Copper and Trace Elements in Gallbladder form Patients with Wilson's Disease Imaged and Determined by Synchrotron X-ray Fluorescence

• Published in: Journal of imaging Vol. 7; no. 12; p. 261
• Main Authors: Osterode, Wolf, Falkenberg, Gerald, Wrba, Fritz
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 03-12-2021; MDPI
• Subjects: Bile; Copper; Damage prevention; Gallbladder; Gastrointestinal system; Investigations; Iron; Liver; Metabolism; Mutation; Physiology; Radiation; Sulfur; sulphur; Synchrotron radiation; synchrotron X-ray fluorescence; Synchrotrons; Toxicity; Trace elements; Wilson’s disease; X ray spectra; X-ray fluorescence; Zinc; Wilson’s disease; gallbladder; synchrotron X-ray fluorescence; sulphur; copper; metallothionein; zinc
• ISSN: 2313-433X; 2313-433X
• DOI: 10.3390/jimaging7120261

Investigations about suspected tissue alterations and the role of gallbladder in Wilson's disease (WD)-an inherited genetic disease with impaired copper metabolism-are rare. Therefore, tissue from patients with genetically characterised WD was investigated by microscopic synchrotron X-ray fluorescence (µSRXRF). For two-dimensional imaging and quantification of elements, X-ray spectra were peak-fitted, and the net peak intensities were normalised to the intensity of the incoming monochromatic beam intensity. Concentrations were calculated by fundamental parameter-based program quant and external standardisation. Copper (Cu), zinc (Zn) and iron (Fe) along with sulphur (S) and phosphorus (P) mappings could be demonstrated in a near histological resolution. All these elements were increased compared to gallbladder tissue from controls. Cu and Zn and Fe in WD-GB were mostly found to be enhanced in the epithelium. We documented a significant linear relationship with Cu, Zn and sulphur. Concentrations of Cu/Zn were roughly 1:1 while S/Cu was about 100:1, depending on the selected areas for investigation. The significant linear relationship with Cu, Zn and sulphur let us assume that metallothioneins, which are sulphur-rich proteins, are increased too. Our data let us suggest that the WD gallbladder is the first in the gastrointestinal tract to reabsorb metals to prevent oxidative damage caused by metal toxicity.