Genotoxicity Assessment of Gadobutrol in Human Lymphocytes by Sister Chromatid Exchange Assay


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Akbaş E., Ünal F., Yüzbaşıoğlu D.

VI. International Scientific and Vocational Studies Congress – Science and Health (BILMES SH 2021), Tokat, Türkiye, 23 Aralık 2021, ss.7-8

  • Yayın Türü: Bildiri / Özet Bildiri
  • Basıldığı Şehir: Tokat
  • Basıldığı Ülke: Türkiye
  • Sayfa Sayıları: ss.7-8
  • Gazi Üniversitesi Adresli: Evet

Özet

Magnetic resonance imaging (MRI) is an important imaging method that provides detailed cross-sectional and three-dimensional anatomical images of tissues and organs and is used in the diagnosis and monitoring of various diseases. In the cases of insufficient resolution and low contrast in MR images, contrast agents are administered to patients. Contrast agents are diagnostic pharmaceutical materials comprising paramagnetic or superparamagnetic metal ions affecting the MR-signal characteristics of tissues, enhancing the image aspect of MRI and the appearance of the internal structure of the body by making clear the density difference between tissues. Since gadolinium (III) is the most widely used heavy metal in MRI contrast agents due to its high magnetic moment and stable structure, gadolinium-based contrast agents (GBCAs) have been commonly used in daily practice. Such widespread use of contrast agents has brought with it some health concerns. Therefore, this study aimed to examine genotoxic effects of Gadobutrol, one of the most used GBCAs in MRI, by Sister Chromatid Exchange (SCE) assay. Lymphocytes taken from three healthy donors were treated with 7,000, 14,000, 28,000, 56,000, and 112,000 μg/mL concentrations of Gadobutrol for 24 and 48 hours. Distilled water and Mitomycin-C were used as the negative and positive control, respectively. After 24 and 48-hour treatments of gadobutrol, all concentrations were found to increase SCEs in human lymphocytes in a dose-dependent manner compared to the negative control. While only 112,000 μg/mL concentration of Gadobutrol was found to be significant for 24-hour treatments, both 56,000 and 112,000 μg/mL were significant for 48-hour treatments. A dose-dependent decrease in the mitotic index (MI) was observed in both the 24-hour and 48-hour treatments compared to the negative control, with concentrations of 56,000 and 112,000 μg/mL being statistically significant. Gadobutrol did not cause a significant difference in the replication index. These results display that Gadobutrol leads to inhibition of mitotic division and induces SCEs at higher concentrations in human lymphocytes in vitro. Besides, other in vitro and in vivo test systems should be carried out with this contrast agent to evaluate its genotoxic potential more clearly.