Sorby-Adams Annabel J, Leonard Anna V, Hoving Jan W, Yassi Nawaf, Vink Robert, Wells Adam J, Turner Renée J
Adelaide Medical School and Adelaide Centre for Neuroscience Research, The University of Adelaide, Adelaide, SA, Australia.
Department of Medicine and Neurology, Melbourne Brain Centre at the Royal Melbourne Hospital, The University of Melbourne, Parkville, VIC, Australia.
Front Neurosci. 2019 Jul 5;13:681. doi: 10.3389/fnins.2019.00681. eCollection 2019.
The morbidity and early mortality associated with stroke is largely attributable to cerebral edema and elevated intracranial pressure (ICP). Existing pharmacotherapies do not target the underlying pathophysiology and are often ineffective in sustainably lowering ICP, whilst decompressive craniectomy (DC) surgery is life-saving yet with surgical/peri-operative risk and increased morbidity in the elderly. Accordingly, there is an urgent need for therapies that directly target the mechanisms of edema genesis. Neurogenic inflammation, mediated by substance P (SP) binding to the tachykinin NK1 receptor (NK1-r), is associated with blood-brain barrier (BBB) disruption, cerebral edema and poor outcome post-stroke. NK1-r antagonist treatment ameliorates BBB dysfunction and cerebral edema in rodent stroke models. However, treatment has not been investigated in a large animal model, an important step toward clinical translation. Consequently, the current study compared the efficacy of NK1-r antagonist treatment to DC surgery in reducing ICP post-stroke in a clinically relevant ovine model. Anesthetized female Merino sheep (65 ± 6 kg, 18-24 months) underwent sham surgery ( = 4) or permanent middle cerebral artery occlusion ( = 22). Stroke animals were randomized into one of 5 treatments: 1×NK1 bolus (4 h), 2×NK1 bolus (4 h;9 h), 3×NK1 bolus (4 h;9 h;14 h), DC surgery (performed at 4 h) or saline vehicle. ICP, blood pressure and blood gasses were monitored for 24 h post-stroke. At 24 h post-stroke anesthetized animals underwent MRI followed by perfusion and brains removed and processed for histological assessment. 2×NK1, 3×NK1 administration or DC surgery significantly ( < 0.05) reduced ICP compared to vehicle. 1×NK1 was ineffective in sustainably lowering ICP. On MRI, midline shift and cerebral edema were more marked in vehicles compared to NK1-r treatment groups. Two or three boluses of NK1-r antagonist treatment reduced ICP comparable to DC surgery, suggesting it may provide a novel alternative to invasive surgery for the management of elevated ICP.
与中风相关的发病率和早期死亡率在很大程度上归因于脑水肿和颅内压(ICP)升高。现有的药物治疗并未针对潜在的病理生理学,而且在持续降低颅内压方面往往无效,而减压性颅骨切除术(DC)虽然能挽救生命,但存在手术/围手术期风险,且会增加老年人的发病率。因此,迫切需要直接针对水肿发生机制的治疗方法。由P物质(SP)与速激肽NK1受体(NK1-r)结合介导的神经源性炎症与血脑屏障(BBB)破坏、脑水肿及中风后不良预后相关。NK1-r拮抗剂治疗可改善啮齿动物中风模型中的血脑屏障功能障碍和脑水肿。然而,尚未在大型动物模型中研究该治疗方法,而这是迈向临床转化的重要一步。因此,本研究在具有临床相关性的绵羊模型中比较了NK1-r拮抗剂治疗与DC手术在降低中风后颅内压方面的疗效。对麻醉的雌性美利奴绵羊(65±6千克,18 - 24个月)进行假手术(n = 4)或永久性大脑中动脉闭塞(n = 22)。中风动物被随机分为5种治疗方法之一:单次NK1推注(4小时)、两次NK1推注(4小时;9小时)、三次NK1推注(4小时;9小时;14小时)、DC手术(在4小时进行)或生理盐水对照。中风后24小时监测颅内压、血压和血气。中风后24小时,对麻醉动物进行MRI检查,随后进行灌注检查,然后取出大脑并进行组织学评估。与对照组相比,两次NK1、三次NK1给药或DC手术显著(P < 0.05)降低了颅内压。单次NK1推注在持续降低颅内压方面无效。在MRI上,与NK1-r治疗组相比,对照组的中线移位和脑水肿更为明显。两剂或三剂NK1-r拮抗剂治疗降低颅内压的效果与DC手术相当,这表明它可能为治疗颅内压升高提供一种替代侵入性手术的新方法。