2016
DOI: 10.3390/molecules21060779
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Chemical Structure and Immunomodulating Activities of an α-Glucan Purified from Lobelia chinensis Lour

Abstract: A neutral α-glucan, named BP1, with a molecular mass of approximately 9.45 kDa, was isolated from Lobelia chinensis by hot-water extraction, a Q-Sepharose Fast Flow column and Superdex-75 column chromatography. Its chemical structure was characterized by monosaccharide analysis, methylation analysis and analysis of its FT-IR, high performance gel permeation chromatography (HPGPC) and 1D/2D-NMR spectra data. The backbone of BP1 consists of The results of the effect of BP1 on mouse macrophage cell line RAW 264.7… Show more

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Cited by 27 publications
(5 citation statements)
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“…Li et al isolated another neutral α-glucan, named BP1 19 (Mol. weight: 9.45 kDa), from Lobelia chinensis by hot-water extraction and studied its immunomodulating activities ( Li et al, 2016 ). The authors proposed that α-glucan BP1 activates Toll-like receptor 4 (TLR4) and exerts immunomodulating effects such as enhancement of the cell proliferation, nitric oxide production, cytokine secretion and phagocytosis in a dose-dependent manner.…”
Section: Introductionmentioning
confidence: 99%
“…Li et al isolated another neutral α-glucan, named BP1 19 (Mol. weight: 9.45 kDa), from Lobelia chinensis by hot-water extraction and studied its immunomodulating activities ( Li et al, 2016 ). The authors proposed that α-glucan BP1 activates Toll-like receptor 4 (TLR4) and exerts immunomodulating effects such as enhancement of the cell proliferation, nitric oxide production, cytokine secretion and phagocytosis in a dose-dependent manner.…”
Section: Introductionmentioning
confidence: 99%
“…Monosaccharide standards ( d -galactose, d -arabinose, l -rhamnose, l -fucose, d -mannose, d -xylose, and d -glucose) were treated as described previously. 52 , 53 Two milligrams of extracted mannans or monosaccharide standards were hydrolyzed with 2 M trifluoroacetic acid at 121 °C for 2 h. After evaporation, the residue was dissolved in 200 μl of H 2 O and reduced with 1 ml of 0.5 mol/l NaBH 4 DMSO solution at 40 °C for 90 min. Then, glacial acetic acid was added dropwise to the reaction tubes.…”
Section: Methodsmentioning
confidence: 99%
“…4), and the results are summarized in Table 2. Based on the chemical shifts, methylation analysis results and reported literature, 37,[40][41][42][43] residues D-H were designated as →4-β-Glcp-1→, α-T-Manp-1→, →2-β-Glcp-1→, →4α-Glcp-1→, and →2-α-Glcp-1→, respectively.…”
Section: Nmr Analysismentioning
confidence: 99%