The antineoplastic agent anacardic 6-pentadecyl salicylic acid produces immunomodulation in vivo via the activation of MAPKs.

Autor: Gnanaprakasam JNR; Department of Toxicology, Centre for Research and Advanced Studies of the National Polytechnic Institute, Av. IPN, 2508, San Pedro Zacatenco, Mexico City 07360, Mexico., Estrada-Muñiz E; Department of Toxicology, Centre for Research and Advanced Studies of the National Polytechnic Institute, Av. IPN, 2508, San Pedro Zacatenco, Mexico City 07360, Mexico., Vega L; Department of Toxicology, Centre for Research and Advanced Studies of the National Polytechnic Institute, Av. IPN, 2508, San Pedro Zacatenco, Mexico City 07360, Mexico. Electronic address: lvega@cinvestav.mx.
Jazyk: angličtina
Zdroj: Toxicology and applied pharmacology [Toxicol Appl Pharmacol] 2019 Aug 01; Vol. 376, pp. 82-92. Date of Electronic Publication: 2019 May 24.
DOI: 10.1016/j.taap.2019.05.017
Abstrakt: Anacardic 6-pentadecyl salicylic acid (6SA) is the active component of Amphipterygium adstringens, a plant used in traditional medicine for the treatment of malaria and vascular diseases and as an anti-bacterial and immune-modulatory agent. However, the effect of 6SA on the immune system remains unclear. In this study, we examined the immune-stimulatory activity of 6SA in 6-8-week-old female BALB/c mice. We found that treatment with 2 mg/kg of 6SA increased the proportions of macrophages after 7 and 14 days of treatment and of natural killer (NK) cells after 14 days of treatment in circulating blood. In lymph nodes, treatment with 6SA for 14 days increased the number of macrophages. In addition, 6SA increases in the systemic levels of pro-inflammatory cytokines such as tumour necrosis factor (TNF)-α, interleukin (IL)-2, IL-12, IL-6 and IL-1β and of nitric oxide (NO). We observed an increase in the secretion of Granulocyte/Macrophage Colony Stimulation Factor (GM-CSF) that could explain the increase in the proportion of macrophages. Moreover, 6SA induced the classical activation of macrophages by increasing their expression of MHC-II and their production of TNF-α. These M1-polarised macrophages presented enhanced phagocytosis and NO secretion. This activation was due to induction of the phosphorylation of MAPKs such as ERK, JNK and p38 because specific inhibitors of the phosphorylation of these MAPKs reduced the 6SA-induced phagocytosis and NO and particularly, the secretion of GM-CSF in macrophages by inhibition of ERK. Despite these effects on macrophages, 6SA does not have any direct effect on the proportion of lymphocytes.
(Copyright © 2019 Elsevier Inc. All rights reserved.)
Databáze: MEDLINE
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