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QA 208 - 199在培养的大鼠胚胎中的细胞色素P - 450依赖性生物转化

Cytochrome P-450-dependent biotransformation of QA 208-199 in cultured rat conceptuses.

作者信息

Terlouw G D, Bechter R

机构信息

Drug Safety Assessment, Toxicology, Sandoz Pharma Ltd, CH-4002 Basle Switzerland.

出版信息

Toxicol In Vitro. 1993 May;7(3):247-58. doi: 10.1016/0887-2333(93)90008-s.

Abstract

It has been shown, using the method of rat post-implantation embryo culture, that the rat conceptus metabolizes the lipoxygenase inhibitor N-hydroxy-N-methyl-7-propoxy-2-naphthalenethan-amine (QA 208-199, QAB) in vitro. The capacity to metabolize QAB and accumulate its main metabolites depends on the developmental stage and length of exposure. In the present study, pregnant Han Wistar dams were given ip injections of either Aroclor 1254 (AC), 3-methylcholanthrene (3-MC) or phenobarbital (PB) before the dissection and culture of 9.5- and 10.5-day-old conceptuses in order to identify possible inducible conceptal cytochrome P-450 species. Conceptuses preinduced in utero were exposed to QAB in vitro for 48 hr, after which metabolites in the culture medium and conceptual tissues were determined with HPLC. Embryotoxic effects were evaluated in the same conceptuses. Preinduction in utero with AC, 3-MC or PB revealed that pretreatment with PB led, after 48 hr of culture, to a statistically significantly increased impairment of embryonic differentiation in 9.5-day-old conceptuses in vitro in comparison with vehicle-induced QAB-exposed conceptuses. Preinduction with PB led to higher levels of QAA, the main metabolite in vivo, in the culture medium. In the conceptal tissues, metabolite levels were significantly lower after preinduction with AC. In vehicle-induced 10.5-day-old embryos QAB caused less embryotoxicity in comparison with 9.5-day-old ones. In all preinduced conceptuses cultured from 10.5 to 12.5 days, yolk-sac vascularization was less affected and fewer embryonic anomalies were found in comparison with conceptuses cultured from 9.5 to 11.5 days. AC and PB pretreatment caused a decreased morphological score without changes in overall growth. Analysis of QAB and its metabolites in culture media and conceptal tissues at 12.5 days showed different levels of metabolites depending on the inducer used. To find further evidence for the involvement of cytochrome P-450 enzymes in the conceptal metabolism of QAB, conceptuses preinduced in utero (3-MC or PB) were exposed to QAB in vitro and gassed during the second half of the culture period with a mixture containing 35% carbon monoxide (CO), an inhibitor of cytochrome P-450 enzymes. CO treatment led to an inhibition of conceptal metabolism of QAB in comparison with that in conceptuses cultured under normal gassing conditions (without CO). These results strongly suggest the involvement of cytochrome P-450-dependent monooxygenases in the conceptal metabolism of QAB in vitro. 10.5-day-old conceptuses, after preexposure in utero to PB, were less susceptible to QAB embryotoxicity in vitro than were 9.5-day-old ones. In addition, the response to preinduction appeared to be age dependent.

摘要

采用大鼠植入后胚胎培养方法已表明,大鼠孕体在体外可代谢脂氧合酶抑制剂N-羟基-N-甲基-7-丙氧基-2-萘乙胺(QA 208-199,QAB)。代谢QAB并积累其主要代谢产物的能力取决于发育阶段和暴露时间。在本研究中,在解剖和培养9.5日龄及10.5日龄的孕体之前,给妊娠的Han Wistar母鼠腹腔注射艾氏剂1254(AC)、3-甲基胆蒽(3-MC)或苯巴比妥(PB),以确定可能被诱导的孕体细胞色素P-450种类。子宫内预先诱导的孕体在体外暴露于QAB 48小时,之后用高效液相色谱法测定培养基和孕体组织中的代谢产物。在相同的孕体中评估胚胎毒性作用。子宫内用AC、3-MC或PB预先诱导显示,与溶剂诱导的暴露于QAB的孕体相比,在体外培养48小时后,用PB预处理导致9.5日龄孕体的胚胎分化损伤在统计学上显著增加。用PB预先诱导导致培养基中体内主要代谢产物QAA的水平升高。在孕体组织中,用AC预先诱导后代谢产物水平显著降低。在溶剂诱导的10.5日龄胚胎中,与9.5日龄胚胎相比,QAB引起的胚胎毒性较小。在所有从10.5日龄培养至12.5日龄的预先诱导的孕体中,与从9.5日龄培养至11.5日龄的孕体相比,卵黄囊血管形成受影响较小,发现的胚胎异常较少。AC和PB预处理导致形态学评分降低,但总体生长无变化。在12.5日龄时对培养基和孕体组织中的QAB及其代谢产物进行分析表明,取决于所使用的诱导剂,代谢产物水平不同。为了找到细胞色素P-450酶参与QAB孕体代谢的进一步证据,将子宫内预先诱导(3-MC或PB)的孕体在体外暴露于QAB,并在培养期的后半段用含35%一氧化碳(CO)的混合物通气,CO是细胞色素P-450酶的抑制剂。与在正常通气条件下(无CO)培养的孕体相比,CO处理导致QAB的孕体代谢受到抑制。这些结果有力地表明,细胞色素P-450依赖性单加氧酶参与了体外QAB的孕体代谢。子宫内预先暴露于PB的10.5日龄孕体在体外对QAB胚胎毒性的敏感性低于9.5日龄孕体。此外,对预先诱导的反应似乎与年龄有关。

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