Efficacy of Telmisartan in Pristane Induced Arthritis Rat Model

Quratulain Mehdi
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Abstract

Introduction: Rheumatoid arthritis is one of the most common systemic inflammatory diseases characterized by progressive damage to the joints. There is rising evidence that Renin Angiotensin Aldosterone System signaling is also involved in the inflammatory response in rheumatoid arthritis and its blockers possess anti-arthritic properties. Telmisartan is an angiotensin receptor blocker and PPAR-? agonist and its anti-arthritic effects were evaluated. Aims & Objectives: This experimental study was designed to evaluate the anti-arthritic efficacy of telmisartan in pristane induced rat model of arthritis in adult female rats. Place and duration of study: The study was conducted in the Department of Pharmacology, Army Medical College, Rawalpindi, in collaboration with National Institute of Health and Armed Forces Institute of Pathology from July 2020 to August 2020. Material & Methods: Twenty four (24) adult non-pregnant female Sprague Dawley rats were divided in three groups (n=8) designated as Group A (normal control), Group B (arthritic control) and Group C (telmisartan group) & maintained on standard diet and water adlibitum. Rheumatoid arthritis was induced in each rat of Groups B &C by a single intradermal injection of 0.5ml pristane at the base of its tail on day 0 and the disease developed in two weeks. All 3 groups were given distilled water 2.5 ml/kg from 2-4 weeks and Group C was additionally given dissolved telmisartan orally at 2 mg/kg/day. Anti-arthritic efficacy was determined by assessing arthrogram score and total leukocyte count on day 0, 14 and 28 along with histological examination done at the end of the study. Data analysis was done using SPSS version 25. Results: Healthy rats in group A maintained a unremarkable arthogram & histogram score & TLC count of 6675±350/?l during the entire study period. Telmisartan administration in Group C for two weeks after pristane induction resulted in significant reduction in arthrogram score (AS) 9.5±3.66, total leukocyte count (TLC) 7350±550/?l and histological score (HS) to 6.88±1.24 as compared to (AS) 14.50±2.07, WBC 10150±350/?L & (HS) 10.75±2.05 in Group B, left untreated with pristane alone. The intergroup comparison showed significant p value < 0.05 respectively. Conclusion: Anti-arthritic effect was shown by telmisartan as it was able to ameliorate the changes induced by pristane.
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替米沙坦对普里坦性关节炎大鼠模型的影响
类风湿关节炎是最常见的系统性炎症性疾病之一,其特征是关节的进行性损伤。越来越多的证据表明肾素血管紧张素醛固酮系统信号也参与类风湿关节炎的炎症反应,其阻滞剂具有抗关节炎的特性。替米沙坦是一种血管紧张素受体阻断剂和PPAR-?评价激动剂及其抗关节炎作用。目的:本实验旨在评价替米沙坦对普里斯坦诱导的成年雌性大鼠关节炎模型的抗关节炎作用。研究地点和时间:该研究于2020年7月至2020年8月在拉瓦尔品第陆军医学院药学系与国家卫生研究所和武装部队病理研究所合作进行。材料与方法:将24只成年未孕雌性Sprague Dawley大鼠分为A组(正常对照组)、B组(关节炎对照组)和C组(替米沙坦组)3组(n=8),给予标准饮食和饮水。B、c组大鼠于第0天尾底单次皮下注射普利斯坦0.5ml诱导类风湿关节炎,2周发病。3组均于2 ~ 4周给予蒸馏水2.5 ml/kg, C组在此基础上口服溶解替米沙坦2 mg/kg/d。通过评估关节造影评分和第0、14和28天的总白细胞计数以及研究结束时的组织学检查来确定抗关节炎疗效。数据分析采用SPSS 25。结果:A组健康大鼠的直方图评分和TLC计数均维持在6675±350/?L在整个研究期间。C组替米沙坦在普里斯坦诱导后给予2周,关节图评分(AS) 9.5±3.66,总白细胞计数(TLC) 7350±550/?组织学评分(HS)为6.88±1.24,而as为14.50±2.07,WBC为10150±350/?B组L & (HS) 10.75±2.05,单药不给药。组间比较p值均< 0.05。结论:替米沙坦能改善普里斯坦引起的关节炎,具有抗关节炎作用。
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