腹腔注射

A型肉毒毒素腹腔注射对大鼠小肠通过速度及胆碱酯酶和P物质表达的影响

Effects of intraperitoneal injection of botulinum toxin A on passage velocity in small intestine and expression of acetylcholinesterase and substance P in rats

结果经口投予和腹腔注射VES均可明显降低B（a）P诱导的小鼠前胃癌的发生。

Can decrease the development of B ( a ) P-induced forestomach cancer in mice .

腹腔注射1，25（OH）2D3对调节性T细胞及大鼠肾移植存活的影响

Effect of 1,25-dihydroxyvitamin D3 on regulatory T cell in vivo and survival of rat renal allograft

方法腹腔注射蛙皮素制成AP大鼠模型。

[ Methods ] AP was induced by injection of Cerulein .

B组和C组通过腹腔注射链脲佐菌素（Streptozocin，STZ）建立糖尿病模型。

The model was established through injection with streptozotocin ( STZ ) .

N组和DM组给予等容积0.9%灭菌氯化钠腹腔注射。

N group and DM group was given equal volume of 0.9 % sterile sodium chloride intraperitoneally .

结论：①孕鼠腹腔注射LPS可诱发早产；

Conclusion : Preterm delivery can be induced by LPS .

大鼠腹腔注射精氨酸加压素，50μg／kg，每天1次，共1周；

Wistar rats were intraperitoneally injected with 50 μ g / kg arginine vasopressin once a day for one week .

方法腹腔注射递增剂量的盐酸吗啡使雄性SD大鼠形成吗啡依赖，并用纳洛酮催促戒断。

Methods Nucleus accumbens was dissected out from morphine dependent and naloxone precipitated withdrawal rats .

方法：通过腹腔注射LPS建立感染性休克小鼠模型。

METHODS : Septic shock mice model was induced by intraperitoneal injection of LPS .

腹腔注射胍乙啶20毫克/公斤后5小时，NA已近耗尽；

Intraperitoneal injection of guanethidine sulphate 20 mg / kg caused a well-nigh complete depletion in 5 hours .

方法大肠杆菌腹腔注射制备猪ARDS模型。

Methods ARDS model was reproduced by intraperitoneal injection of E.

方法D-半乳糖腹腔注射〔50mg/（kg·d）〕，连续6周。

Methods D galactose was daily injected into abdominal cavity for six weeks 〔 50 mg / ( kg · d )〕 .

瘤龄7天后腹腔注射GCV30mg／kg／天，共14天。

When the tumor was 7 days old , 30mg / kg / day of GCV was intraperitoneally injected for 14 days .

方法给SD大鼠先后腹腔注射氯化锂、匹罗卡品，制成癫疒间动物模型；

Methods Models of epilepsy of SD rats were established by intraperitoneal injection with lithium chloride and pilocarpine .

结果：小鼠腹腔注射松针挥发油的LD（50）为3.738ml／kg；

Results : the LD50 injecting essential oils to mice 's abdominal cavity is 3 . 738ml / kg ;

正常对照组与模型组小鼠腹腔注射等体积的PBS。

The nomal control and model group received an equal volume of PBS .

结果：腹腔注射氟哌啶醇使SD大鼠口部异常运动增加明显，第5周达峰值；

RESULTS : Haloperidol could facilitate orofacial dyskinesia movement of rats to reach the peak value at the fifth week ;

SD大鼠腹腔注射卵蛋白制成哮喘模型，分别予相应方法治疗，并与必可酮气雾剂比较。

SD rats were modeled into asthmatic rats by abdominal injection of egg albumin , and then treated by aforementioned methods ;

方法：选用清洁级昆明小鼠腹腔注射脂多糖（LPS）制备内毒素休克动物模型，①观察内毒素休克前后Tβ4变化情况。

Methods : LPS ( lipopolysaccharide ) was intraperitoneally injected into clean Kunming mice to establish the animal model .

方法链脲佐菌素（STZ）单次腹腔注射制作SD大鼠糖尿病模型。

Methods SD rat model of diabetes was established by intraperitoneal injection of streptozotocin ( STZ ) .

感染后12h腹腔注射氟康唑；

Intraperitoneal injection with fluconazole 12h after the infection ;

结论（1）D-gal1.4g/kg腹腔注射可以很好构建SD大鼠急性肝衰竭模型。

Conclusion ( 1 ) Acute hepatic failure of rats can be induced with D-gal at the dose of 1.4g/kg very well .

方法采用立体定向术将LPS注入大鼠单侧黑质后分别于注射后2、3、4周经腹腔注射阿朴吗啡诱发动物旋转行为；

The circling behavior was observed by intraperitoneal-injection of apomorphine during the intervals of 2,3 and 4 weeks after injection .

腹腔注射脂多糖（LPS）制备小鼠脓毒症模型，用流式细胞仪检测DC表面分子CD11c、CD86和主要组织相容性抗原复合物（MHC）的表达；

The sepsis model of mice was reproduced by the injection of lipopolysaccharides ( LPS ) .

腹腔注射组各时间点外周血中EPC的数量均显著增加，而结膜下注射组EPC的数量与注射前差异无统计学意义。

The numbers of EPCs in peripheral blood of intraperitoneal injection group were significantly increased at different time points .

除正常对照组外，各组小鼠均采用利血平复制脾虚证动物模型，腹腔注射利血平0.2mg/（kg·d）。

Except mice in normal control group , model mice of spleen deficiency syndrome were established by injecting 0.2 mg / ( kg · d ) reserpine intravenously .

方法分别利用CCL4腹腔注射和皮下注射的方法制备大鼠肝纤维化模型。

Methods CCL4 was injected intraperitoneally or subcutaneously to make rat liver fibrosis model .

方法：以健康成年雄性Sprague-Dawley白色大鼠为研究对象。所有药物均经腹腔注射。

Method : We selected healthy male adult Sprague-Dawley white rats as research objects .

方法连续7d腹腔注射Mor建立小鼠依赖模型。

Methods The model of Mor - dependent mice was established by intraperitoneal ( i.p. )