目的改良豚鼠灌胃给药的方法。
Objective To modify the method of gavage administration in guinea pigs.
采用灌胃法测定曼陀罗对小鼠的毒性。
方法白酒灌胃法建立酒精性肝病大鼠模型。
Methods The model of alcoholic hepatic disorder was established by feeding alcohol liquor.
方法米非司酮配伍米索前列醇灌胃早孕大鼠。
METHORDS Mifepristone and Misoprostol were given to early-pregnancy rats orally.
建立家兔拟除虫菊酯类农药灌胃染毒致死模型。
To develop a pyrethroid intragastric administration death model.
青年组和老龄组给予相应剂量的蒸馏水灌胃8周。
In the young and the old group, rats were given the same dose distilled water for 8 weeks.
方法：采用灌胃脂肪乳剂建立大鼠的高脂血症模型。
Method: The rat hyperlipidemia model was set up by ig lipid emulsion.
采用大鼠进行动物实验，糖浆灌胃后检测血糖水平。
Experimental rats were fed with the grouped saccharides for assessment of blood sugar level.
小鼠灌胃SCC粉末混悬液可缩短出血和凝血时间。
SCC powder suspension on po administration can contract bleeding and coagulation time.
目的观察溶石胶囊灌胃给药后对结石大鼠的治疗作用。
Objective To observe treatment effects of Rongshi capsules with gastric infusion on experimental renal calculus in rats.
灌胃期满后即做迷宫实验及跳台实验以测学习、记忆能力。
The learning and remembering ability was tested by Y-maze test and jumping table experiment.
与静脉注射相比，灌胃和腹腔注射后的药动学特性发生显著改变。
After ig or IP administration, pharmacokinetic characteristics were significantly changed, compared with iv route.
方法：灌胃给药5次，观察睡眠实验、中枢兴奋实验和耐缺氧实验。
Methods: Sleep experiment, CNS excitability and ability to bear anoxic were observed by giving FXKQY and QTY 5 times.
方法：灌胃给药5次，观察睡眠实验、中枢兴奋实验和耐缺氧实验。
Methords: Observed sleep experiment, central excitation experiment, hypoxia tolerance after giving drugs 5 times.
方法采用亚慢性毒性试验方法，大鼠经口灌胃染毒，试验期为6周。
Methods Subchronic toxicity test was applied. The rats were exposed to arsenic by oral perfusion at gradient doses for 6 weeks respectively.
以最大剂量的腐植酸静脉、皮下注射或灌胃后，对胃肠推进运动无影响。
The propulsive motility was not affected when the humic acid was given Intraveneously, subcutaneously or introduced into the stomach.
灌胃期满将大鼠麻醉后断头处死，立即在冰盘中开颅取脑制备组织匀浆。
On the expiration of gastric perfusion, the rats were sacrificed after anesthetized and the brain was collected on ice plate to prepare tissue homogenate.
急性经口毒性试验采用一次灌胃，急性皮肤刺激试验在家兔皮肤上进行。
Its acute toxicity was tested by single oral injection, and the acute skin stimulation test was conducted directly on rabbits' skin.
结果急性毒性实验小鼠灌胃给药最大耐受量相当于人临床日用量的160倍。
ResultsIn the experiment of acute toxicity, the maximum tolerance dosage by gavage in mice was 160 times of the clinical dosage in humans.
灌胃给药8周后分别测定其对大鼠肾质量、肾功能及尿白蛋白排泄量的影响。
After 8 weeks of administration, the weight of rat kidney, renal function and the excretion of urine albumin were measured.
分组后连续4周灌胃给花粉多糖，同时各组大鼠继续给予高脂颗粒饲料喂饲。
Then they were fed with pollen polysaccharide and high-lipid pellet feed in the meantime for 4 weeks.
本文选用麻醉大鼠进行一次口服灌胃炔诺酮肟(NETO)的急性毒性实验。
Norethisterone oxime (NETO) was given orally to anesthetized rats in single dose to observe acute toxicity.
方法：采用小鼠注射d -半乳糖制成衰老模型。马齿苋水提液灌胃30d。
Methods: The senile mouse models induced by D-gal were prepared and given water extract of Machixian for 30 days.
除正常组外，其余各组连续灌胃给药7天后，ANIT诱发肝内胆汁淤积模型。
Except group a, the other groups were given corresponding medicines for 7 days and then additionally administered ANIT to induce cholestasis.
方法：采取灌胃和外敷两种给药方式，高效液相色谱法测定不同时项点的血药浓度。
METHODS: Two ways of drug given intragastral and usum externum were adopted, and the blood concentration of tetrandrine was detected by high performance liquid chromatography.
连续灌胃14周后，用10 %福尔·马林灌注后，取主动脉做形态学观察及图像分析。
After treating 14 weeks, all the mice were filled with 10% formalin and the aortas were stripped for morphological research and photograph analysis.
方法：用玉泉茶浸提液分别对四氧嘧啶和肾上腺素所致高血糖小鼠灌胃观察并设对照组。
Method: the extracted liquid from Yuquan Tea was poured into the intestine of small rats with hyperglycemia due to alloxan and adrenalin and then was observed, and then set as the controlled group.
模型建立后将高脂组大鼠分为干预组与非干预组，干预组采用灌胃方式进行药物干预8周。
Model high-fat group were divided into intervention group and non-intervention group, intervention approach to drug intervention by gavage for 8 weeks.
但穿山龙总皂苷组和文迪雅组比较，灌胃后各生化指标没有明显差别（P均＞0.05）。
Compared Wendiya to Dioscorea nipponica Makino total saponin group, there were no significant differences in biochemical markers after gavaging(P>0.05).
选择不同抗氧化活性的水果汁进行一次性灌胃实验，动态观察大鼠外周血抗氧化活性的变化。
Several fruits with different antioxidant capacity were selected for gavage experiment in rats, in which the dynamic changes of serum antioxidant capacity were determined after gavage.
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