β Mangostin suppress LPS-induced inflammatory response in RAW 264.7 macrophages in vitro and carrageenan-induced peritonitis in vivo

被引:44
|
作者
Syam, Suvitha [1 ,4 ]
Bustamam, Ahmad [1 ]
Abdullah, Rasedee [2 ]
Sukari, Mohamed Aspollah [3 ]
Hashim, Najihah Mohd [4 ]
Mohan, Syam [5 ]
Looi, Chung Yeng [6 ]
Wong, Won Fen [7 ]
Yahayu, Maizatul Akmal [8 ]
Abdelwahab, Siddig Ibrahim [5 ]
机构
[1] Univ Putra Malaysia, Inst Biosci, UPM MAKNA Canc Res Lab, Serdang 43400, Selangor, Malaysia
[2] Univ Putra Malaysia, Fac Vet, Dept Vet Pathol & Microbiol, Serdang 43400, Selangor, Malaysia
[3] Univ Putra Malaysia, Fac Sci, Dept Chem, Serdang 43400, Selangor, Malaysia
[4] Univ Malaya, Fac Med, Dept Pharm, Kuala Lumpur 50603, Malaysia
[5] Jazan Univ, Med Res Ctr, Jazan, Saudi Arabia
[6] Univ Malaya, Fac Med, Dept Pharmacol, Kuala Lumpur 50603, Malaysia
[7] Univ Malaya, Fac Med, Dept Med Microbiol, Kuala Lumpur, Malaysia
[8] Univ Teknol Malaysia, Inst Bioprod Dev, Johor Baharu, Johor, Malaysia
关键词
β Mangostin; Garcinia mangostana; iNOS; NF-kappa B; COX-2; Cytokines; NF-KAPPA-B; NITRIC-OXIDE; ANTIINFLAMMATORY ACTIVITY; GARCINIA-MANGOSTANA; SIGNALING PATHWAYS; COX-2; INHIBITORS; TNF-ALPHA; CELLS; PROTEIN; MICE;
D O I
10.1016/j.jep.2014.02.051
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: The fruit hull of Garcinia mangostana Linn. has been used in traditional medicine for treatment of various inflammatory diseases. Hence, this study aims to investigate the in vitro and in vivo anti-inflammatory effect of beta mangostin (beta M), a major compound present in Garcinia mangostana. Materials and methods: The in silico analysis of inflammatory mediators such as cyclooxygenase (COX) and nuclear factor-kappa B (NF-kappa B) were performed via molecular docking. Further evaluation of anti-inflammatory effect was conducted in lipopolysaccharide (LPS) induced RAW 264.7 macrophages. Suppression of activated NF-kappa B was analyzed by high content screening. beta M triggered inhibition of COX-1 and COX-2 in vitro were studied using biochemical kit The in vivo model used in this study was carrageenan-induced peritonitis model, where reduction in carrageenan-induced peritonitis is measured by leukocyte migration and vascular permeability. In addition, the evaluation of beta M's effect on carrageenan induced TNF-alpha and IL-1 beta release on peritoneal fluid was also carried out Results: Treatment with beta M could inhibit the LPS-induced NO production but not the viability of RAW 264.7. Similarly, beta M inhibited PGE(2) production and the cytokines: TNF-beta and IL-6. The COX catalyzed prostaglandin biosynthesis assay had showed selective COX-2 inhibition with a 53.0 +/- 6.01% inhibition at 20 mu g/ml. Apart from this, beta M was capable in repressing translocation of NF-kappa B into the nucleus. These results were concurrent with molecular docking which revealed COX-2 selectivity and NF-kappa B inhibition. The in vivo analysis showed that after four hours of peritonitis, beta M was unable to reduce vascular permeability, yet could decrease the total leukocyte migration; particularly, neutrophils. Meanwhile, dexamethasone 0.5 mg/kg, successfully reduced vascular permeability. The levels of TNIF-alpha and IL-1 beta in peritoneal fluid was reduced significantly by beta M treatment. Conclusion: The current study supports the traditional use of Garcinia mangostana fruit hull for treatment of inflammatory conditions. In addition, it is clear that the anti-inflammatory efficacy of this plant is not limited to the presence of a and gamma, but beta also with significant activity. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:435 / 445
页数:11
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