1.Studies on the structural features and anticoagulant activity of the polysaccharide from Aeodes orbitosa
Shunchun WANG ; Songshan SHI ; Yingqi WENG ; Zhengtao WANG ; Zhibi HU
Chinese Journal of Marine Drugs 1994;0(04):-
Objective To study the structural features and anticoagulant activity of the polysaccharide isolated from Aeodes orbitosa.Methods Sugar composition analysis,methylation analysis and IR were used to characterize the structural features.The anticoagulant activity of the polysaccharide was evaluated by cutting tail and capillary methods.Results The polysaccharide was composed of 3,6-anhydrous-galactose,6-methyl-galactose,2-methyl-galactose,galactose,xylose and glucose in the molar ratios of 6.4∶0.9∶5.8∶1.6∶84.1∶1.2.The content of Sulfate group was 37.5%. The main linkage model of the polysaccharide were 1,3 and 1,4 linkages,branch point located at O-2 and 6 of galactose residues.Sulfate group located at 2 and 6 position of 1,4 linked galactose residue and 2 position of 1,3 linked galactose residue.The polysaccharide showed significant activities to extend bleeding time and coagulation time in mice.Conclusion The polysaccharide from Aeodes orbitosa was a sulfate galactan with strong anticoagulant activity.
2.Protection of Grateloupia filicina polysaccharide against hepatotoxicity induced by Dioscorea bulbifera L.
Yibo MA ; Lili JI ; Shunchun WANG ; Songshan SHI ; Zhengtao WANG
Acta Pharmaceutica Sinica 2013;48(8):1253-8
The present study was designed to observe the protection of Grateloupia filicina polysaccharide (GFP) against hepatotoxicity induced by Dioscorea bulbifera L in mice and its underlying mechanism. GFP was intragastrically (ig) given to mice at various doses. After 6 days, the mice were treated with ethyl acetate extract of Dioscorea bulbifera L (EF, ig). Serum levels of alanine/aspartate aminotransferase (ALT/AST), alkaline phosphatase (ALP), total bilirubin (TB) were measured, and liver histological evaluation was conducted. Furthermore, reductions of liver glutathione (GSH) amount and glutamate cysteine ligase (GCL) activity were tested. The expressions of GCL-c, GCL-m, and HO-1 (heme oxygenase-1) in liver were observed by Western-blot. The results showed that GFP (600 mg x kg(-1)) decreased EF-induced the increase of serum ALT, AST and TB, and GFP (400, 600 mg x kg(-1)) inhibited EF-induced the increase of serum ALP. Liver histological evaluation showed that the liver injury induced by EF was relieved after treated with GFP. GFP further increased liver GSH amount and reversed EF-induced the decrease of GCL activity. The Western-blot result showed that GFP augmented EF-induced the increase of HO-1, and reversed EF-induced the decrease of GCL-c. In conclusion, GFP can act against the oxidative stress liver injury induced by Dioscorea bulbifera L in mice.
3.A new triterpenoid tetrasaccharide from the root of Scrophularia ningpoensis.
Liuqiang ZHANG ; Fujiang GUO ; Shunchun WANG ; Yiming LI
Acta Pharmaceutica Sinica 2012;47(10):1358-62
A new oleanane-type triterpenoid glycoside, 3beta-O-(f-D-xylopyranosyl-(1-->2)-[beta-D-glucopyranosyl (1-->4)-beta-D-glucopyranosyl-(1 -->3)]-beta-D-fucopyranosyl-11, 13(18) diene-olean-23alpha, 28 diol (1), along with three known phenylethyl glycosides (2-4), was isolated from the root of traditional Chinese medicine Scrophularia ningpoensis. Among them, compounds 2 and 3 were obtained from Scrophularia genus for the first time. The structure of compound 1 was elucidated on the basis of spectroscopic method including 1D, 2D NMR and HR-ESI-MS.
5.Advances in the preparation and structural characterization of rhamnogalacturonan II
Yupeng LIU ; Songshan SHI ; Yingxuan BU ; Huan GONG ; Huijun WANG ; Shunchun WANG
Journal of China Pharmaceutical University 2024;55(4):432-442
Abstract: Rhamnogalacturonan II (RG-II) is one of the structural domains of pectin whose structure is highly conserved among species. The main chain of RG-II consists of approximately nine galacturonic acids linked by α-1,4 glycosidic bonds, with six well-defined side chains replacing them (A−F). The structures of the disaccharide side chains C and D and the monosaccharide side chains E and F in RG-II from different sources remain essentially the same. In contrast, the oligosaccharide side chains A and B showed slight variability. Structural characterization of RG-II can be achieved by molecular weight, monosaccharide composition, and mass spectrometry. The polysaccharides containing RG-II structural domains in traditional Chinese medicines (TCMs) have high medicinal value. Isolation of RG-II can be achieved using endo-polygalacturonase (Endo-PG) and Penicillium oxalicum. A substantial number of RG-II standards can be rapidly prepared from red wine for the development of new quantitative methods to realize the quality control of active polysaccharides from traditional Chinese medicines and to promote the research process of polysaccharides from traditional Chinese medicines.