糖皮质激素与前列腺素:地塞米松对大鼠肺6-酮前列腺素F1α合成无抑制作用

Michael Y. Tsai
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引用次数: 9

摘要

给孕鼠大剂量地塞米松(1 ~ 12 mg/kg,每日2次),连续2天。在妊娠第21天检测地塞米松对胎儿和母体肺前列腺素代谢的影响。所有剂量的地塞米松治疗均显著增加胎儿和母亲肺匀浆中[14C]-花生四烯酸向6-酮前列腺素Fα的转化。这一发现与我们早期使用低剂量地塞米松的发现相似,表明地塞米松可以增强肺前列腺素合成酶活性。由于已知地塞米松可以抑制磷脂酶的活性,我们还测量了肺免疫反应性6-酮前列腺素Fα。结果表明,即使在最高剂量(12 mg/kg)下,地塞米松治疗也没有降低肺6-酮前列腺素F1α水平。这些结果表明,大剂量地塞米松,如临床治疗感染性休克时使用的地塞米松,不会抑制肺前列腺素的合成。
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Glucocorticoid and prostaglandin: lack of an inhibitory effect by dexamethasone on the synthesis of 6-ketoprostaglandin F1α in rat lung

High doses of dexamethasone (1–12 mg/kg twice daily) were administered to pregnant rats for 2 days. The effect of dexamethasone on fetal and maternal lung prostaglandin metabolism was examined on day 21 of gestation. Dexamethasone treatment at all dosages significantly increased conversion of [14C]-arachidonic acid to 6-ketoprostaglandin Fα in both fetal and maternal lung homogenates. This finding is similar to our earlier finding using lower dosages of dexamethasone and suggests that dexamethasone enhances lung prostaglandin synthetase activity. Because dexamethasone is known to inhibit the activity of phospholipases, we also measured lung immunoreactive 6-ketoprostaglandin Fα. The results showed that dexamethasone treatment did not diminish lung 6-keto-prostaglandin F level even at the highest dosage used (12 mg/kg). These results suggest that high dosages of dexamethasone, such as those used in the clinical treatment of septic shock, do not inhibit synthesis of lung prostaglandin.

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