4.7 Article

Effects of early experience on female behavioural and reproductive development in rhesus macaques

Journal

PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES
Volume 272, Issue 1569, Pages 1243-1248

Publisher

ROYAL SOC
DOI: 10.1098/rspb.2005.3059

Keywords

rhesus macaques; early experience; maternal care; female reproductive maturation; interest in infants

Funding

  1. NCRR NIH HHS [RR 00165, P51 RR000165] Funding Source: Medline
  2. NIMH NIH HHS [K02 MH 63097, R01 MH062577, R01 MH 62577, R01 MH 57249, K02 MH063097] Funding Source: Medline

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A growing body of research on humans suggests that exposure to a stressful family environment or father absence from home during childhood is associated with early female puberty and greater interest in infants among adolescent girls. This effect may be mediated by early exposure to harsh and inconsistent maternal care, but the mechanisms by which maternal care affects female reproductive maturation are not known. The present study reports sex differences in interest in infants among juvenile rhesus macaques similar to those observed in human adolescents. Furthermore, juvenile females that were exposed to harsh and inconsistent maternal care in infancy showed higher interest in infants than controls. Evidence from cross-fostered females indicated that these effects resulted from early experience and not genetic inheritance from the mother. There were no significant differences in female age at first conception in relation to the quality of maternal care received during infancy. Macaque females exposed to harsh and inconsistent maternal care in infancy tended to have higher cortisol responses to stress and to corticotropin-releasing hormone than controls in the first three years of life. Furthermore, females with higher cortisol responses to stress exhibited higher interest in infants. These findings suggest that some of the effects of early parental care on female reproductive maturation may be mediated by developmental changes in the activity of the hypothalamic-pituitary-adrenal axis.

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