Maternal absence and stability of individual differences in CSF 5-HIAA concentrations in rhesus monkey infants

Am J Psychiatry. 2005 Sep;162(9):1658-64. doi: 10.1176/appi.ajp.162.9.1658.

Abstract

Objective: Early life events often lead to deficits in CNS serotonin function, which underlie a number of reoccurring psychopathological disorders. Studies using rhesus macaques have demonstrated that early maternal deprivation reduces CNS serotonin turnover, as measured by cisternal CSF 5-HIAA concentrations. In addition, individual differences in CSF 5-HIAA remain stable from the first year of life through adulthood. The purpose of this study was to assess 1) the impact of rearing environment on the early development (<6 months of age) of the serotonin system, and 2) at what stage of early development individual differences in CSF 5-HIAA concentrations stabilize.

Method: The subjects were 256 infant rhesus macaques reared in three different conditions (mother-reared, peer-reared, and surrogate/peer-reared). Cisternal CSF was obtained at 14, 30, 60, 90, 120, and 150 days of age.

Results: No differences in CSF 5-HIAA concentrations were observed between peer only- and surrogate/peer-reared infants, and these groups combined exhibited lower 5-HIAA concentrations than mother-reared infants throughout early development. CSF 5-HIAA concentrations declined with increasing age regardless of rearing condition. Within each rearing condition, individual differences in CSF 5-HIAA concentrations remained stable from 14 to 150 days of age.

Conclusions: Early maternal deprivation reduces CNS serotonin turnover, and individual differences in CSF 5-HIAA concentrations are trait-like and appear to stabilize in infancy.

Publication types

  • Comparative Study

MeSH terms

  • Age Factors
  • Animals
  • Animals, Newborn
  • Behavior, Animal / physiology
  • Biomarkers
  • Disruptive, Impulse Control, and Conduct Disorders / etiology
  • Disruptive, Impulse Control, and Conduct Disorders / physiopathology
  • Female
  • Humans
  • Hydroxyindoleacetic Acid / cerebrospinal fluid*
  • Hydroxyindoleacetic Acid / metabolism
  • Individuality
  • Macaca mulatta / cerebrospinal fluid*
  • Macaca mulatta / growth & development
  • Male
  • Maternal Deprivation*
  • Models, Animal
  • Mood Disorders / etiology
  • Mood Disorders / physiopathology
  • Serotonin / metabolism
  • Serotonin / physiology
  • Social Behavior
  • Social Environment*
  • Stress, Psychological / cerebrospinal fluid
  • Stress, Psychological / metabolism

Substances

  • Biomarkers
  • Serotonin
  • Hydroxyindoleacetic Acid