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血液炎性介质和药理学工具对冠状小静脉屏障功能的调节:新型微血管壁模型的研究进展。

Regulation of coronary venular barrier function by blood borne inflammatory mediators and pharmacological tools: insights from novel microvascular wall models.

机构信息

Dept. of Physiology, Univ. of Munich (LMU), Schillerstr. 44, 80336 Munich, Germany.

出版信息

Am J Physiol Heart Circ Physiol. 2012 Feb 1;302(3):H567-81. doi: 10.1152/ajpheart.00360.2011. Epub 2011 Nov 11.

Abstract

We hypothesized that postcapillary venules play a central role in the control of the tightness of the coronary system as a whole, particularly under inflammatory conditions. Sandwich cultures of endothelial cells and pericytes of precapillary arteriolar or postcapillary venular origin from human myocardium as models of the respective vascular walls (sandwich cultures of precapillary arteriolar or postcapillary venular origin) were exposed to thrombin and components of the acutely activatable inflammatory system, and their hydraulic conductivity (L(P)) was registered. L(P) of SC-PAO remained low under all conditions (3.24 ± 0.52·10(-8)cm·s(-1)·cmH(2)O(-1)). In contrast, in the venular wall model, PGE(2), platelet-activating factor (PAF), leukotriene B(4) (LTB(4)), IL-6, and IL-8 induced a prompt, concentration-dependent, up to 10-fold increase in L(P) with synergistic support when combined. PAF and LTB(4) released by metabolically cooperating platelets, and polymorphonuclear leucocytes (PMNs) caused selectively venular endothelial cells to contract and to open their clefts widely. This breakdown of the barrier function was preventable and even reversible within 6-8 h by the presence of 50 μM quercetin glucuronide (QG). LTB(4) synthesis was facilitated by biochemical involvement of erythrocytes. Platelets segregated in the arterioles and PMNs in the venules of blood-perfused human myocardium (histological studies on donor hearts refused for heart transplantation). Extrapolating these findings to the coronary microcirculation in vivo would imply that the latter's complex functionality after accumulation of blood borne inflammatory mediators can change rapidly due to selective breakdown of the postcapillary venular barrier. The resulting inflammatory edema and venulo-thrombosis will severely impair myocardial performance. The protection afforded by QG could be of particular relevance in the context of cardiosurgical intervention.

摘要

我们假设,在后毛细血管静脉中,起着控制整个冠状动脉系统的紧密性的核心作用,特别是在炎症条件下。从人类心肌中提取的小动脉前毛细血管或后毛细血管起源的内皮细胞和周细胞的三明治培养物作为各自血管壁的模型(小动脉前毛细血管或后毛细血管起源的三明治培养物),暴露于凝血酶和急性激活炎症系统的成分,并记录它们的水力传导性(L(P))。在所有条件下,SC-PAO 的 L(P) 保持低值(3.24 ± 0.52·10(-8)cm·s(-1)·cmH(2)O(-1))。相比之下,在后毛细血管壁模型中,PGE(2)、血小板激活因子 (PAF)、白三烯 B(4) (LTB(4))、IL-6 和 IL-8 诱导 L(P) 迅速、浓度依赖性增加,当联合使用时,协同支持增加 10 倍。代谢合作的血小板和多形核白细胞 (PMN) 释放的 PAF 和 LTB(4) 选择性地引起后毛细血管内皮细胞收缩,并使其裂孔广泛开放。这种屏障功能的破坏可以通过存在 50 μM 槲皮素葡萄糖醛酸苷 (QG) 来预防,甚至在 6-8 小时内逆转。LTB(4) 的合成通过红细胞的生化参与得到促进。血小板在前小动脉中分离,PMN 在血流灌注的人类心肌中的后小静脉中分离(拒绝用于心脏移植的供体心脏的组织学研究)。将这些发现外推到体内冠状动脉微循环中,意味着在血液炎症介质积累后,后者的复杂功能可以由于后毛细血管静脉屏障的选择性破坏而迅速改变。由此产生的炎症性水肿和静脉血栓形成将严重损害心肌功能。QG 提供的保护在心脏手术干预的背景下可能具有特别重要的意义。

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