Clinical studies have proven that a reduction in body weight improves health parameters and prevents disease development in young and middle aged adults. Basic research studies on yeast cells, worms, flies and mice indicated that calorie restriction in the diet can increase the lifespan across different species. In monkeys, however, results were more ambiguous: calorie restriction improved health parameters (such as blood pressure and blood lipids) but did not lead to an elongation of the survival. “These outcomes appear to be contradictory – a possible explanation was that calorie restriction has beneficial effects on health parameters at middle age but exerts adverse effects during advanced aging”, indicate Pavlos Missios, Medical Doctor of the University of Tübingen and first author of the study.
The new data from the Leibniz Institute for Age Research – Fritz-Lipmann-Institute (FLI) in Jena point to a possible explanation. During aging, cells lose the ends of their chromosome – the telomeres. Telomeres shorten as a consequence of cell divisions and it is known that this mechanism limits the proliferative capacity of human cells and the regenerative capacity of aging tissue.
Modified caloric intake depending on age
Studies on mice, wildlife birds and human blood donors revealed a correlation between telomere shortening and a shortened lifespan. The new study from the group of Lenhard Rudolph at FLI reveals experimental evidence that telomere shortening increases the energy demand of cells and tissue leading to an increased requirement of glucose substitution in old mice with short telomeres in order to maintain energy homeostasis and body functions. “Should these results hold true for humans, this would indicate that we need a different composition of our diet at old age in order to prolong the maintenance of both energy homeostasis and body functions”, indicates Lenhard Rudolph, director of the institute and lead author of the current study.
Aging mice with short telomeres that were switched to a glucose-rich diet exhibited a 20% increase in overall lifespan compared to mice on normal diet. “These results were very surprising and could provide an explanation for the change in correlation of body weight and lifespan in old compared to middle aged individuals”, explains Dr. Bernhard Böhm, co-initiator of the studies at Ulm University and director of Metabolic Medicine at NTU Singapore und Imperial College London. Indeed, increased body weight at mid age is associated with and increased risk of disease development and early death. In contrast, at advanced age it is the opposite, and more than 30% of geriatric patients exhibit signs of malnutrition associating with a shortened lifespan compared to old people with higher body weight.
„It now needs to be tested whether the results of our study hold true in humans. If so, we may need to change the composition of our diet at advanced age in order to maintain the functionality of our cells and tissues exhibiting an increased demand of glucose substitution for energy production“, explains Rudolph. First human trials have been initiated with Dr. Stephan C. Bischoff, M.D. and nutrition scientist from the University of Stuttgart Hohenheim. “It will be important to determine the influence of energy supplementation in controlled settings within clinical trials and to develop biomarkers that indicate the optimization of energy homeostasis”. In the end it could come down to the question whether butter-cream cakes at old age may be equally important as calorie restriction at middle age in order to achieve a maximization of our health span?
++++ NOT FOR PUBLIC RELEASE BEFORE September 18, 2014 at 11 a.m. EST +++
Pavlos Missios, Yuan Zhou, Luis Miguel Guachalla, Guido von Figura, Andre Wegner, Sundaram Reddy Chakkarappan, Tina Binz, Anne Gompf, Götz Hartleben, Martin D. Burkhalter, Veronika Wulff, Cagatay Günes, Rui Wang Sattler, Zhangfa Song, Thomas Illig, Susanne Klaus, Bernhard O. Böhm, Tina Wenz, Karsten Hiller & K. Lenhard Rudolph. Glucose substitution prolongs maintenance of energy homeostasis and lifespan of telomere dysfunctional mice. Nature Communications 2014, doi: 10.1038/ncomms5924. www.nature.com/naturecommunications
About the FLI
The Leibniz Institute for Age Research – Fritz Lipmann Institute (FLI) is the first German research organization dedicated to biomedical aging research since 2004. More than 330 members from over 30 nations explore the molecular mechanisms underlying aging processes and age-associated diseases. For more information, please visit www.fli-leibniz.de.
About the Leibniz Association
The Leibniz Association connects 89 independent research institutions that range in focus from the natural, engineering and environmental sciences via economics, spatial and social sciences to the humanities. Leibniz institutes address issues of social, economic and ecological relevance. They conduct knowledge-driven and applied basic research, maintain scientific infrastructure and provide research-based services. The Leibniz Association identifies focus areas for knowledge transfer to policy-makers, academia, business and the public. Leibniz institutions collaborate intensively with universities – in the form of “WissenschaftsCampi” (thematic partnerships between university and non-university research institutes), for example – as well as with industry and other partners at home and abroad. They are subject to an independent evaluation procedure that is unparalleled in its transparency. Due to the importance of the institutions for the country as a whole, they are funded jointly by the Federation and the Länder, employing some 17,200 individuals, including 8,200 researchers. The entire budget of all the institutes is approximately 1.5 billion EUR. For more information, please visit www.leibniz-gemeinschaft.de/en.
Dr. Kerstin Wagner
Leibniz Institute for Age Research – Fritz Lipmann Institute (FLI)
Beutenbergstr. 11, 07745 Jena
Phone: 03641-656378, e-mail: firstname.lastname@example.org