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人参皂苷 Rd 治疗可改善炎症性肠病大鼠模型的组织学和功能恢复。

Ginsenoside Rd therapy improves histological and functional recovery in a rat model of inflammatory bowel disease.

机构信息

Department of Gastroenterology, The Second Affiliated Hospital of Harbin Medical University, Harbin, China.

Department of Spleen and Stomach Disease, The First Affiliated Hospital of Heilongjiang University of Chinese Medicine, Harbin, China.

出版信息

Phytother Res. 2020 Nov;34(11):3019-3028. doi: 10.1002/ptr.6734. Epub 2020 May 28.

Abstract

Ginsenoside Rd (GRd) is a biologically active component of ginseng that stimulates the proliferation of endogenous stem cells. The objective of our research was to evaluate the utility of GRd in gastrointestinal mucosal regeneration in a rat model of inflammatory bowel disease (IBD) and to clarify whether GRd exerts its pharmacological effects by modulating endogenous intestinal stem cells. The IBD rat model was established via subcutaneous injection of indomethacin, and 10, 20, or 40 mg/kg GRd or an equal volume of physiological saline was then administered orally to rats in different groups every day for seven consecutive days. We observed that GRd treatment, especially 20 mg/kg GRd, significantly reduced indomethacin-induced damage compared with that in the control group. By measuring the mRNA and protein levels of the intestinal stem cell markers Bmi and Msi-1 and the intestinal epithelial cell marker CDX-2 as well as by double-labelling these markers with 5-bromo-2-deoxyuridine (BrdU), we inferred that GRd could stimulate the proliferation and differentiation of endogenous intestinal stem cells in IBD model rats, leading to improved recovery of intestinal function.

摘要

人参皂苷 Rd(GRd)是人参中具有生物活性的成分,可刺激内源性干细胞增殖。我们的研究目的是评估 GRd 在炎症性肠病(IBD)大鼠模型中胃肠黏膜再生的应用价值,并阐明 GRd 是否通过调节内源性肠干细胞发挥其药理作用。通过皮下注射消炎痛建立 IBD 大鼠模型,然后将不同剂量(10、20 或 40mg/kg)GRd 或等量生理盐水每天口服给予各组大鼠,连续 7 天。我们观察到,与对照组相比,GRd 治疗(特别是 20mg/kg GRd)可显著减轻消炎痛诱导的损伤。通过测量肠干细胞标志物 Bmi 和 Msi-1 以及肠上皮细胞标志物 CDX-2 的 mRNA 和蛋白水平,并通过 BrdU 对这些标志物进行双标记,我们推断 GRd 可刺激 IBD 模型大鼠内源性肠干细胞的增殖和分化,从而改善肠功能的恢复。

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