Remedial effects of novel 2,3-disubstituted thiazolidin-4-ones in chemical mediated inflammation

被引:9
|
作者
Mudgal, Jayesh [1 ]
Gowdra, Vasantharaju S. [2 ]
Mathew, Geetha [1 ]
Nayak, Pawan G. [1 ]
Reddy, Nitin D. [1 ]
Namdeo, Neelesh [1 ]
Kumar, Ravilla R. [1 ]
Kantamaneni, Chaitanya [1 ]
Chamallamudi, Mallikarjuna R. [1 ]
Nampurath, Gopalan K. [1 ]
机构
[1] Manipal Univ, Manipal Coll Pharmaceut Sci, Dept Pharmacol, Manipal 576104, Karnataka, India
[2] Manipal Univ, Manipal Coll Pharmaceut Sci, Dept Pharmaceut Qual Assurance, Manipal 576104, Karnataka, India
关键词
Thiazolidin-4-one; Cytokines; Cyclo-oxygenase; Prostaglandins; Myeloperoxidase; Inflammation; BIOLOGICAL EVALUATION; DERIVATIVES; INHIBITION; EFFICACY; ASSAY; RAT; AIR;
D O I
10.1016/j.cbi.2013.12.012
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Three thiazolidin-4-one derivatives were synthesized, purified and characterized by chromatographic and spectroscopic methods. In the in vitro assays, these compounds inhibited reactive oxygen species (ROS), nitrite and cytokine generation in RAW 264.7 murine macrophages and whole blood. These derivatives attenuated carrageenan-induced acute inflammation in rats. The most effective compound 4C possessed identical anti-inflammatory action at two doses (50 and 100 mg/kg). Further, the effect of compound 4C on locally induced inflammatory mediators was investigated in carrageenan-induced air pouch inflammation in rats. In this model, compound 4C inhibited the cytokines, tumor necrosis factor (TNF)-alpha and interleukin (IL)-6 (systemic and local). Additionally, compound 4C was able to reduce locally elevated prostaglandin-E-2 (PGE(2)). Inhibition of leukocyte infiltration by compound 4C was correlated with reduced locally released myeloperoxidase (MPO). To conclude, compound 4C corrected the inflammatory condition by negative effect on cytokine (TNF-alpha, IL-6) network and prostaglandin-E-2 generation. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:34 / 42
页数:9
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