Stewart Randolph H
Department of Veterinary Physiology and Pharmacology, Michael E. DeBakey Institute, Texas A&M University, College Station, TX, United States.
Front Vet Sci. 2020 Nov 5;7:609583. doi: 10.3389/fvets.2020.609583. eCollection 2020.
Increases in the volume of the interstitial space are readily recognized clinically as interstitial edema formation in the loose connective tissue of skin, mucosa, and lung. However, the contents and the hydrostatic pressure of this interstitial fluid can be very difficult to determine even in experimental settings. These difficulties have long obscured what we are beginning to appreciate is a dynamic milieu that is subject to both intrinsic and extrinsic regulation. This review examines current concepts regarding regulation of interstitial volume, pressure, and flow and utilizes that background to address three major topics of interest that impact IV fluid administration. The first of these started with the discovery that excess dietary salt can be stored non-osmotically in the interstitial space with minimal impact on vascular volume and pressures. This led to the hypothesis that, along with the kidney, the interstitial space plays an active role in the long-term regulation of blood pressure. Second, it now appears that hypovolemic shock leads to systemic inflammatory response syndrome principally through the entry of digestive enzymes into the intestinal interstitial space and the subsequent progression of enzymes and inflammatory agents through the mesenteric lymphatic system to the general circulation. Lastly, current evidence strongly supports the non-intuitive view that the primary factor leading to inflammatory edema formation is a decrease in interstitial hydrostatic pressure that dramatically increases microvascular filtration.
间质间隙容积的增加在临床上很容易被识别为皮肤、黏膜和肺的疏松结缔组织中的间质水肿形成。然而,即使在实验环境中,这种间质液的成分和静水压也可能很难确定。长期以来,这些困难掩盖了我们开始认识到的一个动态环境,这个环境受到内在和外在的调节。这篇综述探讨了关于间质容积、压力和流量调节的当前概念,并利用这一背景来讨论影响静脉输液的三个主要感兴趣的话题。其中第一个话题始于发现过量的饮食盐分可以以非渗透方式储存在间质间隙中,对血管容积和压力的影响最小。这导致了一个假说,即间质间隙与肾脏一起在血压的长期调节中发挥积极作用。其次,现在看来,低血容量性休克主要通过消化酶进入肠间质间隙,以及随后酶和炎症介质通过肠系膜淋巴系统进入体循环,从而导致全身炎症反应综合征。最后,目前的证据有力地支持了一个非直观的观点,即导致炎症性水肿形成的主要因素是间质静水压的降低,这会显著增加微血管滤过。