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没食子酸乙酯对比去甲肾上腺素治疗铜绿假单胞菌脓毒症性休克犬心血管崩溃的疗效。

Benefits of ethyl gallate versus norepinephrine in the treatment of cardiovascular collapse in Pseudomonas aeruginosa septic shock in dogs.

机构信息

Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran, Mexico.

出版信息

Crit Care Med. 2012 Feb;40(2):560-72. doi: 10.1097/CCM.0b013e318232d8a6.

Abstract

INTERVENTIONS

Vasopressor therapy is required in septic shock to maintain tissue perfusion in the face of hypotension. Unfortunately, there are significant side effects of current vasopressors, and newer agents need to be developed. We recently discovered that ethyl gallate, a nonflavonoid phenolic antioxidant found in food substances, could reverse low mean arterial pressure found in an experimental model of septic shock due to inhibition of hydrogen peroxide signaling. In the present study, we compared the hemodynamic and biochemical effects of ethyl gallate vs. those of the commonly used vasopressor, norepinephrine, in a bacteremic canine model of Pseudomonas aeruginosa sepsis in two protocols.

MEASUREMENTS AND MAIN RESULTS

We performed these studies in anesthetized and mechanically ventilated dogs. In the early treatment protocol, we infused P. aeruginosa until mean arterial pressure first decreased to ∼60 mm Hg (about 2-3 hrs), after which we stopped the infusion and randomly administered ethyl gallate or norepinephrine in respective groups. In the late treatment protocol, we administered ethyl gallate or norepinephrine after a sustained ∼5-hr decrease in mean arterial pressure to 60 mm Hg and continued the infusion for the duration of the experiment. We followed parameters for over 10 hrs after the initiation of P. aeruginosa in both groups. We measured stroke work, urine output, serum creatinine, among other parameters, and used serum troponin T as an index of myocardial injury. We found that in both protocols, ethyl gallate and norepinephrine improved mean arterial pressure and stroke work to similar extents over the duration of the study. Particularly in the late treatment protocol, ethyl gallate resulted in a lower heart rate, a lower troponin T, and a greater urine output as compared with norepinephrine (p < .05).

CONCLUSIONS

These results suggest that phenolic antioxidants, such as ethyl gallate, that inhibit hydrogen peroxide signaling, may represent an alternative class of vasopressors for use in septic shock.

摘要

干预措施

在感染性休克中需要升压治疗以维持低血压情况下的组织灌注。不幸的是,目前的升压药有明显的副作用,需要开发新的药物。我们最近发现,没食子酸乙酯,一种在食物中发现的非类黄酮酚类抗氧化剂,可以通过抑制过氧化氢信号来逆转感染性休克实验模型中发现的低平均动脉压。在本研究中,我们在两种方案中比较了没食子酸乙酯与常用升压药去甲肾上腺素在犬绿脓假单胞菌感染性败血症模型中的血流动力学和生化效应。

测量和主要结果

我们在麻醉和机械通气的犬中进行了这些研究。在早期治疗方案中,我们输注绿脓假单胞菌,直到平均动脉压首次降至约 60mmHg(约 2-3 小时),然后停止输注,并在相应组中随机给予没食子酸乙酯或去甲肾上腺素。在晚期治疗方案中,我们在平均动脉压持续下降至 60mmHg 并持续 5 小时后给予没食子酸乙酯或去甲肾上腺素,并在整个实验过程中继续输注。在两组中,我们在开始输注绿脓假单胞菌后超过 10 小时测量了心搏量、尿量、血清肌酐等参数,并使用血清肌钙蛋白 T 作为心肌损伤的指标。我们发现,在两种方案中,没食子酸乙酯和去甲肾上腺素在研究期间均能在相似程度上提高平均动脉压和心搏量。特别是在晚期治疗方案中,与去甲肾上腺素相比,没食子酸乙酯导致心率更低、肌钙蛋白 T 更低和尿量更多(p <.05)。

结论

这些结果表明,抑制过氧化氢信号的酚类抗氧化剂,如没食子酸乙酯,可能代表感染性休克中使用的一类新型升压药。

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