Morgan Ruth, Keen John, Halligan Daniel, O'Callaghan Alan, Andrew Ruth, Livingstone Dawn, Abernethie Amber, Maltese Giorgia, Walker Brian, Hadoke Patrick
University/ BHF Centre for Cardiovascular Science, The Queen's Medical Research Institute, University of Edinburgh, Edinburgh, United Kingdom.
Royal (Dick) School of Veterinary Studies, University of Edinburgh, Edinburgh, United Kingdom.
PLoS One. 2018 Feb 15;13(2):e0192746. doi: 10.1371/journal.pone.0192746. eCollection 2018.
Glucocorticoids are potent inhibitors of angiogenesis in the rodent in vivo and in vitro but the mechanism by which this occurs has not been determined. Administration of glucocorticoids is used to treat a number of conditions in horses but the angiogenic response of equine vessels to glucocorticoids and, therefore, the potential role of glucocorticoids in pathogenesis and treatment of equine disease, is unknown. This study addressed the hypothesis that glucocorticoids would be angiostatic both in equine and murine blood vessels.The mouse aortic ring model of angiogenesis was adapted to assess the effects of cortisol in equine vessels. Vessel rings were cultured under basal conditions or exposed to: foetal bovine serum (FBS; 3%); cortisol (600 nM), cortisol (600nM) plus FBS (3%), cortisol (600nM) plus either the glucocorticoid receptor antagonist RU486 or the mineralocorticoid receptor antagonist spironolactone. In murine aortae cortisol inhibited and FBS stimulated new vessel growth. In contrast, in equine blood vessels FBS alone had no effect but cortisol alone, or in combination with FBS, dramatically increased new vessel growth compared with controls. This effect was blocked by glucocorticoid receptor antagonism but not by mineralocorticoid antagonism. The transcriptomes of murine and equine angiogenesis demonstrated cortisol-induced down-regulation of inflammatory pathways in both species but up-regulation of pro-angiogenic pathways selectively in the horse. Genes up-regulated in the horse and down-regulated in mice were associated with the extracellular matrix. These data call into question our understanding of glucocorticoids as angiostatic in every species and may be of clinical relevance in the horse.
糖皮质激素在啮齿动物体内和体外都是血管生成的有效抑制剂,但其作用机制尚未明确。糖皮质激素的给药被用于治疗马匹的多种病症,但马血管对糖皮质激素的血管生成反应以及糖皮质激素在马疾病发病机制和治疗中的潜在作用尚不清楚。本研究探讨了糖皮质激素在马和鼠血管中均具有血管抑制作用这一假说。对小鼠主动脉环血管生成模型进行了改进,以评估皮质醇对马血管的影响。血管环在基础条件下培养或暴露于:胎牛血清(FBS;3%);皮质醇(600 nM),皮质醇(600 nM)加FBS(3%),皮质醇(600 nM)加糖皮质激素受体拮抗剂RU486或盐皮质激素受体拮抗剂螺内酯。在小鼠主动脉中,皮质醇抑制而FBS刺激新血管生长。相反,在马血管中,单独的FBS没有作用,但单独的皮质醇或与FBS联合使用时,与对照组相比显著增加了新血管生长。这种作用被糖皮质激素受体拮抗作用阻断,但未被盐皮质激素拮抗作用阻断。小鼠和马血管生成的转录组显示,皮质醇在两个物种中均诱导炎症途径下调,但在马中选择性地上调促血管生成途径。在马中上调而在小鼠中下调的基因与细胞外基质有关。这些数据使我们对糖皮质激素在每个物种中均具有血管抑制作用的理解受到质疑,并且可能在马的临床中具有相关性。