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Materials and Methods: From January of 2007 through December of 2007, 6 patients underwent subcutaneous liposuction with shaving for bromhidrosis.

目的与目标:藉由病理组织切片观察顶浆腺的数量来评估皮下脂肪抽取术结合旋转刀刮除术能否有效治疗狐臭。

Methods: form january 1995 to january 2005, 42 patients with acute respiratory failure (acute respiratory failure group) and 84 random sampling after esophagectomy and cardiectomy were studied. age, sex, smoke index, preoperative respiratory function, preoperative pulmonary and the other complications, hypoproteinemia, the site of anastomosis, duration of operation, postoperative analgesia, postoperative other complications were compared by logistic regression analysis.

将1995年1月~2005年1月期间食管癌、贲门癌术后发生arf的42例患者临床资料,与按1∶2比例随机抽取的同期手术后未发生arf的84例食管癌、贲门癌患者的资料做对照,应用logistic回归分析比较两组患者的年龄、性别、吸烟指数、术前肺功能、术前有无肺部合并症和其它合并症、术前有无低蛋白血症、吻合口位置、手术时间、术后是否镇痛、术后有无其它并发症等与术后发生arf的相关强度,推测可能导致术后arf发生的危险因素。

Carnosine was added to the drinking and addition dose atⅠto Ⅳgroups were 0,20,40 and 60 mg/L respectively for 6 weeks.6 broilers from each group were randomly selected to pick the blood respectively at the each weekend.

于每周末每组随机抽取6只鸡采血,测定血清中超氧化物歧化酶、过氧化氢酶、谷胱甘肽过氧化物酶的活力和丙二醛的含量。

There were 12 rabbits (24 articular genus) in every group. Osteoarthritis model was established by injection of caroid in articular genu intracavitary. Rabbits with osteoarthritis were interfered by Duhuojisheng decoction. The expression of IL-1 and TNF from synovial fluid in rabbit with osteoarthritis were measured by double antibody sandwich ELISA 1, 3, 5 weeks after treatment.

将24只兔随机分为2组,即对照组和治疗组,各12只,24个膝关节,采用兔膝关节腔内注入木瓜蛋白酶造成骨关节炎的病理模型,以独活寄生汤浓缩液餵食饲养,於治疗后1、3、5 周分别抽取关节液,采用双抗体夹心酶联免疫吸附法,分别测定兔膝关节液中IL-1及TNF 表达水平。

Methods 24 rabbits were randomly divided into control and treatment groups. There were 12 rabbits (24 articular genus) in every group. Osteoarthritis model was established by injection of caroid in articular genu intracavitary. Rabbits with osteoarthritis were interfered by Duhuojisheng decoction.

将24只兔随机分为2组,即对照组和治疗组,各12只,24个膝关节,采用兔膝关节腔内注入木瓜蛋白酶造成骨关节炎的病理模型,以独活寄生汤浓缩液喂食饲养,于治疗后1、3、5 周分别抽取关节液,采用双抗体夹心酶联免疫吸附法,分别测定兔膝关节液中IL-1及TNF 表达水平。

The re were 12 rabbits (24 articular genus) in every group. Osteoarthritis model was established by injection of caroid in articular genu intracavitary. Rabbits with osteoarthritis were interfered by Duhuojisheng decoction. The expression of IL-1 and TNF from synovial fluid in rabbit with osteoarthritis were measured by double antibody sandwich ELISA 1, 3, 5 weeks after treatment.

将24只兔随机分为2组,即对照组和治疗组,各12只,24个膝关节,采用兔膝关节腔内注入木瓜蛋白酶造成骨关节炎的病理模型,以独活寄生汤浓缩液喂食饲养,于治疗后1、3、5 周分别抽取关节液,采用双抗体夹心酶联免疫吸附法,分别测定兔膝关节液中IL-1及TNF 表达水平。

There were 12 rabbits (24 articular genus) in every group. Osteoarthritis model was established by injection of caroid in articular genu intracavitary. Rabbits with osteoarthritis were interfered by Duhuojisheng decoction. The expression of IL-1 and TNF from synovial fluid in rabbit with osteoarthritis were measured by double antibody sandwich ELISA 1, 3, 5 weeks after treatment.

将24只兔随机分为2组,即对照组和治疗组,各12只,24个膝关节,采用兔膝关节腔内注入木瓜蛋白酶造成骨关节炎的病理模型,以独活寄生汤浓缩液喂食饲养,于治疗后1、3、5 周分别抽取关节液,采用双抗体夹心酶联免疫吸附法,分别测定兔膝关节液中IL-1及TNF 表达水平。

Osteoarthritis model was established by injection of caroid in articular genu intracavitary. Rabbits with osteoarthritis were interfered by Duhuojisheng decoction. The expression of IL-1 and TNF from synovial fluid in rabbit with osteoarthritis were measured by double antibody sandwich ELISA 1, 3, 5 weeks after treatment.

将24只兔随机分为2组,即对照组和治疗组,各12只,24个膝关节,采用兔膝关节腔内注入木瓜蛋白酶造成骨关节炎的病理模型,以独活寄生汤浓缩液喂食饲养,于治疗后1、3、5 周分别抽取关节液,采用双抗体夹心酶联免疫吸附法,分别测定兔膝关节液中IL-1及TNF 表达水平。

Notice the packed cell volume from the centesis fluid exceeds the packed cell volume taken from the peripheral vein.

注意的穿刺液红细胞压积从超过红细胞压积静脉抽取周边。

Bone marrow was drawn from rabbit by density gradient centrifugate in 70% Percoll fluid, the rate of cell survival was evaluated with trypan blue staining;The cells have been induced,differentiated and transfered of culture in vitro for five weeks; MSCs was seed onto BMG and continued to be cultured six weeks in vitro,then the compound was carried out to observe collagen by Masson staining.

抽取兔骨髓,用70% Percoll液,经密度梯度离心法分离MSCs,台盼蓝染色观察细胞存活率;诱导分化,传代,体外培养5周;复合BMG,继续体外培养6周,Masson染色观察胶原合成情况。

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