被抑制的

NO could be synthezied for maintaining the resting cerebrovascular tonus in normoal condition and was involved in the vasodilatation mechanism under hypoxia. In these 2 aspects, the NO effects could be inhibited by L-NNA.

在静息状态时，NO有维持离体基底动脉血管条基态张力的作用；低氧时，NO在脑血管的舒张反应中也占有重要地位，两种作用都可以被L-NNA抑制。

Was bounded to 4-(2-aminoethylphenol), followed by labeling the 911-Tyr with fluorescein-5-isothiocyanate at the secondary amino group. High-performance size-exclusion chromatography , ultraviolet/visible spectroscopy and nuclear magnetic resonance spectroscopy demonstrated the binding of tyramine to 911 and the labeling of FITC to 911-Tyr respectively.

911抗HIV-1分子作用机制的研究利用表面等离子体共振生物传感器与流式细胞仪研究了海洋硫酸多糖911在抑制HIV-1粘附与进入宿主细胞过程中与两个潜在重要靶点（HIV-1外被膜糖蛋白rgp120及宿主细胞CD4受体）的相互作用。

Acetoin was shown to function as an inducer for the expression of aco genes, whereas glucose exhibited a repression effect.

被认定为诱导物的乙醯甲基甲醇可刺激启动区的表现，而葡萄糖则表现抑制现象。

Efaroxan 10 μmol· L^-1 inhibit proliferation effect of agmatine on neural stem cell.

结果从新生大鼠海马分离得到的细胞可以持续分裂增殖形成细胞克隆；胍丁胺1、10μmol·L^-1可以显著促进神经前体细胞的增殖，并且这种促增殖作用可以被依法克生所抑制。

Most of thesete1lurites and tellurates in these deposits are found to be products of coeval oxidationof calaverite, altaite and sufides, by Which "refractory gold" of Au tellurides will bereleased as naive gold. Most native gold released through oxidation of tellurides,however, will be trapped in the telluraes or tellurites; or be combined by Te intellurites or tellurates, which prevent gold of hyPergene from secondaxy enrichmentunder the supergene oxidation environrnenis.

研究表明，这些碲含氧盐大多数为碲金矿、碲铅矿与硫化物共同氧化的产物，&难溶金&矿物在氧化条件下发生分解，一般释放出自然金；由于金要么以自然金形式被&捕获&于这些含氧盐，要么重新与碲形成Au－Te含氧盐，所以抑制了金的次生富集。

The synthesis, types of antioxidant s and their antioxygenation mechanism were reviewed.

抗氧化剂被广泛应用于制药、功能化妆品等的生产、加工和贮藏过程中，其通过抑制生物机体活性氧簇的产生，或阻止其进一步链式氧化反应达到抗氧化目的。

When transplanted into CCl4 injured severe combined immunodeficiency mice, these cells integrated into the mouse liver and expressed human alpha-1 antitrypsin for at least 2 months.

当移植到被CCl4严重损害的免疫缺陷的小鼠中，细胞能整合进入小鼠肝细胞中并且表达人α1-胰蛋白酶抑制剂至少2个月。

However, Treatment with NMDA resulted in Giα2 phosphorylation. This phosphorylation could reversed by APV or chelerythrine chloride .

但NMDA可明显增加细胞内Giα2的磷酸化水平，这一作用可被NMDA受体的拮抗剂以及PKC抑制剂所阻断。

The 20-HETE-induced increases in [Ca2+]i, whole-cell L-type Ca2+ channel currents and the amplitudes of Ca2+ transients were blocked by extracellular application of chelerythrine (an inhibitor of protein kinase C, PKC) and H-89 (an inhibitor of cAMP-dependent protein kinase, PKA).

上述20-HETE诱导的[Ca2+]i、全细胞L-型钙离子通道电流、钙瞬变幅度的增加等效应，可被蛋白激酶C抑制剂白屈菜红碱和cAMP依赖蛋白激酶抑制剂H-89阻滞。

The synthetic and release of excitory amino acids are greatly increased after cerebral ischemia and the balance btween excitory amino acids and inhibitory acids are broken.

脑缺血性损伤时，脑内兴奋性氨基酸的合成、释放明显增加，兴奋性/抑制性氨基酸的动态平衡被打破。

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。