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.

Archives of Toxicology
|October 4, 2023
PubMed

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.