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Abstract
Caloric restriction and hormone treatment delay
reproductive senescence in female mammals, but a natural
model of decelerated reproductive aging does not presently
exist. In addition to describing such a model, this study
shows that an abiotic signal (photoperiod) can induce
physiological changes that slow senescence. Relative to
animals born in April, rodents born in September delay
their first reproductive effort by up to 7 months, at
which age reduced fertility is expected. We tested the
hypothesis that the shorter day lengths experienced by
late-born Siberian hamsters ameliorate the reproductive
decline associated with advancing age. Short-day females
(10 h light/day) achieved puberty at a much later age than
long-day animals (14 h light/day) and had twice as many
ovarian primordial follicles. At 10 months of age 86% of
females previously maintained in short day lengths
produced litters, compared to 58% of their long day
counterparts. Changes in pineal gland production of
melatonin appear to mediate the effects of day length on
reproductive aging; only 30% of pinealectomized females
housed in short days produced litters. Exposure to short
days induces substantial decreases in voluntary food
intake and body mass, reduced ovarian estradiol secretion,
and enhanced production of melatonin. One or more of these
changes may account for the protective effect of short day
lengths on female reproduction. In delaying reproductive
senescence, the decrease in day length after the summer
solstice is of presumed adaptive significance for
offspring born late in the breeding season that first
breed at an advanced chronological age.
Key words:
Female Reproductive Tract
Ovary
Aging
Melatonin
Pineal
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