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When MPa was given to the rats and mice model by the method of ip and ig,MPa was found with antiinflammatory action at different extent in the delayed footpad reaction with formaldehyde in rats and in the reaction of pinnae tumefaction with xylene in mice.

河蚌多糖对小鼠灌胃给药,能显著增强腹腔巨噬细胞吞噬能力;对大鼠和小鼠ip和ig给予MPa时,分别对甲醛引起的大鼠足跖反应和二甲苯引起的小鼠耳廓肿胀,具有不同程度的抗炎作用

Ulex Europeus was used as a probe to study the expression of α L Fucose in mouse uterus during early pregnancy,pseudopregnancy and estrous cycle.

应用免疫荧光技术以生物素化的荆豆素-为探针,检测其结合位点α-L-岩藻糖在小鼠妊娠 1~ 8d、假孕 1~ 6 d及发情周期子宫中的表达情况,并以摘除卵巢的小鼠为模型观察雌激素、孕酮对小鼠子宫α-L-岩藻糖表达的影响。

Can accelerate the bone marrow cell from G1 phase into S phase when we measure it's Cell cycle, it make S phase rate was increased .thus it promoted DNA synthesize and repaired. Mice irradiated at dose of 5.5 Gy gamma-irradiation showed timed-related decreases and restores in peripheral blood picture at day 1 through day 21, the counts of WBC of these group had taken drug has various degree to increase than irradiation control group in day 1. Grugs failed to protected the peripheral blood cell at lowest point, but seems promote their rescovery.9803 treated group was distinct. At 7days after mice were radiated in 3.5 Gy. we observed drug can Significantly hold back the decreased number of hematopoietic progenitors colony forming radiation induced. These findings indicated 9803 have a certain radioprotective activity against gammer irradiation in mice.

给药组的 CFU-S 数量较照射对照组明显增加,3.5Gy 照后第七天观察给药9803组对小鼠骨髓造血组细胞集落生成能力的影响,给药组的造血祖细胞集落的形成能力强于照射对照组,并且9803组明显优于523组。5.5Gy 照射引起的小鼠的外周血细胞数量的降低以 WBC 发生最早,照后24小时给药组的 WBC 数量均比照射对照组有不同程度的升高,以9803各给药组最为明显,药物未能使照射引起的外周血细胞最低值升高,而有降低的趋势,但给药对照射后期外周血象的总体恢复有较好的促进作用。7.5Gy 照射后第七天测定小鼠骨髓细胞周期的测定中发现9803具有促进骨髓细胞由 G1期进入 S 期的效应,致使 G0/G1期细胞显著减少, S 期细胞比率显著增加,这利于促进 DNA 合成修复,即促进骨髓细胞增殖,骨髓细胞 DNA 含量给药组显著高于照射对照组。

Gelsemium total alkaloids improved some blood and immune function of mice when it less than 0.30mg/kg body weight, but more than 1.5mg/kg body weight, the gelsemium total alkaloids can reduced some blood and immune function of mice; below the dose of 3%, GEB"s power can improve some blood and immune function of broilers, but GEB"s power can reduce some blood and immune function of broilers above the dose of 6%.

结论是:钩吻对小鼠和肉鸡的血液学及免疫功能的影响均存在着剂量差别,钩吻总碱稀释液在0.30mg/kg剂量以下,能够提高小鼠的某些血液指标与免疫功能(p<0.05),而在1.5mg/kg以上,则降低小鼠的某些血液指标与免疫功能(p<0.05);3%以下的钩吻干粉能够提高肉鸡的某些血液指标与免疫功能,而6%以上的钩吻干粉则降低某些血液指标与免疫功能。

Then the mice were killed in different time after given the medicine wine, and the wounded limbs were got follow the articular genua, and the limbs were put in the 10% formaldehyde solution to fix them, then the histopathologic sides were done, and the change in the tissue structure were observed in light microscope.

于给药后不同时段分别处死小鼠,然后沿膝关节部位剪取小鼠的击伤腿置于10 %甲醛溶液中固定,作病理组织切片,光镜下观察组织结构形态学变化评价,评价永康宁骨康宁药酒对小鼠击伤腿肿胀有无消肿作用。

Results E-jiao hematinic ointment could make the hemoglobin and erythrocyte of the posthemorrhagic anemia mice increase obviously, which had significant difference to the model control group; it could also increase the clearance rate of carbon particle, which had an enhancement effect of nonspecific immunity of mice.

结果阿胶补血膏小鼠灌胃给药可使失血性贫血小鼠血红蛋白及红细胞明显回升,与模型对照组比较有显著性差异;可明显增加碳粒廓清速率,对小鼠非特异性免疫有增强作用。

Results Xinsheng capsule could enhance delayed hypersensitivity in mice,increase the num-ber of antibody-producing cells,the level of serum hemolysin and the activity of NK cells.

结果 新生胶囊能促进小鼠的迟发型变态反应,提高小鼠的抗体生成细胞、血清溶血素水平,提高小鼠的NK细胞活性。

Results: Mouse body weights were significantly lower in high and low dose groups than that of control group (P.05); Spleen index in middle dose group (P.05) and hemolysin titer in high dose group (P.01) were obviously higher than those in control group.

结果:与对照组比较,高、低剂量组小鼠体重明显下降(P.05),中剂量组小鼠脾脏指数明显升高(P.05),高剂量组小鼠的溶血素效价显著升高(P.01)。

Methods The anti?nociceptive site of CAD was analysed with mice formalin test and mice hotplate test after intracerebroventricular administration;the concentration of nitric oxide in serum and β?

利用小鼠福尔马林实验及侧脑室注射CAD对小鼠热板痛反应潜伏期的影响以分析CAD的镇痛作用部位;观察CAD对甲醛所致伤害性疼痛模型小鼠血清一氧化氮和脑组织中β?

The donor was C57BL/6 mice in the control group and F1 hybridism mice in the experimental group.

将48只造模小鼠随机分为2组,对照组供鼠为C57BL/6小鼠,实验组供鼠为F1小鼠

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