胶原诱导关节炎对实验室大鼠抗溶血性链球菌素试验的影响

M. Spasov, I. Gjorgoski
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引用次数: 0

摘要

类风湿性关节炎(RA)是一种严重的健康挑战,具有严重的健康后果,并可能导致永久性残疾。大多数作者指出,这种疾病的发生及其持续存在的原因是多因素的,但最重要的是,它是一种遗传易感性,是免疫系统控制机制被破坏的结果。这种疾病可以发生在任何年龄,但最常见于60岁以上的患者,他们患有关节损伤,导致运动受损,工作能力下降,生产力低下和生活质量差。类风湿关节炎疾病研究中的动物模型有助于研究和评价潜在抗关节炎药物的作用。由于类风湿病和类风湿病在发病和发展上有很大的相似性,动物模型的研究为类风湿病和类风湿病提供了有用的信息。我们的研究旨在了解ii型胶原蛋白诱导的关节炎如何对免疫系统产生影响,特别是在免疫接种的第30天和第60天,雌雄Wistar大鼠的ASTO。ASTO也用于诊断继发于链球菌感染的类风湿性关节炎。Wistar大鼠,健康的七周龄雄性和雌性动物,根据pmfskopje实验室动物农场实验动物的标准条件饲养,用于研究。实验动物分为四组;雄性动物对照组(n=20),雌性动物对照组(n=20),试验组雄性动物(n=30),用ii型胶原蛋白治疗,试验组雌性动物(n=30)也用胶原蛋白治疗。在试验的第30天和第60天进行等分分析。我们将高纯度ii型胶原蛋白按照明确的方案应用于右腿后关节。我们在免疫后的第30天和第60天采血进行分析。ASTO样品在电脑化和恒温的Mini NEF TM Duinding Fait装置上进行测试。该方法的原理是基于A群致病性溶血链球菌产生溶血素O,从而刺激机体产生抗溶血素。效价大于1/200为阳性。从对胶原诱导型关节炎对两性动物ASTO值的影响的研究来看,在两个实验期间,所有组和两性的ASTO值都在正常值的范围内。均<59,430IU/ml。总的来说,这些在动物模型中进行的RA研究为RA在人群中的病程和发展提供了很好的平行。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
EFFECT OF COLLAGEN INDUCED ARTHRITIS ON ANTISTREPTOLYSIN TEST IN THE WHITE LABORATORY RAT
Rheumatoid arthritis (RA) is a serious health challenge as a disease with serious health consequences andthe potential to result in permanent disability. Most of the authors state that the reason for the occurrence of thedisease and its persistence is multifactorial, but above all it is a genetic predisposition as a result of the disruption ofthe control mechanisms of the immune system. The disease can occur at any age, but it is most common in patientsover sixty years of age who suffer from damage to the joints, resulting in impaired locomotion, reduced workcapacity, unproductive and poor quality of life. Animal models in RA disease research are useful for studying andevaluating the effect of potential antiarthritic drugs. The study of the disease in animal models provides usefulinformation about rheumatoid diseases and RA in humans because of the great similarity in their onset anddevelopment.Our research aimed to see how collagen type-II induced arthritis would cause an effect on the immune system andinter alia on ASTO in Wistar rats of both sexes, on the thirtieth and sixtieth days of immunization. ASTO is alsoused to diagnose RA secondary to streptococcal infections. Wistar rats, healthy seven-week-old male and femaleanimals, bred according to standard conditions for experimental animals at the laboratory animal farm at PMFSkopjewere used for the research. The experimental animals were divided into four groups; control group of maleanimals (n=20), control group of female animals (n=20), experimental group of male animals (n=30), which weretreated with collagen type-II and experimental group of female animals (n=30), which were also treated withcollagen. Analyzes of aliquots were performed on the thirtieth and sixtieth day of the test. We apply the highlypurified collagen type-II according to a defined protocol in the joint of the back right leg. We took blood for analysison the thirtieth and sixtieth day after immunization. The ASTO samples were tested on the computerized andthermostated Mini NEF TM Duinding Fait apparatus. The principle of the method is based on the fact thatpathogenic beta-hemolytic streptococci of group A produce streptolysin O, which stimulate the body to produceantistreptolysin. A titer greater than 1/200 is a positive value. From the studies that were done on the influence ofcollagen induced arthritis type-II on the value of ASTO in both sexes of animals, in both experimental periods, it canbe concluded that they are within the limits of normal values in all groups and in both sexes. All were <59,430IU/ml. In general, these studies of RA performed in animal models provide a good parallel for the course anddevelopment of RA in the human population.
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