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淋巴液:交换机制与调节。

Lymphatic fluid: exchange mechanisms and regulation.

机构信息

University of Missouri School of Medicine, Department of Physiology, MA 415 Medical Sciences Bldg, Columbia, MO 65212-0001, USA.

出版信息

J Physiol. 2011 Jun 15;589(Pt 12):2935-43. doi: 10.1113/jphysiol.2011.208298. Epub 2011 Apr 26.

Abstract

Regulation of fluid and material movement between the vascular space of microvessels penetrating functioning organs and the cells therein has been studied extensively. Unanswered questions as to the regulatory mechanisms and routes remain. Significantly less is known about the lymphatic vascular system given the difficulties in seeing, no less isolating, these vessels lying deeper in these same tissues. It has become evident that the exchange microvasculature is not simply a passive biophysical barrier separating the vascular and interstitial compartments but a dynamic, multicellular structure subject to acute regulation and chronic adaptation to stimuli including inflammation, sepsis, diabetes, injury, hypoxia and exercise. Similarly lymphatic vessels range, in their simplest form, from lymphatic endothelium attached to the interstitial matrix, to endothelia and phasic lymphatic smooth muscle that act as Starling resistors. Recent work has demonstrated that among the microvascular lymphatic elements, the collecting lymphatics have barrier properties similar to venules, and thus participate in exchange. As with venules, vasoactive agents can alter both the permeability and contractile properties thereby setting up previously unanticipated gradients in the tissue space and providing potential targets for the pharmacological prevention and/or resolution of oedema.

摘要

微血管腔内的血管空间与穿透功能器官的细胞之间的液体和物质运动的调节已经得到了广泛的研究。然而,对于调节机制和途径,仍存在一些尚未解答的问题。由于这些位于更深层组织中的淋巴管难以观察,更不用说分离了,因此人们对淋巴管系统的了解要少得多。显然,交换性微血管系统不仅仅是一个将血管和间质隔离开来的被动生物物理屏障,而是一个动态的、多细胞的结构,它受到包括炎症、败血症、糖尿病、损伤、缺氧和运动等刺激的急性调节和慢性适应。同样,淋巴管系统的最简单形式从附着在间质基质上的淋巴管内皮细胞,到作为 Starling 阻力的内皮细胞和时相性淋巴平滑肌。最近的研究表明,在微血管淋巴管中,收集淋巴管具有与小静脉相似的屏障特性,因此参与了交换。与小静脉一样,血管活性物质可以改变通透性和收缩性,从而在组织间隙中建立以前未预料到的梯度,并为药理学预防和/或解决水肿提供潜在的靶点。

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