Inhibition of Endogenous Thyroid Hormone Receptor- β and Peroxisome Proliferator-Activated Receptor- α Activities by Humic Acid in a Human-Derived Liver Cell Line

Abstract

Humic acid (HA), know to be ubiquitous in the natural environment, is present in almost all soil, surface water, and plants. Earlier studies indicate that HA can affect thyroid economy via binding with iodide, inhibiting both thyroid peroxidase and hepatic 5′-deiodinase in rodents. However, the effect of HA, a peroxisome proliferator in rodents, on thyroid hormone receptor (TR) and peroxisome proliferator-activated receptor (PPAR) in human cells has not yet been examined. In this study, we demonstrate that the malic enzyme activity and the transcriptional activities of endogenous TR and PPAR were inhibited after treatment with HA in human hepatocyte Chang liver cell line. Although the protein expression levels of TR-β, PPAR-α and retinoid X receptor-α (RXRα) were not changed significantly by HA treatment, both the binding abilities of endogenous TR-β on thyroid hormone response element (TRE) and PPAR-α on the PPAR response element (PPRE) were inhibited by HA treatment. The study of the subcellular distribution of HA, relying on the inherent HA fluorescence, showed that HA distributed in the intracellular compartments including cytoplasm and nucleus. The 50% binding inhibition values (CI₅₀) of HA on ME-TRE (malic enzyme gene-TRE) and ACOX-PPRE (acylCoA oxidase gene-PPRE) were 19.31 and 19.94 μg/mL, respectively. These results suggest that HA-induced endemic goiter may link in part to the disruption of TRβ and PPARα function in human Chang liver cells. This model may be useful in the investigation of environmental goitrogens.