Differential Organ Distribution of 7-(Deoxyadenosin- <i>N</i> <sup>6</sup> -yl)-aristolactam I in Mice Exposed to Aristolochic Acid I: Insights from Acute and Chronic Exposure Studies

The distribution of 7-(deoxyadenosin-<i>N</i><sup>6</sup>-yl)-aristolactam I (ALI-dA) in mice treated with the same amount of aristolochic acid I (AA-I) at different dosage rates was investigated. The results showed a distinct organ distribution pattern of ALI-dA, with the highest adduct levels observed in the bladders of mice that received chronic doses of AA-I. In contrast, in mice that received AA-I acutely, the highest levels were found in the kidneys and were over ten times higher than those observed with chronic exposure. These results indicate that, in addition to the cumulative dose, the rate at which humans are exposed to AA-I is an under-recognized risk factor in the development of aristolochic acid nephropathy.

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Publication Details

Journal
Chemical Research in Toxicology
Published
2026-01-05
DOI
https://doi.org/10.1021/acs.chemrestox.5c00511
Citations
1
Primary Topic
Nephrotoxicity and Medicinal Plants
Type
article
Field-Weighted Citation Impact
31.92
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article

Differential Organ Distribution of 7-(Deoxyadenosin- N 6 -yl)-aristolactam I in Mice Exposed to Aristolochic Acid I: Insights from Acute and Chronic Exposure Studies

Shuangshuang Wang, Hong-Ching Kwok, Yat-Hing Ham, Wan Chan
1 citations
Chemical Research in Toxicology
Nephrotoxicity and Medicinal Plants
31.92
article

Differential Organ Distribution of 7-(Deoxyadenosin- N 6 -yl)-aristolactam I in Mice Exposed to Aristolochic Acid I: Insights from Acute and Chronic Exposure Studies

Shuangshuang Wang, Hong-Ching Kwok, Yat-Hing Ham, Wan Chan
article en
1 citations

Abstract

The distribution of 7-(deoxyadenosin-<i>N</i><sup>6</sup>-yl)-aristolactam I (ALI-dA) in mice treated with the same amount of aristolochic acid I (AA-I) at different dosage rates was investigated. The results showed a distinct organ distribution pattern of ALI-dA, with the highest adduct levels observed in the bladders of mice that received chronic doses of AA-I. In contrast, in mice that received AA-I acutely, the highest levels were found in the kidneys and were over ten times higher than those observed with chronic exposure. These results indicate that, in addition to the cumulative dose, the rate at which humans are exposed to AA-I is an under-recognized risk factor in the development of aristolochic acid nephropathy.

Chemical Research in ToxicologyVol. 39(1)
Hong Kong University of Science and Technology (HK)
Good health and well-being
Openalex Percentile: Top 3%
Nephrotoxicity and Medicinal Plants
31.92
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