1996
DOI: 10.2133/dmpk.11.481
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Pharmacokinetic Studies of 3-Methyl-1-phenyl-2-pyrazolin-5-one(MCI-186) in rats. (2). Blood and Plasma Levels, Distribution, Metabolism, Excretion and Accumulation during and after Repeated Intravenous Administration.

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(2 citation statements)
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“…A sufficient concentration of edaravone for the inhibition of IL‐6 from MH‐S cells ranged from 10–100 µmol/L. At 5 min after a single intravenous administration of edaravone (2 mg/kg/day: roughly equivalent to the daily human dose) to male rats, edaravone levels in plasma and lung tissue were about 1 and 0.5 µmol/L, respectively 15 . To inhibit pro‐inflammatory cytokine production by LPS, concentrations of edaravone 10–100 times higher than the daily human dose might be necessary.…”
Section: Discussionmentioning
confidence: 99%
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“…A sufficient concentration of edaravone for the inhibition of IL‐6 from MH‐S cells ranged from 10–100 µmol/L. At 5 min after a single intravenous administration of edaravone (2 mg/kg/day: roughly equivalent to the daily human dose) to male rats, edaravone levels in plasma and lung tissue were about 1 and 0.5 µmol/L, respectively 15 . To inhibit pro‐inflammatory cytokine production by LPS, concentrations of edaravone 10–100 times higher than the daily human dose might be necessary.…”
Section: Discussionmentioning
confidence: 99%
“…The main adverse effects of edaravone are renal failure and liver dysfunction 15 . No significant effect on heart rate or blood pressure at the dose of 450 mg/kg of edaravone was reported 16 .…”
Section: Discussionmentioning
confidence: 99%