Suppr超能文献

[日本血吸虫尾蚴经皮肤侵入机制的研究及预防药物的筛选]

[A study on mechanism of skin penetration by cercaria of S. japonicum and screening of preventive drugs].

作者信息

Wang Y S, Chen J Y, Song P Z, Wang W N, Zhou X K, Hu H Q

出版信息

Hua Xi Yi Ke Da Xue Xue Bao. 1989 Mar;20(1):18-20.

PMID:2793135
Abstract

Mice pretreated with PG cyclo-oxygenase inhibitor aspirin, at 300 mg/kg/d x 5, and ibuprofen, at 100 mg/kg/d x 5 orally and 20 mg/kg/d x 3 intraperitoneally revealed moderate chemoprophylactic effects and the reduction of the penetration of worms by 23% when compared to controls. Daily oral administration of aspirin, at 300 mg/kg for 15 days the worms reduction increased to 41.7%. In estimation of PGE1 in cercariae of S. japonicum by radioimmunoassay, the PGE1 was 49 pg/100 cercariae. In normal mouse skin PGE1 has been measured to amount to 3105 +/- 691.7 pg/10 mg on average. In cercarial penetrated mouse skin, 1.5 hours after exposure the PGE1 assessed in 100 and 250 cercariae in the infected skin were 5506 +/- 1127.1 and 12085 +/- 2622.9 pg/10 mg respectively, which were significantly higher than that of the non-penetrated skin. These studies in conjunction with our previous work indicate that: 1.PGs, similar to S. mansoni, were probably necessary for cercarial penetration. 2.PG inhibitors could reduce cercarial penetration. Receptors antagonist etc. e.g. diphenhydramine, chlorpheniramine, atropine, practolol could not reduce cercarial penetration, but praziquantel in the pretreated mice could reduce cercarial penetration significantly. e.g. 400 mg/kg orally 2 hours prior to affection of cercariae about 100% reduction of the penetration, but if pretreated with praziquantel, 4, 8, 24, 36 hours prior to the affection the reduction penetration decreased to 51.7, 46.1, 9.4, 8.9% respectively.

摘要

用PG环氧化酶抑制剂阿司匹林(300mg/kg/d,连续5天口服)和布洛芬(100mg/kg/d,连续5天口服,20mg/kg/d,连续3天腹腔注射)预处理的小鼠显示出中度的化学预防效果,与对照组相比,蠕虫的穿透率降低了23%。每天口服300mg/kg的阿司匹林,持续15天,蠕虫减少率增加到41.7%。通过放射免疫测定法估计日本血吸虫尾蚴中的PGE1,PGE1为49pg/100尾蚴。在正常小鼠皮肤中,PGE1的平均含量为3105±691.7pg/10mg。在尾蚴穿透的小鼠皮肤中,暴露1.5小时后,感染皮肤中100只和250只尾蚴中的PGE1分别为5506±1127.1和12085±2622.9pg/10mg,显著高于未穿透皮肤的PGE1。这些研究与我们之前的工作表明:1.与曼氏血吸虫一样,PG可能是尾蚴穿透所必需的。2.PG抑制剂可以降低尾蚴的穿透率。受体拮抗剂等,如苯海拉明、氯苯那敏、阿托品、心得宁不能降低尾蚴的穿透率,但在预处理的小鼠中吡喹酮可以显著降低尾蚴的穿透率。例如,在感染尾蚴前2小时口服400mg/kg,穿透率降低约100%,但如果在感染前4、8、24、36小时用吡喹酮预处理,穿透率降低分别降至51.7%、46.1%、9.4%、8.9%。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验