Natural chromones as potential anti-inflammatory agents: Pharmacological properties and related mechanisms

Chromones are a group of natural substances with a diversity of biological activities. Herein we assessed the pharmacological potential of three chromones (1, 2 and 3) isolated from Dictyoloma vandellianum as anti-inflammatory agents using in vitro and in vivo approaches. During in vitro screening,...

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Veröffentlicht in:International immunopharmacology 2019-07, Vol.72, p.31-39
Hauptverfasser: Opretzka, Luiza Carolina França, Espírito-Santo, Renan Fernandes do, Nascimento, Olívia Azevedo, Abreu, Lucas Silva, Alves, Iura Muniz, Döring, Eva, Soares, Milena Botelho Pereira, Velozo, Eudes da Silva, Laufer, Stefan A., Villarreal, Cristiane Flora
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Sprache:eng
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Zusammenfassung:Chromones are a group of natural substances with a diversity of biological activities. Herein we assessed the pharmacological potential of three chromones (1, 2 and 3) isolated from Dictyoloma vandellianum as anti-inflammatory agents using in vitro and in vivo approaches. During in vitro screening, the production of NO and cytokines by macrophages stimulated with LPS and IFN-γ was inhibited by all chromones at concentrations (5–20 μM) that did not induce cytotoxicity. Analysis of pharmacokinetic parameters (in vitro half-life and intrinsic clearance) using human liver microsomes revealed that 3 has a superior pharmacokinetic profile, compared to 1 and 2. Treatment with 3 (100 mg/kg, ip) did not affect the mice motor performance, while 1 and 2 induced motor deficit. Taking into account the pharmacokinetic profile and absence of motor impairment, 3 was selected for further pharmacological characterization. Corroborating the data from in vitro screening, treatment of cell cultures with 3 (5–20 μM) reduced TNF-α, IL-6 and IL-1β production by stimulated macrophages. In the complete Freund's adjuvant-induced paw inflammation model in mice, 3 (25 and 50 mg/kg, ip) inhibited mechanical hyperalgesia, edema and cytokine production/release (IL-1β, IL-6 and TNF-α). 3 (5–20 μM) also reduced the transcriptional activity of NF-κB in stimulated macrophages. Furthermore, treatment with RU486, a glucocorticoid receptor (GR) antagonist, partially prevented the inhibitory effect of 3 on macrophages, indicating that this chromone exerts its anti-inflammatory effects in part through the activation of GR. The results presented herein demonstrate the pharmacological potential of natural chromones, highlighting 3 as a possible candidate for the drug discovery process targeting new anti-inflammatory drugs. •Chromones from Dictyoloma vandellianum have consistent anti-inflammatory properties.•Natural chromones have favorable in vitro pharmacokinetic profile.•Anti-inflammatory effects of chromones involve glucocorticoid receptors activation.•Inhibition of NF-κB may contribute to the anti-inflammatory effects of chromones.
ISSN:1567-5769
1878-1705
DOI:10.1016/j.intimp.2019.03.044