Maternal caloric restriction partially rescues the deleterious effects of advanced maternal age on offspring
Maternal caloric restriction partially rescues the deleterious effects of advanced maternal age on offspring
Date
2014-03-24
Authors
Gribble, Kristin E.
Jarvis, George
Bock, Martha
Mark Welch, David B.
Jarvis, George
Bock, Martha
Mark Welch, David B.
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DOI
10.1111/acel.12217
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Keywords
Aging
Caloric restriction
Maternal effect
Monogonont rotifer
Caloric restriction
Maternal effect
Monogonont rotifer
Abstract
While many studies have focused on the detrimental effects of advanced maternal age and harmful prenatal environments on progeny, little is known about the role of beneficial non-Mendelian maternal inheritance on aging. Here, we report the effects of maternal age and maternal caloric restriction (CR) on the life span and health span of offspring for a clonal culture of the monogonont rotifer Brachionus manjavacas. Mothers on regimens of chronic CR (CCR) or intermittent fasting (IF) had increased life span compared with mothers fed ad libitum (AL). With increasing maternal age, life span and fecundity of female offspring of AL-fed mothers decreased significantly and life span of male offspring was unchanged, whereas body size of both male and female offspring increased. Maternal CR partially rescued these effects, increasing the mean life span of AL-fed female offspring but not male offspring and increasing the fecundity of AL-fed female offspring compared with offspring of mothers of the same age. Both maternal CR regimens decreased male offspring body size, but only maternal IF decreased body size of female offspring, whereas maternal CCR caused a slight increase. Understanding the genetic and biochemical basis of these different maternal effects on aging may guide effective interventions to improve health span and life span.
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© The Author(s), 2014. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Aging Cell 13 (2014): 623–630, doi:10.1111/acel.12217.
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Aging Cell 13 (2014): 623–630