盐酸苯胺处理大鼠腭裂的诱导:母体高铁血红蛋白缺氧的可能影响

Kiyoshi Matsumoto, N. Seki, K. Fukuta, Y. Ooshima
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引用次数: 3

摘要

盐酸苯胺(Aniline hydrochloride, AH)是一种刺激高铁血红蛋白形成的物质,其剂量为520 mg/kg,不会引起明显的胎儿死亡,在妊娠第14、15或16天皮下注射一次,以评估腭裂诱导的阶段特异性。同时,在妊娠第15天给药260、390、520和650 mg/kg的剂量,研究了剂量-反应与胎儿腭裂和母体高铁血蛋白血症诱导的关系。在分期特异性研究中,经AH治疗的水坝出现苍白、体重增加减少和高铁血红蛋白浓度升高。在胎儿检查中,虽然所有AH处理组的体重都有所下降,但只有在妊娠第15天处理的母鼠中才观察到腭裂。在剂量依赖性研究中,妊娠第15天给药剂量分别为260、390、520和650 mg/kg时,AH诱导母体高铁血红蛋白血症,降低胎儿体重,增加腭裂发生率。此外,亚甲基蓝(一种预防高铁血红蛋白血症的物质)对AH处理的小鼠的治疗改善了母体高铁血红蛋白血症,降低了胎儿腭裂的发生率。综上所述,我们认为AH期特异性诱导大鼠腭裂,而腭裂不是由AH的直接致畸作用引起的,而是由高铁血红蛋白血症引起的母体缺氧引起的。
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Induction of cleft palate in aniline hydrochloride‐treated rats: Possible effect of maternal methemoglobinemic hypoxia
ABSTRACT  Aniline hydrochloride (AH), a methemoglobin formation‐stimulating substance, at a dosage level of 520 mg/kg which does not induce apparent fetal death, was injected subcutaneously into pregnant rats once on day 14, 15 or 16 of gestation in order to assess the stage specificity of cleft palate induction. Also, doses of 260, 390, 520 and 650 mg/kg were administered to pregnant rats on day 15 of gestation, and the dose‐response relationships with respect to fetal cleft palate and maternal methemo‐globinemia induction were studied. In the stage‐specificity study, paleness, decreased body weight gain and elevated methemoglobin concentration were noted in the dams treated with AH. Upon fetal examinations, although reduced body weight was noted in all AH‐treated groups, cleft palate was observed only in fetuses from those dams treated on day 15 of gestation. In the dose‐dependency study, AH induced maternal methemoglobinemia, decreased fetal body weight and increased the incidence of cleft palate dose dependently when administered at dosage levels of 260, 390, 520 and 650 mg/kg on day 15 of gestation. Additionally, administration of methylene blue, a methemoglobinemia‐preventing substance, to the AH‐treated dams ameliorated maternal methemoglobinemia and reduced the incidence of fetal cleft palate. In summation, it is considered that AH stage‐specifically induces cleft palate in rats and that cleft palate is caused not by a direct teratogenic effect of AH but by maternal hypoxia due to methemoglobinemia.
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