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断头

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Methods (1) The influence on the rats with non-bacterial prostatitis of 1.5% carrageenin. Rats were divided randomly into the normal control group, the model control group, the Qianliean low-dose group (1.5 g/kg), mid-dose group (3.0 g/kg), high-dose group (6.0 g/kg), with 10 rats in each group. All groups were treated continuously for 7 days, once a day. The model control group was given distilled water, 30mins after the last medication, injects 1.5% carrageenin 0.05ml in each rat's prostate, after 24hs, behead execute the rats and record the white blood cell number and Lecithin density.(2) the influence on the swelling ears of rats.

方法(1)对1.5%角叉菜胶致大鼠非细菌性前列腺炎的影响:将大鼠随机分为正常对照组、模型对照组、前列安颗粒小剂量组(1.5 g/kg)、前列安颗粒中剂量组(3.0 g/kg)、前列安颗粒大剂量组(6.0 g/kg)及阳性药前列舒乐颗粒组(2.4 g/kg)6组,每组10只,各给药组大鼠连续灌胃给药7日,每日1次,模型对照组给予等容量蒸馏水,末次给药后30 min,在每鼠前列腺内注入1.5%角叉菜胶0.05 mL,24 h后断头处死大鼠,取致炎前列腺组织,镜下记录白细胞数和卵磷脂小体密度。

Objective To conduct Pharmacodynamics research of Qianliean pellet and provide the basis for the clinical medication. Methods (1) The influence on the rats with non-bacterial prostatitis of 1.5% carrageenin. Rats were divided randomly into the normal control group, the model control group, the Qianliean low-dose group (1.5 g/kg), mid-dose group (3.0 g/kg), high-dose group (6.0 g/kg), with 10 rats in each group. All groups were treated continuously for 7 days, once a day. The model control group was given distilled water, 30mins after the last medication, injects 1.5% carrageenin 0.05ml in each rat's prostate, after 24hs, behead execute the rats and record the white blood cell number and Lecithin density.

方法(1)对1.5%角叉菜胶致大鼠非细菌性前列腺炎的影响:将大鼠随机分为正常对照组、模型对照组、前列安颗粒小剂量组(1.5 g/kg)、前列安颗粒中剂量组(3.0 g/kg)、前列安颗粒大剂量组(6.0 g/kg)及阳性药前列舒乐颗粒组(2.4 g/kg)6组,每组10只,各给药组大鼠连续灌胃给药7日,每日1次,模型对照组给予等容量蒸馏水,末次给药后30 min,在每鼠前列腺内注入1.5%角叉菜胶0.05 mL,24 h后断头处死大鼠,取致炎前列腺组织,镜下记录白细胞数和卵磷脂小体密度。

This may result in yarns that are considerably weaker in some areas than in others, caus in g breakage to occur easily at the weak po in ts.

从而引起应力的不均匀分配。纱线某段的强度比其它段要低,在纱线的弱段容易产生断头

The picture they took has the caption "Illustration of the Decapitation of Violent Chinese Soldiers."

照片了,他们有摄",说明了断头暴力中国士兵"。

Methods The gasp time of mice was observed after decapitation in mouse decapitation model.

方法应用小鼠断头张口喘气模型观察喘气时间的变化

We recorded the gasping time of the mice subjected to decapitation.

采用断头方法考察人参皂苷Re对小鼠全脑缺血后喘息时间的影响。

METHODS: Total 60 male Wistar rats were randomly divided into 6 groups, i.e., normal control group , DMN model group , large dose treatment group , middle dose treatment group, small dose treatment group and Dongbao gantai treatment group. The liver fibrotic model was induced by i.p. dimethylnitrosamine for 4wk. The relative herbs were given after model establishment in each treatment group and the administration lasted for 6 weeks. Decollate to get the blood and The serum hepatofibrosis indexes, hyaluronic acid, collagen IV, pro-collagen type III and laminin were measuredwith radioimmunoassay. SOD and MDA were measured with biochemistry method. The liver pathological changes were observed in each group of rats.

将60只雄性Wistar大鼠随即机分正常对照组、模型对照组、实验大剂量组(20ml/kg/d)、实验中剂量组(10ml/kg/d)、实验小剂量组(5ml/kg/d)及东宝肝泰药物对照组;腹腔注射二甲基亚硝胺制备大鼠肝纤维化模型,连续灌胃6周,断头取血,生化检测血清SOD、MDA;放射免疫法测定血清HA、LN、PCIII及IV-C;取肝左叶做HE染色和Mallory胶原染色,观察肝病理组织学改变。

CMC is used as woof trimming agent replacing traditional starch paste material, which can reduce pollution of woof during sizing and desizing. At the same time, CMC can form a membrane on woof which reduces"drop woof"and "decollation" sign.

CMC作为织物的整理剂,用于取代传统的淀粉浆料,大大减少了在织物上浆及退浆中对环境的污染,同时CMC在织物纤维上形成薄膜;而CMC薄膜具有吸湿性,增加了织物的塑性,减少高速织机上"跳纱"、"断头"现象。

The main direction to reduce decollation rate of yarn is to control and stabilize yarn tension, increase the yarn mightiness and reduce weakness tache rate, especially cut down the break tension and mightiness weakness point to reduce the cross rate of tension wave crest and mightiness wave trough.

由气圈理论的研究我们可以得知:降低断头率的主攻方向是控制和稳定张力,提高纺纱强力、降低强力不匀率,尤其是减少突变张力和强力薄弱环节,以减少张力与强力的波峰与波谷交叉机率。

Methods Twenty guinea pigs with gentamicin-induced hearing loss were randomized equally into IGF-1 group and control group. In both groups, scala tympani fenestration was performed for injection of IGF-l (10μ1) or artificial perilymphatic fluid (10μl). Auditory brainstem responses test was performed before and 7 and 14 days after surgery, respectively, and the cochlea was removed by decollation of 3 guinea pigs from each group after ABR test for observing the changes in the hair cells using scanning electron microscope.

豚鼠20只,施用庆大霉素致耳聋后均分为IGF-1组和对照组,行鼓阶开窗术,微孔技术注入试剂(IGF-1组注入鼠重组IGF-1,对照组注入人工生理外淋巴液)10μ1,分别在术前和术后7、14d行ABR测试;测试完后每组3只断头取听泡,在扫描电镜下观察耳蜗毛细胞改变。

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然而,正如其名字所指出的那样,CD盘不能写,也不能用任何方式改变其内容。

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