The hypothalamic-pituitary-gonadal axis is target of cadmium toxicity. An update of recent studies and potential therapeutic approaches

Food Chem Toxicol. 2013 Sep:59:395-404. doi: 10.1016/j.fct.2013.06.024. Epub 2013 Jun 26.

Abstract

This review presents an overview of neuroendocrine disruption induced by cadmium on the hypothalamic-pituitary-gonadal (HHG) axis. This review focuses on a number of hypotheses: (1) the HHG axis is a physiological target on cadmium toxicity; (2) cadmium could induce chronotoxicity on this neuroendocrine axis by disrupting the daily pattern of the HHG axis activity; (3) cadmium exposure throughout life could contribute to the oxidative stress and the circadian rhythms disruption induced by aging on the HHG; and (4) cadmium induces oxidative stress in the HHG axis so antioxidants could prevent or reduce cadmium toxicity in this system. Cadmium disrupts the regulatory mechanisms of this physiological axis, by altering neurotransmitters involved in this regulation at the hypothalamic level, altering gonadotropin hormone secretion, and by affecting testicular or ovarian structure and activity. These effects are age-dependent and they could be related to the circadian rhythms of this physiological axis. Several antioxidant agents could have a protective action against the neuroendocrine toxicity of cadmium on the reproductive system. A comprehensive view of the physiological axis may provide a better understanding about the neuroendocrine toxicity of cadmium on the reproductive system, so this perspective is recommended for undertaking further studies.

Keywords: Cadmium; Hypothalamic–pituitary–gonadal axis; Neuroendocrine toxicity.

Publication types

  • Review

MeSH terms

  • Age Factors
  • Animals
  • Antioxidants / therapeutic use*
  • Cadmium / chemistry
  • Cadmium / toxicity*
  • Cadmium Poisoning / drug therapy*
  • Cadmium Poisoning / metabolism
  • Cadmium Poisoning / physiopathology
  • Circadian Rhythm / drug effects
  • Female
  • Humans
  • Hypothalamo-Hypophyseal System / drug effects*
  • Hypothalamo-Hypophyseal System / metabolism
  • Hypothalamo-Hypophyseal System / physiopathology
  • Male
  • Models, Biological*
  • Neurosecretory Systems / drug effects
  • Neurosecretory Systems / metabolism
  • Neurosecretory Systems / physiopathology
  • Ovary / drug effects*
  • Ovary / metabolism
  • Ovary / physiopathology
  • Oxidative Stress / drug effects
  • Testis / drug effects*
  • Testis / metabolism
  • Testis / physiopathology

Substances

  • Antioxidants
  • Cadmium