首页> 美国卫生研究院文献>Frontiers in Neuroscience >NK1-r Antagonist Treatment Comparable to Decompressive Craniectomy in Reducing Intracranial Pressure Following Stroke
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NK1-r Antagonist Treatment Comparable to Decompressive Craniectomy in Reducing Intracranial Pressure Following Stroke

机译:NK1-r拮抗剂治疗可与减压颅骨切除术相比降低中风后颅内压

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Background and Purpose: 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.Methods: Anesthetized female Merino sheep (65 ± 6 kg, 18–24 months) underwent sham surgery (n = 4) or permanent middle cerebral artery occlusion (n = 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.Results: 2×NK1, 3×NK1 administration or DC surgery significantly (p < 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.Conclusion: 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.
机译:背景和目的: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。现有的药物治疗并不针对潜在的病理生理学,并且常常无法持续降低ICP,而减压颅骨切除术(DC)可以挽救生命,但具有手术/围手术期风险,并且老年人的发病率增加。因此,迫切需要直接针对水肿发生机制的疗法。由与速激肽NK1受体(NK1-r)结合的P物质(SP)介导的神经源性炎症与血脑屏障(BBB)破坏,脑水肿和中风后不良预后有关。 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。但是,尚未在大型动物模型中研究治疗方法,这是迈向临床翻译的重要一步。因此,当前研究在临床相关的绵羊模型中比较了NK1-r拮抗剂治疗与DC手术在降低卒中后ICP方面的​​功效。方法:麻醉的雌性美利奴绵羊(65±6 kg,18 –24个月)接受了假手术(n = 4)或永久性大脑中动脉阻塞(n = 22)。将中风动物随机分为5种治疗方法之一:1次NK1推注(4 h),2次NK1推注(4 h; 9 h),3次NK1推注(4 h; 9 h; 14 h),DC手术(进行在4小时)或生理盐水。中风后24小时监测ICP,血压和血气。脑卒中后24 h,对动物进行MRI,然后进行灌注,取出大脑并进行组织学评估。结果: 2×NK1、3×NK1给药或DC手术显着降低了ICP(p <0.05)与车辆相比。 1×NK1在持续降低ICP方面无效。在MRI上,与NK1-r治疗组相比,媒介物在中线移位和脑水肿方面更显着。结论:与DC手术相比,两次或三次大剂量NK1-r拮抗剂治疗可使ICP降低,这可能提供了一种新的替代方法,以解决ICP升高的侵入性手术。

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