Impact of Chronodisruption during Primate Pregnancy on the Maternal and Newborn Temperature Rhythms
Author
dc.contributor.author
Serón Ferré, María
es_CL
Author
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Forcelledo, María Luisa
es_CL
Author
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Torres Farfán, Claudia
es_CL
Author
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Valenzuela, Francisco J.
es_CL
Author
dc.contributor.author
Rojas, Auristela
es_CL
Author
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Vergara, Marcela
es_CL
Author
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Rojas García, Pedro
es_CL
Author
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Recabarren, Mónica P.
Author
dc.contributor.author
Valenzuela, Guillermo J.
Admission date
dc.date.accessioned
2014-02-06T19:32:08Z
Available date
dc.date.available
2014-02-06T19:32:08Z
Publication date
dc.date.issued
2013
Cita de ítem
dc.identifier.citation
PLoS ONE 8(2): e57710
en_US
Identifier
dc.identifier.other
doi:10.1371/journal.pone.0057710
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/129262
General note
dc.description
Artículo de publicación ISI
en_US
Abstract
dc.description.abstract
Disruption of the maternal environment during pregnancy is a key contributor to offspring diseases that develop in adult
life. To explore the impact of chronodisruption during pregnancy in primates, we exposed pregnant capuchin monkeys to
constant light (eliminating the maternal melatonin rhythm) from the last third of gestation to term. Maternal temperature
and activity circadian rhythms were assessed as well as the newborn temperature rhythm. Additionally we studied the effect
of daily maternal melatonin replacement during pregnancy on these rhythms. Ten pregnant capuchin monkeys were
exposed to constant light from 60% of gestation to term. Five received a daily oral dose of melatonin (250 mg kg/body
weight) at 1800 h (LL+Mel) and the other five a placebo (LL). Six additional pregnant females were maintained in a 14:10
light:dark cycles and their newborns were used as controls (LD). Rhythms were recorded 96 h before delivery in the mother
and at 4–6 days of age in the newborn. Exposure to constant light had no effect on the maternal body temperature rhythm
however it delayed the acrophase of the activity rhythm. Neither rhythm was affected by melatonin replacement. In
contrast, maternal exposure to constant light affected the newborn body temperature rhythm. This rhythm was entrained in
control newborns whereas LL newborns showed a random distribution of the acrophases over 24-h. In addition, mean
temperature was decreased (34.060.6 vs 36.160.2uC, in LL and control, respectively P,0.05). Maternal melatonin
replacement during pregnancy re-synchronized the acrophases and restored mean temperature to the values in control
newborns. Our findings demonstrate that prenatal melatonin is a Zeitgeber for the newborn temperature rhythm and
supports normal body temperature maintenance. Altogether these prenatal melatonin effects highlight the physiological
importance of the maternal melatonin rhythm during pregnancy for the newborn primate.