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印楝素减轻致癌物苯并(a)芘诱导的HepG2细胞DNA损伤、细胞周期阻滞、凋亡、炎症、代谢及氧化应激。

Azadirachtin Attenuates Carcinogen Benzo(a) Pyrene-Induced DNA Damage, Cell Cycle Arrest, Apoptosis, Inflammatory, Metabolic, and Oxidative Stress in HepG2 Cells.

作者信息

John Annie, Raza Haider

机构信息

Department of Biochemistry and Molecular Biology, College of Medicine and Health Sciences, United Arab Emirates University, 5th Postal Region, Al Ain P.O. Box 15551, United Arab Emirates.

出版信息

Antioxidants (Basel). 2023 Nov 14;12(11):2001. doi: 10.3390/antiox12112001.

Abstract

Azadirachtin (AZD), a limonoid from the versatile, tropical neem tree (Azadirachta indica), is well known for its many medicinal, and pharmacological effects. Its effects as an anti-oxidant, anti-inflammatory, and anti-cancer agent are well known. However, not many studies have explored the effects of AZD on toxicities induced by benzo(a)pyrene (B(a)P), a toxic component of cigarette smoke known to cause DNA damage and cell cycle arrest, leading to different kinds of cancer. In the present study, using HepG2 cells, we investigated the protective effects of Azadirachtin (AZD) against B(a)P-induced oxidative/nitrosative and metabolic stress and mitochondrial dysfunction. Treatment with 25 µM B(a)P for 24 h demonstrated an increased production of reactive oxygen species (ROS), followed by increased lipid peroxidation and DNA damage presumably, due to the increased metabolic activation of B(a)P by CYP 450 1A1/1A2 enzymes. We also observed intrinsic and extrinsic apoptosis, alterations in glutathione-dependent redox homeostasis, cell cycle arrest, and inflammation after B(a)P treatment. Cells treated with 25 µM AZD for 24 h showed decreased oxidative stress and apoptosis, partial protection from DNA damage, and an improvement in mitochondrial functions and bioenergetics. The improvement in antioxidant status, anti-inflammatory potential, and alterations in cell cycle regulatory markers qualify AZD as a potential therapeutic in combination with anti-cancer drugs.

摘要

印楝素(AZD)是一种从用途广泛的热带印楝树(Azadirachta indica)中提取的柠檬苦素,因其多种药用和药理作用而闻名。其作为抗氧化剂、抗炎剂和抗癌剂的作用广为人知。然而,关于印楝素对苯并(a)芘(B(a)P)诱导的毒性影响的研究并不多,苯并(a)芘是香烟烟雾中的一种有毒成分,已知会导致DNA损伤和细胞周期停滞,进而引发各种癌症。在本研究中,我们使用HepG2细胞,研究了印楝素(AZD)对B(a)P诱导的氧化/亚硝化和代谢应激以及线粒体功能障碍的保护作用。用25 μM B(a)P处理24小时后,活性氧(ROS)的产生增加,随后脂质过氧化和DNA损伤增加,这可能是由于CYP 450 1A1/1A2酶对B(a)P的代谢活化增加所致。我们还观察到B(a)P处理后细胞发生内源性和外源性凋亡、谷胱甘肽依赖性氧化还原稳态改变、细胞周期停滞和炎症。用25 μM AZD处理24小时的细胞显示氧化应激和凋亡减少,对DNA损伤有部分保护作用,线粒体功能和生物能量学得到改善。抗氧化状态的改善、抗炎潜力以及细胞周期调节标志物的改变使印楝素成为与抗癌药物联合使用的潜在治疗药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ddc/10669168/5cc563663064/antioxidants-12-02001-g001.jpg

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