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预先口服盐酸氨基葡萄糖/硫酸软骨素/抗坏血酸锰组合对大鼠实验性关节炎的影响。

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

作者信息

Beren J, Hill S L, Diener-West M, Rose N R

机构信息

Department of Pathology, The Johns Hopkins Medical Institutions, Baltimore, Maryland 21205, USA.

出版信息

Exp Biol Med (Maywood). 2001 Feb;226(2):144-51. doi: 10.1177/153537020122600213.

Abstract

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 [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 (HI) scoring of lesions, T-cell proliferation, and serological studies for antibody classes and subclasses. Both the AI 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%, chi2 analysis P = 0.001). Rats fed the NC/GCM also exhibited a significant decrease in the severity of autoimmune arthritis in both the AI and HI compared to control Group 2 (immunized-NC) (chi2 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-II collagen, indicating that its effects are not due to alteration of the antigen-specific immune response.

摘要

在胶原诱导的自身免疫性关节炎(CIA)大鼠模型中,研究了一种营养补充剂的治疗效果,该补充剂由盐酸氨基葡萄糖(FCHG49)、纯化硫酸软骨素钠(TRH122)和抗坏血酸锰(GCM)3组成。将GCM化合物与可口的营养膏(Nutri-cal [NC])混合。在免疫前10天开始对26只大鼠口服给予NC/GCM化合物,并持续至处死当天。一组12只对照大鼠不给予口服制剂;另一组12只对照大鼠仅接受NC。评估包括由三名独立评估者进行的关节炎指数(AI)评分、病变的组织学指数(HI)评分、T细胞增殖以及抗体类别和亚类的血清学研究。与联合对照组(96%,卡方分析P = 0.001)相比,AI和HI标准均显示,用NC/GCM预处理的大鼠中CIA的患病率有统计学显著降低(54%)。与对照组2(免疫-NC)相比,喂食NC/GCM的大鼠在AI和HI方面自身免疫性关节炎的严重程度也显著降低(卡方分析P < 0.05)。组织学研究证实,与对照组2相比,NC/GCM组关节炎的发病率降低。GCM治疗未能改变对牛II型胶原的T细胞增殖和抗体产生,表明其作用不是由于抗原特异性免疫反应的改变。

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