Pregnenolone, dehydroepiandrosterone, and schizophrenia: alterations and clinical trials

CNS Neurosci Ther. 2010 Spring;16(1):32-44. doi: 10.1111/j.1755-5949.2009.00118.x.

Abstract

Neurosteroids, such as pregnenolone (PREG), dehydroepiandrosterone (DHEA), and their sulfates (PREGS and DHEAS) are reported to have a modulatory effect on neuronal excitability and synaptic plasticity. They also have many other functions associated with neuroprotection, response to stress, mood regulation, and cognitive performance. Furthermore, these neurosteroids have been linked to, and their levels are altered in, neuropsychiatric disorders. This review highlights what is currently known about the metabolism and mode of action of PREG and DHEA, as well as about alterations of these neurosteroids in schizophrenia. This review also provides substantial information about clinical trials with DHEA and PREG augmentation with of antipsychotic agents in schizophrenia.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adjuvants, Immunologic / metabolism
  • Adjuvants, Immunologic / pharmacology
  • Adjuvants, Immunologic / therapeutic use*
  • Animals
  • Antipsychotic Agents / pharmacology
  • Antipsychotic Agents / therapeutic use
  • Central Nervous System / drug effects
  • Central Nervous System / metabolism
  • Clinical Trials as Topic
  • Dehydroepiandrosterone / metabolism
  • Dehydroepiandrosterone / pharmacology
  • Dehydroepiandrosterone / therapeutic use*
  • Humans
  • Neuroprotective Agents / pharmacology
  • Neuroprotective Agents / therapeutic use
  • Pregnenolone / metabolism
  • Pregnenolone / pharmacology
  • Pregnenolone / therapeutic use*
  • Receptors, Neurotransmitter / metabolism
  • Schizophrenia / drug therapy*
  • Schizophrenia / physiopathology

Substances

  • Adjuvants, Immunologic
  • Antipsychotic Agents
  • Neuroprotective Agents
  • Receptors, Neurotransmitter
  • Dehydroepiandrosterone
  • Pregnenolone