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从普洱茶(Camellia sinensis)中分离得到的Strictinin 的抗菌和通便活性。

Antibacterial and laxative activities of strictinin isolated from Pu'er tea (Camellia sinensis).

机构信息

Graduate Institute of Biotechnology, National Chung-Hsing University, Taichung, Taiwan, ROC.

Department of Biotechnology, National Formosa University, Yunlin, Taiwan, ROC.

出版信息

J Food Drug Anal. 2016 Oct;24(4):722-729. doi: 10.1016/j.jfda.2016.03.014. Epub 2016 Jun 21.

Abstract

Strictinin, the major phenolic compound in Pu'er teas produced from young leaves and buds of wild trees, was isolated to evaluate its antibacterial and laxative activities. The minimum inhibitory concentrations of strictinin against Propionibacterium acnes and Staphylococcus epidermidis were determined as 250 μM and 2000 μM, respectively, apparently higher than those of several antibiotics commonly used for bacterial infections. The additive and synergistic effects on the inhibitory activities of strictinin combined with other commercial antibiotics were observed in two bacteria tested in this study via the analysis of fractional inhibitory concentrations. Laxative activity was observed on defecation of the rats fed with strictinin. Further analysis showed that the laxative effect of strictinin was presumably caused by accelerating small intestinal transit, instead of enhancing gastric emptying, increasing food intake, or inducing diarrhea in the rats. Taken together with the antiviral activities demonstrated previously, it is suggested that strictinin is one of the active ingredients responsible for the antiviral, antibacterial, and laxative effects of wild Pu'er tea, and has the potential to be developed as a mild natural substitute for antibiotics and laxatives.

摘要

严格因,是从野生茶树的幼叶和芽制成的普洱茶中的主要酚类化合物,被分离出来以评估其抗菌和通便活性。严格因对痤疮丙酸杆菌和表皮葡萄球菌的最小抑菌浓度分别为 250μM 和 2000μM,明显高于几种常用于细菌感染的抗生素。通过分析部分抑菌浓度,观察到在本研究中测试的两种细菌中,严格因与其他商业抗生素联合使用具有相加和协同作用。在给予严格因的大鼠的排便中观察到通便活性。进一步的分析表明,严格因的通便作用可能是通过加速小肠转运引起的,而不是通过增强胃排空、增加食物摄入或引起大鼠腹泻。结合先前证明的抗病毒活性,表明严格因是导致野生普洱茶抗病毒、抗菌和通便作用的活性成分之一,具有作为温和天然抗生素和泻药替代品的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62ff/9337302/fdbc1eb38952/jfda-24-04-722f1.jpg

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