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子宫内给予α-二氟甲基鸟氨酸对大鼠胚胎发育的抑制作用。

Inhibition of rat embryonic development by the intrauterine administration of alpha-difluoromethylornithine.

作者信息

Méndez J D, Diaz-Flores M, Durán G, Hicks J J

出版信息

Contraception. 1983 Jul;28(1):93-8. doi: 10.1016/s0010-7824(83)80010-9.

Abstract

Decarboxylation of L-ornithine by L-ornithine decarboxylase (ODC; E.C.4.1.1.17.) is the initial step in the biosynthesis of putrescine, ODC activity is generally low in most tissues, marked increases are associated with rapid tissue growth and particularly with mammalian embryogenesis. 0.5 mg/kg of DL-alpha-difluoromethylornithine (DFMO) (irreversible inhibitor of ODC) was administered to uterine horns of Long-Evans adult rats during the 4th day of pregnancy. As control material, saline (0.15 M) was administered to contralateral uterine horn. The animals were sacrificed on different days, the uterine horns were removed and the number of implant of implanted embryos were counted. DNA, RNA, protein and dry weight content in implantation sites (5th day of pregnancy) indicated that decidualization following DFMO took place normally but that embryonic growth was arrested in the treated horn. When 100 micrograms of putrescine were added together with DFMO, the embryotoxic effect was absent.

摘要

L-鸟氨酸脱羧酶(ODC;E.C.4.1.1.17.)催化L-鸟氨酸脱羧是腐胺生物合成的第一步。在大多数组织中,ODC活性通常较低,其显著增加与组织快速生长特别是与哺乳动物胚胎发育有关。在妊娠第4天,给成年Long-Evans大鼠子宫角注射0.5mg/kg的DL-α-二氟甲基鸟氨酸(DFMO)(ODC的不可逆抑制剂)。作为对照,给对侧子宫角注射生理盐水(0.15M)。在不同时间处死动物,取出子宫角并计数着床胚胎的数量。着床部位(妊娠第5天)的DNA、RNA、蛋白质和干重含量表明,DFMO处理后蜕膜化正常发生,但处理侧子宫角的胚胎生长停滞。当与DFMO一起添加100微克腐胺时,胚胎毒性作用消失。

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