gene was homozygous,the / gene could not inhibit the expression of it.

根据认叭真秋刀6078各衍生分离世代中典型不育株和正常可育株所占比例推断：基因型中仅包含1对杂合的Rf基因时，I对Rf的表达起完全抑制作用；基因型中包含2对杂合的Rf基因时，I仅对Rf的表达起削弱作用；当基因型中包含3对杂合的对基因时，I对Rf的表达不起抑制作用；I对纯合位点的Rf的表达不起抑制作用。

The preliminary bioassays indicated that, at 500 g/mL, 1-(o-tolyl-4-(4-chloro-3-ethyl-1-methylpyrazol-5-ylcarbonyl)semicarbazide (4g) and 1-(2,4-dimethyl- phenyl)-4-(4-chloro-3-ethyl-1-methylpyrazol-5-ylcarbonyl)semicarbazide (4k) showed inhibitory activities 90% and 80% against Blumeria graminis, respectively; and at 25 g/mL, 4-phenyl-4-(4-chloro-3-ethyl-1- methylpyrazol-5-ylcarbonylsemicarbazide (4c) showed inhibitory activity 70.1% against Botrytis cinerea and 1-2-nitro-phenyl-4-(4-chloro-3-ethyl-1-methylpyrazol-5-ylcarbonylsemicarbazide (4d) showed inhibi-tory activitiy 51.3% against Pyricularia oryzae.

初步生物活性实验结果表明，在500 mg/mL浓度下，化合物1-(4-氯-3-乙基-1-甲基-1H-吡唑-5-甲酰基)-4-(2-甲基苯基)氨基脲(4g)， 1-(4-氯-3-乙基-1-甲基-1H-吡唑-5-甲酰基)-4-(2，4-二甲基苯基)氨基脲(4k)对小麦白粉病菌的抑制率分别达到90%和80%；在25 mg/mL浓度下，化合物1-(4-氯-3-乙基-1-甲基-1H-吡唑-5-甲酰基)-4-苯基氨基脲(4c)对黄瓜灰霉病菌的抑制率达到70.1%；化合物1-(4-氯-3-乙基-1-甲基-1H-吡唑-5-甲酰基)-4-苯基氨基脲(4c)和1-(4-氯-3-乙基-1-甲基-1H-吡唑-5-甲酰基)-4-(2-硝基苯基)氨基脲(4d)对稻瘟病菌的抑制率均达到51.3%。

For improve altogether mould inhibit than,in before the high altogether mould inhibit output altogether mould voltage feedback to shouldering by ends public of power also among the amplifiers than instrument in grade, make it put power voltage until mould input voltage float , setover voltage follow mould inputs the voltage into together very much each altogether not to transport, thus improved together mould inhibit to.

为提高共模抑制比，在前级高共模抑制比仪器放大器中还将输出共模电压反馈到正负电源的公共端，使运放电源电压随共模输入电压浮动，各极偏置电压都跟踪共模输入电压，从而提高了共模抑制比。

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。