Microvascular experimental evidence on the relative significance of restoring oxygen carrying capacity vs. blood viscosity in shock resuscitation

被引:31
作者
Vazquez, Beatriz Y. Salazar [1 ,2 ]
Wettstein, Reto [3 ]
Cabrales, Pedro [4 ]
Tsai, Amy G. [1 ,4 ]
Intaglietta, Marcos [1 ]
机构
[1] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
[2] Univ Juarez Estado Durango, Fac Med, Victoria De Durango 34000, Durango, Mexico
[3] Univ Hosp Geneva, Dept Plast & Reconstruct Surg, Geneva, Switzerland
[4] La Jolla Bioengn Inst, La Jolla, CA 92037 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEINS AND PROTEOMICS | 2008年 / 1784卷 / 10期
关键词
Plasma expander; Blood viscosity; Oxygen carrying capacity; Blood substitute; Hemorrhagic shock; Microcirculation;
D O I
10.1016/j.bbapap.2008.04.020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The development of volume replacement fluids for resuscitation in hemorrhagic shock comprises oxygen carrying and non carrying fluids. Non oxygen carrying fluids or plasma expanders are used up to the transfusion trigger, and upon reaching this landmark either blood, and possibly in the near future oxygen carrying blood substitutes, are used. An experimental program in hemorrhagic shock using the hamster chamber window model allowed to compare the relative performance of most fluids proposed for shock resuscitation. This model allows investigating simultaneously the microcirculation and systemic reactions, in the awake condition, in a tissue isolated from the environment. Results from this program show that in general plasma expanders such as Ringer's lactate and dextran 70 kDa do not sufficiently restore blood viscosity upon reaching the transfusion trigger, causing microvascular collapse. This is in part restored by a blood transfusion, independently of the oxygen carrying capacity of red blood cells. These results lead to the proposal that effective blood substitutes must be designed to prevent microvascular collapse, manifested in the decrease of functional capillary density. Achievement of this goal, in combination with the increase of oxygen affinity, significantly postpones the need for a blood transfusion, and lowers the total requirement of restoration of intrinsic oxygen carrying capacity. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:1421 / 1427
页数:7
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