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首页> 外文期刊>Journal of Veterinary Pharmacology and Therapeutics >Effects of enrofloxacin on cytochromes P4501A and P4503A in Carassius auratus gibelio (crucian carp)
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Effects of enrofloxacin on cytochromes P4501A and P4503A in Carassius auratus gibelio (crucian carp)

机译:恩诺沙星对Car鱼细胞色素P4501A和P4503A的影响

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摘要

Currently, although enrofloxacin (EF) as a widely used veterinary medicine has begun to apply to treating fish bacterial infections, the researches on the effects of EF on their main drug metabolic enzymes are limited. To investigate the effects of EF on fish cytochromes P450 (CYPs) 1A and 3A, the enzymatic activities and expressions (mRNA and protein) of crucian carp CYP1A and CYP3A after EF administration were examined. For CYP1A, in the in vivo experiments, EF exhibited potent inhibition on the CYP1A-related ethoxyresorufin-O-deethylase (EROD) activity, as well as CYP1A expressions at both protein and mRNA levels, at 24 h after administration with different EF dosages (3, 10, 30, and 60 mg/kg); Furthermore, CYP1A enzymatic activity and expressions at both protein and mRNA levels decreased more with increasing EF dosages. Additionally, the in vitro experimental results showed that, after incubated with microsomes, EF did not change the EROD activity through interacting directly with CYP1A. For CYP3A, the in vitro and in vivo experimental results demonstrated that EF could inhibit the CYP3A-related erythromycin N-demethylase activity in a time-and dose-dependent manner, while it did not suppress CYP3A expressions at both protein and mRNA levels after administration with EF for a short period (no more than 24 h); however, after injection with EF at a high dose (10 mg/kg) for a long period, the CYP3A protein and mRNA reached their lowest levels at 96 and 48 h, respectively. These results indicate that EF can suppress CYP1A expressions in a dose-dependent manner, thereby inhibiting further its catalytic activity; meanwhile, both the interactions of EF with CYP3A and the expressions decrease (protein and mRNA) caused by EF contribute to the CYP3A inhibition.
机译:目前,尽管恩诺沙星(EF)作为广泛使用的兽药已开始用于治疗鱼类细菌感染,但关于EF对其主要药物代谢酶的作用的研究仍然有限。为了研究EF对鱼类细胞色素P450(CYPs)1A和3A的影响,检查了EF施用后cru鱼CYP1A和CYP3A的酶活性和表达(mRNA和蛋白质)。对于CYP1A,在体内实验中,在以不同的EF剂量给药后24小时,EF对CYP1A相关的乙氧基间苯二酚-O-脱乙基酶(EROD)活性以及蛋白和mRNA水平上的CYP1A表达均表现出有效的抑制作用( 3、10、30和60 mg / kg);此外,随着EF剂量的增加,CYP1A酶活性和蛋白和mRNA水平的表达均下降更多。此外,体外实验结果表明,在与微粒体温育后,EF不会通过直接与CYP1A相互作用而改变EROD活性。对于CYP3A,体内外实验结果表明EF可以以时间和剂量依赖性的方式抑制CYP3A相关的红霉素N-去甲基酶活性,而在给药后在蛋白和mRNA水平上均未抑制CYP3A的表达。在短时间内使用EF(不超过24小时);然而,在长期以高剂量(10 mg / kg)EF注射后,CYP3A蛋白和mRNA分别在96 h和48 h达到最低水平。这些结果表明EF可以剂量依赖的方式抑制CYP1A的表达,从而进一步抑制其催化活性。同时,EF与CYP3A的相互作用以及EF引起的表达降低(蛋白质和mRNA)均对CYP3A产生抑制作用。

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