Study of potential inhibitors of thyroid iodide uptake by using CHO cells stably expressing the human sodium/iodide symporter (hNIS) protein

J Endocrinol Invest. 2011 Mar;34(3):170-4. doi: 10.1007/BF03347061. Epub 2010 May 17.

Abstract

Background: Thyroid gland is highly dependent on dietary intake of iodine for normal function, so it is particularly subjected to "endocrine disruptor" action. The human sodium/iodide symporter (hNIS) is an integral plasma membrane glycoprotein mediating the active transport of iodide into thyroid follicular cells, a crucial step for thyroid hormone biosynthesis. Beyond to perchlorate and thyocianate ions a few other inhibitors of iodide uptake have been described.

Aim: The aim of this study was to investigate if 10 substances usually used as drugs in clinical practice were able to inhibit NIS-mediated iodide uptake in vitro.

Materials and methods: A CHO cell line stably expressing hNIS was used to test any inhibition of NIS-mediated iodide uptake exerted by drugs. Perchlorate and thyocianate ions were used as positive controls.

Results: None of the analyzed substances was able to significantly inhibit iodide uptake in our system. As we expected, perchlorate and thyocianate ions were able to inhibit iodide uptake in a dose-dependent manner.

Conclusions: In conclusion, we carried out an in vitro assay to evaluate the potential inhibitory effect of common drugs on NISmediated iodide uptake by using CHO-hNIS cells. None of the analyzed substances was able to inhibit iodide uptake; only perchlorate and thyocianate were able to inhibit iodide uptake in a dose-dependent manner.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 14-alpha Demethylase Inhibitors / chemistry
  • 14-alpha Demethylase Inhibitors / pharmacology
  • Amphotericin B / chemistry
  • Amphotericin B / pharmacology
  • Animals
  • Anti-Allergic Agents / chemistry
  • Anti-Allergic Agents / pharmacology
  • Anti-Infective Agents / chemistry
  • Anti-Infective Agents / pharmacology
  • Anti-Inflammatory Agents / chemistry
  • Anti-Inflammatory Agents / pharmacology
  • Atropine / chemistry
  • Atropine / pharmacology
  • Biotin / chemistry
  • Biotin / pharmacology
  • Buspirone / chemistry
  • Buspirone / pharmacology
  • CHO Cells / drug effects
  • CHO Cells / metabolism*
  • Cricetinae
  • Cricetulus
  • Econazole / chemistry
  • Econazole / pharmacology
  • Humans
  • Hydrocortisone / chemistry
  • Hydrocortisone / pharmacology
  • Iodides / metabolism*
  • Metronidazole / chemistry
  • Metronidazole / pharmacology
  • Muscarinic Antagonists / chemistry
  • Muscarinic Antagonists / pharmacology
  • Papaverine / chemistry
  • Papaverine / pharmacology
  • Perchlorates / pharmacology
  • Phosphodiesterase Inhibitors / chemistry
  • Phosphodiesterase Inhibitors / pharmacology
  • Promethazine / chemistry
  • Promethazine / pharmacology
  • Serotonin Receptor Agonists / chemistry
  • Serotonin Receptor Agonists / pharmacology
  • Sulfadiazine / chemistry
  • Sulfadiazine / pharmacology
  • Symporters / genetics
  • Symporters / metabolism*
  • Thiocyanates / pharmacology
  • Thyroid Gland / drug effects
  • Thyroid Gland / metabolism*

Substances

  • 14-alpha Demethylase Inhibitors
  • Anti-Allergic Agents
  • Anti-Infective Agents
  • Anti-Inflammatory Agents
  • Iodides
  • Muscarinic Antagonists
  • Perchlorates
  • Phosphodiesterase Inhibitors
  • Serotonin Receptor Agonists
  • Symporters
  • Thiocyanates
  • Sulfadiazine
  • Metronidazole
  • sodium-iodide symporter
  • Biotin
  • Econazole
  • Atropine
  • Amphotericin B
  • Papaverine
  • Promethazine
  • Buspirone
  • perchlorate
  • Hydrocortisone