Subscribe to RSS
DOI: 10.1055/s-2002-23133
© Georg Thieme Verlag Stuttgart · New York
Structural Features of an Immunostimulating and Antioxidant Acidic Polysaccharide from the Seeds of Cuscuta chinensis
Publication History
March 16, 2001
August 4, 2001
Publication Date:
25 March 2002 (online)
![](https://www.thieme-connect.de/media/plantamedica/200203/lookinside/thumbnails/10.1055-s-2002-23133-1.jpg)
Abstract
Three crude polysaccharide fractions, named CS-A, CS-B and CS-C, were prepared from the seeds of Cuscuta chinensis by hot water extraction and diluted alkali extraction subsequently, then EtOH precipitation, and tested for lymphocyte proliferation activity. CS-A showed a stimulating effect on concanavalin A or lipopolysaccharide induced mitogenic activity of lymphocytes. An acidic polysaccharide (CS-A-3β) was purified from CS-A by anion exchange and gel filtration chromatography. The polysaccharide showed potent stimulating effects on lymphocyte proliferation and antibody production, but did not significantly influence the serum IgG level. Its structural features were elucidated by methylation analysis, partial acid hydrolysis, 1D and 2D NMR and ESI-mass spectroscopy. The data obtained indicated that CS-A-3β had a backbone consisting of α-D-1,4-linked GalpA residues and β-L-1,2-linked Rhap residues with branches at C-4 of Rhap residues and C-3 of GalpA residues, composed of arabinogalactan and glucobiose. This structure is typical for a pectic polysaccharide of the rhamnogalacturonan type. In addition, the effect of CS-A, CS-B, CS-C and CS-A-3β on hydrogen peroxide induced cell lesion in rat pheochromocytoma line PC 12 was investigated. The results indicated that, besides its immunostimulating activity, CS-A-3β had a protective effect against free radical-induced cell toxicity.
Key words
Cuscuta chinensis - Convolvulaceae - acidic polysaccharide - lymphocyte proliferation - antibody production - free radical - PC12 cell
References
- 1 Miyahara K, Du X M, Watanabe M, Sugimura C, Yahara S, Nohara T. Two novel acetylated trisaccharides related to resin glycoside from the seeds of Cuscuta chinensis . Chemical and Pharmaceutical Bulletin. 1996; 44 481-5
- 2 Yahara S, Domoto H, Sugimura C, Nohara T, Niiho Y, Nakajima Y, Ito H. An alkaloid and two lignans from Cuscuta chinensis . Phytochemistry. 1994; 37 1755-7
- 3 Jin X, Li J S, Yan M W. Studies on flavonoids in the seeds of Cuscuta chinensis Lam. Journal of Chinese Materia Medica. 1992; 17 292-4
- 4 Wang Z, Fang J N, Ge D L, Li X Y. Chemical characterization and immunological activities of an acid polysaccharide isolated from the seeds of Cuscuta Chinensis Lam. Acta Pharmacologica Sinica. 2000; 21 1136-40
- 5 Xu R S. Natural Products Chemistry, 9. Saccharides. In: Pan DJ, editor Chinese Science Press Beijing; 1993: 475
- 6 Dong Q, Ding S W, Yang X, Fang J N. Structural features of a heteroxylan from Sophora subprostrata roots. Phytochemistry. 1999; 50 81-4
- 7 Kimberley A T, Jock G BS. A clorimetric method for the quantitation of uronic acids and a specific assay for galacturonic acid. Analytical Biochemistry. 1992; 201 190-6
- 8 Gerwig G J, Kamerling J P, Vliegenthart J FG. Determination of the D and L configuration of neutral monosaccharides by high-resolution capiliary GLC. Carbohydrate Research. 1978; 62 349-57
- 9 Tomoda M, Shimizu N, Shimada K, Suga M. Isolation and structural features of two glucans from the rhizomes of Crinum latifolium . Chemical and Pharmaceutical Bulletin. 1985; 33 16-21
- 10 Tomoda M, Ichikawa M, Shimizu N. The major pectin from the roots of Angelica acutilobba . Chemical and Pharmaceutical Bulletin. 1986; 34 4992-6
- 11 Tayor A B, Courad H E. Stoichiometric depolymerization of polysaccharides and glycosaminoglycuronans to monosaccharides following reduction of their carodiimide-activated carboxyl grouos. Biochemistry. 1972; 11 1385-8
- 12 Needs P W, Selvendran R R. A voiding oxidative degradation during sodium hydroxide/methyl idodide-mediated carbohydrate methylation in dimethyl sulfoxide. Carbohydrate Research. 1993; 245 1-10
- 13 Bao X F, Liu C P, Fang J N, Li X Y. Structural and immunological studies of a major polysaccharide from spores of Ganoderma lucidum (Fr.) Karst. Carbohydrate Research. 2001; 332 67-74
- 14 Sweet D P, Shapiro R H, Albersheim P. Quantitative analysis by various GLC response-factor theories for partially methylated and partially ethylated alditol acetates. Carbohydrate Research. 1975; 40 217-25
- 15 Heek K, Reimann J, Kabelitz D, Hardt C, Wagner H. A rapid colorimetric assay for the determination of IL-2-producing helper T cell frequencies. Journal of Immunological Methods. 1985; 77 237-46
- 16 Li X Y, Wang J F, Zhu P P, Lin L, Ge J B, Yang S X. Immune enhancement of a polysaccharide peptide isolated from Coriolus versicolor . Acta Pharmacololgica Sinica. 1990; 11 542-5
- 17 Xiang D B, Li X Y. Antitumor activity and immuno-potentiating actions of Achyranthes bidentata polysaccharides. Acta Pharmacologica Sinica. 1993; 14 556-61
- 18 Xiao X Q, Jian W Y, Tang X C. Huperzine A protects rat pheochromocytoma cells against hydrogen peroxide-induced injury. Neuroscience Letters. 1999; 275 73-6
- 19 Cui W W, Eskin M NA, Biliaderis C G, Marat K. NMR characterization of a 4-O-methyl-β-D-glucuronic acid-containing rhamnogalacturonan from yellow mustard (Sinapis alba L.) mucilage. Carbohydrate Research. 1996; 292 173-83
- 20 Rougeaux H, Talaga P, Carlos R W, Guezennec J. Structural studies of an exopolysaccharide produced by Acteromonas macleodii subsp. Fijiensis originating from a deep-sea hydrothermal vent. Carbohydrate Research. 1998; 312 53-9
- 21 Dumitriu S. Polysaccharides: structural diversity and functional versatility, 12. Pectin. In: Rolin C, Nielsen BU, Glahn PE, editors Marcel dekker New York; 1999: 391-5
- 22 Kiyohara H, Takemoto N, Zhao J F, Kawamura H, Yamada H. Pectic polysaccharides from roots of Glycyrrhiza uralensis: possible contribution of neutral region to anti-complementary and mitogenic activities. Planta Medica. 1996; 62 14-9
Prof. Ji-nian Fang
Shanghai Institute of Materia Medica
Shanghai Institute for Biological Sciences
Chinese Academy of Sciences
294 Tai-Yuan Road
Shanghai 200031
People’s Republic of China
Email: jnfang@mail.shcnc.ac.cn
Fax: +86-21-64370269
Phone: +86-21-64311833 ext.601