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The Cardioprotective Effect of Hypertonic Saline Is Associated with Inhibitory Effect on Macrophage Migration Inhibitory Factor in Sepsis

机译:高渗盐水的心脏保护作用与对脓毒症中巨噬细胞迁移抑制因子的抑制作用有关。

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摘要

Sepsis can cause myocardial dysfunction, which contributes to the high mortality of sepsis. Hypertonic saline (HS) has been reported to increase myocardial contractility in sepsis. In the present study, mechanisms of action of HS resuscitation (4 mL of 7.5% NaCl per kilogram) on cardiac function have been evaluated in septic rats. HS was administered 1 h after LPS (10 mg/kg, i.v.) challenge. The mean arterial blood pressure significantly decreased 4 h after LPS challenge, and septic shock was observed at the end of experiment (6 h). Posttreatment with HS prevented hypotension caused by LPS and significantly improved cardiac function, evidenced by increases in left ventricular developed pressure, mean +dP/dt and −dP/dt. The amplitude of electrical-stimulated intracellular Ca2+ transient in isolated single cardiomyocytes was significantly reduced after 6 h LPS insult, which was recovered by HS. In addition, LPS resulted in significant increases in neutrophil myeloperoxidase activity, macrophage migration inhibitory factor (MIF), and NF-κB phospho-p65 protein levels in myocardium at 6 h, which were significantly attenuated by HS. In conclusion, HS improved myocardial contractility and prevented circulatory failure induced by endotoxemia, which may attribute to improvement of intracellular calcium handling process and inhibitory effects on neutrophil infiltration and MIF production in hearts.
机译:败血症可引起心肌功能障碍,从而导致败血症的高死亡率。据报道高渗盐水(HS)可增加败血症中的心肌收缩力。在本研究中,已经在脓毒症大鼠中评估了HS复苏(每公斤4 µmL的7.5%NaCl)对心脏功能的作用机制。 LPS(10μmg/ kg,i.v.)攻击后1h给予HS。 LPS攻击后4 h,平均动脉血压显着下降,在实验结束时(6 h)观察到败血性休克。 HS的后处理可预防LPS引起的低血压,并显着改善心脏功能,左室发达压力,平均+ dP / dt和-dP / dt升高可证明这一点。 LPS损伤6h后,分离的单个心肌细胞中电刺激的细胞内Ca 2 + 瞬变幅度明显降低,并通过HS恢复。此外,LPS导致心肌在6 h时嗜中性粒细胞髓过氧化物酶活性,巨噬细胞迁移抑制因子(MIF)和NF-κB磷酸化p65蛋白水平显着增加,而HS则显着降低了其水平。总之,HS改善了心肌的收缩力并防止了由内毒素血症引起的循环衰竭,这可能归因于细胞内钙处理过程的改善以及对心脏中性粒细胞浸润和MIF产生的抑制作用。

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