Osman Afaf Sayed, Labib Dina Ahmed, Kamel Mahmoud M
Medical Pharmacology Department, Faculty of Medicine, Cairo University, Egypt.
Medical Pharmacology Department, Faculty of Medicine, Cairo University, Egypt.
Int Immunopharmacol. 2017 Sep;50:243-250. doi: 10.1016/j.intimp.2017.07.004. Epub 2017 Jul 12.
Rheumatoid arthritis treatment aims to control joint damage and any associated complications such as cardiovascular disease. Most anti-inflammatory drugs have a high tendency to cause gastro-intestinal irritation. The present study is designed to investigate the anti-inflammatory effect of carvedilol and to study its effect on gastric mucosa.
Lornoxicam (1.3mg/kg) or carvedilol (10mg/kg) was administrated orally 1h before histamine injection into animals of a histamine-induced paw edema model and orally daily for 11days into animals of a formaldehyde-induced arthritis model. Tumor necrosis factor-α and prostaglandin E were measured in animals of the formaldehyde-induced arthritis model. The effect of lornoxicam and carvedilol on gastric mucosa was assessed in normal rats and after induction of cold stress ulcer.
Carvedilol succeeded in reducing hind paw edema in both histamine-induced paw edema and formaldehyde-induced arthritis and in reducing the elevated level of tumor necrosis factor-α and prostaglandin E nearly with near equal efficacy compared with lornoxicam. Carvedilol did not show any ulcerative effect on the gastric mucosa of normal rats, and its use was associated with an improvement of both the gross and histopathological pictures of gastric ulcers in animals of the cold stress ulcer model compared with lornoxicam treated rats.
The current findings support the use of carvedilol both in the management of inflammation as well as the prevention of cardiovascular complications in rheumatoid arthritis patients. The use of carvedilol was not associated with any gastro-intestinal tract irritation.
类风湿性关节炎的治疗旨在控制关节损伤及任何相关并发症,如心血管疾病。大多数抗炎药极易引起胃肠道刺激。本研究旨在探究卡维地洛的抗炎作用,并研究其对胃黏膜的影响。
在向组胺诱导的爪肿胀模型动物注射组胺前1小时,口服氯诺昔康(1.3mg/kg)或卡维地洛(10mg/kg),并在甲醛诱导的关节炎模型动物中每日口服给药,持续11天。在甲醛诱导的关节炎模型动物中测量肿瘤坏死因子-α和前列腺素E。在正常大鼠以及诱导冷应激溃疡后,评估氯诺昔康和卡维地洛对胃黏膜的影响。
与氯诺昔康相比,卡维地洛成功减轻了组胺诱导的爪肿胀和甲醛诱导的关节炎中后爪的肿胀,并降低了肿瘤坏死因子-α和前列腺素E的升高水平,且疗效相近。卡维地洛对正常大鼠胃黏膜未显示出任何溃疡作用,与氯诺昔康治疗的大鼠相比,在冷应激溃疡模型动物中,使用卡维地洛可改善胃溃疡的大体和组织病理学表现。
目前的研究结果支持卡维地洛可用于类风湿性关节炎患者的炎症管理及心血管并发症预防。使用卡维地洛未出现任何胃肠道刺激。