Guineensine increases the production of pro-inflammatory cytokines in activated M1 macrophages and shows inhibitory effects on resting and M2 macrophages
PDF (Español (España))

Keywords

Guineensine
Inflammation
Cytokines
Macrophages

Métricas de PLUMX 

Abstract

Guineensine, a natural compound isolated from several species of pepper plants, is an inhibitor of endocannabinoid uptake and probably an indirect CB1 receptor (CB1R) agonist.  As an inhibitor of cellular uptake of AEA and 2-AG, guineensine has been shown to exhibit cannabimimetic effects; however, the role of this compound in the control of inflammation and macrophage activation is not yet clear. Here we used the human macrophages-like THP-1 cell line to study guineensine. When stimulated with lipopolysaccharide (LPS) and IFN-γ, guineensine increases production of IL-1β, TNF-α, and monocyte chemoattractant protein (MCP)-1 (the latter two up to 2.5-fold). Interestingly, when resting macrophage-like or macrophage-like stimulated with IL- 4 and IL-13 (M2) were exposed to guineensine, MCP-1 and IL-8 levels were significantly decreased. No significant differences between phagocytosis and respiratory burst (ROS production) in activated macrophages treated with guineensine were found. These results suggest a differential outcome between M1, M2 and resting macrophages-like and immune response when exposed to guineensine.

https://doi.org/10.15741/revbio.13.e1886
PDF (Español (España))

References

Borriello, F., Iannone, R., Di Somma, S., Loffredo, S., Scamardella, E., Galdiero, M. R., Varricchi, G., Granata, F., Portella, G., & Marone, G. (2017). GM-CSF and IL-3 Modulate Human Monocyte TNF-α Production and Renewal in In Vitro Models of Trained Immunity. Frontiers in Immunology, 7(1), 1–12. https://doi.org/10.3389/fimmu.2016.00680

Borriello, F., Longo, M., Spinelli, R., Pecoraro, A., Granata, F., Staiano, R. I., Loffredo, S., Spadaro, G., Beguinot, F., Schroeder, J., & Marone, G. (2015). IL-3 synergises with basophil-derived IL-4 and IL-13 to promote the alternative activation of human monocytes. European Journal of Immunology, 45(7), 2042–2051. https://doi.org/10.1002/eji.201445303

Carlisle, S. J., Marciano-Cabral, F., Staab, A., Ludwick, C., & Cabral, G. A. (2002). Differential expression of the CB2 cannabinoid receptor by rodent macrophages and macrophage-like cells in relation to cell activation. International Immunopharmacology, 2(1), 69–82. https://doi.org/10.1016/S1567-5769(01)00147-3

Chimal-Ramírez, G. K., Espinoza-Sánchez, N. A., Chávez-Sánchez, L., Arriaga-Pizano, L., & Fuentes-Pananá, E. M. (2016). Monocyte Differentiation towards Protumor Activity Does Not Correlate with M1 or M2 Phenotypes. Journal of Immunology Research, 2016(1), 1–16. https://doi.org/10.1155/2016/6031486

Di Marzo, V., Bisogno, T., De Petrocellis, L., Melck, D., Orlando, P., Wagner, J. A., & Kunos, G. (1999). Biosynthesis and inactivation of the endocannabinoid 2-arachidonoylglycerol in circulating and tumoral macrophages. European Journal of Biochemistry, 264(1), 258–267. https://doi.org/10.1046/j.1432-1327.1999.00631.x

Gonsiorek, W., Lunn, C., Fan, X., Narula, S., Lundell, D., & Hipkin, R. W. (2000). Endocannabinoid 2-arachidonyl glycerol is a full agonist through human type 2 cannabinoid receptor: antagonism by anandamide. Molecular Pharmacology, 57(5), 1045–1050. https://doi.org/10.1016/S0026-895X(24)26516-0

Han, K. H., Lim, S., Ryu, J., Lee, C. W., Kim, Y., Kang, J. H., Kang, S. S., Ahn, Y. K., Park, C. S., & Kim, J. J. (2009). CB1 and CB2 cannabinoid receptors differentially regulate the production of reactive oxygen species by macrophages. Cardiovascular Research, 84(3), 378–386. https://doi.org/10.1093/cvr/cvp240

Kishimoto, S., Kobayashi, Y., Oka, S., Gokoh, M., Waku, K., & Sugiura, T. (2004). 2-Arachidonoylglycerol, an endogenous cannabinoid receptor ligand, induces accelerated production of chemokines in HL-60 cells. Journal of Biochemistry, 135(4), 517–524. https://doi.org/10.1093/jb/mvh063

Lee, S. W., Rho, M. C., Nam, J. Y., Lim, E. H., Kwon, O. E., Kim, Y. H., Lee, H. S., & Kim, Y. K. (2004). Guineensine, an Acyl-CoA: cholesterol acyltransferase inhibitor, from the fruits of Piper longum. Planta Medica, 70(7), 678–679. https://doi.org/10.1055/s-2004-827193

Mai, P., Tian, L., Yang, L., Wang, L., Yang, L., & Li, L. (2015). Cannabinoid receptor 1 but not 2 mediates macrophage phagocytosis by G(α)i/o/RhoA/ROCK signaling pathway. Journal of Cellular Physiology, 230(7), 1640–1650. https://doi.org/10.1002/jcp.24911

Mantovani, A., Sica, A., Sozzani, S., Allavena, P., Vecchi, A., & Locati, M. (2004). The chemokine system in diverse forms of macrophage activation and polarization. Trends in Immunology, 25(12), 677–686. https://doi.org/10.1016/j.it.2004.09.015

Marazzi, J., Kleyer, J., Paredes, J. M., & Gertsch, J. (2011). Endocannabinoid content in fetal bovine sera – unexpected effects on mononuclear cells and osteoclastogenesis. Journal of Immunological Methods, 373(1), 219–228. https://doi.org/10.1016/j.jim.2011.08.021

Murray, P. J., Allen, J. E., Biswas, S. K., Fisher, E. A., Gilroy, D. W., Goerdt, S., Gordon, S., Hamilton, J. A., Ivashkiv, L. B., Lawrence, T., Locati, M., Mantovani, A., Martinez, F. O., Mege, J. L., Mosser, D. M., Natoli, G., Saeij, J. P., Schultze, J. L., Shirey, K. A., Sica, A., & Wynn, T. A. (2014). Macrophage activation and polarization: nomenclature and experimental guidelines. Immunity, 41(1), 14–20. https://doi.org/10.1016/j.immuni.2014.06.008

Muthumalage, T., & Rahman, I. (2019). Cannabidiol differentially regulates basal and LPS-induced inflammatory responses in macrophages, lung epithelial cells, and fibroblasts. Toxicology and Applied Pharmacology, 382(1), 1–13. https://doi.org/10.1016/j.taap.2019.114713

Nicolussi, S., Viveros-Paredes, J. M., Gachet, M. S., Rau, M., Flores-Soto, M. E., Blunder, M., & Gertsch, J. (2014). Guineensine is a novel inhibitor of endocannabinoid uptake showing cannabimimetic behavioral effects in BALB/c mice. Pharmacological Research, 80(1), 52–65. https://doi.org/10.1016/j.phrs.2013.12.010

Okogun, J. I., & Ekong, D. E. U. (1974). Extracts from the fruits of Piper guineense Schum. and Thonn. Journal of the Chemical Society, Perkin Transactions 1, 1(0), 2195–2198. https://doi.org/10.1039/P19740002195

Pullela, S. V., Tiwari, A. K., Vanka, U. S., Vummenthula, A., Tatipaka, H. B., Dasari, K. R., Khan, I. A., & Janaswamy, M. R. (2006). HPLC-assisted chemobiological standardization of alpha-glucosidase-I enzyme inhibitory constituents from Piper longum Linn. Journal of Ethnopharmacology, 108(3), 445–449. https://doi.org/10.1016/j.jep.2006.06.004

Reynoso-Moreno, I., Najar-Guerrero, I., Escareño, N., Flores-Soto, M. E., Gertsch, J., & Viveros-Paredes, J. M. (2017). An Endocannabinoid Uptake Inhibitor from Black Pepper Exerts Pronounced Anti-Inflammatory Effects in Mice. Journal of Agricultural and Food Chemistry, 65(43), 9435–9442. https://doi.org/10.1021/acs.jafc.7b02979

Saqib, U., Sarkar, S., Suk, K., Mohammad, O., Baig, M. S., & Savai, R. (2018). Phytochemicals as modulators of M1–M2 macrophages in inflammation. Oncotarget, 9(25), 17937–17950. https://doi.org/10.18632/oncotarget.24788

Shiratsuchi, A., Watanabe, I., Yoshida, H., & Nakanishi, Y. (2008). Involvement of cannabinoid receptor CB2 in dectin-1-mediated macrophage phagocytosis. Immunology and Cell Biology, 86(2), 179–184. https://doi.org/10.1038/sj.icb.7100121

Silva, M., Videira, P. A., & Sackstein, R. (2018). E-Selectin Ligands in the Human Mononuclear Phagocyte System: Implications for Infection, Inflammation, and Immunotherapy. Frontiers in Immunology, 8(1), 1–17. https://doi.org/10.3389/fimmu.2017.01878

Singh, G., Marimuthu, P., Catalán, C. A., & de Lampasona, M. (2004). Chemical, antioxidant, and antifungal activities of volatile oil of black pepper and its acetone extract. Journal of the Science of Food and Agriculture, 84(14), 1878–1884. https://doi.org/10.1002/jsfa.1863

Staiano, R. I., Loffredo, S., Borriello, F., Iannotti, F. A., Piscitelli, F., Orlando, P., Secondo, A., Granata, F., Lepore, M. T., Fiorelli, A., Varricchi, G., Santini, M., Triggiani, M., Di Marzo, V., & Marone, G. (2016). Human lung-resident macrophages express CB1 and CB2 receptors whose activation inhibits the release of angiogenic and lymphangiogenic factors. Journal of Leukocyte Biology, 99(4), 531–540. https://doi.org/10.1189/jlb.3HI1214-584R

Sugiura, T., Kondo, S., Kishimoto, S., Miyashita, T., Nakane, S., Kodaka, T., Suhara, Y., Takayama, H., & Waku, K. (2000). Evidence that 2-arachidonoylglycerol but not N-palmitoylethanolamine or anandamide is the physiological ligand for the cannabinoid CB2 receptor. Journal of Biological Chemistry, 275(1), 605–612. https://doi.org/10.1074/jbc.275.1.605

Tarique, A. A., Logan, J., Thomas, E., Holt, P. G., Sly, P. D., & Fantino, E. (2015). Phenotypic, functional, and plasticity features of classical and alternatively activated human macrophages. American Journal of Respiratory Cell and Molecular Biology, 53(5), 676–688. https://doi.org/10.1165/rcmb.2015-0012OC

Yeisley, D. J., Arabiyat, A. S., & Hahn, M. S. (2021). Cannabidiol-Driven Alterations to Inflammatory Protein Landscape of Lipopolysaccharide-Activated Macrophages In Vitro May Be Mediated by Autophagy and Oxidative Stress. Cannabis and Cannabinoid Research, 6(3), 253–263. https://doi.org/10.1089/can.2020.0109

Licencia Creative Commons
Revista Bio Ciencias by Universidad Autónoma de Nayarit under Creative Commons Attribution-NonCommercial 3.0 Unported License.
Based on work of http://biociencias.uan.edu.mx/.
Further permits not covered by this licence can be found at http://editorial.uan.edu.mx/index.php/BIOCIENCIAS.