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血小板活化因子对微血管水力通透性的调节作用。

Modulation of microvascular hydraulic permeability by platelet-activating factor.

作者信息

Victorino Gregory P, Newton Christopher R, Curran Brian

机构信息

Department of Surgery, University of California San Francisco-East Bay, Alameda County Medical Center, Oakland, California 94602, USA.

出版信息

J Trauma. 2004 Feb;56(2):379-84. doi: 10.1097/01.TA.0000042156.89779.6C.

DOI:10.1097/01.TA.0000042156.89779.6C
PMID:14960983
Abstract

BACKGROUND

Platelet-activating factor (PAF) is a modulator of the inflammatory response to shock. Edema formation and intravascular fluid loss have been associated with PAF. The increase in microvessel permeability caused by PAF may be related to direct endothelial cell activation and leukocyte activation. We hypothesized that PAF increases hydraulic permeability by means of the direct activation of endothelial cells.

METHODS

Hydraulic permeability (Lp) was measured in rat mesenteric venules using the modified Landis micro-occlusion technique. After baseline Lp measurements, paired measures of Lp were obtained during PAF perfusion at doses of 0.1 nmol/L (n = 6), 1.0 nmol/L (n = 6), 10 nmol/L (n = 6), and 50 nmol/L (n = 6). The temporal effects of pulse administration of PAF and repeated exposures to PAF were also assessed.

RESULTS

Compared with baseline values (Lp = 1.16 +/- 0.11), the Lp of the microvessels significantly increased at PAF doses of 0.1 nmol/L (Lp = 1.46 +/- 0.1) (p < 0.002), 1 nmol/L (Lp = 2.0 +/- 0.11) (p < 0.004), 10 nmol/L (Lp = 4.09 +/- 0.09) (p < 0.005), and 50 nmol/L (Lp = 5.13 +/- 0.07) (p < 0.0001). All units for Lp are given as +/- SE x 10 -7 cm s-1. cm H2O-1.

CONCLUSION

PAF increased microvessel permeability in a dose-dependent manner. The permeability-increasing effect of PAF was transient even with continuous endothelial exposure to PAF. This study emphasizes the ability of PAF to directly modulate microvascular permeability and increase venular permeability.

摘要

背景

血小板活化因子(PAF)是休克炎症反应的调节剂。水肿形成和血管内液体丢失与PAF有关。PAF引起的微血管通透性增加可能与内皮细胞直接活化和白细胞活化有关。我们假设PAF通过直接激活内皮细胞来增加水通透性。

方法

采用改良的兰迪斯微闭塞技术测量大鼠肠系膜小静脉的水通透性(Lp)。在测量基线Lp后,在0.1 nmol/L(n = 6)、1.0 nmol/L(n = 6)、10 nmol/L(n = 6)和50 nmol/L(n = 6)剂量的PAF灌注期间获得Lp的配对测量值。还评估了PAF脉冲给药和重复暴露于PAF的时间效应。

结果

与基线值(Lp = 1.16 +/- 0.11)相比,在0.1 nmol/L(Lp = 1.46 +/- 0.1)(p < 0.002)、1 nmol/L(Lp = 2.0 +/- 0.11)(p < 0.004)、10 nmol/L(Lp = 4.09 +/- 0.09)(p < 0.005)和50 nmol/L(Lp = 5.13 +/- 0.07)(p < 0.0001)剂量的PAF作用下,微血管的Lp显著增加。Lp的所有单位均表示为+/- SE x 10 -7 cm s-1.cm H2O-1。

结论

PAF以剂量依赖性方式增加微血管通透性。即使内皮细胞持续暴露于PAF,PAF的通透性增加作用也是短暂的。本研究强调了PAF直接调节微血管通透性和增加小静脉通透性的能力。

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