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冬凌草甲素通过抑制黄嘌呤氧化酶活性对双酚 A 诱导的大鼠肝损伤的保护作用。

Hepatoprotective effects of oridonin against bisphenol A induced liver injury in rats via inhibiting the activity of xanthione oxidase.

机构信息

Key Laboratory of Advanced Drug Preparation Technologies, Ministry of Education of China, Co-innovation Center of Henan Province for New drug R & D and preclinical Safety, School of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, Henan 450001, PR China.

Henan Joint International Research Laboratory of Chronic Liver Injury, Henan Key Laboratory of Rehabilitation Medicine, Department of Pediatrics, the Fifth Affiliated Hospital, Zhengzhou University, Kangfuqian Street, Zhengzhou, Henan 450052, PR China.

出版信息

Sci Total Environ. 2021 May 20;770:145301. doi: 10.1016/j.scitotenv.2021.145301. Epub 2021 Jan 21.

Abstract

Bisphenol A (BPA) is widely used to manufacture packaging materials for various daily necessities and causes harmful effects in organs, especially liver injury, by generating oxidative stress. Oridonin, an active diterpenoid isolated from Rabdosia rubescens (Hemsl.) Hara, has been reported to possess a wide range of pharmacological activities including anti-inflammatory, antioxidative and antiapoptotic effects. However, the role of oridonin in BPA--induced liver injury and its potential protective mechanism have not been well characterized. In this research, we explored the metabolic alterations in the liver tissue of rats after exposure to BPA with or without pretreatment with oridonin for 14 days by metabolomics analysis based on UPLC-MS/MS. Rats were randomly divided into groups as follows: Control, Vehicle, Oridonin (10 mg/kg), Bisphenol A (500 mg/kg), bisphenol A + Oridonin (500 + 10 mg/kg), Bisphenol A + Diammonium glycyrrhizinate (500 + 40 mg/kg). The biochemical results showed that oridonin significantly reduced the levels of AST and ALT (P < 0.05), ameliorated the abnormal histopathological changes and reduced hepatic apoptosis compared with the BPA group. Furthermore, metabolomics results revealed that purine metabolism, phenylalanine, tyrosine and tryptophan biosynthesis and phenylalanine metabolism were reprogrammed, based on 28 identified significant differential metabolites among the Vehicle, BPA and BPA + oridonin groups. In-depth studies demonstrated that pretreatment with oridonin may play a protective role by restoring BPA-induced changes in oxidative stress and the activity of oxidase (XOD) (P < 0.05). Additionally, oridonin could inhibit the activity of XOD by binding to it, therefore decreasing the reactive oxygen species (ROS) level, upregulating the content of hypoxanthine and xanthine, and reducing the level of uric acid in the liver (P < 0.05). This research presents the potential protective mechanisms of oridonin on BPA-induced liver injury at the metabolic level, which might be used to identify new protective agents that prevent BPA-induced liver injury.

摘要

双酚 A(BPA)被广泛用于制造各种日用品的包装材料,通过产生氧化应激,对器官尤其是肝脏造成有害影响。冬凌草甲素是从冬凌草(Hemsl.)中分离得到的一种活性二萜类化合物,已被报道具有广泛的药理活性,包括抗炎、抗氧化和抗凋亡作用。然而,冬凌草甲素在 BPA 诱导的肝损伤中的作用及其潜在的保护机制尚未得到很好的描述。在这项研究中,我们通过基于 UPLC-MS/MS 的代谢组学分析,研究了暴露于 BPA 后大鼠肝脏组织的代谢变化,以及用冬凌草甲素预处理 14 天后的变化。大鼠随机分为以下几组:对照组、载体组、冬凌草甲素(10mg/kg)组、双酚 A(500mg/kg)组、双酚 A+冬凌草甲素(500+10mg/kg)组、双酚 A+甘草酸二铵(500+40mg/kg)组。生化结果表明,与 BPA 组相比,冬凌草甲素显著降低了 AST 和 ALT 的水平(P<0.05),改善了异常的组织病理学变化,并减少了肝凋亡。此外,代谢组学结果显示,基于在载体组、BPA 组和 BPA+冬凌草甲素组之间鉴定的 28 种显著差异代谢物,嘌呤代谢、苯丙氨酸、酪氨酸和色氨酸生物合成以及苯丙氨酸代谢发生了重新编程。深入研究表明,冬凌草甲素预处理可能通过恢复 BPA 诱导的氧化应激和氧化酶(XOD)活性的变化发挥保护作用(P<0.05)。此外,冬凌草甲素可以通过与 XOD 结合来抑制 XOD 的活性,从而降低活性氧(ROS)水平,上调次黄嘌呤和黄嘌呤的含量,并降低肝脏中尿酸的水平(P<0.05)。本研究从代谢水平上揭示了冬凌草甲素对 BPA 诱导的肝损伤的潜在保护机制,这可能有助于识别新的保护剂,以防止 BPA 诱导的肝损伤。

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