Department of Physiology and Pharmacology, Inflammation Research Network and Smooth Muscle Research Group, Snyder Institute of Infection, Immunity, and Inflammation, University of Calgary, Alberta, Canada.
Ann N Y Acad Sci. 2010 Oct;1207 Suppl 1:E69-74. doi: 10.1111/j.1749-6632.2010.05715.x.
The role of the lymphatic circulation to actively remove fluid, cells, proteins, and other particles from the interstitium to prevent mounting edema is well appreciated, but whether and how this function is compromised during inflammation has been scarcely investigated. We discuss here the mechanisms of lymphatic pumping and their modulation in inflammatory conditions or by inflammatory mediators in the context of inflammatory bowel disease (IBD), an ensemble of disorders typically described with abnormal or dysfunctional intestinal or mesenteric lymphatic vessels. We report our findings showing impaired mesenteric lymphatic contractile activity in an animal model of intestinal inflammation that recapitulates some features of IBD and suggests a role for prostanoids in this dysfunction. With the knowledge that prostaglandin E(2) and prostacyclin are implicated in IBD pathogenesis and induce a potent inhibition of lymphatic pumping, we established the pharmacological profile for these prostaglandin receptors in mesenteric lymphatic vessels and their respective role in pumping inhibition. Inhibition of mesenteric lymphatic pumping during inflammation may be a cause of edema, compromised immune response, and granuloma associated with IBD.
淋巴循环在积极清除间质中的液体、细胞、蛋白质和其他颗粒以防止水肿方面发挥着重要作用,但在炎症期间,这一功能是否以及如何受到影响,尚未得到充分研究。我们在这里讨论了淋巴泵的机制及其在炎症条件下或炎症介质调节下的机制,炎症性肠病(IBD)就是一个典型的例子,它通常描述为肠道或肠系膜淋巴血管异常或功能障碍。我们报告了我们的发现,即在一种模拟 IBD 某些特征的肠道炎症动物模型中,肠系膜淋巴收缩活动受损,并提示前列腺素在这种功能障碍中起作用。我们了解到前列腺素 E2 和前列环素参与 IBD 的发病机制,并导致淋巴泵的强烈抑制,因此我们确定了这些前列腺素受体在肠系膜淋巴血管中的药理学特征及其在泵送抑制中的各自作用。在炎症期间,肠系膜淋巴泵的抑制可能是导致水肿、免疫反应受损和与 IBD 相关的肉芽肿的原因。