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In no brassiere condition had higher FVC and less effects at respiratory function than fashion brassiere condition.

无胸罩支撑型式比一般胸罩支撑型式产生较低的外在压力,在安静期间肺功能测验中有较高的用力肺活量,较不影响呼吸功能。

I have problems with low blood pressure, and sometimes chest tightness, breathlessness, the (I am just 30 years old) how can I treat?

我血压低的问题,有时胸闷,呼吸困难,在(我只是30岁)我如何对待?

Objective To investigate the effects of selenium and iodine deficiency on the contractibility of rat thoracic aorta and probe into its mechanisms.

目的 研究低硒、低碘对大鼠离体胸主动脉收缩力的作用并探讨其机制。

objective to discuss perioperative complication and management of patient with high risk copd following esophagectomy.methods 45 patients with high risk copd underwent esophagectomy with epidural block combined with general anesthesia.perioperative treatment included smoking cessation,chest physiotherapy,prevention and control of infection of air way and appropriate bronchodilators of air way,breathing exercises,nutrition support and oxygen therapy.painkiller was instilled after surgery,early exercises,ensuring unobstruction of the air way,mechanical ventilation was applied when needed.results 3 had hypoxaemia in operation.after surgery,all patients had spo2 somewhat declined.6 had lung infection.6 were removed of bronchial secretion by bronchoscope.2 were supported by ventilator by using intubation.2 underwent tracheotomy.1 had disturbances of acid base balance and treated by using hydrochloric acid muriatic acid.all patients recovered rather smoothly and discharged from hospital.conclusion high risk copd is not the absolute contraindication of esophagectomy.active management before and after surgery ensures the safety and recovery of patients.

目的 探讨重度慢性阻塞性肺疾病简称慢阻肺病人食管切除术围手术期常见并发症及其处理。方法 45例重度慢阻肺的病人在全麻联合硬膜外阻滞下进行开胸食管切除手术,围手术期处理包括术前戒烟、胸部理疗、预防和控制呼吸道感染、解痉化痰、呼吸功能锻炼、营养支持和氧疗;术后硬膜外镇痛、早期锻炼、保持呼吸道通畅,部分病人予以呼吸支持。结果术中3例出现低氧血症。术后所有病人pao2均有不同程度的下降,6例出现肺部感染,6例行纤维支气管镜吸痰,2例通过气管插管给予呼吸机支持,2例行气管切开术,1例酸碱平衡紊乱使用盐酸精氨酸治疗。所有病人均痊愈出院。结论重度慢阻肺病人并非开胸食管切除手术的绝对禁忌证,积极的术前准备和严格的术后管理可减少和控制术后急性发作,有助于确保此类病人的围手术期安全和康复。

Methods Twenty-six NZW rabbits were randomly divided into three groups: a normal control group (fed on normal commercial rabbit diet, n =6), a hyperlipidemic group fed on high-fat ma total cholesterol (TC concentration at the beginning and the 12-week end point of the experiment determined,and all the experimental rabbits were sacrificed, and endothelial function test were performed on thoracic aortic rings prepared from the isolated aorta using the vascular endothelium-dependent relaxation parameter in response to acetylcholine The aortic atherosclerotic lesion expression of LOX-1 mRNA and protein were examined by RTPCR and Western blotting respectively.

方法新西兰大白兔随机分为正常对照组(普通饮食,6只),高脂饮食组(高脂饮食,10只)及普罗布考组(高脂饮食+普罗布考200mg/kg·d,10只)。实验开始前及第12周分别耳缘静脉采血测定血清总胆固醇。第12周处死动物,取胸主动脉,制备离体胸主动脉环对乙酰胆碱的反应以检查内皮功能,RT-PCR与免疫印迹检测凝集素样氧化低密度脂蛋白受体-1(LOX-1)基因与蛋白质表达水平。

As the rapid development of contemporary biochemistry technology, new-style beautiful breast cosmetic is increasing also, apparent to beautiful breast effect biochemistry additive appears ceaselessly, if placenta extracts albumen of content, royal jelly, collagen, serum to wait, curative effect of product of these biology beautiful breast is apparent and safety does not have side-effect; Product of the natural plant that is a delegate with Chinese herbal medicine beautiful breast its characteristic is safety, effect good, cost is low; Have already in product of a few series can make make the same score pectoral ridgy abundant breast element, have again in the light of Female The bounce elite element with flabby, flagging breast, still have gel of be good at bosom, agent of sparge of be good at bosom.

随着现代生化技术的迅速发展,新型的美乳化妆品也越来越多,对美乳效果明显的生化添加剂不断出现,如胎盘提取物、蜂王浆、胶原蛋白、血清等,这些生物型美乳产品疗效明显且安全无副作用;以中草药为代表的天然植物型美乳产品其特点是安全、效果好、成本低;一些系列产品中既有可使平胸隆起的丰乳素,又有针对女性乳房松弛、下垂的弹力精华素,还有健胸凝胶,健胸喷雾剂等。

Methods 40 ICR mice were divided into four groups: the control,the low(0.5 mg /kg),the middle(4 mg/kg) and the high(20 mg/kg),intragastric through mouth for 21 d,detected the thymocyte apoptosis by flow cytometry,observed the fas protein expression in thymus by immunohistochemistry.

方法ICR种小鼠体重20~25 g,雄、雌各半,共40只,随机分为4组,每组10只,即1个对照组和低、中和高3个组,经口灌胃21 d,流式细胞仪检测胸腺细胞凋亡状况,免疫组化染色,观察Fas蛋白在胸腺的表达。

Methods: Eighty mice were randomly divided into high, middle, and low dosage groups which were orally given 1.5 g/kg, 0.75 g/kg, 0. 375 g/kg of ant powder respectively, twice a day for 10 days. A blank control group was set up which was given water instead. Body weight, thymus weight and spleen weight were measured. Thymus indexes and spleen index were calculated. Neutrophil phagocytose rate, Ea and Et rosette formation rate of T lymphocytes, and hemolysin titre were detected. QHS values were achieved with spleen cell mediated sheep red cell spectrophotometer quantitative assay.

根据黑蚂蚁的用药量将小鼠分成高、中、低剂量及空白对照组,黑蚂蚁粉给药量按小鼠体重1.5g/kg、0.75g/kg、0.375g/kg计算,连续10d灌胃给药后,测定各组小鼠的体重、胸腺和脾脏重量,计算胸脾指数;检测中性粒细胞的吞噬率、T淋巴细胞E花环形成率及小鼠的溶血素效价和脾细胞介导的羊红细胞分光光度计定量测定法。

A blank control group was set up which was given water instead. Body weight, thymus weight and spleen weight were measured. Thymus indexes and spleen index were calculated. Neutrophil phagocytose rate, Ea and Et rosette formation rate of T lymphocytes, and hemolysin titre were detected. QHS values were achieved with spleen cell mediated sheep red cell spectrophotometer quantitative assay.

根据黑蚂蚁的用药量将小鼠分成高、中、低剂量及空白对照组,黑蚂蚁粉给药量按小鼠体重1.5 g/kg、0.75 g/kg、0.375 g/kg计算,连续10 d灌胃给药后,测定各组小鼠的体重、胸腺和脾脏重量,计算胸脾指数;检测中性粒细胞的吞噬率、T淋巴细胞E花环形成率及小鼠的溶血素效价和脾细胞介导的羊红细胞分光光度计定量测定法。

Methods: A total of 21 young swines were randomly divided into untreated group, low-dose salvianolate group and high-dose salvianolate group (7 in each group). AMI was induced by ligaturing left anterior descending coronary artery. After the operation, 400 or 200 mg salvianolate dissolved in 250 mL 5% glucose saline was administered by intravenous drip to swines in the HS group and the LS group respectively for 7 days. The swines in the untreated group were administered with 250 mL 5% glucose saline.

苏中幼猪21只,随机分为模型组和低、高剂量丹参多酚酸盐组。3组均经开胸结扎冠状动脉左前降支制作心肌梗死模型,造模成功后当日,高剂量丹参多酚酸盐组给予400mg丹参多酚酸盐加250mL 5%写葡萄糖生理盐水静脉滴注;低剂量丹参多酚酸盐组给予200mg丹参多酚酸盐加250mL 5%葡萄糖生理盐水静脉滴注;模型组给予等体积的5%葡萄糖生理盐水静脉滴注。1次/d,连续给药7d。

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