AI Article Synopsis

  • Madder color (MC) has shown potential to cause cancer in rat kidneys, linked to various cellular changes and increased renal damage markers.
  • In a study, male F344 rats were fed different components of MC, revealing that the metabolite rubiadin (Rub) led to significant kidney damage after 26 weeks, specifically inducing atypical tubules, which are precursors to cancer.
  • While rubiadin appears to be a strong carcinogenic factor of MC, other metabolites and components may also contribute to kidney cancer through mechanisms like increased oxidative stress.

Article Abstract

Madder color (MC) has been shown to exert carcinogenic potential in the rat kidney in association with degeneration, karyomegaly, increased cell proliferation of renal tubule cells and increased renal 8-OHdG levels. To clarify the causal relationship of components and metabolites of MC to renal carcinogenesis, male F344 rats were fed lucidin-3-O-primeveroside (LuP) or alizarin (Alz), and the genotoxic LuP metabolites lucidin (Luc) or rubiadin (Rub) for up to 26 weeks. After one week and four weeks, Luc did not induce any renal changes. In contrast, after one week, cortical tubule degeneration was apparent in the Alz and LuP groups, and cytoplasmic swelling with basophilic change and karyomegaly in the outer medulla was observed only in the Rub group. LuP and Rub increased the proliferative activity of tubule cells in the outer medulla, and Alz and LuP increased renal 8-OHdG levels. After 26 weeks, Rub but not Alz induced atypical tubules, a putative preneoplastic lesion, and karyomegaly in the outer medulla. These results indicate that Rub may be a potent carcinogenic metabolite of MC, targeting proximal tubule cells in the outer medulla, although oxidative stress increased by Alz or LuP might also be involved in renal carcinogenesis by MC.

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http://dx.doi.org/10.1016/j.fct.2009.01.003DOI Listing

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