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马兜铃酸 I 暴露诱导贫血和 DNA 加合物形成中的正反馈机制:对巴尔干地方性肾病的影响。

Positive Feedback Mechanism in Aristolochic Acid I Exposure-Induced Anemia and DNA Adduct Formation: Implications for Balkan Endemic Nephropathy.

机构信息

Department of Chemistry, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong.

Medical Faculty, University of Niš, 18000 Niš, Serbia.

出版信息

J Agric Food Chem. 2024 Aug 14;72(32):18155-18161. doi: 10.1021/acs.jafc.4c03508. Epub 2024 Aug 1.

Abstract

Balkan endemic nephropathy (BEN) is a chronic kidney disease that predominantly affects inhabitants of rural farming communities along the Danube River tributaries in the Balkans. Long-standing research has identified dietary exposure to aristolochic acids (AAs) as the principal toxicological cause. This study investigates the pathophysiological role of anemia in BEN, noting its earlier and more severe manifestation in BEN patients compared to those with other chronic kidney diseases. Utilizing a mouse model, our research demonstrates that prolonged exposure to aristolochic acid I (AA-I) (the most prevalent AA variant) leads to significant red blood cell depletion through DNA damage, such as DNA adduct formation in bone marrow, prior to observable kidney function decline. Furthermore, experiments with kidney cells exposed to lowered oxygen and pH conditions mimicking an anemia environment show enhanced DNA adduct formation, suggesting increased AA-I mutagenicity and carcinogenicity. These findings indicate for the first time a positive feedback mechanism of AA-induced anemia, DNA damage, and kidney impairment in BEN progression. These results not only advance our understanding of the underlying mechanisms of BEN but also highlight anemia as a potential target for early BEN diagnosis and therapy.

摘要

巴尔干地方性肾病(BEN)是一种慢性肾病,主要影响巴尔干地区多瑙河支流沿岸农村农业社区的居民。长期以来的研究已经确定膳食暴露于马兜铃酸(AAs)是主要的毒理学原因。本研究探讨了贫血在 BEN 中的病理生理作用,注意到与其他慢性肾脏病患者相比,BEN 患者的贫血表现更早且更严重。利用小鼠模型,我们的研究表明,长时间暴露于马兜铃酸 I(AA-I)(最常见的 AA 变体)会导致骨髓中 DNA 加合物形成等 DNA 损伤,从而导致红细胞大量减少,然后才出现可观察到的肾功能下降。此外,对暴露于低氧和低 pH 条件下的肾细胞进行的实验模拟了贫血环境,显示出 DNA 加合物形成增加,提示 AA-I 的突变性和致癌性增强。这些发现首次表明 AA 诱导的贫血、DNA 损伤和肾脏损害在 BEN 进展中的正反馈机制。这些结果不仅提高了我们对 BEN 潜在机制的理解,还强调了贫血作为早期 BEN 诊断和治疗的潜在靶点。

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