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不同剂量阿利吉仑在大鼠炎症模型中的抗炎作用

The Anti-Inflammatory Effect of Different Doses of Aliskiren in Rat Models of Inflammation.

作者信息

Aziz Tavga Ahmed, Kareem Ahmed Azad, Othman Hemn Hassan, Ahmed Zheen Aorahman

机构信息

Department of Pharmacology and Toxicology, College of Pharmacy, University of Sulaimani, Sulaimani, Kurdistan Region, Iraq.

出版信息

Drug Des Devel Ther. 2020 Jul 20;14:2841-2851. doi: 10.2147/DDDT.S255607. eCollection 2020.

Abstract

OBJECTIVE

The present study was designed to evaluate the anti-inflammatory effects of different doses of aliskiren in two animal models of inflammation.

METHODOLOGY

Sixty-six Wistar rats were allocated into five groups: the first group (six rats) was treated with the vehicle only, without induction of paw edema and granulomatous inflammation, and served as a negative control; the second group (12 rats) was allocated into two subgroups and treated with the vehicle only, with induction of paw edema and granulomatous inflammation, and served as a positive control; the third group (36 rats) was allocated into six subgroups and treated with different doses of aliskiren (15, 30, and 60 mg/kg) in both models; the fourth group (12 rats) was treated with dexamethasone (1 mg/kg) in both models of inflammation. Serum concentrations of tumor necrosis factor-α (TNF-α), interleukin-10 (IL-10), vascular cell adhesion molecule-1 (VCAM-1), and high sensitivity C-reactive protein (hs-CRP) were measured. Skin samples were also sent for histopathological examination.

RESULTS

Aliskiren, in a dose-dependent pattern, significantly decreased inflammation in rat models of inflammation, by attenuating the percentage of exudate, granuloma, and paw edema. Furthermore, it significantly reduced serum concentrations of TNF-α, VCAM-1, and hs-CRP and restored the serum concentration of IL-10. Additionally, significant improvement was seen in the histopathological findings.

CONCLUSION

In the current study, aliskiren was successful in decreasing inflammation in both models. These findings suggest that aliskiren is a good candidate for the treatment of inflammatory diseases.

摘要

目的

本研究旨在评估不同剂量阿利吉仑在两种炎症动物模型中的抗炎作用。

方法

66只Wistar大鼠被分为五组:第一组(6只大鼠)仅接受赋形剂处理,未诱导爪肿胀和肉芽肿性炎症,作为阴性对照;第二组(12只大鼠)分为两个亚组,仅接受赋形剂处理,诱导爪肿胀和肉芽肿性炎症,作为阳性对照;第三组(36只大鼠)分为六个亚组,在两种模型中用不同剂量的阿利吉仑(15、30和60mg/kg)处理;第四组(12只大鼠)在两种炎症模型中用 dexamethasone(1mg/kg)处理。测量血清肿瘤坏死因子-α(TNF-α)、白细胞介素-10(IL-10)、血管细胞粘附分子-1(VCAM-1)和高敏C反应蛋白(hs-CRP)的浓度。皮肤样本也送去进行组织病理学检查。

结果

阿利吉仑以剂量依赖性方式显著减轻大鼠炎症模型中的炎症,通过降低渗出物、肉芽肿和爪肿胀的百分比。此外,它显著降低了TNF-α、VCAM-1和hs-CRP的血清浓度,并恢复了IL-10的血清浓度。另外,组织病理学结果有显著改善。

结论

在本研究中,阿利吉仑在两种模型中均成功减轻了炎症。这些发现表明阿利吉仑是治疗炎症性疾病的良好候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c11/7381093/7991388b612f/DDDT-14-2841-g0001.jpg

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