抑制作用的

In the toxicity inhibition test, the accumulated amount of oxygen uptake of BAC was decreased with the increase of Monochloroacetic acid dosages, especially when concentration of MCAA over 100 μg/L. It can be concluded that high concentration of MCAA can inhibit the microorganism's metabolism.

在毒性抑制方面，随著添加加氯消毒副产物一氯醋酸的浓度增加，微生物之累积摄氧有降低趋势，尤其是浓度高於100 μg/L后更为明显，显示MCAA在高浓度下对BAC附著微生物的代谢机制有抑制作用。

We show that the Wnt signaling actiator 6-bromoindirubin-3'-monoxime releases MSCs from the osteoinhibitory effects of Dickkopf-1, whereas LiCl treatment does not.

我们也发现Wnt信号激活剂BIO会解除DDK1对MSC的成骨抑制作用，而LiCl处理则无这种作用。

Our findings show:rrALR could inhibit the effect of gentamicin which induced NRK-52E cells apoptosis (P.05),which indicate that ALR probably protect renal tubular cell from nephrotoxic drugs injury by inhibiting its apoptosis.

1、ALR对庆大霉素诱导的NRK-52E细胞凋亡具有抑制作用，表明ALR可能通过抑制肾小管上皮细胞凋亡而减轻肾毒性药物对小管上皮细胞的损伤。

Imaging research in nude mice bearing human breast cancer exhibited that radioactivity has been accumulated in tumor site, While only slightly visualized or nonvisualized in the control group of mice.(4) Compared with the negative control group, the 〓I-EGF trial groups remarkably suppressed the growth of tumor.

〓I-EGF静脉和瘤内注射对荷瘤裸鼠有较强的肿瘤抑制作用，病理组织检查及透射电镜细胞超微结构观察发现肿瘤细胞发生一系列不可逆损害变化，而〓I或〓I-白蛋白无此作用； 6。

New antifungal agents have been developed over the past years based on the discovery of many new target sites of Candida albicands. For example, Echinocandins, aiming at the cell wall of Candida albicands, showed strong antifungal activities to fluconazole resistant candidas and fungal biofilm. Moreover, because β-glucan synthase does not exist on the cell membrane of mammalian cells, Echinocandins has a low toxicity and a promising clinical future. Though the mechanism of Histatin is not clear, it has strong activity not only on candida resistant of polyene and azole, but also to Candida parapsilosis, Candida krusei and Cry ptococcus neoformans. Berberine and Ocimum gratissimum L. were also found to have prominent anti-fungi activities.

近年来相继提出了许多抗白念珠菌药物作用的新靶点并成功开发出一些活性强大，疗效确切的抗真菌药，如以真菌细胞壁为靶点开发出棘白菌素类药物卡泊芬净、米卡芬净等，该类药物主要抑制β-葡聚糖合成酶，体外对氟康唑耐药的念珠菌属及真菌生物被膜表现出强大的抗菌活性，又由于β-葡聚糖合成酶在哺乳类动物细胞内不存在，故具有高效低毒的临床效果，是一极具前途的新型抗真菌药；以真菌细胞膜为靶点开发出Histatin类药物，虽然作用机制目前还不完全明了，但其作用不同于临床常用的多烯类和氮唑类，并已经发现Histatin5对两性霉素B和氮唑类耐药的念珠菌有效，并且对非白念珠菌如光滑念珠菌、克柔氏念株菌、隐球菌等也有杀灭作用；通过对植物药物的研究发现黄连素和丁香罗勒Ocimum gratissimum L。

In the initial stage of the bioleaching, when the bacteria are not active, the chemical oxidation of ferric irons to the solid sulfide minerals is primary; While in the whole course of the bioleaching, it is very limited; ferric irons inhibit the bacterial activity, lower the oxidational ability of the bacteria to ferrous irons in the liquid phase; ferric irons and their precipitations reduce the quantities of the attached bacteria and their activity, and have bad influence on the direct bioleaching action.

结果表明，在浸出的初始阶段，Fe3+的化学氧化作用是主要的；但在整个金属浸出过程中，Fe3+的化学氧化作用是很有限的；Fe3+对T.f菌有一定的抑制作用，降低了它们对液相中Fe2+的氧化能力；Fe3+及其沉淀使细菌在固体矿物颗粒表面的吸附量减少，降低了吸附细菌的活性，从而影响了细菌的直接氧化浸出作用。

Objective To investgate the inhibitory effect of Phyllanthus Urinaria L compound on proliferation of hepatoma cell HePG2 in vitro and to explore its mechanism.

目的 观察叶下珠复方对人肝癌HePG2细胞体外增殖的抑制作用并探讨其作用机制。

The inhibitory rate of metabolites produced by TD103-UV-4 against RS was more than 80%, and the antibiotic production capacity increased by 47.1%, meanwhile, its metabolites had a strong inhibition against other phytopathogenic fungi, such as Botrytis cinerea.

其中菌株TD103-UV-4发酵液对立枯丝核菌的抑制率在80%以上，并且对灰葡萄孢菌等植物病原菌有较强的抑制作用，产抗生素能力比出发菌株提高了47.1%。

As the chitosan is an alkaline polyose, it can be degradated in conjuction with polylactic acid and can suppress that polylactic acid generates pH pulses on environment in degradation process, increasing the cell affinity of the surface of polylactic acid material.

由于壳聚糖是一种碱性多糖，它与聚乳酸同时降解，还可以对聚乳酸降解过程中对环境产生pH脉冲作用起到抑制作用，提高了聚乳酸材料表面的细胞亲和性。

ResultsLoureirin B inhibits the TTXR peak sodium currents in a dose-dependent model and the inhibition is reversible. 0.2mmol/L loureirin B accelerates the inactive process of the TTXR sodium currents and delays the revivable process but does not affect the activitive process.

结果龙血素B对TTXR钠电流呈浓度依赖性抑制，且抑制作用可逆；高浓度的龙血素B（0.2 mmol/L）加速TTX-R钠通道电流的失活过程，延迟其复活过程，对激活过程无显著影响。

This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。