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Review: Novel insights into the regulation of vascular tone by sphingosine 1-phosphate

机译:综述:鞘氨醇1-磷酸调节血管张力的新见解

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摘要

Endothelial dysfunction leading to increased vascular tone is implicated in the pathogenesis of cardiovascular disease, hypertension and pregnancy-related complications like preeclampsia and intrauterine growth restriction. Vascular tone is regulated by a balance between vasoconstrictor and vasodilator signals. Some vascular mediators circulate in blood, whereas others are produced by the endothelium and are delivered to the underlying vascular smooth muscle cells (VSMCs). It is proposed that increased permeability of resistance arteries in preeclampsia allows access of circulating vasoactive factors to VSMCs leading to increased vascular tone. This review focuses on the role of sphingosine 1-phosphate (SIP). This sphingolipid enhances the endothelial barrier, but it can also disrupt the barrier under certain conditions. These SIP-mediated effects on the endothelial barrier have been demonstrated in cultured endothelial cells and in isolated venules. They depend on SIP concentrations, the SIP receptors expressed and the vascular bed. However, no studies have examined if vascular tone is regulated by SIP in resistance arteries through changes in endothelial permeability and the leakage of circulating vasoconstrictors. Our recent studies using the pressure myograph system show that access of infused vasoconstrictors to VSMCs is blocked under low SIP concentrations. Pathophysiological levels of infused SIP disrupt the barrier and maximally increase vascular tone by facilitating access of itself and a co-infused vasoconstrictor to the VSMCs. Interestingly, infusion of an intermediate physiological concentration of SIP showed a small increase in endothelial permeability with controlled leakage of a co-infused vasoconstrictor that led to sub-maximal vascular tone development. These and other studies delineate the important role of SIP in the regulation of vascular tone and emphasize how dysfunction of this regulation can lead to pregnancy-related disorders.
机译:导致血管紧张度增加的内皮功能障碍与心血管疾病,高血压和与妊娠有关的并发症(如先兆子痫和子宫内生长受限)的发病机制有关。血管紧张度由血管收缩剂和血管扩张剂信号之间的平衡调节。一些血管介导物在血液中循环,而另一些则由内皮产生,并被输送至下面的血管平滑肌细胞(VSMC)。提出先兆子痫中抵抗动脉的通透性增加允许循环的血管活性因子进入VSMC,导致血管紧张度增加。这篇综述集中于1-磷酸鞘氨醇(SIP)的作用。这种鞘脂可增强内皮屏障,但在某些情况下也会破坏屏障。这些SIP介导的对内皮屏障的作用已在培养的内皮细胞和分离的小静脉中得到证实。它们取决于SIP浓度,表达的SIP受体和血管床。但是,尚无研究检查SIP是否通过抵抗性动脉中的内皮通透性变化和循环血管收缩剂的渗漏来调节血管张力。我们最近使用压力肌成像仪系统进行的研究表明,在低SIP浓度下,输注血管收缩剂无法进入VSMC。注入的SIP的病理生理学水平通过促进自身和共注入的血管收缩剂进入VSMC来破坏屏障并最大程度地增加血管张力。有趣的是,中度生理浓度的SIP输注显示内皮通透性略有增加,同时输注的血管收缩剂渗漏受到控制,导致血管张力降低至最大。这些研究和其他研究描述了SIP在调节血管张力中的重要作用,并强调了该调节功能障碍如何导致妊娠相关疾病。

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