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实验模型中失血性休克复苏期间改变血液血红蛋白氧亲和力的微循环效应

Microcirculatory effects of changing blood hemoglobin oxygen affinity during hemorrhagic shock resuscitation in an experimental model.

作者信息

Villela Nivaldo R, Cabrales Pedro, Tsai Amy G, Intaglietta Marcos

机构信息

Department of Bioengineering, University of California-San Diego, La Jolla, California 92093-0412, USA.

出版信息

Shock. 2009 Jun;31(6):645-52. doi: 10.1097/SHK.0b013e31818bb98a.

Abstract

Microvascular responses to blood volume restitution using red blood cells (RBCs) with modified hemoglobin (Hb) oxygen affinity were studied in the hamster window chamber model during resuscitation from hemorrhagic shock. Allosteric effectors inositol hexaphosphate and 5-hydroxymethyl-2-furfural were introduced into the RBCs by electroporation to decrease and increase Hb-oxygen affinity. In vitro P50s (partial pressure of oxygen at 50% Hb saturation) were modified to 10 and 50 mmHg (normal P50, 32 mmHg). Awake hamsters were subjected to hemorrhage of 50% of blood volume, followed by a shock period of 1 h, and then resuscitated with 25% blood volume with high or low P50 RBCs (hematocrit, 50%). After resuscitation, base excess was significantly lower than baseline in the high-P50 RBC group (HP50; 0.3 +/- 2 vs. 5.0 +/- 1.7 mM) and MAP was lower than baseline in the low-P50 RBC group (LP50; 93 +/- 6 vs. 109 +/- 6 mM). Arteriolar diameter and flow were significantly lower in the HP50. Functional capillary density in the HP50 was significantly lower than LP50 at 60 and 90 min after resuscitation. There was no significantly difference in arteriolar PO2. Tissue PO2, venular PO2, and oxygen delivery were higher in LP50 than in HP50. There was no significant difference in oxygen extraction. Oxygen extraction ratio (oxygen extraction/oxygen delivery) x 100 was significantly higher in HP50 than in LP50. These results suggest that lowering blood P50 in resuscitation provides improved microvascular function in comparison with higher P50.

摘要

在仓鼠窗式小室模型中,研究了在失血性休克复苏过程中,使用具有修饰血红蛋白(Hb)氧亲和力的红细胞(RBC)对血容量恢复的微血管反应。通过电穿孔将变构效应剂肌醇六磷酸和5-羟甲基-2-糠醛引入红细胞,以降低和增加Hb-氧亲和力。体外P50(Hb饱和度为50%时的氧分压)分别调整为10和50 mmHg(正常P50为32 mmHg)。清醒的仓鼠失血50%血容量,随后经历1小时的休克期,然后用高或低P50的红细胞(血细胞比容50%)以25%血容量进行复苏。复苏后,高P50红细胞组(HP50)的碱剩余显著低于基线(0.3±2 vs. 5.0±1.7 mM),低P50红细胞组(LP50)的平均动脉压低于基线(93±6 vs. 109±6 mmHg)。HP50组的小动脉直径和血流量显著降低。复苏后60和90分钟时,HP50组的功能性毛细血管密度显著低于LP50组。小动脉PO2无显著差异。LP50组的组织PO2、小静脉PO2和氧输送高于HP50组。氧摄取无显著差异。氧摄取率(氧摄取/氧输送)×100在HP50组显著高于LP50组。这些结果表明,与较高的P50相比,复苏时降低血液P50可改善微血管功能。

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