Suppr超能文献

迷迭香酸纳米囊泡通过调节 NLRP3 炎性小体对急性结肠炎的抗炎作用。

Anti-Inflammatory Effects of Rosmarinic Acid-Loaded Nanovesicles in Acute Colitis through Modulation of NLRP3 Inflammasome.

机构信息

Health Sciences Center, Federal University of Recôncavo da Bahia, Santo Antônio de Jesus 44430-400, Brazil.

Department of Normal and Pathological Cytology and Histology, Universidad de Sevilla, 41009 Seville, Spain.

出版信息

Biomolecules. 2021 Jan 26;11(2):162. doi: 10.3390/biom11020162.

Abstract

Ulcerative colitis (UC), one of the two main types of inflammatory bowel disease, has no effective treatment. Rosmarinic acid (RA) is a polyphenol that, when administered orally, is metabolised in the small intestine, compromising its beneficial effects. We used chitosan/nutriose-coated niosomes loaded with RA to protect RA from gastric degradation and target the colon and evaluated their effect on acute colitis induced by 4% dextran sodium sulphate (DSS) for seven days in mice. RA-loaded nanovesicles (5, 10 and 20 mg/kg) or free RA (20 mg/kg) were orally administered from three days prior to colitis induction and during days 1, 3, 5 and 7 of DSS administration. RA-loaded nanovesicles improved body weight loss and disease activity index as well as increased mucus production and decreased myeloperoxidase activity and TNF-α production. Moreover, RA-loaded nanovesicles downregulated protein expression of inflammasome components such as NLR family pyrin domain-containing 3 (NLRP3), adaptor protein (ASC) and caspase-1, and the consequent reduction of IL-1β levels. Furthermore, nuclear factor erythroid 2-related factor 2 (Nrf2) and heme oxygenase-1 (HO-1) protein expression increased after the RA-loaded nanovesicles treatment However, these mechanistic changes were not detected with the RA-free treatment. Our findings suggest that the use of chitosan/nutriose-coated niosomes to increase RA local bioavailability could be a promising nutraceutical strategy for oral colon-targeted UC therapy.

摘要

溃疡性结肠炎(UC)是两种主要类型的炎症性肠病之一,目前尚无有效治疗方法。迷迭香酸(RA)是一种多酚,口服时在小肠中代谢,从而降低其有益作用。我们使用壳聚糖/营养糖包被的尼奥斯ome 负载 RA 来保护 RA 免受胃降解,并靶向结肠,并评估它们对用 4%葡聚糖硫酸钠(DSS)诱导的急性结肠炎的影响,在小鼠中持续 7 天。RA 负载的纳米囊泡(5、10 和 20mg/kg)或游离 RA(20mg/kg)在结肠炎诱导前三天开始口服,并在 DSS 给药的第 1、3、5 和 7 天给药。RA 负载的纳米囊泡改善了体重减轻和疾病活动指数,增加了粘液产生,并降低了髓过氧化物酶活性和 TNF-α产生。此外,RA 负载的纳米囊泡下调了炎症小体成分的蛋白表达,如 NOD 样受体家族 pyrin 域包含 3(NLRP3)、衔接蛋白(ASC)和半胱天冬酶-1,以及随之而来的 IL-1β 水平降低。此外,在 RA 负载的纳米囊泡处理后,核因子红细胞 2 相关因子 2(Nrf2)和血红素加氧酶-1(HO-1)蛋白表达增加。然而,在游离 RA 处理中没有检测到这些机制变化。我们的研究结果表明,使用壳聚糖/营养糖包被的尼奥斯ome 来增加 RA 的局部生物利用度可能是一种有前途的用于口服结肠靶向 UC 治疗的营养策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d61/7912577/ad55f9312dbd/biomolecules-11-00162-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验