Late-life dietary folate restriction reduces biosynthesis without compromising healthspan in mice

Author:

Blank Heidi M1ORCID,Hammer Staci E1,Boatright Laurel12,Roberts Courtney1ORCID,Heyden Katarina E3,Nagarajan Aravindh24,Tsuchiya Mitsuhiro5,Brun Marcel6,Johnson Charles D6ORCID,Stover Patrick J178,Sitcheran Raquel9,Kennedy Brian K1011,Adams L Garry12ORCID,Kaeberlein Matt513ORCID,Field Martha S3ORCID,Threadgill David W14814,Andrews-Polymenis Helene L24,Polymenis Michael147ORCID

Affiliation:

1. Department of Biochemistry and Biophysics, Texas A&M University

2. Department of Microbial Pathogenesis and Immunology, School of Medicine, Texas A&M University

3. Division of Nutritional Sciences, Cornell University, Ithaca, NY, USA

4. Interdisciplinary Program in Genetics, Texas A&M University

5. Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, USA

6. Texas A&M Agrilife Research, Genomics and Bioinformatics Service, College Station, TX, USA

7. Institute for Advancing Health Through Agriculture, Texas A&M University

8. Department of Nutrition, Texas A&M University

9. Department of Cell Biology and Genetics, School of Medicine, Texas A&M University

10. Departments of Biochemistry and Physiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore

11. Healthy Longevity Translational Research Programme, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore

12. Department of Veterinary Pathobiology, College of Veterinary Medicine, Texas A&M, College Station, TX, USA

13. Optispan, Inc., Seattle, WA, USA

14. Texas A&M Institute for Genome Sciences and Society, Texas A&M University

Abstract

Folate is a vitamin required for cell growth and is present in fortified foods in the form of folic acid to prevent congenital abnormalities. The impact of low-folate status on life-long health is poorly understood. We found that limiting folate levels with the folate antagonist methotrexate increased the lifespan of yeast and worms. We then restricted folate intake in aged mice and measured various health metrics, metabolites, and gene expression signatures. Limiting folate intake decreased anabolic biosynthetic processes in mice and enhanced metabolic plasticity. Despite reduced serum folate levels in mice with limited folic acid intake, these animals maintained their weight and adiposity late in life, and we did not observe adverse health outcomes. These results argue that the effectiveness of folate dietary interventions may vary depending on an individual’s age and sex. A higher folate intake is advantageous during the early stages of life to support cell divisions needed for proper development. However, a lower folate intake later in life may result in healthier aging.

Funder

HHS | NIH | National Institute of General Medical Sciences

HHS | NIH | National Heart, Lung, and Blood Institute

HHS | NIH | National Institute of Allergy and Infectious Diseases

Publisher

Life Science Alliance, LLC

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