Higher Reliance on Glycolysis Limits Glycolytic Responsiveness in Degenerating Glaucomatous Optic Nerve

Assraa Hassan Jassim, Lucy Coughlin, Mohammad Harun-Or-Rashid, Patrick T. Kang, Yeong Renn Chen, Denise M. Inman

Research output: Contribution to journalArticle

Abstract

Metabolic dysfunction accompanies neurodegenerative disease and aging. An important step for therapeutic development is a more sophisticated understanding of the source of metabolic dysfunction, as well as to distinguish disease-associated changes from aging effects. We examined mitochondrial function in ex vivo aging and glaucomatous optic nerve using a novel approach, the Seahorse Analyzer. Optic nerves (ON) from the DBA/2J mouse model of glaucoma and the DBA/2-Gpnmb+ control strain were isolated, and oxygen consumption rate (OCR) and extracellular acidification rate (ECAR), the discharge of protons from lactate release or byproducts of substrate oxidation, were measured. The glial-specific aconitase inhibitor fluorocitrate was used to limit the contribution of glial mitochondria to OCR and ECAR. We observed significant decreases in maximal respiration, ATP production, and spare capacity with aging. In the presence of fluorocitrate, OCR was higher, with more ATP produced, in glaucoma compared to aged ON. However, glaucoma ON showed lower maximal respiration. In the presence of fluorocitrate and challenged with ATPase inhibition, glaucoma ON was incapable of further upregulation of glycolysis to compensate for the loss of oxidative phosphorylation. Inclusion of 2-deoxyglucose as a substrate during ATPase inhibition indicated a significantly higher proportion of ECAR was derived from TCA cycle substrate oxidation than glycolysis in glaucoma ON. These data indicate that glaucoma axons have limited ability to respond to increased energy demand given their lower maximal respiration and inability to upregulate glycolysis when challenged. The higher ATP output from axonal mitochondria in glaucoma optic nerve compensates for this lack of resiliency but is ultimately inadequate for continued function.

Original languageEnglish
Pages (from-to)7097-7112
Number of pages16
JournalMolecular Neurobiology
Volume56
Issue number10
DOIs
StatePublished - 1 Oct 2019

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Glycolysis
Optic Nerve
Glaucoma
Oxygen Consumption
Respiration
Adenosine Triphosphate
Neuroglia
Adenosine Triphosphatases
Mitochondria
Up-Regulation
Aconitate Hydratase
Smegmamorpha
Inbred DBA Mouse
Oxidative Phosphorylation
Deoxyglucose
Neurodegenerative Diseases
Axons
Protons
Lactic Acid
fluorocitrate

Keywords

  • DBA/2J
  • Fluorocitrate
  • Glaucoma
  • Mitochondria
  • Optic nerve
  • Seahorse analyzer

Cite this

Jassim, Assraa Hassan ; Coughlin, Lucy ; Harun-Or-Rashid, Mohammad ; Kang, Patrick T. ; Chen, Yeong Renn ; Inman, Denise M. / Higher Reliance on Glycolysis Limits Glycolytic Responsiveness in Degenerating Glaucomatous Optic Nerve. In: Molecular Neurobiology. 2019 ; Vol. 56, No. 10. pp. 7097-7112.
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Higher Reliance on Glycolysis Limits Glycolytic Responsiveness in Degenerating Glaucomatous Optic Nerve. / Jassim, Assraa Hassan; Coughlin, Lucy; Harun-Or-Rashid, Mohammad; Kang, Patrick T.; Chen, Yeong Renn; Inman, Denise M.

In: Molecular Neurobiology, Vol. 56, No. 10, 01.10.2019, p. 7097-7112.

Research output: Contribution to journalArticle

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