Literature DB >> 34477202

Age-Related Increase in Lactate Dehydrogenase Activity in Skeletal Muscle Reduces Life Span in Drosophila.

Liam C Hunt1, Fabio Demontis1.   

Abstract

Metabolic adaptations occur with aging but the significance and causal roles of such changes are only partially known. In Drosophila, we find that skeletal muscle aging is paradoxically characterized by increased readouts of glycolysis (lactate, NADH/NAD+) but reduced expression of most glycolytic enzymes. This conundrum is explained by lactate dehydrogenase (LDH), an enzyme necessary for anaerobic glycolysis and whose expression increases with aging. Experimental Ldh overexpression in skeletal muscle of young flies increases glycolysis and shortens life span, suggesting that age-related increases in muscle LDH contribute to mortality. Similar results are also found with overexpression of other glycolytic enzymes (Pfrx/PFKFB, Pgi/GPI). Conversely, hypomorphic mutations in Ldh extend life span, whereas reduction in PFK, Pglym78/PGAM, Pgi/GPI, and Ald/ALDO levels shorten life span to various degrees, indicating that glycolysis needs to be tightly controlled for optimal aging. Altogether, these findings indicate a role for muscle LDH and glycolysis in aging.
© The Author(s) 2021. Published by Oxford University Press on behalf of The Gerontological Society of America. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  zzm321990 Drosophilazzm321990 ; Aging; Glycolysis; LDH; Life span; Skeletal muscle

Mesh:

Substances:

Year:  2022        PMID: 34477202      PMCID: PMC8824701          DOI: 10.1093/gerona/glab260

Source DB:  PubMed          Journal:  J Gerontol A Biol Sci Med Sci        ISSN: 1079-5006            Impact factor:   6.591


  52 in total

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4.  Overexpression of the cytosolic form of phosphoenolpyruvate carboxykinase (GTP) in skeletal muscle repatterns energy metabolism in the mouse.

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Review 6.  Role of myokines in exercise and metabolism.

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Review 7.  Non-canonical functions of enzymes facilitate cross-talk between cell metabolic and regulatory pathways.

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8.  Activating transcription factor 4-dependent lactate dehydrogenase activation as a protective response to amyloid beta toxicity.

Authors:  Teresa Niccoli; Fiona Kerr; Inge Snoeren; Daniel Fabian; Benjamin Aleyakpo; Dobril Ivanov; Oyinkan Sofola-Adesakin; Adam Cryar; Jennifer Adcott; Janet Thornton; Linda Partridge
Journal:  Brain Commun       Date:  2021-03-26

9.  Antagonistic control of myofiber size and muscle protein quality control by the ubiquitin ligase UBR4 during aging.

Authors:  Liam C Hunt; Bronwen Schadeberg; Jared Stover; Benard Haugen; Vishwajeeth Pagala; Yong-Dong Wang; Jason Puglise; Elisabeth R Barton; Junmin Peng; Fabio Demontis
Journal:  Nat Commun       Date:  2021-03-03       Impact factor: 14.919

10.  Tissue-specific down-regulation of S-adenosyl-homocysteine via suppression of dAhcyL1/dAhcyL2 extends health span and life span in Drosophila.

Authors:  Andrey A Parkhitko; Richard Binari; Nannan Zhang; John M Asara; Fabio Demontis; Norbert Perrimon
Journal:  Genes Dev       Date:  2016-06-16       Impact factor: 11.361

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