Tarshis Samantha, Maltzahn Joanne, Loomis Zoe, Irwin David C
Kendall Regional Medical Center of the Miami Emergency Department, University of Colorado School of Medicine, Aurora, CO, USA.
Aerosp Med Hum Perform. 2016 Dec 1;87(12):1031-1035. doi: 10.3357/AMHP.4571.2016.
High altitude cerebral edema (HACE) is a fulminant, deadly, and yet still unpredictable brain disease. A new prophylactic treatment for HACE and its predecessor, acute mountain sickness (AMS), needs to be developed without the contraindications or adverse effect profiles of acetazolamide and dexamethasone. Since neovascularization signals are likely key contributors to HACE/AMS, our approach was to examine already existing anti-angiogenic drugs to inhibit potential initiating HACE pathway(s). This approach can also reveal crucial early steps in the frequently debated mechanism of HACE/AMS pathogenesis.
We exposed four rat cohorts to hypobaric hypoxia and one to sea level (hyperbaric) conditions. The cohorts were treated with saline controls, an anti-angiogenesis drug (motesanib), a pro-angiogenesis drug (deferoxamine), or an intraperitoneal version of the established AMS prophylaxis drug, acetazolamide (benzolamide). Brain tissue was analyzed for cerebrovascular leak using the Evans Blue Dye (EVBD) protocol.
We observed significantly increased EVBD in the altitude control and pro-angiogenesis (deferoxamine) cohorts, and significantly decreased EVBD in the anti-angiogenesis (motesanib), established treatment (benzolamide), and sea-level cohorts.
Anti-angiogenesis-treated cohorts demonstrated less cerebrovascular extravasation than the altitude control and pro-angiogenesis treated rats, suggesting promise as an alternative prophylactic HACE/AMS treatment. The leak exacerbation with pro-angiogenesis treatment and improvement with anti-angiogenesis treatment support the hypothesis of early neovascularization signals provoking HACE. We demonstrate statistically significant evidence to guide further investigation for VEGF- and HIF-inhibitors as HACE/AMS prophylaxis, and as elucidators of still unknown HACE pathogenesis.Tarshis S, Maltzahn J, Loomis Z, Irwin DC. Preventing high altitude cerebral edema in rats with repurposed anti-angiogenesis pharmacotherapy. Aerosp Med Hum Perform. 2016; 87(12):1031-1035.
高原脑水肿(HACE)是一种暴发性、致命且仍不可预测的脑部疾病。需要开发一种针对HACE及其前身急性高原病(AMS)的新预防性治疗方法,且没有乙酰唑胺和地塞米松的禁忌症或不良反应。由于新血管生成信号可能是HACE/AMS的关键促成因素,我们的方法是研究现有的抗血管生成药物,以抑制潜在的引发HACE的途径。这种方法还可以揭示HACE/AMS发病机制中经常争论的关键早期步骤。
我们将四组大鼠暴露于低压低氧环境,一组暴露于海平面(高压)环境。这些组分别用生理盐水对照、抗血管生成药物(莫特桑尼)、促血管生成药物(去铁胺)或已确立的AMS预防药物乙酰唑胺(苯甲酰胺)的腹腔注射版本进行治疗。使用伊文思蓝染料(EVBD)方案分析脑组织的脑血管渗漏情况。
我们观察到,在高原对照组和促血管生成(去铁胺)组中,EVBD显著增加,而在抗血管生成(莫特桑尼)组、既定治疗(苯甲酰胺)组和海平面组中,EVBD显著降低。
接受抗血管生成治疗的组显示出比高原对照组和接受促血管生成治疗的大鼠更少的脑血管外渗,这表明有望作为HACE/AMS的替代预防性治疗方法。促血管生成治疗导致渗漏加剧,而抗血管生成治疗则使其改善,这支持了早期新血管生成信号引发HACE的假说。我们展示了具有统计学意义的证据,以指导进一步研究VEGF和HIF抑制剂作为HACE/AMS的预防措施,以及作为仍未知的HACE发病机制的阐释者。塔希斯S、马尔茨ahn J、卢米斯Z、欧文DC。用重新利用的抗血管生成药物疗法预防大鼠高原脑水肿。航空航天医学与人类表现。2016;87(12):1031 - 1035。