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Cited by 474

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The neuroprotective pharmacology of methylprednisolone

Hall, Edward D.·1992·Journal of Neurosurgery

Abstract

✓ A 24-hour intensive intravenous dosing regimen with the glucocorticoid steroid methylprednisolone has recently been shown to be effective in enhancing neurological recovery in spinal cord-injured patients when initiated within 8 hours after injury. The state of knowledge concerning the neuroprotective pharmacology of methylprednisolone, including mechanism(s) of action, dosing requirements, and time-action considerations is reviewed, as are the results of studies with high doses in experimental and clinical head injury, subarachnoid hemorrhage, and cerebral ischemia. A primary neuroprotective mechanism of action in each of these cases is hypothesized to involve the ability of high doses of methylprednisolone to inhibit oxygen free radical-induced lipid peroxidation, although additional mechanisms may contribute. Unresolved issues are also addressed, including the therapeutic window, optimum duration of treatment, and rational combination with other neuroprotective agents. A newer methylprednisolone pro-drug with improved solution stability is discussed, together with a brief consideration of novel nonglucocorticoid steroids that surpass methylprednisolone's lipid antioxidant effects without unwanted glucocorticoid properties.

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Metadata

Authors
Hall, E. D.
Venue
Journal of Neurosurgery
Published
1992-01
Volume
76
Issue
1
Pages
13-22
ISSN
0022-3085 (ISSN-L)
OpenAlex
W1996449070
Cited by
474
References
0
FWCI
16.07
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: The neuroprotective pharmacology of methylprednisolone. https://app.cochat.ai/papers/10.3171/jns.1992.76.1.0013
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Hall, E. D. (1992). The neuroprotective pharmacology of methylprednisolone. Journal of Neurosurgery. https://doi.org/10.3171/jns.1992.76.1.0013

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.