Uterotrophic Bioassay in Rodents (UT assay) (OECD TG 440) (including OECD GD 71 on the procedure to test for anti-estrogenicity)

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引用次数: 1

Abstract

650. This assay is a short-term in vivo screening assay in female rodents for chemicals that interact with the estrogen receptor (ER). It is based on the increase in uterine weight (or uterotrophic response) that is elicited by ER agonists in animal models where endogenous estrogen levels are minimal. There are two variants of the assay; one uses immature animals, the other uses ovariectomised animals. The immature rodent assay may detect modalities acting via mechanisms other than ER, as the animals have an intact hypothalamic/pituitary/gonadal (HPG) axis, but the ability to detect these is limited. The assay may be conducted using rats or mice, but the there is more experience with the rat assay and this species was used in the OECD validation of this assay (OECD, 2006). Route of administration of test substance is via oral gavage or subcutaneous injection. This assay has been considered to be the “gold standard” bioassay screen for identifying ER agonists. A recently curated database of bioactivity with results from over 2 500 Uterotrophic Bioassays in rats and mice provides comprehensive information on this assay (Kleinstreuer et al., 2016).
啮齿类动物子宫营养生物测定(UT测定)(OECD TG 440)(包括OECD GD 71关于抗雌激素试验程序的规定)
650. 这是一项短期的雌性啮齿动物体内筛选试验,用于寻找与雌激素受体(ER)相互作用的化学物质。这是基于内源性雌激素水平极低的动物模型中内源性雌激素受体激动剂引起的子宫重量增加(或子宫营养反应)。该化验有两种变体;一个用未成熟的动物,另一个用切除卵巢的动物。由于动物具有完整的下丘脑/垂体/性腺(HPG)轴,因此未成熟啮齿动物实验可以检测通过内质网以外的机制作用的模式,但检测这些的能力是有限的。该试验可以用大鼠或小鼠进行,但对大鼠试验有更多的经验,并且该物种被用于经合组织对该试验的验证(经合组织,2006年)。试验物质的给药途径是口服灌胃或皮下注射。该试验被认为是鉴别内质网激动剂的“金标准”生物测定筛选。最近建立了一个生物活性数据库,其中包含了对大鼠和小鼠进行的2500多次子宫营养生物测定的结果,提供了有关该测定的全面信息(Kleinstreuer等,2016)。
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