Effects of Astragalus heteropolysaccharides on erythrocyte immune adherence function of mice with adjuvant-induced arthritis.
- Author:
Li-Hu YANG
1
;
Jian-Dong QIU
;
Hong-Quan LI
Author Information
1. College of Animal Science and Veterinary Medicine, Agricultural University of Shanxi, Taigu 030801, China.
- Publication Type:Journal Article
- MeSH:
Animals;
Antigen-Antibody Complex;
blood;
metabolism;
Arthritis, Experimental;
metabolism;
pathology;
Astragalus Plant;
chemistry;
Dose-Response Relationship, Drug;
Erythrocytes;
immunology;
Knee Joint;
pathology;
Male;
Mice;
Plant Roots;
chemistry;
Plants, Medicinal;
chemistry;
Polysaccharides;
administration & dosage;
isolation & purification;
pharmacology;
Random Allocation;
Receptors, Complement;
blood;
Synovial Membrane;
immunology
- From:
Acta Pharmaceutica Sinica
2009;44(12):1364-1370
- CountryChina
- Language:Chinese
-
Abstract:
Astragalus heteropolysaccharides (AHPS) is obtained from the dried roots of Astragalus membranaceus (Fisch.) Bunge var. mongholious (Bunge) Hsiao. In the present study, we observed its effects on erythrocyte immune adherence function in mice with adjuvant-induced arthritis (AA). The mice were treated intragastrically with AHPS of 1 000, 500, and 250 mg x kg(-1) x d(-1) separately and treated with tripterygium glycosides (TG) of 60 mg x kg(-1) x d(-1) as positive control. The number of complement receptor type 1 (CR1) on erythrocyte, the concentration of circulating immune complex (CIC) in serum and the amount of immune complex (IC) deposition in synovium of knee joint were determined by flow cytometry, polyethylene glycol (PEG-6000) precipitation and ponceau S (P-S) staining and fluorescent immunohistochemistry respectively. The pathological change of knee joint was evaluated by histological section. The results showed that both AHPS and TG improved significantly the primary and secondary local or systemic symptoms of the mice with AA and reduced the synovium hyperplasia, inflammatory cell infiltrate, pannus and cartilage demolish of knee joint, and AHPS of 1 000, 500, and 250 mg x kg(-1) x d(-1) could significantly increase the number of CR1 on erythrocyte, improve the elimination of CIC in the peripheral blood and reduce the deposition of IC in joint synovium in a dose-dependent manner (P < 0.01 or P < 0.05). The results indicate that one of the therapeutic effective mechanisms of AHPS on mice with AA could be to increase gene expression of CR1 of mice with AA.
