Metyrapone reduces rat brain damage and seizures after hypoxia-ischemia: An effect independent of modulation of plasma corticosterone levels?

HJ Krugers*, RHA Kemper, J Korf, GJ Ter Horst, S Knollema

*Corresponding author for this work

    Research output: Contribution to journalArticleAcademicpeer-review

    Abstract

    Hypoxia-ischemia is accompanied by abundant corticosterone secretion that could exacerbate train damage after the insult. The authors demonstrate that the steroid syn thesis inhibitor metyrapone (150 mg/kg subcutaneously) suppresses the hypoxia-ischemia-induced rise of plasma corticosterone levels (17.3 +/- 3.6 mu g/dL) when compared with corticosterone-treated animals (72.2 +/- 4.8 mu g/dL) immediately after hypoxia-ischemia In parallel, metyrapone reduced brain damage (P <0.05). Moreover, none of the metyrapone-treated animals displayed seizures, whereas seven of eight corticosterone-treated animals had seizures after hypoxia-ischemia. Although corticosterone administration in metyrapone-treated animals elevated plasma corticosterone levels (39.0 +/- 5.3 mu g/dL), this did not result in a subsequent increase in brain damage and seizures when compared with metyrapone-treated animals. The authors conclude that metyrapone reduces brain damage and the incidence of seizures after hypoxia-ischemia but that this effect might partially be independent from its effect on modulating plasma corticosterone levels.

    Original languageEnglish
    Pages (from-to)386-390
    Number of pages5
    JournalJournal of Cerebral Blood Flow and Metabolism
    Volume18
    Issue number4
    Publication statusPublished - Apr-1998

    Keywords

    • brain damage
    • corticosterone
    • epilepsy
    • hippocampus
    • ischemia
    • EXCITATORY AMINO-ACIDS
    • HIPPOCAMPAL ASTROCYTES
    • KAINIC ACID
    • ADRENALECTOMY
    • ACCUMULATION
    • EXPOSURE
    • NEURONS
    • NUMBER
    • INJURY

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