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胡桃隔多糖:提取工艺优化、抗肿瘤及免疫增强作用。

Polysaccharides from Diaphragma juglandis fructus: Extraction optimization, antitumor, and immune-enhancement effects.

机构信息

State Key Laboratory of Food Science and Technology, Jiangnan University, Wuxi, Jiangsu 214122, PR China; School of Food Science and Technology, Jiangnan University, Wuxi, Jiangsu 214122, PR China; Beijing Advanced Innovation Center for Food Nutrition and Human Health, Beijing Technology and Business University, Beijing 100048, PR China; Department of Food, Nutrition and Packaging Sciences, Clemson University, Clemson, SC 29634, USA.

Department of Food, Nutrition and Packaging Sciences, Clemson University, Clemson, SC 29634, USA.

出版信息

Int J Biol Macromol. 2018 Aug;115:835-845. doi: 10.1016/j.ijbiomac.2018.04.121. Epub 2018 Apr 27.

Abstract

This study discusses the optimization of the microwave-assisted extraction of polysaccharides from Diaphragma juglandis (DJPs). One main fraction (DJP-2) was successfully purified by ion-exchange chromatography and gel-permeation chromatography. The results showed that the optimal extraction conditions with DJP extraction yield of 4.7 ± 0.28% were water to raw material ratio of 20 mL/g, extraction time of 40 min, and microwave extraction power of 400 W. Bioassays indicated that DJP-2 could effectively suppress the proliferation of HepG2 and BGC-82 cell lines. In addition, DJP-2 could significantly enhance phagocytosis; stimulate the production of NO, tumor necrosis factor-α (TNF-α), and interleukins (IL-6 and IL-1β); and promote their corresponding mRNA expression levels in a dose-dependent manner. Meanwhile, CR3, MR, and TLR2 were confirmed to be the major membrane receptors of DJP-2 on RAW 264.7. All these results indicated that DJP-2 could be a potential antitumor and immunomodulatory agent in the field of pharmacology.

摘要

本研究探讨了从山茱萸中多糖的微波辅助提取的优化。通过离子交换色谱和凝胶渗透色谱成功地对一个主要级分(DJP-2)进行了纯化。结果表明,DJP 提取收率为 4.7±0.28%的最佳提取条件为水与原料比为 20 mL/g、提取时间为 40 min、微波提取功率为 400 W。生物测定表明,DJP-2 能有效抑制 HepG2 和 BGC-82 细胞系的增殖。此外,DJP-2 能显著增强吞噬作用;以剂量依赖性方式刺激 NO、肿瘤坏死因子-α(TNF-α)和白细胞介素(IL-6 和 IL-1β)的产生;并促进其相应的 mRNA 表达水平。同时,CR3、MR 和 TLR2 被确认为 DJP-2 在 RAW 264.7 上的主要膜受体。所有这些结果表明,DJP-2 可能是药理学领域中一种有潜力的抗肿瘤和免疫调节剂。

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