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Intranasal Delivery of Curcumin Nanoparticles Improves Neuroinflammation and Neurological Deficits in Mice with Intracerebral Hemorrhage.

Zhongxin Duan, Wenjie Zhou, Shi He, Wanyu Wang, Hongyi Huang et al.
Other Small methods 2024 22 اقتباسات
PubMed DOI
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Study Design

نوع الدراسة
Other
المجتمع المدروس
Intracerebral hemorrhage mouse model
التدخل
Intranasal Delivery of Curcumin Nanoparticles Improves Neuroinflammation and Neurological Deficits in Mice with Intracerebral Hemorrhage. None
المقارن
ICH model controls
النتيجة الأولية
Neuroinflammation and neurological deficits post-ICH
اتجاه التأثير
Positive
خطر التحيز
Unclear

Abstract

Intracerebral hemorrhage (ICH) represents one of the most severe subtypes of stroke. Due to the complexity of the brain injury mechanisms following ICH, there are currently no effective treatments to significantly improve patient functional outcomes. Curcumin, as a potential therapeutic agent for ICH, is limited by its poor water solubility and oral bioavailability. In this study, mPEG-PCL is used to encapsulate curcumin, forming curcumin nanoparticles, and utilized the intranasal administration route to directly deliver curcumin nanoparticles from the nasal cavity to the brain. By inhibiting pro-inflammatory neuroinflammation of microglia following ICH in mice, reprogramming pro-inflammatory microglia toward an anti-inflammatory function, and consequently reducing neuronal inflammatory death and hematoma volume, this approach improved blood-brain barrier damage in ICH mice and promoted the recovery of neurological function post-stroke. This study offers a promising therapeutic strategy for ICH to mediate neuroinflammatory microenvironments.

باختصار

By inhibiting pro‐inflammatory neuroinflammation of microglia following ICH in mice, reprogramming pro‐inflammatory microglia toward an anti‐inflammatory function, and consequently reducing neuronal inflammatory death and hematoma volume, this approach improved blood‐brain barrier damage in ICH mice and promoted the recovery of neurological function post‐stroke.

Used In Evidence Reviews

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