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优化小鼠接触敏感性的剂量和时间研究。

Dose and timing studies for the optimization of contact sensitivity in the mouse.

作者信息

Brown W R, Shivji G M

机构信息

Division of Dermatology, University of Toronto, Canada.

出版信息

Acta Derm Venereol. 1991;71(1):44-7.

PMID:1676214
Abstract

We investigated the effectiveness of very low doses of the contact sensitizer dinitrofluorobenzene in sensitizing BALB/cJ mice. Surprisingly, the ear swelling reactions were greater with lower dinitrofluorobenzene doses, down to one-twentieth of doses commonly used. Although it is common practice to use much lower doses at challenge than at sensitization, we found greater reactions with lower doses at sensitization than at challenge. We also studied the timing of the development and waning of reactivity to dinitrofluorobenzene, dinitrochlorobenzene and oxazolone. Reactivity peaked at day 5 for dinitrofluorobenzene and dinitrochlorobenzene, and at day 3 for oxazolone. Reactivity waned by 3 weeks with dinitrofluorobenzene and oxazolone, and by day 7 with dinitrochlorobenzene. Pretreatment with cyclophosphamide caused a delay in the development and waning of reactivity.

摘要

我们研究了极低剂量的接触性致敏剂二硝基氟苯对BALB/cJ小鼠的致敏效果。令人惊讶的是,二硝基氟苯剂量越低,耳部肿胀反应越大,低至常用剂量的二十分之一。虽然通常在激发时使用比致敏时低得多的剂量,但我们发现致敏时较低剂量的反应比激发时更大。我们还研究了对二硝基氟苯、二硝基氯苯和恶唑酮反应性的发展和消退时间。二硝基氟苯和二硝基氯苯的反应性在第5天达到峰值,恶唑酮在第3天达到峰值。二硝基氟苯和恶唑酮的反应性在3周内减弱,二硝基氯苯在第7天减弱。用环磷酰胺预处理会导致反应性发展和消退的延迟。

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