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腹腔注射和口服一水合6-巯基嘌呤的微核试验。

Micronucleus test with 6-mercaptopurine monohydrate administered intraperitoneally and orally.

作者信息

Hara T, Makita T, Horiya N, Ozawa S, Ohba M, Naito J, Shibuya T

机构信息

Hatano Research Institute, Food and Drug Safety Center, Kanagawa, Japan.

出版信息

Mutat Res. 1989 Aug;223(4):349-52. doi: 10.1016/0165-1218(89)90083-9.

Abstract

The effect of route of administration on the induction of micronucleated polychromatic erythrocytes (MNPCEs) was examined. 6-Mercaptopurine monohydrate (6-MP) was administered intraperitoneally (i.p.) or orally (p.o.) to 2 strains of mice, MS/Ae and CD-1. From the results of an acute toxicity test and a pilot micronucleus test, the doses selected for the final micronucleus test were 12.5-100 mg/kg for the i.p. route and 25-200 mg/kg for the p.o. route. The sampling time was 48 h. Frequencies of MNPCEs increased dose-dependently by the i.p. route but peaked at 50 or 100 mg/kg for the p.o. route. 6-MP induced MNPCEs more efficiently after p.o. administration than after i.p. treatment in both strains.

摘要

研究了给药途径对诱导微核多染性红细胞(MNPCEs)的影响。将一水合6-巯基嘌呤(6-MP)经腹腔注射(i.p.)或口服(p.o.)给予2个品系的小鼠,即MS/Ae和CD-1。根据急性毒性试验和预试验微核试验的结果,最终微核试验选择的剂量为腹腔注射途径12.5 - 100 mg/kg,口服途径25 - 200 mg/kg。取样时间为48小时。微核多染性红细胞的频率经腹腔注射途径呈剂量依赖性增加,但经口服途径在50或100 mg/kg时达到峰值。在两个品系中,6-MP口服给药后诱导微核多染性红细胞的效率均高于腹腔注射给药后。

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