Oral quercetin nanoparticles in hydrogel microspheres alleviate high-altitude sleep disturbance based on the gut-brain axis
[Display omitted] •Quercetin was entrapped in zein nanoparticles to form QNPs.•QNPs were embedded in calcium alginate hydrogel microspheres to form QNP@HMs.•Oral QNP@HMs had long colon retention.•Oral QNP@HMs prevented the sleep disturbance of mice at high altitudes. High-altitude sleep disturbance...
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Veröffentlicht in: | International journal of pharmaceutics 2024-06, Vol.658, p.124225-124225, Article 124225 |
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Sprache: | eng |
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•Quercetin was entrapped in zein nanoparticles to form QNPs.•QNPs were embedded in calcium alginate hydrogel microspheres to form QNP@HMs.•Oral QNP@HMs had long colon retention.•Oral QNP@HMs prevented the sleep disturbance of mice at high altitudes.
High-altitude sleep disturbance is a common symptom of acute mountain sickness, which can be alleviated via modulation of the gut-brain axis. Quercetin (Que) is used to modulate gut microbiota and serves as a potential drug to regulate the gut-brain axis, but the poor solubility and bioavailability affect its biological functions. Here, Que nanoparticles (QNPs) were prepared with zein using an antisolvent method, and QNP-loaded calcium alginate hydrogel microspheres (QNP@HMs) were prepared using electrospinning technology to improve the gastrointestinal stability and intestinal adhesion of QNPs. In the mouse model of high-altitude sleep disturbance, oral administration of QNP@HMs before the mice entering high altitude prolonged sleep duration, improved blood cell recovery, spontaneous behavior and short-term memory, and reduced such inflammation factors as TNF-α and iNOS. Moreover, QNP@HMs enhanced the abundance of probiotics in the gut, including Lactobacillus and Lachnospira, and reduced intestinal inflammation. However, in the mice after gut sterilization by long-term oral antibiotics, QNP@HMs showed no therapeutic effect. QNP@HMs are a promising medication for the prevention of high-altitude sleep disturbance based on the gut-brain axis. |
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ISSN: | 0378-5173 1873-3476 |
DOI: | 10.1016/j.ijpharm.2024.124225 |