Fetal alcohol spectrum disorder-associated depression: evidence for reductions in the levels of brain-derived neurotrophic factor in a mouse model

Pharmacol Biochem Behav. 2008 Oct;90(4):614-24. doi: 10.1016/j.pbb.2008.05.004.

Abstract

Prenatal ethanol exposure is associated with an increased incidence of depressive disorders in patient populations. However, the mechanisms that link prenatal ethanol exposure and depression are unknown. Several recent studies have implicated reduced brain-derived neurotrophic factor (BDNF) levels in the hippocampal formation and frontal cortex as important contributors to the etiology of depression. In the present studies, we sought to determine whether prenatal ethanol exposure is associated with behaviors that model depression, as well as with reduced BDNF levels in the hippocampal formation and/or medial frontal cortex, in a mouse model of fetal alcohol spectrum disorder (FASD). Compared to control adult mice, prenatal ethanol-exposed adult mice displayed increased learned helplessness behavior and increased immobility in the Porsolt forced swim test. Prenatal ethanol exposure was associated with decreased BDNF protein levels in the medial frontal cortex, but not the hippocampal formation, while total BDNF mRNA and BDNF transcripts containing exons III, IV or VI were reduced in both the medial frontal cortex and the hippocampal formation of prenatal ethanol-exposed mice. These results identify reduced BDNF levels in the medial frontal cortex and hippocampal formation as potential mediators of depressive disorders associated with FASD.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Behavior, Animal / physiology
  • Brain Chemistry / drug effects
  • Brain Chemistry / physiology*
  • Brain-Derived Neurotrophic Factor / metabolism*
  • Central Nervous System Depressants / blood
  • Cyclophilin A / metabolism
  • DNA Primers
  • DNA, Complementary / biosynthesis
  • DNA, Complementary / genetics
  • Depressive Disorder / etiology
  • Depressive Disorder / metabolism*
  • Depressive Disorder / psychology*
  • Ethanol / blood
  • Exons / genetics
  • Female
  • Fetal Alcohol Spectrum Disorders / metabolism*
  • Fetal Alcohol Spectrum Disorders / psychology*
  • Helplessness, Learned
  • Hypoxanthine Phosphoribosyltransferase / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Motor Activity / drug effects
  • Pregnancy
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • Swimming / psychology

Substances

  • Brain-Derived Neurotrophic Factor
  • Central Nervous System Depressants
  • DNA Primers
  • DNA, Complementary
  • RNA, Messenger
  • Ethanol
  • Hypoxanthine Phosphoribosyltransferase
  • Cyclophilin A