Effect of pre-loading oral glucosamine HCI/chondroitin sulfate/manganese ascorbate combination on experimental arthritis in rats

被引:33
作者
Beren, J
Hill, SL
Diener-West, M
Rose, NR
机构
[1] Johns Hopkins Med Inst, Dept Pathol, Baltimore, MD 21205 USA
[2] Johns Hopkins Med Inst, W Harry Feinstone Dept Mol Microbiol & Immunol, Baltimore, MD 21205 USA
[3] Johns Hopkins Med Inst, Dept Biostat, Baltimore, MD 21205 USA
关键词
glucosamine hydrochloride; sodium chondroitin sulfate; arthritis;
D O I
10.1177/153537020122600213
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 [基础医学];
摘要
The therapeutic effect of a nutritional supplement consisting of a combination of glucosamine hydrochloride (FCHG49), purified sodium chondroitin sulfate (TRH122), and manganese ascorbate (GCM)(3) was investigated in the rat model of collagen-induced autoimmune arthritis (CIA). The GCM compound was mixed with a palatable nutritional paste (Nutri-cal(R) [NC]). Oral administration of the NC/GCM compound was initiated in 26 rats 10 days before immunization and continued until the day of sacrifice. One group of 12 control rats was given no oral agents; a second group of 12 control rats received NC only. Evaluations included arthritis index (AI) scoring by three independent evaluators, histologic index (Hr) scoring of lesions, T-cell proliferation, and serological studies for antibody classes and sub-classes, Both the Al and HI criteria showed a statistically significant reduction in the prevalence of CIA in rats pretreated with the NC/GCM (54%) compared to the combined control groups (96%, chi (2) analysis P = 0.001), Rats fed the NC/GCM also exhibited a significant decrease in the severity of autoimmune arthritis in both the Al and HI compared to control Group 2 (immunized-NC) (chi (2) analysis P < 0.05), Histological studies verified the decreased incidence of arthritis in the NC/GCM group compared to control Group 2. GCM treatment failed to alter T-cell proliferation and antibody production to bovine type-if collagen, indicating that its effects are not due to alteration of the antigen-specific immune response.
引用
收藏
页码:144 / 151
页数:8
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