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基于冻干开菲尔乳的自纳米乳化系统通过微生物群-肠-脑轴对认知增强的影响。

Impact of Lyophilized Milk Kefir-Based Self-Nanoemulsifying System on Cognitive Enhancement via the Microbiota-Gut-Brain Axis.

作者信息

Anwar Mai M, Boseila Amira A, Mabrouk Abeer A, Abdelkhalek Abdelfattah A, Amin Amr

机构信息

Department of Biochemistry, National Organization for Drug Control and Research (NODCAR)/Egyptian Drug Authority (EDA), Giza 12654, Egypt.

Department of Pharmaceutics, National Organization for Drug Control and Research (NODCAR)/Egyptian Drug Authority (EDA), Giza 12654, Egypt.

出版信息

Antioxidants (Basel). 2024 Oct 7;13(10):1205. doi: 10.3390/antiox13101205.

Abstract

Chronic inflammatory bowel disorders (IBDs) are characterized by altered intestinal permeability, prompting inflammatory, oxidative stress, and immunological factors. Gut microbiota disorders impact brain function via the bidirectional gut-brain axis, influencing behavior through inflammatory cascades, oxidative stress, and neurotransmitter levels. This study highlights the potential effect of integrating lyophilized milk kefir alone and lyophilized milk kefir as solid carriers loaded with a self-nanoemulsifying self-nanosuspension (SNESNS) of licorice extract on an induced chronic IBD-like model in rats. Licorice-SNESNS was prepared by the homogenization of 30 mg of licorice extract in 1 g of the selected SNEDDS (30% Caraway oil, 60% Tween 20, and 10% propylene glycol (/)). Licorice-SNESNS was mixed with milk kefir and then freeze-dried. Dynamic TEM images and the bimodal particle size curve confirmed the formation of the biphasic nanosystems after dilution (nanoemulsion and nanosuspension). Daily oral administration of lyophilized milk kefir (100 mg/kg) loaded with SNESNS (10 mg/kg Caraway oil and 1 mg/kg licorice) restored normal body weight and intestinal mucosa while significantly reducing submucosal inflammatory cell infiltration in induced rats. Importantly, this treatment demonstrated superior efficacy compared to lyophilized milk kefir alone by leading to a more significant alleviation of neurotransmitter levels and improved memory functions, thereby addressing gut-brain axis disorders. Additionally, it normalized fecal microbiome constituents, inflammatory cytokine levels, and oxidative stress in examined tissues and serum. Moreover, daily administration of kefir-loaded SNESNS normalized the disease activity index, alleviated histopathological changes induced by IBD induction, and partially restored the normal gut microbiota. These alterations are associated with improved cognitive functions, attributed to the maintenance of normal neurotransmitter levels and the alleviation of triggered inflammatory factors and oxidative stress levels.

摘要

慢性炎症性肠病(IBDs)的特征是肠道通透性改变,引发炎症、氧化应激和免疫因素。肠道微生物群紊乱通过双向肠-脑轴影响脑功能,通过炎症级联反应、氧化应激和神经递质水平影响行为。本研究强调了单独使用冻干乳开菲尔以及将冻干乳开菲尔作为负载甘草提取物自纳米乳化自纳米混悬液(SNESNS)的固体载体对诱导的大鼠慢性IBD样模型的潜在作用。甘草-SNESNS是通过将30mg甘草提取物在1g选定的自纳米乳化药物传递系统(SNEDDS)(30%葛缕子油、60%吐温20和10%丙二醇(/))中均质化制备的。甘草-SNESNS与乳开菲尔混合,然后冻干。动态透射电镜图像和双峰粒径曲线证实了稀释后双相纳米系统(纳米乳液和纳米混悬液)的形成。每日口服负载SNESNS(10mg/kg葛缕子油和1mg/kg甘草)的冻干乳开菲尔(100mg/kg)可恢复正常体重和肠黏膜,同时显著减少诱导大鼠黏膜下炎症细胞浸润。重要的是,与单独使用冻干乳开菲尔相比,这种治疗方法显示出更高的疗效,可更显著地缓解神经递质水平并改善记忆功能,从而解决肠-脑轴紊乱问题。此外,它使所检查组织和血清中的粪便微生物群成分、炎性细胞因子水平和氧化应激正常化。此外,每日给予负载SNESNS的开菲尔可使疾病活动指数正常化,减轻IBD诱导引起的组织病理学变化,并部分恢复正常肠道微生物群。这些改变与认知功能改善有关,这归因于正常神经递质水平的维持以及引发的炎症因子和氧化应激水平的减轻。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/853b/11504727/6697f7cf9340/antioxidants-13-01205-g001.jpg

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