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^125I—血管活性肠肽在小鼠体内的分布实验
引用本文:李前伟,谭天秩.^125I—血管活性肠肽在小鼠体内的分布实验[J].华西医科大学学报,1998,29(3):281-284.
作者姓名:李前伟  谭天秩
摘    要:为探讨高兹放活性血管活性肠肽(^125I-VIP)在正常小鼠体内的分布特性,取纯系昆明种小鼠30只,随机分为6组,每组5只,在尾静脉注入^125I-VIP0.2ml(74kBq)后180分钟内的不同时相,将小鼠断头处死,收集血液、肺、肝、肠和肾,称重并测定其放射性,最后换算为每克组织的ID%。另取纯系昆明种小鼠30只,分组同上,尾静脉分别注入含10、20和40μgVIP的^125I-VIP溶液,于

关 键 词:血管活性肠肽  药物分布  动物实验  胃肠道肿瘤

A biodistribution experiment on 125 I-VIP in mice]
Y Zhao,J Yang.A biodistribution experiment on 125 I-VIP in mice][J].Journal of West China University of Medical Sciences,1998,29(3):281-284.
Authors:Y Zhao  J Yang
Institution:Department of Nuclear Medicine, First Affiliated Hospital, Changdhu.
Abstract:This experiment was designed to investigate the biodistribution characters of 125 I-vasoactive intestinal peptide (VIP) with high specific activity in normal mice and the effect of VIP on the distributive test. After intravenous injection of 125 I-VIP, the mice were killed during 180 min. Blood, lungs, liver, intestine and kidneys were collected respectively and measured in 7 counter, finally the measurements of their radioactivity (cpm) were converted into ID%/g tissue and the results were expressed as mean+/-s. The effect on VIP on distributive test was evaluated by simultaneously injection of 125 I-VIP (74kBq) which contained 10,20 and 40 microgram VIP respectively; the mice were killed at 5 and 20 min. respectively, the collection of tissues and the management of data were the same as above. Most of the 125 I-VIP was distributed in the lungs rapidly, the radioactivity was mainly eliminated through kindneys; the T1/2 of activity in blood was shorter than 20 min; the difference in activity between liver and blood was not significant after 20 min. (P >0.05); the activity intestine remained lower during the experiment. The uptake of 125 I-VIP in lungs, liver and intestine was inhibited by VIP in dose dependence. The rates of inhibitory effectiveness of 10, 20 and 40 microgram VIP in lungs were 45.12%, 56.64% and 68.12% respectively at 5 min., and 53.65%, 71.03% and 79.03% respectively at 20 min. The present study indicated that the uptake of 125 I-VIP in various tissues of the mice possesses the character mediated by VIP receptor, 125 I-VIP is mainly accumulated by lungs, eliminated through kidneys, and the hepatobiliary system cannot remove it. The biodistribution character of 125 I-VIP is helpful to 131I (123I)-VIP imaging in the detection of gastrointestinal tumor.
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