Detecting cadmium during ultrastructural characterization of hepatotoxicity

J Trace Elem Med Biol. 2020 Dec:62:126644. doi: 10.1016/j.jtemb.2020.126644. Epub 2020 Sep 9.

Abstract

Background: The threat of cadmium (Cd), which is the cause of itai-itai disease in Japan, is still complicated and confusing, especially for digestive system, such as liver disease. One of the most keys of this problem is demonstrating that the hepatotoxicity is indeed induced by Cd. Therefore, we attempt detecting Cd at microscale during ultrastructural imaging of liver tissue.

Methods: 12 rats were divided randomly into two experimental groups: control and Cd-treated. Treated rats were intraperitoneal injected with 1 mg/kg body weight cadmium chloride (CdCl2) for 4 weeks (5 P.M each day for 6 days/week). At the end of the exposure period, liver tissue samples were processed into ultrathin sections for analysis of advanced analytical transmission electron microscopy and X-ray energy dispersive spectroscopy (TEM/X-EDS) investigations. Ultrastructural images and X-ray energy dispersive spectrum were acquired at microscale.

Results: Cd can cause changes in the structure of the organelle, including the collapse of the membrane structure in the cell, the destruction of the internal structure of the organelle, the mitochondrial swelling, the expansion of the endoplasmic reticulum, and the appearance of inclusions. Cadmium bioaccumulation is detected in the mitochondria at microscale by TEM/X-EDS, which is the visual evidence of morphological changes of mitochondria related to Cd.

Conclusion: The combination of detailed ultrastructure and microscale X-ray energy dispersive spectroscopy (X-EDS) characterization of cadmium hepatotoxicity demonstrate that cadmium indeed leads to mitochondrial damage, which is helpful for further investigation of the pathological mechanism of cadmium hepatotoxicity.

Keywords: Cadmium (Cd); Hepatotoxicity; Organelles; Transmission electron microscopy (TEM); Ultrastructure; X-ray energy dispersive spectroscopy (X-EDS).

MeSH terms

  • Animals
  • Cadmium / toxicity*
  • Cadmium Chloride / toxicity
  • Japan
  • Liver / drug effects
  • Liver / metabolism
  • Liver / ultrastructure
  • Male
  • Microscopy, Electron, Transmission
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Mitochondria / ultrastructure
  • Rats
  • Rats, Sprague-Dawley
  • Spectrometry, X-Ray Emission

Substances

  • Cadmium
  • Cadmium Chloride