NK1-r Antagonist Treatment Comparable to Decompressive Craniectomy in Reducing Intracranial Pressure Following Stroke
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Updated: Jan 21, 2026

Optimized Management of Endovascular Treatment for Acute Ischemic Stroke
Published on: January 18, 2018
Annabel J Sorby-Adams1, Anna V Leonard1, Jan W Hoving2,3
1Adelaide Medical School and Adelaide Centre for Neuroscience Research, The University of Adelaide, Adelaide, SA, Australia.
Insights
Two or three doses of NK1-receptor antagonist effectively lowered intracranial pressure (ICP) post-stroke in sheep, comparable to decompressive craniectomy surgery. This offers a potential non-surgical alternative for managing elevated ICP after stroke.
Area of Science:
- Neuroscience
- Neurosurgery
- Pharmacology
Background:
- Stroke-induced cerebral edema and elevated intracranial pressure (ICP) significantly contribute to morbidity and mortality.
- Current treatments for elevated ICP are often ineffective or carry substantial risks.
- Neurogenic inflammation, involving substance P (SP) and the NK1 receptor (NK1-r), plays a role in stroke-related brain swelling and poor outcomes.
Purpose of the Study:
- To evaluate the efficacy of NK1-receptor (NK1-r) antagonist treatment in reducing elevated ICP in a large animal model of stroke.
- To compare the effectiveness of NK1-r antagonist treatment with decompressive craniectomy (DC) surgery in managing post-stroke ICP.
Main Methods:
- Permanent middle cerebral artery occlusion was induced in ovine models.
- Animals received either NK1-r antagonist (1, 2, or 3 doses), decompressive craniectomy (DC), or saline vehicle.
- Intracranial pressure (ICP), blood pressure, and blood gases were monitored for 24 hours; MRI and histological assessments were performed.
Main Results:
- Two or three doses of NK1-r antagonist, as well as DC surgery, significantly reduced ICP compared to the vehicle group (p < 0.05).
- Single-dose NK1-r antagonist treatment did not sustainably lower ICP.
- MRI revealed reduced midline shift and cerebral edema in NK1-r antagonist-treated groups compared to vehicle controls.
Conclusions:
- Repeated administration of NK1-r antagonist effectively reduces elevated ICP post-stroke in a large animal model.
- NK1-r antagonist treatment demonstrated comparable efficacy to decompressive craniectomy in lowering ICP.
- NK1-r antagonist therapy presents a potential novel, non-invasive alternative to surgical intervention for managing elevated ICP following stroke.
Abstract:
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.
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