地塞米松与氨基胍联合应用对内毒素血症大鼠的影响。

C C Wu, M H Yen
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引用次数: 0

摘要

研究了诱导型一氧化氮合酶(iNOS)合成抑制剂地塞米松(DEX)和iNOS活性抑制剂氨基胍(AG)联合用药对内毒素(脂多糖,LPS)麻醉大鼠的影响。此外,我们还研究了LPS对一氧化氮(NO)形成的完全抑制是否能预防低血压,使血管低反应性恢复正常,提高生存率。DEX (LPS前30分钟3 mg/kg)加AG (LPS后2小时15 mg/kg)联合用药可抑制硝酸盐(NO指标)的过量产生,防止迟发性低血压的发生,但在LPS处理6小时后,进一步增强了大鼠的速搏。此外,内毒素大鼠对去甲肾上腺素(NE)的血管低反应性仅部分恢复。在实验期间,DEX + AG处理的LPS-大鼠的存活率也比仅LPS处理的大鼠有所提高。DEX + AG联合治疗对内毒素血症大鼠的有益作用,表明(i) DEX + AG联合治疗动物可能减少LPS的一些有害影响,(ii) NO仅部分导致内毒素休克时血管反应性降低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Combined effects of dexamethasone and aminoguanidine on rats with endotoxemia.

The effects of a combination of dexamethasone (DEX, an inhibitor of inducible nitric oxide synthase (iNOS) synthesis) and aminoguanidine (AG, an inhibitor of iNOS activity) on the anesthetized rat treated with endotoxin (lipopolysaccharide, LPS) were examined. In addition, we investigated whether a complete inhibition of nitric oxide (NO) formation caused by LPS prevents the hypotension, restores the vascular hyporeactivity to normal and improves the survival rate. The combination of DEX (3 mg/kg at 30 min prior to LPS) plus AG (15 mg/kg at 2 h after LPS) inhibited the overproduction of nitrate (an indicator of NO) and prevented the development of delayed hypotension, but further enhanced tachycardia in rats treated with LPS for 6 h. In addition, the vascular hyporeactivity to norepinephrine (NE) was, however, only partially restored in endotoxemic rats treated with DEX plus AG. During the experimental period, the survival rate of LPS-rats treated with DEX plus AG was also improved when compared to that of rats treated with LPS only. The beneficial effects of the combined therapy with DEX plus AG on rats with endotoxemia, suggesting that (i) combined treatment of animals with DEX plus AG may reduce some of the detrimental effects of LPS and (ii) NO only partially contributes to the vascular hyporeactivity in endotoxic shock.

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