Division of Cardiology, Pulmonology, and Vascular Medicine, University Duesseldorf, Medical Faculty, Duesseldorf, Germany.
Division of Cardiology, Pulmonology, and Vascular Medicine, University Duesseldorf, Medical Faculty, Duesseldorf, Germany; CARID - Cardiovascular research Institute Duesseldorf, University Duesseldorf, Duesseldorf, Germany.
Free Radic Biol Med. 2018 Dec;129:520-531. doi: 10.1016/j.freeradbiomed.2018.10.399. Epub 2018 Oct 15.
Collateral expansion is an important compensatory mechanism to alleviate tissue ischemia after arterial occlusion. We investigated the efficacy and mechanisms of temporary remote hindlimb occlusion to stimulate contralateral blood flow and collateral expansion after hindlimb ischemia in mice and evaluated translation to peripheral artery disease in humans.
We induced unilateral hindlimb ischemia via femoral artery excision in mice. We studied central hemodynamics, blood flow, and perfusion of the ischemic hindlimb during single and repetitive remote occlusion (RRO) of the contralateral non-ischemic hindlimb with a pressurized cuff. Similar experiments were performed in patients with unilateral peripheral artery disease (PAD). Contralateral occlusion of the non-ischemic hindlimb led to an acute increase in blood flow to the ischemic hindlimb without affecting central blood pressure and cardiac output. The increase in blood flow was sustained even after deflation of the pressure cuff. RRO over 12 days (8/day, each 5 min) led to significantly increased arterial inflow, lumen expansion of collateral arteries, and increased perfusion of the chronically ischemic hindlimb as compared to control. In NOS3 and after inhibition of NOS (L-NAME), and NO (ODQ), the acute and chronic effects of contralateral occlusion were abrogated and stimulation of guanylyl cyclase with cinaciguate exhibited a similar response as RRO and was not additive. Pilot studies in PAD patients demonstrated that contralateral occlusion increased arterial inflow to ischemic limbs and improved walking distance.
Repetitive remote contralateral occlusion stimulates arterial inflow, perfusion, and functional collateral expansion in chronic hindlimb ischemia via an eNOS-dependent mechanism underscoring the potential of remote occlusion as a novel treatment option in peripheral artery disease.
侧支扩张是缓解动脉闭塞后组织缺血的重要代偿机制。我们研究了通过短暂性远程后肢阻断来刺激对侧血流和侧支扩张的效果和机制,以评估其在小鼠后肢缺血和人类外周动脉疾病中的应用。
我们通过股动脉切除在小鼠中诱导单侧后肢缺血。我们研究了在加压袖带单次和重复阻断对侧非缺血后肢时,中央血流动力学、血流和缺血后肢灌注情况。在单侧外周动脉疾病(PAD)患者中进行了类似的实验。非缺血后肢的对侧阻断导致缺血后肢的血流急性增加,而不影响中心血压和心输出量。即使在压力袖带放气后,血流量仍持续增加。与对照组相比,12 天(每天 8 次,每次 5 分钟)的 RRO 导致动脉流入增加、侧支动脉管腔扩张和慢性缺血后肢灌注增加。与对照组相比,NOS3 缺失和 NOS 抑制(L-NAME)和 NO(ODQ)后,急性和慢性阻断效果消失,用西那卡塞刺激鸟苷酸环化酶也表现出与 RRO 相似的反应,而没有叠加作用。在 PAD 患者的初步研究中,发现对侧阻断增加了缺血肢体的动脉流入并改善了步行距离。
重复远程对侧阻断通过 eNOS 依赖机制刺激慢性后肢缺血中的动脉流入、灌注和功能性侧支扩张,突出了远程阻断作为外周动脉疾病新治疗选择的潜力。