G6PD protects from oxidative damage and improves healthspan in mice.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 26976705.
- Also identified by DOI 10.1038/ncomms10894 and PMC identifier 4796314.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Reactive oxygen species (ROS) are constantly generated by cells and ROS-derived damage contributes to ageing. Protection against oxidative damage largely relies on the reductive power of NAPDH, whose levels are mostly determined by the enzyme glucose-6-phosphate dehydrogenase (G6PD). Here, we report a transgenic mouse model with moderate overexpression of human G6PD under its endogenous promoter. Importantly, G6PD-Tg mice have higher levels of NADPH, lower levels of ROS-derived damage, and better protection from ageing-associated functional decline, including extended median lifespan in females. The G6PD transgene has no effect on tumour development, even after combining with various tumour-prone genetic alterations. We conclude that a modest increase in G6PD activity is beneficial for healthspan through increased NADPH levels and protection from the deleterious effects of ROS.
Medical subject headings
- Aging
- Glucosephosphate Dehydrogenase
- Longevity
- NADP
- Oxidative Stress
- Reactive Oxygen Species