Abstract

Seven new triterpenoid saponins (1–7), together with three known ones (8–10), were isolated from Ilex pubescens. Elucidation of their structures was performed based on high-resolution electrospray ionisation mass spectrometry (HR-ESI-MS), infrared spectra (IR), and nuclear magnetic resonance (NMR) spectroscopic data. The anti-inflammatory activity of the isolates toward lipopolysaccharide (LPS)-stimulated RAW264.7 macrophages was investigated. The results demonstrated that compounds 3, 5, and 6 inhibited the expression of inducible nitric oxide synthase (iNOS) protein in comparison with LPS stimulation in RAW264.7 cells.

Highlights

  • Ilex pubescens, belonging to the plant family Aquifoliaceae, is widely distributed throughout the south of China

  • Pubescenoside E (1) (Figure 1) was isolated as a white amorphous powder, and the molecular formula was deduced to be C47 H74 O17 based on the quasi-molecular ion peak [M + COOH]− at m/z

  • nuclear magnetic resonance (NMR) spectra, we identified the structure of compound

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Summary

Introduction

Ilex pubescens, belonging to the plant family Aquifoliaceae, is widely distributed throughout the south of China. The primary components that have been reported from this plant include triterpenoids [4], phenolic glycosides [5], lignan glycosides [6], hemiterpene glycosides [7], and flavonoids [8]. All of the components described above play an important role related to several bioactivities, such as anti-inflammatory [9,10,11,12], anticoagulant [13], and antithrombotic activities [14]. Lipopolysaccharide (LPS)-induced macrophages are widely used to study inflammatory responses in vitro [15]. Macrophages are versatile cells that play many roles, and can be activated by external stimuli, such as LPS, to release excessive amounts of inflammatory mediators, including prostaglandin E2

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