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首页> 外文期刊>Archives of Toxicology >Intralaboratory validation of alternative endpoints in the murine local lymph node assay for the identification of contact allergic potential: primary ear skin irritation and ear-draining lymph node hyperplasia induced by topical chemicals.
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Intralaboratory validation of alternative endpoints in the murine local lymph node assay for the identification of contact allergic potential: primary ear skin irritation and ear-draining lymph node hyperplasia induced by topical chemicals.

机译:在实验室进行的鼠局部淋巴结测定法中替代终点的实验室验证,用于确定接触性过敏潜力:局部化学物引起的原发性耳部皮肤刺激和引流淋巴结增生。

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We validated a two-tiered murine local lymph node assay (LLNA) with a panel of standard contact (photo)allergens and (photo)irritants with the aim of improving the discrimination between contact (photo) allergenic potential and true skin (photo)irritation potential. We determined ear weights to correlate chemical-induced skin irritation with the ear-draining lymph node (LN) activation potential. During tier I LLNAs, a wide range of concentrations were applied on three consecutive days to the dorsum of both ears. Mice were exposed to UVA light immediately after topical application to determine the photoreactive potential of some test chemicals. Mice were killed 24 h after the last application to determine ear and LN weights and LN cell counts. It was possible to classify the tested chemicals into three groups according to their threshold concentrations for LN activation and skin irritation: (1) chemicals with a low LN activation potential and no or very low skin irritation potential; (2) chemicals with a marked LN activation potential higher than a distinct skin irritation potential; and (3) chemicals with LN activation potential equal to or lower than their skin irritation potential. Group 1 consisted only of contact allergens, indicating that LN activation in the absence of skin irritation points to a contact allergenic activity. Since groups 2 and 3 comprised irritants and contact allergens, a tier II LLNA protocol was used to finally differentiate between true irritants and contact allergens. Briefly, mice were pretreated with mildly to moderately irritating concentrations of the chemical to the shaved back and after 12 days were challenged on the ears as described above in order to elicit a contact allergenic response in the ear skin and the ear-draining LN. With this approach, tier II LLNAs have to be conducted only in cases for which skin irritation potential is in the range of LN activation potential and no structure-activity relationship data indicating a contact allergenic hazard are available.
机译:我们验证了一组标准接触(光)过敏原和(光)刺激物的两层鼠局部淋巴结测定法(LLNA),目的是提高对接触(光)过敏原潜力和真实皮肤(光)刺激之间的区别。潜在。我们确定了耳重,以将化学诱导的皮肤刺激与引流淋巴结(LN)的激活潜力相关联。在第一级LLNA中,连续三天对两只耳朵的背部施加了广泛的浓度。局部应用后,立即将小鼠暴露于UVA光下,以确定某些测试化学品的光反应电位。最后一次施用后24小时处死小鼠以确定耳和LN重量以及LN细胞计数。可以根据其对LN活化和皮肤刺激的阈值浓度将测试的化学品分为三类:(1)具有低LN活化潜能且无或非常低的皮肤刺激潜能的化学品; (2)具有明显的LN活化潜能高于明显的皮肤刺激潜能的化学物质; (3)LN活化潜能等于或低于其皮肤刺激潜能的化学物质。第1组仅由接触性过敏原组成,表明在没有皮肤刺激的情况下LN激活指向接触性致敏活性。由于第2组和第3组包含刺激物和接触性过敏原,因此使用II级LLNA协议最终区分真正的刺激物和接触性过敏原。简而言之,用轻度至中度刺激性浓度的化学物质对小鼠进行剃刮预处理,并如上所述对小鼠的耳朵进行12天攻击,以引起耳朵皮肤和排液LN中的接触变应原反应。使用这种方法,仅在皮肤刺激潜力在LN活化潜力范围内且没有表明接触性变应性危害的结构活性关系数据可用的情况下,才需要进行II级LLNA。

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