Inhibitory Effect of Fruit Juices on the Doxorubicin Metabolizing Activity of Carbonyl Reductase 1.

Takeshi Miura, Katsutoshi Nagai, Shingo Kaneshiro, Ayako Taketomi, Toshikatsu Nakabayashi, Hiroki Konishi, Toru Nishinaka, Tomoyuki Terada
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引用次数: 2

Abstract

Background and objective: Doxorubicin, an anthracycline anti-cancer drug, is effective for breast cancer and childhood lymphoma. Chronic cardiotoxicity has been known as a critical adverse effect of doxorubicin and is attributed to its metabolite doxorubicinol produced by carbonyl reductase 1 (CBR1, SDR21C1). Some flavonoids have been reported to act as inhibitors for CBR1, therefore, commercially available juices containing flavonoids are likely to be applicable as a prophylactic treatment against doxorubicin-induced cardiotoxicity by suppression of doxorubicinol production. In the study, fruit juices containing flavonoids were investigated for inhibitory effects on CBR1.

Method: Recombinant CBR1 protein was subjected to in vitro enzymatic assays with/without juices. An apple juice and a grapefruit juice were selected in the present study as candidates capable of inhib-iting CBR1.

Results: The enzymatic assays revealed that both juices potently inhibit the CBR1-mediated metabolic conversion of doxorubicin to doxorubicinol in concertation-dependent manner. The concentrations required for obtaining 50% inhibition (IC50) were 0.0012% (v/v) and 0.0014% (v/v) for apple and grapefruit juices, respectively. Additionally, it is worth noting that these juices showed inhibitory effects on doxorubicin metabolism by CBR1 even at very low concentrations (0.0001% (v/v)).

Conclusion: An apple juice and a grape fruit juice showed strong inhibitory effects on doxorubicin metabolism by CBR1 in vitro. These results suggest that the intake of flavonoid-containing juices can be a promising measure for protection against doxorubicin-induced cardiac toxicity, enabling patients to keep higher adherence with routine use in light of safety, economic performance and stable supply to market.

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果汁对阿霉素羰基还原酶代谢活性的抑制作用
背景与目的:阿霉素是一种蒽环类抗癌药物,对乳腺癌和儿童淋巴瘤有较好的疗效。慢性心脏毒性被认为是阿霉素的一个重要不良反应,并归因于其代谢产物阿霉素由羰基还原酶1 (CBR1, SDR21C1)产生。据报道,一些黄酮类化合物可作为CBR1的抑制剂,因此,市售的含有黄酮类化合物的果汁可能可通过抑制阿霉素的产生,预防阿霉素引起的心脏毒性。本研究考察了含黄酮类化合物果汁对CBR1的抑制作用。方法:对重组CBR1蛋白进行体外酶促实验,加/不加果汁。在本研究中,苹果汁和葡萄柚汁被选为能够抑制CBR1的候选物。结果:酶促实验显示,两种果汁均能以浓度依赖的方式抑制cbr1介导的阿霉素到阿霉素醇的代谢转化。苹果汁和葡萄柚汁获得50%抑制(IC50)所需浓度分别为0.0012% (v/v)和0.0014% (v/v)。此外,值得注意的是,即使在非常低的浓度(0.0001% (v/v))下,这些果汁也显示出CBR1对阿霉素代谢的抑制作用。结论:苹果汁和葡萄果汁对体外CBR1对阿霉素代谢有较强的抑制作用。这些结果表明,摄入含黄酮类化合物的果汁可能是防止阿霉素引起的心脏毒性的一种有希望的措施,使患者在安全、经济和稳定的市场供应的情况下保持较高的依从性。
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来源期刊
Drug metabolism letters
Drug metabolism letters Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
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发文量
12
期刊介绍: Drug Metabolism Letters publishes letters and research articles on major advances in all areas of drug metabolism and disposition. The emphasis is on publishing quality papers very rapidly by taking full advantage of the Internet technology both for the submission and review of manuscripts. The journal covers the following areas: In vitro systems including CYP-450; enzyme induction and inhibition; drug-drug interactions and enzyme kinetics; pharmacokinetics, toxicokinetics, species scaling and extrapolations; P-glycoprotein and transport carriers; target organ toxicity and interindividual variability; drug metabolism and disposition studies; extrahepatic metabolism; phase I and phase II metabolism; recent developments for the identification of drug metabolites.
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