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细胞色素P450及其与血红素生物合成途径的相互作用。

Cytochrome P450 and its interactions with the heme biosynthetic pathway.

作者信息

De Matteis F, Marks G S

机构信息

Instituto di Farmacologica, Facolta di Medicina e Chirugia, Universita di Torino, Italy.

出版信息

Can J Physiol Pharmacol. 1996 Jan;74(1):1-8.

PMID:8963944
Abstract

An important factor in disruption of hepatic heme biosynthesis by porphyrinogenic drugs appears to be interaction with one or several cytochrome P450 isozymes. Clarification of the nature of the interaction between porphyrinogenic drugs and cytochrome P450 isozymes, as well as identification of the isozymes involved, will be helpful in extrapolating the results of animal experimentation to humans. Administration of griseofulvin to mice results in accumulation in the liver of two N-alkylated protoporphyrins (PPs). The major N-alkyl PP, N-griseofulvin PP, which is devoid of ferrochelatase-inhibitory activity, was shown to be the precursor of N-methyl PP, which is a potent ferrochelatase inhibitor. N-Griseofulvin PP was present predominantly as the Nc regioisomer rather than the anticipated NA regioisomer. Progesterone (PG) 6 beta-hydroxylase and androstenedione (AD) 6 beta-hydroxylase, diagnostic markers for cytochrome P450 3A1/2 activity in rat liver, were identified in chick embryo liver. The in ovo administration of 3,5-diethoxycarbonyl-1,4-dihydro-2,6-dimethyl-4-ethylpyridine (4-ethyl DDC) and 3-[2-(2,4,6-trimethylphenyl)thioethyl]-4-methylsydnone (TTMS) caused inactivation of chick embryo hepatic PG and AD 6 beta-hydroxylases. Ascorbate was shown to inhibit uroporphyrin accumulation in cultures of chick embryos treated with porphyrinogenic drugs and in the livers of an ascorbate-requiring rat strain treated with a porphyrinogenic combination of chemicals. Ascorbate appears to act by inhibiting oxidation of uroporphyrinogen to uroporphyrin. Avian hepatocytes were cultured in 48-well plates and directly assayed within the wells for the activity of 7-ethoxyresorufin O-deethylation (EROD), and for porphyrin and protein concentration by a fluorescence plate reader. Uroporphyrin was the main porphyrin to accumulate in response to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in chick embryos, pheasants, ducks, and herring gulls; heptacarboxylated porphyrin predominated in turkey hepatocytes. The EROD-inducing potential of complex mixtures of polyhalogenated aromatic hydrocarbons from herring gull eggs was assessed and compared with that of TCDD. A nuclear heme pool appears to regulate the transcription of the cytochrome P450 2B1/2B2 genes in rat liver, by modulating binding of a transcription factor(s) that appears to be involved in the transcriptional activation by phenobarbitone.

摘要

致卟啉药物破坏肝脏血红素生物合成的一个重要因素似乎是与一种或几种细胞色素P450同工酶相互作用。阐明致卟啉药物与细胞色素P450同工酶之间相互作用的性质,以及确定所涉及的同工酶,将有助于把动物实验结果外推至人类。给小鼠服用灰黄霉素会导致肝脏中两种N-烷基化原卟啉(PPs)蓄积。主要的N-烷基PP,即N-灰黄霉素PP,没有亚铁螯合酶抑制活性,已证明它是N-甲基PP的前体,而N-甲基PP是一种有效的亚铁螯合酶抑制剂。N-灰黄霉素PP主要以Nc区域异构体形式存在,而非预期的NA区域异构体。孕酮(PG)6β-羟化酶和雄烯二酮(AD)6β-羟化酶是大鼠肝脏中细胞色素P450 3A1/2活性的诊断标志物,在鸡胚肝脏中也被鉴定出来。在鸡胚中给予3,5-二乙氧羰基-1,4-二氢-2,6-二甲基-4-乙基吡啶(4-乙基DDC)和3-[2-(2,4,6-三甲基苯基)硫代乙基]-4-甲基-3-亚甲基异噁唑烷酮(TTMS)会导致鸡胚肝脏PG和AD 6β-羟化酶失活。已证明抗坏血酸可抑制用致卟啉药物处理的鸡胚培养物以及用致卟啉化学物组合处理的需要抗坏血酸的大鼠品系肝脏中的尿卟啉蓄积。抗坏血酸似乎是通过抑制尿卟啉原氧化为尿卟啉起作用。将禽肝细胞培养在48孔板中,并直接在孔内测定7-乙氧基异吩恶唑酮O-脱乙基酶(EROD)活性,以及用荧光酶标仪测定卟啉和蛋白质浓度。尿卟啉是鸡胚、雉鸡、鸭和银鸥中对2,3,7,8-四氯二苯并对二恶英(TCDD)产生反应而蓄积的主要卟啉;七羧化卟啉在火鸡肝细胞中占主导。评估了银鸥蛋中多卤代芳烃复杂混合物的EROD诱导潜力,并与TCDD的进行了比较。核血红素池似乎通过调节一种转录因子的结合来调控大鼠肝脏中细胞色素P450 2B1/2B2基因的转录,该转录因子似乎参与苯巴比妥的转录激活。

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