Milner P, Bodin P, Burnstock G
Department of Anatomy and Developmental Biology, University College London, UK.
J Vasc Res. 1996 Mar-Apr;33(2):139-45. doi: 10.1159/000159142.
Chronic rather than acute changes in the autonomic innervation of the vasculature are a feature of ageing and several cardiovascular disorders. To investigate the long-term influence of perivascular innervation on the vascular endothelium, the release of vasoactive substances which have been localized in endothelial cells, namely ATP, endothelin, substance P and vasopressin, was monitored from cells isolated from adult rat thoracic aorta following neonatal guanethidine sympathectomy. The endothelial cells were initially perfused at 0.5 ml/min and exposed to two periods of increased flow at 3.0 ml/min. Cells isolated from control rats released significantly more ATP on both occasions of switching from the lower to higher flow rate and significantly more endothelin on the second exposure to the higher flow rate. In contrast, endothelial cells isolated from sympathectomised rats showed no increased release of either ATP or endothelin with increase flow, although the release of endothelin at the initial flow rate of 0.5 ml/min was higher than in the controls. Substance P and vasopressin levels in the perfusate were the same in controls and after sympathectomy. In summary, long-term sympathectomy suppresses increased flow-induced release of selected vasoactive substances from the endothelium, thus shear-stress-induced changes in local blood flow may be impaired when there are chronic disturbances in the autonomic innervation.
血管自主神经支配的慢性而非急性变化是衰老和几种心血管疾病的一个特征。为了研究血管周围神经支配对血管内皮的长期影响,对新生大鼠进行胍乙啶交感神经切除术后,从成年大鼠胸主动脉分离的细胞中监测了定位于内皮细胞的血管活性物质(即三磷酸腺苷(ATP)、内皮素、P物质和血管加压素)的释放情况。内皮细胞最初以0.5毫升/分钟的速度灌注,并经历两个流速增加至3.0毫升/分钟的阶段。在从较低流速切换到较高流速的两种情况下,从对照大鼠分离的细胞释放的ATP显著更多,并且在第二次暴露于较高流速时释放的内皮素显著更多。相比之下,从交感神经切除的大鼠分离的内皮细胞在流速增加时,ATP或内皮素的释放均未增加,尽管在初始流速0.5毫升/分钟时内皮素的释放高于对照组。灌注液中P物质和血管加压素的水平在对照组和交感神经切除术后相同。总之,长期交感神经切除术会抑制流速增加引起的内皮细胞中特定血管活性物质的释放,因此当自主神经支配存在慢性紊乱时,剪切应力诱导的局部血流变化可能会受到损害。