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Methods: 80 patients with ecchymosis were divided into observation group (40 cases) and control group (40 cases) randomly. Skin of afflicted part was sterilized with iodophor, then washed with normal saline, and pasted comfeel transparent dressing on afflicted part after dry in observation group. Skin of afflicted part was compressed with 50℃, so% magnesium sulfate, 20 minutes each time, twice a day in control group.

将80例皮下出血患者随机分为观察组(40例)和对照组(40例),观察组将患处皮肤先用碘伏消毒穿刺部位再用生理盐水清洗待干后采用康惠尔透明贴贴于患处,根据是否皱折及膜内胶体渗出情况给予更换;对照组采用温度为50℃,50%的硫酸镁热湿敷处理,每次20min,2次/d。

Methods: Fifty-five male adult SD rats were randomly divided into a normal control group, a saline control group and a heroin dependence group. Heroin-dependent rat models were set up by subcutaneous injection of heroin and the hypophysis were excised on the 10, 17, 24, 31, and 38 days after models were set up. Immunohistochemical SABC method, imagine analysis, and radioimmunoassay were used in the research.

成年雄性SD大鼠55只,随机分为正常对照组、盐水对照组及海洛因依赖组;皮下注射海洛因建立海洛因依赖大鼠模型,分别于模型建立的第10、17、24、31、38天取垂体组织,应用免疫组织化学SABC法、图像分析法观察大鼠垂体远侧部β-内啡肽表达。

The biocompatibility of poly(3-hydroxybutyrate-co-hydroxyocatanoate), a new biodegradable co-polymer scaffold, was evaluated with a series of tests, including cytotoxicity test, acute systemic toxicity test, hemolysis test, pyrogen test, genetic toxicity test, intracutaneous stimulation test and subcutaneous implantation test.

文章选用细胞毒性实验、急性全身毒性实验、溶血实验、热源实验、皮内刺激实验、遗传毒性实验和皮下植入实验等7个生物相容性实验对生物可降解支架材料羟基丁酸与羟基辛酸共聚体的生物相容性进行评价。

Syringe aspiration: At the up-left and right-down two regions, needle with 20 mL in volume used for extracting fat was used.

电动脂肪抽吸法:在左下、右上两个区域,用电动脂肪特制抽吸管置入待抽吸区域皮下脂肪组织内,调节负压为-75kPa,防止漏气以保持相对稳定的负压,往返抽动抽吸管12次,抽吸脂肪约30mL。

METHODS Sterile polyvinyl alcohol sponge discs which were labeled as physiological saline group and sinapine groups were implanted into the subcutaneous part of rat.

方法将聚乙烯醇海绵盘随机分为生理盐水对照组和不同剂量芥子碱组,植入小鼠皮下,构建盘状血管生成模型,观察术后12d的血管生成情况及组织生成情况,以蛋白定量检测试剂盒检测在海绵组织中的可溶性蛋白含量,对海绵冰冻切片行苏木精-伊红染色,应用计算机图像处理分析系统分析海绵内组织生长情况。

The positive hybridizations with COCH gene cRNA probe were detected in the mouse mesenchymic cell surroundding the endolymphic sac epithelium, the level of expression was similar to the fibrocytes underlying crista ampullaris sense epithellium, and inferior to the fibrocytes of spiral ligament.

成年小鼠内淋巴囊周围间质细胞COCH基因表达阳性,其原位杂交染色平均积分光密度为0.4±0.25(〓±SD,单位:U/mm〓),与壶腹嵴感觉上皮下间质细胞的0.47±0.21相似,弱于耳蜗螺旋韧带成纤维细胞的0.77±0.19。

To explore the influence on the expression of orexin A in the hypothalamus and orexin type 1 receptor (OX1R) in the medulla of neonatal rats after prenatal nicotine exposure, the 20 pregnant rats were divided into 2 groups randomly. Either nicotine (6 mg/kg per day) or normal saline solution (as same volume as nicotine group) was administered into the pregnant rats hypodermically from the fifth day to the end of gestation.

为了观察出生前尼古丁暴露对新生大鼠下丘脑orexin A及延髓内orexin 1型受体(OX1R)表达的影响,本实验将20只雌性成年大鼠随机均分为二组,怀孕后第5 d开始每天分别皮下注射尼古丁6 mg/kg或等量的生理盐水,直至分娩。

Methods: The rats were injected with thioacetamide 600mg/kg twice at same time for two days to induce the model of acute hepatic failure rat except the normal group injected with the normal saline hypodermically.

按600mg/kg的剂量经皮下注射硫代乙酰胺1次,24小时后按相同剂量重复注射1次,造成大鼠急性肝衰竭模型,于实验前3天至实验结束分别给予各组大鼠生理盐水,不同剂量丹黄方及促肝细胞生长素,观察造模后48小时内大鼠病死率,并于造模48小时后经腹主动脉采血测定ALT、AST、TBil、TNF-α、IL-6,取肝组织作病检。

Methods:The subcutaneous adipose tissue was obtained from the fold inguen of four SD rats, then digested with collagenase type Ⅰ and cultured in endothelial medium for seven days.

获取4只雄性SD大鼠鼠蹊部皮下脂肪,通过机械分割和组织消化法获取脂肪基质细胞,在内皮细胞培养液中培养7d后,经免疫细胞化学及透射电镜鉴定证实95%以上细胞已具内皮细胞表型特征,再将这些细胞进行成脂(DMEM/F-12培养基内加入0.5mmol/L1-甲基-3-异丁基-黄嘌呤,1μmol/L地塞米松,10μmol/L胰岛素,200μmol/L吲哚美星)定向诱导7d,形态学观察和油红O特殊染色鉴定诱导后的细胞。

A total of 1762 patients were enrolled within 48 hours of stroke symptom onset and randomized to receie either 40 mg daily of enoxaparin gien subcutaneously or 5000 IU of heparin twice daily for 10 days plus or minus 4 days — depending on when the patient was able to be ambulated.

总共1762名患者在出现中风征兆48小时内随机接受了每天40毫克伊诺肝素皮下注射或者每天两次5000国际单位肝素的治疗,治疗时间为10天或6天,这取决于患者何时能够行走。

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