Immunomodulatory Effect of Petroleum Ether Extract and Ethyl Acetate Fraction of Bengkoang (Pachyrhizus erosus (L.) Urban) In Vitro
Abstract
Bengkoang (Pachyrhizus erosus (L.) Urban) contains phytosterol and the isoflavone daidzein, which are thought to have immunomodulatory activity. There have been no studies reporting on the immunomodulatory effects of bengkoang extract containing polar and semi-polar compounds, such as phytosterols and isoflavone-like compounds. The objective of this study was to evaluate the immunomodulatory effects of bengkoang extracts, including petroleum ether extract (PEE), methanol extract (ME), and the ethyl acetate fraction (EAF) of bengkoang, in vitro. The immunomodulatory effects of PEE, ME, and EAF of bengkoang were determined according to the phagocytic activity of macrophages based on phagocytosis of latex beads, lymphocyte proliferation, and detection of cytokine production of tumor necrosis factor-α (TNF-α) interleukin-6 (IL-6), and interleukin-10 (IL-10) levels. Results: The phagocytic index and phagocytic capacity of ME, PEE, and EAF of bengkoang on macrophage cells were significantly increased (p < 0.05), whereas lymphocyte proliferation was unchanged compared with the control (p > 0.05), and ME of bengkoang enhanced the levels of the cytokines TNF-α and IL-6. In contrast, PEE and EAF of bengkoang decreased TNF-α and IL-6 levels compared with the control group. All of the bengkoang extracts decrease the production of the anti-inflammatory cytokine IL-10. In conclusion, this study showed that PEE, ME, and EAF of bengkoang could increase the non-specific immune response (phagocytic activity) but had a lesser effect on the specific immune response (lymphocyte proliferation). The ME of bengkoang acts as an immunostimulant by increasing the levels of the inflammatory cytokines TNF-α and IL-6 and decreasing those of the anti-inflammatory cytokine IL-10.
References
Abbas, A.K., Lichtman, A.H., Pillai, S., 2018. Cellular and molecular immunology e-Book, Ninth, Elsevier, Philadelphia.
Aderem, A., Ulevitch, R.J., 2000. Toll-like receptors in the induction of the innate immune response. Immunol. Lett. 406, 782–787.
Bharanishankar, S., Vishnupriya, V., Ponnulakshmi, R., Gayathri, R., Madhan, K., Shyamaladevi, B., Selvaraj, J., 2019. Effects of beta-sitosterol on inflammatory cytokines in high-fat diet-fed type-2 diabetic rats. Drug Invent. Today. 12, 906–909.
Calpe-Berdiel, L., Escolà-Gil, J.C., Benítez, S., Bancells, C., González-Sastre, F., 2007. Palomer X, Blanco-Vaca F. Dietary phytosterols modulate T-helper immune response but do not induce apparent anti-inflammatory effects in a mouse model of acute, aseptic inflammation. Life Sci. 80, 1951–1956.
Champion, J.A., Walker, A., Mitragotri, S., 2008. Role of particle size in phagocytosis of polymeric microspheres. Pharm. Res. 25, 1815–1821.
Desjardins, M., Griffiths, G., 2003. Phagocytosis: Latex leads the way. Curr. Opin. Cell Biol. 15, 498–503.
Dwiecki, K., Neunert, G., Polewski, P., Polewski, K., 2009. Antioxidant activity of daidzein, a natural antioxidant, and its spectroscopic properties in organic solvents and phosphatidylcholine liposomes. J. Photochem. Photobiol. B, Biol. 96, 242–48.
El-gamal, Y.M., Elmasry, O.A., El-ghoneimy, D.H., 2011. Soliman IM. Immunomodulatory effects of food. Egypt J. Pediatr. Allergy Immunol. 9, 3–13.
Findlay, V.L., Munday, B.L., 2000. The immunomodulatory effects of levamisole on the nonspecific immune system of Atlantic salmon, Salmo salar L. J. Fish Dis. 23, 369–378.
Iyer, S.S., Cheng, G., 2012. Role of interleukin 10 transcriptional regulation in inflammation and autoimmune disease. Crit. Rev. Immunol. 32, 23–63.
Jantan, I., Ahmad, W., Bukhari, S.N.A., 2015. Plant-derived immunomodulators: An insight on their preclinical evaluation and clinical trials. Front. Plant Sci. 6, 1–18.
Jensch, B.E., Pressinotti, L.N., Borges, J.C.S., Da Silva, J.R.M.C., 2006. Characterization of macrophage phagocytosis of the tropical fish Prochilodus scrofa (Steindachner, 1881). Aquaculture. 251, 509–515.
Kaminogawa, S., Nanno, M., 2004. Modulation of immune functions by foods. Evid. Based Complement. Alternat. Med. 1, 241–50.
Kumalasari, I.D., Nishi, K., Harmayani, E., Raharjo, S., Sugahara, T., 2013. Effect of bengkoang (Pachyrhizus erosus) fiber extract on murine macrophage-like J774.1 cells and mouse peritoneal macrophages. J. Funct. Foods 5, 582–589.
Kumalasari, I.D., Nishi, K., Putra, A.B.N., Sugahara, T., 2014. Activation of macrophages stimulated by the Bengkoang fiber extract through toll-like receptor 4. Func. Food 5, 1403–1408.
Li, G.F., Liu, L.B., Tan, Y.L., Liu, L.Z., Deng, H.Z., Wan, H., Zhong, W.Z., Chen, S.J., 2011. In vitro effect of levamisole on the cell viability, phagocytosis and respiratory burst of Barbel chub (Squaliobarbus curriculus) macrophages. Aquac. Nutr. 17, e263–270.
Lukitaningsih, E., 2012. Phytosterol Content in Bengkoang (Pachyrhizus erosus). Pharmacon. 13, 47–54.
Lukitaningsih, E., Ulrike, H., 2014. Bioactive compounds in Bengkoang (Pachyrhizus erosus) as antioxidant and tyrosinase inhibiting agents. Indonesian. J. Pharm. 25, 68–75.
Maji, A.K., Mahapatra, S., Banerjee, D., 2014. In-vivo Immunomodulatory potential of standardized Pueraria Tuberosa extract and its isoflavonoids. Int. J. Pharm. Pharm. Sci. 6, 861–867.
Muralidharan, S., Mandrekar, P., 2013. Cellular stress response and innate immune signaling: Integrating pathways in host defense and inflammation. J. Leuko. Biol. 94, 1167–1184.
Noman, A.S.M., Hoque, M.A., Haque, M.M., Pervin, F., Karim, M.R., 2007. Food chemistry nutritional and anti-nutritional components in Pachyrhizus erosus L.Uber. Food Chem. 102, 1112–1118.
Nurrochmad, A., Ikawati, M., Sari, I.P., Murwanti, R., Nugroho, A.E., 2015. Immunomodulatory effects of ethanolic extract of Thyphonium flagelliforme (Lodd) blume in rats induced by cyclophosphamide. J. Evid. Based. Complementary Altern. Med. 20, 167–172.
Ray, A., Dittel, B.N., 2010. Isolation of mouse peritoneal cavity cells. J. Vis. Exp. 35, 9–11.
Schepetkin, I.A., Quinn, M.T., 2006. Botanical polysaccharides: Macrophage immunomodulation and therapeutic potential. Int. Immunopharmacol. 6, 317–33.
Sharma, A., Rangari, V., 2016. Immunomodulatory activity of methanol extract of Adansonia digitata L. Trop. J. Pharm. Res. 15,1923–1927.
Tsai, W.J., Chen, Y.C., Wu, M.H., Lin, L.C., Chuang. K.A., Chang, S.C., Kuo, Y.C., 2008. Seselin from Plumbago zeylanica inhibits phytohemagglutinin (PHA)-stimulated cell proliferation in human peripheral blood mononuclear cells. J. Ethnopharmacol. 119, 67–73.
Wahdaningsih, S., Wahyuono, S., Riyanto, S., Murwanti, R., 2018. Antioxidant activity of red dragon fruit peel (Hylocereus polyrhizus (F.A.C. weber) britton and rose) isolates using 2,2-diphenyl-1-picrylhydrazyl method. Asian J. Pharm. Clin. Res. 11, 124–128.
Woronzoff-Dashkoff, K.K., 2002. The Wright-Giemsa stain: Secrets revealed. Clin. Lab. Med. 22, 15–23.
Yang, Q., Yu, D., Zhang, Y., 2019. β-Sitosterol attenuates the intracranial aneurysm growth by suppressing TNF-α-mediated mechanism. Pharmacology. 104, 303–311.
Yum, M.K., Jung, M.Y., Cho, D., Kim, T.S., 2011. Suppression of dendritic cells’ maturation and functions by daidzein, a phytoestrogen. Toxicol. Appl. Pharmacol. 257, 174–181.