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Early Detection of Drug-Induced Renal Hemodynamic Dysfunction Using Sonographic Technology in Rats
Published on: March 11, 2016
Site-specific genotoxicity of rubiadin: localization and histopathological changes in the kidneys of rats
Tatsuya Mitsumoto1,2, Yuji Ishii3, Norifumi Takimoto1,4
1Division of Pathology, National Institute of Health Sciences, 3-25-26 Tonomachi, Kawasaki-Ku, Kawasaki-Shi, Kanagawa, 210-9501, Japan.
Abstract:
Rubiadin (Rub) is a genotoxic component of madder color (MC) that is extracted from the root of Rubia tinctorum L. MC induces renal tumors and preneoplastic lesions that are found in the proximal tubule of the outer stripe of the outer medulla (OSOM), suggesting that the renal carcinogenicity of MC is site specific. To clarify the involvement of Rub in renal carcinogenesis of MC, we examined the distribution of Rub in the kidney of male gpt delta rats that were treated with Rub for 28 days. We used desorption electrospray ionization quadrupole time-of-flight mass spectrometry imaging (DESI-Q-TOF-MSI), along with the histopathological analysis, immunohistochemical staining, and reporter gene mutation assays of the kidney. DESI-Q-TOF-MSI revealed that Rub and its metabolites, lucidin and Rub-sulfation, were specifically distributed in the OSOM. Histopathologically, karyomegaly characterized by enlarged nuclear and microvesicular vacuolar degeneration occurred in proximal tubule epithelial cells in the OSOM. The ɤ-H2AX- and p21-positive cells were also found in the OSOM rather than the cortex. Although dose-dependent increases in gpt and Spi- mutant frequencies were observed in both the medulla and cortex, the mutant frequencies in the medulla were significantly higher. The mutation spectra of gpt mutants showed that A:T-T:A transversion was predominant in Rub-induced gene mutations, consistent with those of MC. Overall, the data showed that the distribution of Rub and its metabolites resulted in site-specific histopathological changes, DNA damage, and gene mutations, suggesting that the distribution of genotoxic components and metabolites is responsible for the site-specific renal carcinogenesis of MC.
Insights
Rubiadin, a genotoxic compound from madder color, specifically targets the kidney's outer stripe of the outer medulla (OSOM). This distribution causes site-specific DNA damage and mutations, explaining madder color's kidney carcinogenicity.
Area of Science:
- Toxicology
- Molecular Biology
- Carcinogenesis
Background:
- Rubiadin (Rub) is a genotoxic component of madder color (MC) from Rubia tinctorum L.
- MC induces site-specific renal tumors and preneoplastic lesions in the proximal tubule of the outer stripe of the outer medulla (OSOM).
Purpose of the Study:
- To clarify Rub's role in MC-induced renal carcinogenesis by examining its distribution in the rat kidney.
- To correlate Rub distribution with histopathological, DNA damage, and mutation changes in the kidney.
Main Methods:
- Male gpt delta rats were treated with Rub for 28 days.
- Desorption electrospray ionization quadrupole time-of-flight mass spectrometry imaging (DESI-Q-TOF-MSI) was used to map Rub distribution.
- Histopathological analysis, immunohistochemical staining (ɤ-H2AX, p21), and reporter gene mutation assays were performed.
Main Results:
- DESI-Q-TOF-MSI showed specific distribution of Rub and its metabolites (lucidin, Rub-sulfation) in the OSOM.
- Histopathology revealed karyomegaly and vacuolar degeneration in OSOM proximal tubule cells.
- Increased ɤ-H2AX and p21 expression, along with higher gpt and Spi mutant frequencies, were observed in the OSOM compared to the cortex.
- A:T-T:A transversion was the predominant mutation type, consistent with MC exposure.
Conclusions:
- Rub and its metabolites accumulate specifically in the OSOM, leading to site-specific histopathological changes and DNA damage.
- The distribution of genotoxic components and their metabolites is responsible for the site-specific renal carcinogenesis induced by MC.

