From: Adverse effects and underlying mechanism of rare earth elements
Organ | Element | drug delivery route | Test model | Main effects | References |
---|---|---|---|---|---|
Lung | LaCl3、CeCl3、Nd2O3 | Male Sprague–Dawley rat | Lung fibrosis | [125] | |
Nd2O3 | Nd2O3 exposure on rat NR8383 | Rat NR8383 alveolar macrophages | Caused cell damage and enhanced synthesis and release of inflammatory chemokines | [77] | |
CeO2 NPs | Expose | Alveolar A549 and bronchial BEAS- 2B epithelial cells | Downregulation of gene transcription | [149] | |
CeO2、TiO2 | Oropharyngeal | CD- 1 mice | Lung inflammatory | [88] | |
La2O3 | Expose nose to La2O3 | Male rats | Alveolar protein deposition and pulmonary inflammation | [137] | |
CeO2 | Endotracheal instillation | Male Sprague–Dawley rat | Lung phospholipid deposition and fibrosis | [111] | |
CeO2 | Inhalation | Rat | Lung inflammation | [135] | |
La2O3 | Whole-body inhalation exposure | C57BL/6 J mice | Chronic inflammatory changes and mild fibrosis | [138] | |
CeO2 | Intratracheal instillation | Male Sprague–Dawley | Lung fibrosis | [110] | |
CeO2 | Intratracheal instillation | C57BL/6 J mice | Damage to lung development | [126] | |
Heart | YCl3 | Different concentrations of YCl3 | Rat H9c2 cardiomyocytes | DNA damage | [165] |
YCl3 | Intragastric administration | Male Kunming mice | Lipid peroxidation and inflammation in the heart | [166] | |
Ce | Treated with CeCl3 | Wistar rat | Endomyocardial fibrosis | [90] | |
CeO2 NPs | Nose-only inhalation to CeO2 NPs | C57BL/6 J mice, mice prone to cardiovascular disease and a mouse model of neurological disease | Cardiovascular dysfunction | [41] | |
16 REEs (LaCl3, CeCl3, PrCl3, SmCl3, TbCl3, DyCl3, YbCl3, ScCl3 NdCl3, EuCl3, GdCl3, HoCl3, ErCl3, TmCl3, LuCl3, and YCl3) | Exposure of 16 REEs | Zebrafish embryo | Cardiac hypertrophy and myocardial contraction | [186] | |
Liver | CeO2 NPs | Expose in CeO2 NPs | A549, CaCo2, and HepG2 cell lines | Toxic to all tested cell lines | [39] |
La, Ce, Pd, Nd, and Gd | Intragastric administration | SD rats | The accumulation of REEs in the liver was irreversible | [21] | |
Pr(NO3)3 | Intravenous injection | Female Wistar rats | Fatty livers | [92] | |
CeCl3 | Oral administration | Male CD- 1 mice | Liver inflammation, and hepatocyte necrosis | [34] | |
La | Intragastric administration | Male CD- 1 mice | Impairing liver function | [33] |