Department of Systems Biology and Translational Medicine, Texas A&M Health Science Center College of Medicine, College Station, TX 77843, USA.
Am J Physiol Heart Circ Physiol. 2012 Feb 1;302(3):H643-53. doi: 10.1152/ajpheart.00606.2011. Epub 2011 Dec 9.
Numerous studies on metabolic syndrome (MetSyn), a cluster of metabolic abnormalities, have demonstrated its profound impact on cardiovascular and blood microvascular health; however, the effects of MetSyn on lymphatic function are not well understood. We hypothesized that MetSyn would modulate lymphatic muscle activity and alter muscularized lymphatic function similar to the impairment of blood vessel function associated with MetSyn, particularly given the direct proximity of the lymphatics to the chronically inflamed adipose depots. To test this hypothesis, rats were placed on a high-fructose diet (60%) for 7 wk, and their progression to MetSyn was assessed through serum insulin and triglyceride levels in addition to the expression of metabolic and inflammatory genes in the liver. Mesenteric lymphatic vessels were isolated and subjected to different transmural pressures while lymphatic pumping and contractile parameters were evaluated. Lymphatics from MetSyn rats had significant negative chronotropic effects at all pressures that effectively reduced the intrinsic flow-generating capacity of these vessels by ∼50%. Furthermore, lymphatics were remodeled to a significantly smaller diameter in the animals with MetSyn. Wire myograph experiments demonstrated that permeabilized lymphatics from the MetSyn group exhibited a significant decrease in force generation and were less sensitive to Ca(2+), although there were no significant changes in lymphatic muscle cell coverage or morphology. Thus, our data provide the first evidence that MetSyn induces a remodeling of collecting lymphatics, thereby effectively reducing their potential load capabilities and impairing the intrinsic contractility required for proper lymph flow.
大量关于代谢综合征(MetSyn)的研究表明,代谢异常的聚集对心血管和血液微血管健康有深远影响;然而,MetSyn 对淋巴管功能的影响还不是很清楚。我们假设 MetSyn 会调节淋巴管肌肉活动,并改变肌肉化的淋巴管功能,类似于与 MetSyn 相关的血管功能障碍,特别是考虑到淋巴管与慢性炎症脂肪组织的直接临近关系。为了验证这一假设,将大鼠置于高果糖饮食(60%)中 7 周,并通过血清胰岛素和甘油三酯水平以及肝脏代谢和炎症基因的表达来评估它们向 MetSyn 的进展情况。分离肠系膜淋巴管并施加不同的跨壁压力,同时评估淋巴管的泵送和收缩参数。MetSyn 大鼠的淋巴管在所有压力下都有明显的负变时作用,这有效地降低了这些血管的固有流量产生能力约 50%。此外,MetSyn 动物的淋巴管被重塑为明显较小的直径。电穿孔肌描记实验表明,MetSyn 组的通透性淋巴管的力生成显著降低,对 Ca(2+)的敏感性降低,尽管淋巴管肌肉细胞覆盖率或形态没有明显变化。因此,我们的数据首次提供了证据表明 MetSyn 诱导了收集淋巴管的重塑,从而有效地降低了它们的潜在负载能力,并损害了适当淋巴流动所需的内在收缩性。