Fluoride Affects Dopamine Metabolism and Causes Changes in the Expression of Dopamine Receptors (D1R and D2R) in Chosen Brain Structures of Morphine-Dependent Rats

Int J Mol Sci. 2020 Mar 29;21(7):2361. doi: 10.3390/ijms21072361.

Abstract

Disturbances caused by excess or shortages of certain elements can affect the cerebral reward system and may therefore modulate the processes associated with the development of dependence as was confirmed by behavioural studies on animals addicted to morphine. Earlier publications demonstrated and proved the neurodegenerative properties of both low and high doses of fluoride ions in animal experiments and in epidemiological and clinical studies. The aim of the experiments conducted in the course of the present study was to analyse the effect of pre- and postnatal exposure to 50 ppm F- on the initiation/development of morphine dependence. For this purpose, the following were conducted: behavioural studies, the analysis of concentrations of dopamine and its metabolites, and the analyses of mRNA expression and dopamine receptor proteins D1 and D2 in the prefrontal cortex, striatum, hippocampus, and cerebellum of rats. In this study, it was observed for the first time that pre- and postnatal exposure to fluoride ions influenced the phenomenon of morphine dependence in a model expressing withdrawal symptoms. Behavioural, molecular, and neurochemical studies demonstrated that the degenerative changes caused by toxic activity of fluoride ions during the developmental period of the nervous system may impair the functioning of the dopaminergic pathway due to changes in dopamine concentration and in dopamine receptors. Moreover, the dopaminergic disturbances within the striatum and the cerebellum played a predominant role as both alterations of dopamine metabolism and profound alterations in striatal D1 and D2 receptors were discovered in these structures. The present study provides a new insight into a global problem showing direct associations between environmental factors and addictive disorders.

Keywords: dependence; dopamine; dopamine receptors; fluoride; morphine.

MeSH terms

  • Animals
  • Behavior, Animal
  • Brain / drug effects*
  • Brain / metabolism*
  • Cerebellum / metabolism
  • Corpus Striatum / metabolism
  • Dopamine / metabolism*
  • Female
  • Fluorides / pharmacology*
  • Gene Expression Regulation
  • Hippocampus / metabolism
  • Maternal Exposure / adverse effects
  • Metabolic Networks and Pathways
  • Models, Animal
  • Morphine / pharmacology*
  • Prefrontal Cortex / metabolism
  • Rats
  • Receptors, Dopamine D1 / genetics*
  • Receptors, Dopamine D1 / metabolism
  • Receptors, Dopamine D2 / genetics*
  • Receptors, Dopamine D2 / metabolism
  • Substance Withdrawal Syndrome

Substances

  • Receptors, Dopamine D1
  • Receptors, Dopamine D2
  • Morphine
  • Fluorides
  • Dopamine