Carvedilol alleviates adjuvant-induced arthritis and subcutaneous air pouch edema: Modulation of oxidative stress and inflammatory mediators

被引:59
作者
Arab, Hany H. [1 ,2 ]
El-Sawalhi, Maha M. [2 ]
机构
[1] Taif Univ, Fac Pharm, Dept Pharmacol & Toxicol, Div Biochem, Al Haweiah 21974, Taif, Saudi Arabia
[2] Cairo Univ, Fac Pharm, Dept Biochem, Cairo, Egypt
关键词
Carvedilol; Adjuvant arthritis; Air pouch edema; Oxidative stress; Inflammatory mediators; BETA-ADRENOCEPTOR ANTAGONIST; COLLAGEN-INDUCED ARTHRITIS; RHEUMATOID-ARTHRITIS; NITRIC-OXIDE; MITOCHONDRIAL TOXICITY; ANTIOXIDANT PROTECTION; REACTIVE OXYGEN; LEUKOTRIENE B4; FREE-RADICALS; HUMAN-DISEASE;
D O I
10.1016/j.taap.2013.01.019
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Rheumatoid arthritis (RA) is a systemic inflammatory disease with cardiovascular complications as the leading cause of morbidity. Carvedilol is an adrenergic antagonist which has been safely used in treatment of several cardiovascular disorders. Given that carvedilol has powerful antioxidant/anti-inflammatory properties, we aimed to investigate its protective potential against arthritis that may add further benefits for its clinical usefulness especially in RA patients with concomitant cardiovascular disorders. Two models were studied in the same rat; adjuvant arthritis and subcutaneous air pouch edema. Carvedilol (10 mg/kg/day p.o. for 21 days) effectively suppressed inflammation in both models with comparable efficacy to the standard anti-inflammatory diclofenac (5 mg/kg/day p.o.). Notably, carvedilol inhibited paw edema and abrogated the leukocyte invasion to air pouch exudates. The latter observation was confirmed by the histopathological assessment of the pouch lining that revealed mitigation of immuno-inflammatory cell influx. Carvedilol reduced/normalized oxidative stress markers (lipid peroxides, nitric oxide and protein thiols) and lowered the release of inflammatory cytokines (TNF-alpha & IL-6), and eicosanoids (PGE(2) & LTB4) in sera and exudates of arthritic rats. Interestingly, carvedilol, per se, didn't present any effect on assessed biochemical parameters in normal rats. Together, the current study highlights evidences for the promising anti-arthritic effects of carvedilol that could be mediated through attenuation of leukocyte migration, alleviation of oxidative stress and suppression of proinflammatory cytokines and eicosanoids. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:241 / 248
页数:8
相关论文
共 55 条
[1]
Effects of captopril on interleukin-6, leukotriene B4, and oxidative stress markers in serum and inflammatory exudate of arthritic rats:: Evidence of antiinflammatory activity [J].
Agha, AM ;
Mansour, M .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2000, 168 (02) :123-130
[2]
Nitric oxide and the immune response [J].
Bogdan, C .
NATURE IMMUNOLOGY, 2001, 2 (10) :907-916
[3]
Evidence that cytokines play a role in rheumatoid arthritis [J].
Brennan, Fionula M. ;
McInnes, Iain B. .
JOURNAL OF CLINICAL INVESTIGATION, 2008, 118 (11) :3537-3545
[4]
INFLAMMATION AND COLLAGENASE PRODUCTION IN RATS WITH ADJUVANT ARTHRITIS REDUCED WITH 13-CIS-RETINOIC ACID [J].
BRINCKERHOFF, CE ;
COFFEY, JW ;
SULLIVAN, AC .
SCIENCE, 1983, 221 (4612) :756-758
[5]
Grape seed proanthocyanidin extract (GSPE) attenuates collagen-induced arthritis [J].
Cho, Mi-La ;
Heo, Yu-Jung ;
Park, Mi-Kyung ;
Oh, Hye-Jwa ;
Park, Jin-Sil ;
Woo, Yun-Ju ;
Ju, Ji-Hyeon ;
Park, Sung-Hwan ;
Kim, Ho-Youn ;
Min, Jun-Ki .
IMMUNOLOGY LETTERS, 2009, 124 (02) :102-110
[6]
Cronstein BN, 2007, BULL HOSP JT DIS, V65, pS11
[7]
Leukotriene B4 [J].
Crooks, SW ;
Stockley, RA .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 1998, 30 (02) :173-178
[8]
Beneficial effects of diclofenac therapy on serum lipids, oxidized low-density lipoprotein and antioxidant defenses in rats [J].
Curcelli, Emilio C. ;
Muller, Sergio S. ;
Novelli Filho, Jose Luiz V. B. .
LIFE SCIENCES, 2008, 82 (15-16) :892-898
[9]
Antioxidant activity of carvedilol in cardiovascular disease [J].
Dandona, Paresh ;
Ghanim, Husam ;
Brooks, David P. .
JOURNAL OF HYPERTENSION, 2007, 25 (04) :731-741
[10]
Nitric oxide-mediated chondrocyte cell death requires the generation of additional reactive oxygen species [J].
Del Carlo, M ;
Loeser, RF .
ARTHRITIS AND RHEUMATISM, 2002, 46 (02) :394-403