Neurotrophin regulation of energy homeostasis in the central nervous system

G. R. Jackson, K. Werrbach-Perez, Z. Pan, D. Sampath, J. Perez-Polo

    Research output: Contribution to journalArticle

    40 Citations (Scopus)

    Abstract

    Our hypothesis is that one cause of neuronal cell death and shrinkage in the aged central nervous system is an inability of neurons to maintain oxidant homeostasis in the face of increased levels of reactive oxygen species, decreased endogenous antioxidants, and impaired energy metabolism associated with physiological senescence, Alzheimer's, and Parkinson's diseases. Since treatment with nerve growth factor (NGF) reverses behavioral impairments in aged rats and stimulates cholinergic activity in the basal forebrain, while brain-derived neurotrophic factor appears to play a similar role in the striatum, we propose that neurotrophin-mediated cell-sparing reflects effects on oxidant homeostasis. Neurotrophins may play a similar cell-sparing role in hypoxic/ischemic injury to the nervous system, which also is mediated in part by reactive oxygen species. The degradation of one such species, H2O2, is catalyzed by catalase and glutathione peroxidase (GSH Px). The activity of the latter enzyme is dependent on glutathione reductase and the availability of NADPH for regeneration of reduced GSH. The GSH redox cycle is also regulated by enzymes of the hexose monophosphate shunt. NGF protects PC12 cells from H2O2 injury by stimulating the synthesis of antioxidant enzymes including catalase, GSH Px, glucose-6-phosphate dehydrogenase, and γ-glutamylcysteine synthetase, the rate-limiting enzyme for glutathione synthesis. NGF also enhances recovery from the NAD+ losses occurring as a consequence of H2O2 treatment.

    Original languageEnglish (US)
    Pages (from-to)285-290
    Number of pages6
    JournalDevelopmental Neuroscience
    Volume16
    Issue number5-6
    StatePublished - 1994

    Fingerprint

    Nerve Growth Factors
    Nerve Growth Factor
    Homeostasis
    Central Nervous System
    Enzymes
    Oxidants
    Catalase
    Reactive Oxygen Species
    Antioxidants
    Glutamate-Cysteine Ligase
    Nervous System Trauma
    Pentose Phosphate Pathway
    Glutathione Reductase
    Glucosephosphate Dehydrogenase
    PC12 Cells
    Brain-Derived Neurotrophic Factor
    Glutathione Peroxidase
    NADP
    NAD
    Cholinergic Agents

    Keywords

    • Catalase
    • Glutathione
    • Glutathione peroxidase
    • Hydrogen peroxide
    • Nerve growth factor
    • Neurotrophin
    • Oxidative stress
    • PC12 cells

    ASJC Scopus subject areas

    • Neuroscience(all)

    Cite this

    Jackson, G. R., Werrbach-Perez, K., Pan, Z., Sampath, D., & Perez-Polo, J. (1994). Neurotrophin regulation of energy homeostasis in the central nervous system. Developmental Neuroscience, 16(5-6), 285-290.

    Neurotrophin regulation of energy homeostasis in the central nervous system. / Jackson, G. R.; Werrbach-Perez, K.; Pan, Z.; Sampath, D.; Perez-Polo, J.

    In: Developmental Neuroscience, Vol. 16, No. 5-6, 1994, p. 285-290.

    Research output: Contribution to journalArticle

    Jackson, GR, Werrbach-Perez, K, Pan, Z, Sampath, D & Perez-Polo, J 1994, 'Neurotrophin regulation of energy homeostasis in the central nervous system', Developmental Neuroscience, vol. 16, no. 5-6, pp. 285-290.
    Jackson GR, Werrbach-Perez K, Pan Z, Sampath D, Perez-Polo J. Neurotrophin regulation of energy homeostasis in the central nervous system. Developmental Neuroscience. 1994;16(5-6):285-290.
    Jackson, G. R. ; Werrbach-Perez, K. ; Pan, Z. ; Sampath, D. ; Perez-Polo, J. / Neurotrophin regulation of energy homeostasis in the central nervous system. In: Developmental Neuroscience. 1994 ; Vol. 16, No. 5-6. pp. 285-290.
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