4.3 Article

Steroid hormone concentrations in milk predict sex-specific offspring growth in a nonhuman primate

期刊

AMERICAN JOURNAL OF HUMAN BIOLOGY
卷 31, 期 6, 页码 -

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WILEY
DOI: 10.1002/ajhb.23315

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资金

  1. National Center for Research Resources [P51RR000169, R24RR019970]
  2. National Institutes of Health [P51OD011107, R24OD010962]
  3. National Science Foundation [BCS-0921978]
  4. Stony Brook University
  5. California National Primate Research Center

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Objectives In humans and other mammals, maternal hormones are transferred to offspring during lactation via milk and may regulate postnatal development, including the pace of early growth. Here, we used a nonhuman primate model to test the hypotheses that milk cortisol and dehydroepiandrosterone-sulfate (DHEAS) concentrations reflect maternal characteristics, and that changes in these hormones across lactation are associated with early postnatal growth rates. Methods Demographic information, morphometrics, and milk samples were collected from rhesus macaque mothers and their infants at the California National Primate Research Center in Davis, California. Using linear models, we examined the relationship between maternal traits and milk hormone concentrations (N = 104 females) and explored the effect of milk hormones on the rate of offspring growth (N = 72 mother-infant dyads), controlling for available milk energy. Results Contrary to previous studies, we found that milk cortisol concentrations were categorically higher in multiparous females than in primiparous females. However, milk DHEAS concentrations decreased with maternal parity. Neither milk cortisol nor DHEAS were related to maternal rank. Finally, changes in milk hormones predicted offspring growth in a sex-specific and temporal manner: increases in cortisol from peak to late lactation predicted faster female growth, and increases in DHEAS concentrations from early to peak and peak to late lactation predicted faster male growth. Conclusions Our findings shed light on how hormonal components of milk have sex-specific effects on offspring growth during early postnatal life with varying temporal windows of sensitivity.

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