Anti-inflammatory and antioxidant effects of a combination of cannabidiol and moringin in LPS-stimulated macrophages

被引:87
|
作者
Rajan, Thangavelu Soundara [1 ]
Giacoppo, Sabrina [1 ]
Iori, Renato [2 ]
De Nicola, Gina Rosalinda [2 ]
Grassi, Gianpaolo [3 ]
Pollastro, Federica [4 ]
Bramanti, Placido [1 ]
Mazzon, Emanuela [1 ]
机构
[1] IRCCS Ctr Neurolesi Bonino Pulejo, Via Prov Palermo, I-98124 Messina, Italy
[2] Ctr Ric Colture Ind CREA CIN, Consiglio Ric Agr & Anal Econ Agr, Via Corticella 133, I-40128 Bologna, Italy
[3] Res Ctr Ind Crops CRA CIN, Council Res & Expt Agr, Rovigo, Italy
[4] Univ Piemonte Orientale, Dipartimento Sci Farm, Largo Donegani 2, I-28100 Novara, Italy
关键词
Cannabidiol; Moringin; Combination therapy; Anti-inflammation; LPS; Macrophages; NF-KAPPA-B; ISOTHIOCYANATE; INFLAMMATION; MYROSINASE; RECEPTOR; MODEL;
D O I
10.1016/j.fitote.2016.05.008
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Inflammatory response plays an important role in the activation and progress of many debilitating diseases. Natural products, like cannabidiol, a constituent of Cannabis sativa, and moringin, an isothiocyanate obtained from myrosinase-mediated hydrolysis of the glucosinolate precursor glucomoringin present in Moringa oleifera seeds, are well known antioxidants also endowed with anti-inflammatory activity. This is due to a covalent based mechanism for ITC, while non-covalent interactions underlie the activity of CBD. Since these two mechanisms are distinct, and the molecular endpoints are potentially complementary, we investigated in a comparative way the protective effect of these compounds alone or in combination on lipopolysaccharide-stimulated murine macrophages. Our results show that the cannabidiol (5 mu M) and moringin (5 mu M) combination outperformed the single constituents that, at this dosage had only a moderate efficacy on inflammatory (Tumor necrosis factor-alpha, Interleukin-10) and oxidative markers (inducible nitric oxide synthase, nuclear factor erythroid 2-related factor 2, nitrotyrosine). Significant upregulation of Bcl-2 and downregulation of Bax and cleaved caspase-3 was observed in cells treated with cannabidiol-moringin combination. Treatment with the transient receptor potential vanilloid receptor 1 antagonist was detrimental for the efficacy of cannabidiol, while no effect was elicited by cannabinoid receptor 1 and cannabinoid receptor 2 antagonists. None of these receptors was involved in the activity of moringin. Taken together, our in vitro results testify the anti-inflammatory, antioxidative, and anti-apoptotic effects of the combination of cannabidiol and moringin. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:104 / 115
页数:12
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