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氢化可的松和地塞米松对小鼠花生四烯酸毒性的急性保护作用。

Acute protection against arachidonate toxicity by hydrocortisone and dexamethasone in mice.

作者信息

Rabbani F, Myers A, Ramey E, Ramwell P, Penhos J

出版信息

Prostaglandins. 1981 May;21(5):699-704. doi: 10.1016/0090-6980(81)90227-6.

Abstract
  1. Pharmacologic doses of hydrocortisone sodium succinate (100 mg/kg) has a rapid protective action against arachidonate-induced mortality in mice when administered intravenously 5 to 60 min before intravenous infusion of arachidonate. 2. Intravenous dexamethasone sodium phosphate (4 mg/kg) has a similar protective effect. 3. The time course of the development of the protective effect of intravenous glucocorticoids suggests that DNA transcription and protein synthesis are not involved in the mechanism of this action. 4. Longer pretreatment with glucocorticoids are required to reduce mortality when subcutaneous or intraperitoneal routes of administration of the steroids used.
摘要
  1. 药理剂量的琥珀酸钠氢化可的松(100毫克/千克)在静脉输注花生四烯酸盐前5至60分钟静脉给药时,对花生四烯酸盐诱导的小鼠死亡具有快速保护作用。2. 静脉注射磷酸地塞米松钠(4毫克/千克)具有类似的保护作用。3. 静脉糖皮质激素保护作用的发展时间进程表明,DNA转录和蛋白质合成不参与此作用机制。4. 当使用皮下或腹腔途径给药类固醇时,需要更长时间的糖皮质激素预处理来降低死亡率。

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