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慢性内毒素血症中器官血流的增加可通过抑制一氧化氮合酶而逆转。

Increased organ blood flow in chronic endotoxemia is reversed by nitric oxide synthase inhibition.

作者信息

Meyer J, Hinder F, Stothert J, Traber L D, Herndon D N, Flynn J T, Traber D L

机构信息

Department of Anesthesiology, University of Texas Medical Branch, Galveston 77555-1091.

出版信息

J Appl Physiol (1985). 1994 Jun;76(6):2785-93. doi: 10.1152/jappl.1994.76.6.2785.

DOI:10.1152/jappl.1994.76.6.2785
PMID:7523359
Abstract

We evaluated regional blood flows in a hyperdynamic sepsis model and the reversal of increased flows by blockade of nitric oxide (NO) synthase. Seven awake sheep were continuously infused with Escherichia coli endotoxin [lipopolysaccharide (LPS), 10 ng.kg-1.min-1] for 48 h. The NO synthase inhibitor N omega-nitro-L-arginine methyl ester (L-NAME, 25 mg/kg) was injected after 24 h. Blood flows to systemic organs were determined with the radioactive microsphere technique. LPS induced elevation of cardiac index by 36% (P < 0.05) and a fall in systemic vascular resistance index by 37% (P < 0.05) at 0 h [time of L-NAME administration, 24 h after infusion of LPS had begun] L-NAME administration normalized cardiac index [6.1 +/- 0.5 at 4 h posttreatment, 6.1 +/- 0.5 l.min-1.m-2 at -24 h (baseline)] and systemic vascular resistance index (1,333 +/- 105 at 4 h posttreatment, 1,280 +/- 163 dyn.s.cm-5.m2 at -24 h) and reduced all regional blood flows to near-baseline levels for the remainder of the study period (24 h). O2 consumption was unaffected by treatment.

摘要

我们评估了高动力性脓毒症模型中的局部血流情况,以及通过一氧化氮(NO)合酶阻断对血流增加的逆转作用。七只清醒的绵羊连续48小时输注大肠杆菌内毒素[脂多糖(LPS),10 ng·kg-1·min-1]。24小时后注射NO合酶抑制剂Nω-硝基-L-精氨酸甲酯(L-NAME,25 mg/kg)。用放射性微球技术测定全身各器官的血流。在0小时[L-NAME给药时间,LPS输注开始后24小时],LPS使心脏指数升高36%(P<0.05),全身血管阻力指数下降37%(P<0.05)。L-NAME给药使心脏指数恢复正常[治疗后4小时为6.1±0.5,-24小时(基线)为6.1±0.5 l·min-1·m-2]和全身血管阻力指数(治疗后4小时为1333±105,-24小时为1280±163 dyn·s·cm-5·m2),并在研究期剩余时间(24小时)内将所有局部血流降低至接近基线水平。氧耗不受治疗影响。

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