尾静脉

B组与C组一次性经尾静脉注射阿霉素7mg/kg。

Rats in groups B and C were injected with a single dose of 7mg / kg adriamycin via caudal vein .

本研究旨在探讨MLCK在糖尿病肾病中的作用机制。方法：尾静脉注射链脲佐菌素（STZ）制作糖尿病大鼠模型，糖尿病大鼠再进一步随机分为糖尿病组和胰岛素组。

The aim of this study is to investigate the mechanism of MLCK in diabetic nephropathy . Methods : Diabetes was induced by a caudal vein injection of streptozotocin . The diabetic rats were then randomly divided into diabetic group and insulin group .

尾静脉注射P物质分别反转了雌激素对这两类神经元放电活动的影响。

While SP reversed the effects of estradiol bezonate on the above mentioned neurons .

每只大鼠用硫喷妥钠腹腔注射麻醉后，经鼠尾静脉刺入输液针，验证回血后送入CT室准备灌注扫描。

After intraperitoneal injection of sodium pentothal the tail vein was used as transfusion circuit of perfusion scanning .

采用双侧颈总动脉结扎建立SD大鼠暂时性全脑缺血模型，手术后通过尾静脉注射刺五加注射液或生理盐水。

The temporary cerebral ischemia model was established through common carotid arteries occlusion .

TBI4小时后，B、D组大鼠经尾静脉输注供鼠骨髓细胞作为实验组，A、C组大鼠输注生理盐水作为对照组。

Four hours after TBI , rats of group B and D were injected with donor bone marrow cells via tail vein as test groups .

方法采用44只SD大鼠尾静脉注射链脲霉素的方法，建立超负荷血糖模型。

Methods Hyperglycemia model was made by intravenous injection of streptozocin in 44 SD rats .

结论①尾静脉注射LPS可以复制出大鼠ALI模型。

Conclusion ① ALI model can be duplicated by injection of LPS .

尾静脉注射bFGF对大鼠脊髓损伤的早期影响

The Early Effects of Intravenous bFGF on Injured Spinal Cord

经尾静脉注射鞭毛蛋白以建立大鼠ALI模型。

Rat model of ALI was reproduced by injecting flagellin .

小鼠尾静脉注射细菌SOD，不同组织、器官均有分布，但数量有差异；

The bacterial SOD distributed to many tissue and organs through tail mainline , but the quantity is diversity .

采用上述相同方法尾静脉注射PBS缓冲液。

PBS was injected intravenously into rats with the same way as above .

方法：对SD大鼠一次性尾静脉注射阿霉素（6.5mg／kg），建立阿霉素肾病模型。

Methods : The AIN rats model was induced by adriamycin .

方法60只急性放射性脑损伤模型大鼠（直线加速器6MeV电子束单次照射25Gy）分为单纯照射组和照射前尾静脉注射bFGF组（250ng/kg），并设未照射对照组；

Methods 60 rats were classified into radiation group , bFGF intravenous injection group and contol group .

方法：用油酸尾静脉注射制作小鼠ALI损伤模型，观察其周围血白细胞及肺组织病理改变。

Method Mouse model with oil-acid and observe the change of leukocyte and pathological of lung tissue .

模型组（B组）：LPS每只6mg/kg溶于706代血浆，每只2mL/kg尾静脉注射；

B , the model group , LPS 6 mg / kg dissolves into 706 substitute of blood plasma 2 mL / kg tail iv ;

方法应用尾静脉注射OA复制大鼠ALI模型。

Methods The model of ALI in rats was reproduced by injecting oleic acid into the tail vein .

与尾静脉注射非磁丝裂霉素C纳米球胶体溶液剂的结果比较，外加磁场与磁纳米球的相互作用可大大地提高磁纳米球对肝脏的靶向率。

Compared with the results of tail vein administration mitomycin nanoparticles , interaction between the external magnetic field and magnetic nanoparticles is significantly effective to increase targeting rates of MMC to liver .

20只ICR小鼠经尾静脉途径人工感染泰泽氏菌。

ICR mice were inoculated with Clostridium piliformis via tail vein .

采用尾静脉给药方式，观察给药后48h内小鼠的一般情况及其死亡率。

General physical condition and the death rate of mice were observed within 48 h.

不同剂量BMSC尾静脉输注对小鼠肺组织纤维化的影响

Effects of different dosages of BMSC on lung fibrosis in mice

尾静脉注射Evans蓝检测肠黏膜与血管通透性的变化；

Intravenous inject Evans blue through vena caudalis to observe intestine mucous membrane permeability and vasopermeability ;

B组DFO腹腔注射半小时后ALA尾静脉注射；

Group B were injected with 5-ALA through tail veins half an hour after celiac injection of DFO .

方法：经尾静脉注射LPS（4mg/Kg）建立ALI大鼠模型。

Methods A rat model of ALI was established by injection of LPS with a dose of 4mg / kg .

方法：动物灌胃给药，小鼠尾静脉注射鞣花酸制造高凝动物模型，以剪尾法测定出血时间（BT）；

Methods : The model of blood hypercoagulable state was established by intravenous injection of ellagic acid in mice and rats .

采用尾静脉注射给药的方法，给予SD大鼠不同浓度的Ucn1小时后从胸主动脉取血测血清ACE水平；取大鼠胸主动脉及肺测定组织ACE水平。

One hour after the administration , blood samples were obtained from the thoracic aortas for the determination of serum ACE activity .

B为模型组，LPS6mg／kg／只溶于706代血浆2ml／kg／只尾静脉注射；

B , the model group : each rat received LPS 6mg / kg that was dissolved into 706 2ml / kg by tail intravenous injection ;

结果经筛选的S180肉瘤细胞尾静脉注射可成功建立小鼠血行肺转移模型。

Results A pulmonary metastasis model was successfully established with the selected sarcoma S 180 cells .

连续给药3d后，尾静脉注射绵羊红细胞悬液0.1mL进行致敏。

0.1 mL of sheep erythrocyte suspension was injected via the vena caudalis after 3-day administration to allergize .

对照组2是假手术组，经尾静脉注入LPC。

The rats in control group 2 were subjected to the intravenous infection of LPC with pseudo-operation .