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犬类败血症血管系统对N(ω)-单甲基-L-精氨酸和肾上腺素延长血管加压素治疗的反应。

Response of the septic vasculature to prolonged vasopressor therapy with N(omega)-monomethyl-L-arginine and epinephrine in canines.

作者信息

Freeman B D, Zeni F, Banks S M, Eichacker P Q, Bacher J D, Garvey E P, Tuttle J V, Jurgensen C H, Natanson C, Danner R L

机构信息

Critical Care Medicine Department, Warren G. Magnuson Clinical Center, Veterinary Resource Program, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

Crit Care Med. 1998 May;26(5):877-86. doi: 10.1097/00003246-199805000-00022.

Abstract

OBJECTIVE

To investigate the effect of blocking nitric oxide production on cardiovascular function and survival in canine septic shock treated with or without a conventional vasopressor.

DESIGN

Randomized, controlled trial.

SETTING

An animal research laboratory at the National Institutes of Health.

SUBJECTS

Sixty purpose-bred beagles.

INTERVENTIONS

Fibrin clots containing Escherichia coli were surgically placed into the peritoneal cavity. N(omega)-monomethyl-L-arginine (L-NMMA) 10 mg/kg followed by 0.5, 1.0, or 4.0 mg/kg/hr), epinephrine (1 microg/kg/min), both, or neither were infused for 24 hrs beginning 6 hrs after the onset of infection. All animals received fluid and antibiotic therapy.

MEASUREMENTS AND MAIN RESULTS

Serum nitric oxide metabolites, nitrite and nitrate, increased with infection (p = .024) and decreased with L-NMMA (p = .004, all doses combined). Myocardial nitric oxide synthase activity was ranked as follows: nonsurvivors > survivors > noninfected controls (p < .01). Other tissues examined showed the same pattern. L-NMMA produced sustained increases in systemic vascular resistance index and mean arterial pressure 9 and 24 hrs after the onset of infection (p < or = .04). Left ventricular ejection fraction was depressed by septic shock (p = .01) and further decreased by L-NMMA (p = .02). However, control and L-NMMA cardiac index values were similar (p > .4), perhaps because L-NMMA increased pulmonary artery occlusion pressure (p = .02). From 9 to 24 hrs, epinephrine, in the absence or presence of L-NMMA, blunted recovery of cardiac index (p < .02) and had a diminishing vasopressor effect (p = .05). Neither L-NMMA nor epinephrine, individually or combined, significantly altered survival rates at the doses investigated (p > or = .69).

CONCLUSIONS

The tested doses showed that nitric oxide production was inhibited by L-NMMA in canine septic shock, but mortality and myocardial depression were unaffected. These results suggest that if L-NMMA has a beneficial effect on survival rates in septic shock, it is small.

摘要

目的

研究阻断一氧化氮生成对接受或未接受传统血管升压药治疗的犬脓毒性休克心血管功能及生存率的影响。

设计

随机对照试验。

地点

美国国立卫生研究院的动物研究实验室。

对象

60只专门培育的比格犬。

干预措施

通过手术将含大肠杆菌的纤维蛋白凝块置于腹腔内。感染开始6小时后,输注10mg/kg的N(ω)-单甲基-L-精氨酸(L-NMMA),随后分别以0.5、1.0或4.0mg/kg/小时的剂量持续输注24小时,或输注肾上腺素(1μg/kg/分钟),或两者都输注,或两者都不输注。所有动物均接受液体和抗生素治疗。

测量指标及主要结果

血清一氧化氮代谢产物亚硝酸盐和硝酸盐随感染增加(p = 0.024),而随L-NMMA降低(所有剂量合并,p = 0.004)。心肌一氧化氮合酶活性排序如下:未存活者>存活者>未感染对照(p < 0.01)。检查的其他组织也呈现相同模式。L-NMMA在感染开始后第9小时和24小时使全身血管阻力指数和平均动脉压持续升高(p≤0.04)。脓毒性休克使左心室射血分数降低(p = 0.01),L-NMMA使其进一步降低(p = 0.02)。然而,对照组和L-NMMA组的心指数值相似(p > 0.4),这可能是因为L-NMMA使肺动脉闭塞压升高(p = 0.02)。在第9至24小时,无论有无L-NMMA,肾上腺素均减弱心指数的恢复(p < 0.02),且血管升压作用逐渐减弱(p = 0.05)。在研究的剂量下,单独或联合使用L-NMMA和肾上腺素均未显著改变生存率(p≥0.69)。

结论

所测试的剂量表明,L-NMMA可抑制犬脓毒性休克中一氧化氮的生成,但未影响死亡率和心肌抑制。这些结果提示,若L-NMMA对脓毒性休克的生存率有有益作用,其作用也很小。

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