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载有小檗碱的仿生纳米颗粒通过增强白细胞介素-12表达减轻实验性过敏性哮喘的炎症。

Berberine-Loaded Biomimetic Nanoparticles Attenuate Inflammation of Experimental Allergic Asthma Enhancing IL-12 Expression.

作者信息

Jin Hua, Li Jiale, Zhang Miaoyuan, Luo Renxing, Lu Peishan, Zhang Wenting, Zhang Junai, Pi Jiang, Zheng Weixin, Mai Zesen, Ding Xiaowen, Liu Xinguang, Ouyang Suidong, Huang Gonghua

机构信息

Guangdong Provincial Key Laboratory of Medical Molecular Diagnostics, Guangdong Medical University, Dongguan, China.

College of Pharmacy, Guangdong Medical University, Dongguan, China.

出版信息

Front Pharmacol. 2021 Nov 9;12:724525. doi: 10.3389/fphar.2021.724525. eCollection 2021.

DOI:10.3389/fphar.2021.724525
PMID:34858170
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8630696/
Abstract

Asthma is one of the most common chronic pulmonary disorders, affecting more than 330 million people worldwide. Unfortunately, there are still no specific treatments for asthma so far. Therefore, it is very important to develop effective therapeutics and medicines to deal with this intractable disease. Berberine (Ber) has fabulous anti-inflammatory and antibacterial effects, while its low water solubility and bioavailability greatly limit its curative efficiency. To improve the nasal mucosa absorption of poorly water-soluble drugs, such as Ber, we developed a platelet membrane- (PM-) coated nanoparticle (NP) system (PM@Ber-NPs) for targeted delivery of berberine to the inflammatory lungs. , PM@Ber-NPs exhibited enhanced targeting retention in the inflammatory lungs compared with free Ber. In a mouse model of house dust mite- (HDM-) induced asthma, PM@Ber-NPs markedly inhibited lung inflammation, as evident by reduced inflammatory cells and inflammatory cytokines in the lung compared with free Ber. Collectively, our study demonstrated the inhibitory actions of nasally delivered nanomedicines on HDM-induced asthma, primarily through regulating Th1/Th2 balance by enhancing IL-12 expression which could potentially reduce lung inflammation and allergic asthma.

摘要

哮喘是最常见的慢性肺部疾病之一,全球有超过3.3亿人受其影响。不幸的是,迄今为止仍没有针对哮喘的特效治疗方法。因此,开发有效的治疗方法和药物来应对这种难治性疾病非常重要。黄连素(Ber)具有出色的抗炎和抗菌作用,但其低水溶性和生物利用度极大地限制了其治疗效果。为了提高难溶性药物(如Ber)的鼻粘膜吸收,我们开发了一种血小板膜(PM)包被的纳米颗粒(NP)系统(PM@Ber-NPs),用于将黄连素靶向递送至炎症肺部。与游离Ber相比,PM@Ber-NPs在炎症肺部表现出增强的靶向滞留。在屋尘螨(HDM)诱导的哮喘小鼠模型中,与游离Ber相比,PM@Ber-NPs显著抑制肺部炎症,表现为肺部炎症细胞和炎症细胞因子减少。总的来说,我们的研究证明了经鼻给药的纳米药物对HDM诱导的哮喘具有抑制作用,主要是通过增强IL-12表达来调节Th1/Th2平衡,这可能会减轻肺部炎症和过敏性哮喘。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cff3/8630696/337b25bac248/fphar-12-724525-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cff3/8630696/7c5162b20414/fphar-12-724525-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cff3/8630696/7ca63a744645/fphar-12-724525-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cff3/8630696/221a58b83352/fphar-12-724525-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cff3/8630696/2d88d94b1c03/fphar-12-724525-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cff3/8630696/337b25bac248/fphar-12-724525-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cff3/8630696/7c5162b20414/fphar-12-724525-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cff3/8630696/7ca63a744645/fphar-12-724525-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cff3/8630696/221a58b83352/fphar-12-724525-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cff3/8630696/2d88d94b1c03/fphar-12-724525-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cff3/8630696/337b25bac248/fphar-12-724525-g005.jpg

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