Genotoxicity and subchronic toxicity of Sophorae radix in rats: hepatotoxic and genotoxic potential

Regul Toxicol Pharmacol. 2015 Apr;71(3):379-87. doi: 10.1016/j.yrtph.2015.01.012. Epub 2015 Jan 30.

Abstract

Although Sophorae radix (SR) has been traditionally used as a treatment for various clinical symptoms, a comprehensive investigation of its safety has not yet been carried out. Therefore, we present an evaluation of the toxicity of the SR extract that was performed according to the Organization for Economic Cooperation and Development test guidelines for subchronic toxicity and genotoxicity. In an oral subchronic study for 13 weeks, the repeated treatment of rats with 429 or 1500 mg/kg of the SR extract induced a dose-related change in body weight. In particular, the SR extract was observed to exert a significant increase in liver weight along with an increase in serum alkaline phosphatase and alanine transaminase. A small but statistically significant reductions in red blood cell, hemoglobin, and hematocrit levels in the SR extract-treated rats suggest the possibility that anemia, accompanied by liver injury, was at least partially induced. These findings indicate the no-observed-adverse-effect-level for the SR extract was considered to be 10mg/kg/d. And, the data obtained from the chromosome aberration assay showed that SR extract might be considered to be a weak clastogen although no significant micronucleus induction was observed in vivo. Despite the benefits that SR extract can exhibit, this study indicates that SR extract may possess hepatotoxic and genotoxic potential.

Keywords: Anemia; Genotoxicity; Hepatotoxicity; Liver; Sophorae radix; Subchronic.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Anemia / blood
  • Anemia / chemically induced
  • Animals
  • Biomarkers / blood
  • Body Weight / drug effects
  • Chemical and Drug Induced Liver Injury / blood
  • Chemical and Drug Induced Liver Injury / diagnosis
  • Chemical and Drug Induced Liver Injury / etiology*
  • Chromosome Aberrations / chemically induced*
  • Dose-Response Relationship, Drug
  • Eating / drug effects
  • Female
  • Male
  • Micronuclei, Chromosome-Defective / chemically induced
  • Micronucleus Tests
  • Mutagenicity Tests* / methods
  • No-Observed-Adverse-Effect Level
  • Phytotherapy
  • Plant Extracts / administration & dosage
  • Plant Extracts / toxicity*
  • Plants, Medicinal
  • Rats, Inbred F344
  • Risk Assessment
  • Sophora*
  • Time Factors
  • Toxicity Tests, Subchronic*

Substances

  • Biomarkers
  • Plant Extracts