Mitraphylline inhibits lipopolysaccharide-mediated activation of primary human neutrophils

• Published in: Phytomedicine (Stuttgart) 2016-02, Vol.23 (2), p.141-148
• Main Authors: Montserrat-de la Paz, Sergio, Fernandez-Arche, Angeles, de la Puerta, Rocío, Quilez, Ana M, Muriana, Francisco JG, Garcia-Gimenez, Maria Dolores, Bermudez, Beatriz
• Format: Article
• Language: English
• Subjects: Alkaloids; Anti-Inflammatory Agents - pharmacology; Cat's Claw - chemistry; Cytokines - metabolism; Health aspects; Humans; Indole Alkaloids - pharmacology; Inflammation; Interleukin-6 - metabolism; Interleukin-8 - metabolism; Lipopolysaccharide; Lipopolysaccharides; Mitogens; Mitraphylline; Neutrophils; Neutrophils - cytology; Neutrophils - drug effects; NF-kappa B - metabolism; Oxindoles; Plant Bark - chemistry; Tumor necrosis factor; Tumor Necrosis Factor-alpha - metabolism; Uncaria tomentosa
• ISSN: 0944-7113; 1618-095X
• DOI: 10.1016/j.phymed.2015.12.015

Mitraphylline (MTP) is the major pentacyclic oxindolic alkaloid presented in Uncaria tomentosa. It has traditionally been used to treat disorders including arthritis, heart disease, cancer, and other inflammatory diseases. However, the specific role of MTP is still not clear, with more comprehensivestudies, our understanding of this ancient herbal medicine will continue growing. Some studies provided its ability to inhibit proinflamatory cytokines, such as TNF-α, through NF-κB-dependent mechanism. TNF-α primes neutrophils and modulates phagocytic and oxidative burst activities in inflammatory processes. Since, neutrophils represent the most abundant pool of leukocytes in human blood and play a crucial role in inflammation, we aimed to determine the ability of MTP to modulate neutrophil activation and differentially regulate inflammatory-related cytokines. To determine the mechanism of action of MTP, we investigated the effects on LPS-activated human primary neutrophils responses including activation surface markers by FACS and the expression of inflammatory cytokines, measured by real time PCR and ELISA. Treatment with MTP reduced the LPS-dependent activation effects. Activated neutrophils (CD16+CD62L−) diminished after MTP administration. Moreover, proinflamatory cytokines (TNF-α, IL-6 or IL-8) expression and secretion were concomitantly reduced, similar to basal control conditions. Taken together, our results demonstrate that MTP is able to elicit an anti-inflammatory response that modulates neutrophil activation contributing to the attenuation of inflammatory episodes. Further studies are need to characterize the mechanism by which MTP can affect this pathway that could provide a means to develop MTP as new candidate for inflammatory disease therapies. [Display omitted]