{"title":"非洲爪蛙变态蝌蚪的肝酶诱导及其对甲状腺激素代谢的潜在影响","authors":"Kohei Wada, Takafumi Yamaguchi, Hitoshi Tanaka, Takuo Fujisawa","doi":"10.1002/jat.4672","DOIUrl":null,"url":null,"abstract":"<p>Hepatic enzyme induction, an inherent defense system against xenobiotics, is known to simultaneously affect endocrine system functions in mammals under specific conditions, particularly thyroid hormone (TH) regulation. While this phenomenon has been studied extensively, the pathway leading to this indirect thyroid effect in mammals has unclear applicability to amphibians, despite the importance of amphibian species in assessing thyroid-disruptive chemicals. Here, we investigated the effects of three well-known mammalian enzyme inducers—β-naphthoflavone (BNF), pregnenolone carbonitrile (PCN), and sodium phenobarbital (NaPB)—on the gene expression of phase-I and phase-II metabolizing enzymes in <i>Xenopus laevis</i> tadpoles. Waterborne exposure to BNF and PCN significantly induced the expression of both phase-I (cytochrome P450, CYP) and phase-II enzymes (UDP-glucuronosyltransferase, UGT and sulfotransferase, SULT), but in different patterns, while NaPB exposure induced CYP2B expression without affecting phase-II enzymes in tadpoles, in contrast to mammals. Furthermore, an ex vivo hepatic enzyme activity assay confirmed that BNF treatment significantly increased phase-II metabolic activity (glucuronidation and sulfation) toward TH. These results suggest the potential for certain mammalian enzyme inducers to influence TH clearance in <i>X. laevis</i> tadpoles. Our findings provide insights into the profiles of xenosensing activity and enzyme induction in amphibians, which can facilitate a better understanding of the mechanisms of indirect effects on the thyroid system via hepatic enzyme induction in nonmammalian species.</p>","PeriodicalId":15242,"journal":{"name":"Journal of Applied Toxicology","volume":"44 11","pages":"1773-1783"},"PeriodicalIF":2.7000,"publicationDate":"2024-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Hepatic enzyme induction and its potential effect on thyroid hormone metabolism in the metamorphosing tadpole of Xenopus laevis (African clawed frog)\",\"authors\":\"Kohei Wada, Takafumi Yamaguchi, Hitoshi Tanaka, Takuo Fujisawa\",\"doi\":\"10.1002/jat.4672\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Hepatic enzyme induction, an inherent defense system against xenobiotics, is known to simultaneously affect endocrine system functions in mammals under specific conditions, particularly thyroid hormone (TH) regulation. 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Furthermore, an ex vivo hepatic enzyme activity assay confirmed that BNF treatment significantly increased phase-II metabolic activity (glucuronidation and sulfation) toward TH. These results suggest the potential for certain mammalian enzyme inducers to influence TH clearance in <i>X. laevis</i> tadpoles. 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引用次数: 0
摘要
肝酶诱导是一种针对异种生物的固有防御系统,已知在特定条件下会同时影响哺乳动物的内分泌系统功能,特别是甲状腺激素(TH)的调节。尽管这种现象已被广泛研究,但导致哺乳动物甲状腺间接效应的途径还不清楚是否适用于两栖动物,尽管两栖动物物种在评估甲状腺干扰性化学物质方面非常重要。在这里,我们研究了三种著名的哺乳动物酶诱导剂--β-萘甲黄酮(BNF)、孕烯酮腈(PCN)和苯巴比妥钠(NaPB)--对爪蟾蝌蚪体内I期和II期代谢酶基因表达的影响。水载接触 BNF 和 PCN 会显著诱导 I 期酶(细胞色素 P450,CYP)和 II 期酶(UDP-葡萄糖醛酸基转移酶 UGT 和磺基转移酶 SULT)的表达,但表达模式不同,而接触 NaPB 会诱导 CYP2B 的表达,但不会影响蝌蚪体内的 II 期酶,这与哺乳动物的情况不同。此外,体内外肝脏酶活性测定证实,BNF 处理显著增加了对 TH 的第二阶段代谢活性(葡萄糖醛酸化和硫酸化)。这些结果表明,哺乳动物的某些酶诱导剂可能会影响X.laevis蝌蚪对TH的清除。我们的研究结果提供了对两栖动物体内异种传感活性和酶诱导概况的深入了解,有助于更好地理解非哺乳动物物种通过肝酶诱导间接影响甲状腺系统的机制。
Hepatic enzyme induction and its potential effect on thyroid hormone metabolism in the metamorphosing tadpole of Xenopus laevis (African clawed frog)
Hepatic enzyme induction, an inherent defense system against xenobiotics, is known to simultaneously affect endocrine system functions in mammals under specific conditions, particularly thyroid hormone (TH) regulation. While this phenomenon has been studied extensively, the pathway leading to this indirect thyroid effect in mammals has unclear applicability to amphibians, despite the importance of amphibian species in assessing thyroid-disruptive chemicals. Here, we investigated the effects of three well-known mammalian enzyme inducers—β-naphthoflavone (BNF), pregnenolone carbonitrile (PCN), and sodium phenobarbital (NaPB)—on the gene expression of phase-I and phase-II metabolizing enzymes in Xenopus laevis tadpoles. Waterborne exposure to BNF and PCN significantly induced the expression of both phase-I (cytochrome P450, CYP) and phase-II enzymes (UDP-glucuronosyltransferase, UGT and sulfotransferase, SULT), but in different patterns, while NaPB exposure induced CYP2B expression without affecting phase-II enzymes in tadpoles, in contrast to mammals. Furthermore, an ex vivo hepatic enzyme activity assay confirmed that BNF treatment significantly increased phase-II metabolic activity (glucuronidation and sulfation) toward TH. These results suggest the potential for certain mammalian enzyme inducers to influence TH clearance in X. laevis tadpoles. Our findings provide insights into the profiles of xenosensing activity and enzyme induction in amphibians, which can facilitate a better understanding of the mechanisms of indirect effects on the thyroid system via hepatic enzyme induction in nonmammalian species.
期刊介绍:
Journal of Applied Toxicology publishes peer-reviewed original reviews and hypothesis-driven research articles on mechanistic, fundamental and applied research relating to the toxicity of drugs and chemicals at the molecular, cellular, tissue, target organ and whole body level in vivo (by all relevant routes of exposure) and in vitro / ex vivo. All aspects of toxicology are covered (including but not limited to nanotoxicology, genomics and proteomics, teratogenesis, carcinogenesis, mutagenesis, reproductive and endocrine toxicology, toxicopathology, target organ toxicity, systems toxicity (eg immunotoxicity), neurobehavioral toxicology, mechanistic studies, biochemical and molecular toxicology, novel biomarkers, pharmacokinetics/PBPK, risk assessment and environmental health studies) and emphasis is given to papers of clear application to human health, and/or advance mechanistic understanding and/or provide significant contributions and impact to their field.