<i>Sphaeranthus indicus</i>: Traditional Wisdom to Modern Medicine—An Orally Active, Potent Cytokine Inhibitor for the Management of Inflammatory Disorders — Oak Academic Publishing
Research ArticleOpen AccessGoogle Scholar indexed
<i>Sphaeranthus indicus</i>: Traditional Wisdom to Modern Medicine—An Orally Active, Potent Cytokine Inhibitor for the Management of Inflammatory Disorders
Department of Herbal Development, Piramal Life Sciences India Limited, Mumbai, India
,
Department of Herbal Development, Piramal Life Sciences India Limited, Mumbai, India
,
Department of Herbal Development, Piramal Life Sciences India Limited, Mumbai, India
,
Department of Herbal Development, Piramal Life Sciences India Limited, Mumbai, India
,
Department of Herbal Development, Piramal Life Sciences India Limited, Mumbai, India
,
Department of Herbal Development, Piramal Life Sciences India Limited, Mumbai, India
,
Department of Herbal Development, Piramal Life Sciences India Limited, Mumbai, India
,
Department of Herbal Development, Piramal Life Sciences India Limited, Mumbai, India
,
Department of Herbal Development, Piramal Life Sciences India Limited, Mumbai, India
,
Department of Herbal Development, Piramal Life Sciences India Limited, Mumbai, India
,
Department of Herbal Development, Piramal Life Sciences India Limited, Mumbai, India
1 Department of Herbal Development, Piramal Life Sciences India Limited, Mumbai, India
2 Department of Herbal Development, Piramal Life Sciences India Limited, Mumbai, India
3 Department of Herbal Development, Piramal Life Sciences India Limited, Mumbai, India
4 Department of Herbal Development, Piramal Life Sciences India Limited, Mumbai, India
5 Department of Herbal Development, Piramal Life Sciences India Limited, Mumbai, India
6 Department of Herbal Development, Piramal Life Sciences India Limited, Mumbai, India
7 Department of Herbal Development, Piramal Life Sciences India Limited, Mumbai, India
8 Department of Herbal Development, Piramal Life Sciences India Limited, Mumbai, India
9 Department of Herbal Development, Piramal Life Sciences India Limited, Mumbai, India
10 Department of Herbal Development, Piramal Life Sciences India Limited, Mumbai, India
11 Department of Herbal Development, Piramal Life Sciences India Limited, Mumbai, India
Tumor necrosis factor (TNF- α ) is a key regulator of the inflammatory and tissue destruc-tive pathways in rheumatoid arthritis (RA). The clinical success of anti-TNF- α and an-ti-IL-17 biologics has validated the concept that cytokine blockade is beneficial in RA. However, as these drugs are parenterally administered, our efforts are directed at identifying a novel orally active TNF- α inhibitor with a therapeutic profile similar to that of biologics. Since plants are natural immunomodulators, we explored the immunomodulatory potential of Sphaeranthus indicus extract. In our studies, the extract dose-dependently inhibited the release of cytokines in stimulated human peripheral blood mononuclear cells (hPBMCs), and their spontaneous release in synovial cells derived from patients suffering from RA. TNF- α and IFN- γ induced release of p40 subunit of IL-12/ IL-23, and p19 subunit of IL-23 in differentiated THP-1 cells is potently blocked. The expression of endothelial cell adhesion molecules in TNF- α -stimulated HUVECs was also potently inhibited. The oral treatment significantly and dose-dependently reduced LPS-induced TNF- α and IL-1 β production in mice. Disease regression was seen in collagen-induced arthritis in DBA/1J mice, which was validated along with radiological and histopathological evaluation. Therefore, the extract of Sphaeranthus indicus could be used in the management of inflammatory conditions.
Feldmann, M. (2008) Many Cytokines Are Very Useful Therapeutic Targets in Disease. The Journal of Clinical Investigation, 118, 3533-3536. http://dx.doi.org/10.1172/JCI37346
Taylor, P.C. (2001) Anti-TNF Therapy for Rheumatoid Arthritis and Other Inflammatory Diseases. Molecular Biotechnology, 19, 153-168. http://dx.doi.org/10.1385/mb:19:2:153
Weinblatt, M.E., Keystone, E.C., Furst, D.E., Moreland, L.W., Weisman, M.H., Birbara, C.A. and Teoh, L.A. (2003) Adalimumab, a Fully Human Anti-Tumor Necrosis Factor α Monoclonal Antibody, for the Treatment of Rheumatoid Arthritis in Patients Taking Concomitant Methotrexate: The ARMADA Trial. Arthritis & Rheumatism, 48, 35-45. http://dx.doi.org/10.1002/art.10697
Uyemura, K., Yamamura, M., Fivenson, D.F., Modlin, R.L. and Nickoloff, B.J. (1993) The Cytokine Network in Lesional and Lesion-Free Psoriatic Skin Is Characterized by a T-Helper Type 1 Cell-Mediated Response. Journal of Investigative Dermatology, 101, 701-705. http://dx.doi.org/10.1111/1523-1747.ep12371679
Ettehadi, P., Greaves, M., Wallach, D., Aderka, D. and Camp, R. (1994) Elevated Tumour Necrosis Factor-Alpha (TNF-α) Biological Activity in Psoriatic Skin Lesions. Clinical & Experimental Immunology, 96, 146-151. http://dx.doi.org/10.1111/j.1365-2249.1994.tb06244.x
Mease, P.J., Goffe, B.S., Metz, J., Vander Stoep, A., Finck, B. and Burge, D.J. (2000) Etanercept in the Treatment of Psoriatic Arthritis and Psoriasis: A Randomised Trial. The Lancet, 356, 385-390. http://dx.doi.org/10.1016/S0140-6736(00)02530-7
Reich, K., Nestle, F.O., Papp, K., Ortonne, J.-P., Evans, R., Guzzo, C., Li, S., Dooley, L.T. and Griffiths, C.E. (2005) Infliximab Induction and Maintenance Therapy for Moderate-to-Severe Psoriasis: A Phase III, Multicentre, Double-Blind Trial. The Lancet, 366, 1367-1374. http://dx.doi.org/10.1016/S0140-6736(05)67566-6
Leonardi, C., Matheson, R., Zachariae, C., Cameron, G., Li, L., Edson-Heredia, E., Braun, D. and Banerjee, S. (2012) Anti-Interleukin-17 Monoclonal Antibody Ixekizumab in Chronic Plaque Psoriasis. New England Journal of Medicine, 366, 1190-1199. http://dx.doi.org/10.1056/NEJMoa1109997
Yeilding, N., Szapary, P., Brodmerkel, C., Benson, J., Plotnick, M., Zhou, H., Goyal, K., et al. (2011) Development of the IL-12/23 Antagonist Ustekinumab in Psoriasis: Past, Present, and Future Perspectives. Annals of the New York Academy of Sciences, 1222, 30-39. http://dx.doi.org/10.1111/j.1749-6632.2011.05963.x
Rohit, R., Mahendra, S., Richa, S., Kavitha, M. and Vikram, S.S. (2014) A Clinical Study on the effect of Punarnavadi churna, Singhanada guggulu in the management of Amavata (Rheumatoid Arthritis). International Journal of Ayurveda and Pharma Research, 2, 46-54.
Ramachandran, S. (2013) Review on S. indicus Linn. (Kottaikkarantai). Pharmacognosy Reviews, 7, 157-169. http://dx.doi.org/10.4103/0973-7847.120517
Chakrabarti, D., Suthar, A.S., Jayaraman, G., Muthuvelan, B., Sharma, S. and Padigaru, M. (2012) NPS31807, a Standardized Extract from Sphaeranthus indicus, Inhibits Inflammatory, Migratory and Proliferative Activity in Keratinocytes and Immune Cells. Pharmacology & Pharmacy, 3, 178-194. http://dx.doi.org/10.4236/pp.2012.32025
Jansky, L., Reymanova, P. and Kopecky, J. (2003) Dynamics of Cytokine Production in Human Peripheral Blood Mononuclear Cells Stimulated by LPS, or Infected by Borrelia. Physiological Research, 52, 593-598.
Brennan, F.M., Chantry, D., Jackson, A., Maini, R. and Feldmann, M. (1989) Inhibitory Effect of TNF Alpha Antibodies on Synovial Cell Interleukin-1 Production in Rheumatoid Arthritis. Lancet, 334, 244-247. http://dx.doi.org/10.1016/S0140-6736(89)90430-3
Kamata, M., Tada, Y., Tatsuta, A., Kawashima, T., Shibata, S., Mitsui, H., Asano, Y., Sugaya, M., Kadono, T., Kanda, N., Watanabe, S. and Sato, S. (2013) Ciclosporin A Inhibits Production of Interleukin-12/23p40 and Interleukin-23 by the Human Monocyte Cell Line, THP-1. Clinical and Experimental Dermatology, 38, 545-548. http://dx.doi.org/10.1111/ced.12110
Balachandran, S., Gadekar, P.K., Parkale, S., Yadav, V.N., Kamath, D., Ramaswamy, S., Sharma, S., Vishwakarma, R.A. and Dagia, N.M. (2011) Synthesis and Biological Activity of Novel MIF Antagonists. Bioorganic & Medicinal Chemistry Letters, 21, 1508-1511. http://dx.doi.org/10.1016/j.bmcl.2010.12.127
Béchard, D., Scherpereel, A., Hammad, H., Gentina, T., Tsicopoulos, A., Aumercier, M., Pestel, J., et al. (2001) Human Endothelial-Cell Specific Molecule-1 Binds Directly to the Integrin CD11a/CD18 (LFA-1) and Blocks Binding to Intercellular Adhesion Molecule-1. The Journal of Immunology, 167, 3099-3106. http://dx.doi.org/10.4049/jimmunol.167.6.3099
Kim, K., Choi, Y., Lee, N., Park, K., Kim, G., Park, J., Kim, B., Lim, Y., et al. (2011) 5-Hydroxymethylfurfural from Black Garlic Extract Prevents TNFα-Induced Monocytic Cell Adhesion to HUVECs by Suppression of Vascular Cell Adhesion Molecule-1 Expression, Reactive Oxygen Species Generation and NF-κB Activation. Phytotherapy Research, 25, 965-974. http://dx.doi.org/10.1002/ptr.3351
Moreira, L., Wang, J., Sarno, N. and Kaplan, G. (1997) Thalidomide Protects Mice against LPS-Induced Shock. Brazilian Journal of Medical and Biological Research, 10, 1199-1207. http://dx.doi.org/10.1590/s0100-879x1997001000010
Terato, K., Karen, H., Michael, C., John, S., Alexander, T. and Andrew, K. (1985) Collagen-Induced Arthritis in Mice. Localization of an Arthritogenic Determinant to a Fragment of the Type II Collagen Molecule. The Journal of Experimental Medicine, 162, 637-646. http://dx.doi.org/10.1084/jem.162.2.637
Papp, A., Langley, G., Lebwohl, M., Krueger, G., Szapary, P. and Yeilding, N. (2008) Efficacy and Safety of Ustekinumab, a Human Interleukin-12/23 Monoclonal Antibody, in Patients with Psoriasis: 52-Week Results from a Randomised, Double-Blind, Placebo-Controlled Trial (PHOENIX 2). Lancet, 371, 1675-1684. http://dx.doi.org/10.1016/S0140-6736(08)60726-6
Ding, C., Xu, J. and Li, J. (2008) ABT-874, a Fully Human Monoclonal Anti-IL-12/IL-23 Antibody for the Potential Treatment of Autoimmune Diseases. Current Opinion in Investigational Drugs, 9, 515-522.
Fukuda, T., Sumichika, H., Murata, M., Hanano, T., Adachi, K. and Hisadome, M. (2000) A Novel Dual Regulator of Tumour Necrosis Factor-α and Interleukin-10 Protects Mice from Endotoxin-Induced Shock. European Journal of Pharmacology, 391, 317-320. http://dx.doi.org/10.1016/S0014-2999(00)00096-0
Wooley, H., Luthra, S., Krco, J., Stuart, M. and David, S. (1984) Type II Collagen—Induced Arthritis in Mice. Arthritis & Rheumatism, 27, 1010-1017. http://dx.doi.org/10.1002/art.1780270907
Simmonds, R.E. and Foxwell, B.M. (2008) Signalling, Inflammation and Arthritis: NF-κB and Its Relevance to Arthritis and Inflammation. Rheumatology, 5, 584-590. http://dx.doi.org/10.1093/rheumatology/kem298
Klimiuk, P., Sierakowski, S., Latosiewicz, R., Cylwik, J., Cylwik, B., Skowronski, J. and Chwiecko, J. (2002) Soluble Adhesion Molecules (ICAM-1, VCAM-1, and E-Selectin) and Vascular Endothelial Growth Factor (VEGF) in Patients with Distinct Variants of Rheumatoid Synovitis. Annals of the Rheumatic Diseases, 9, 804-809. http://dx.doi.org/10.1136/ard.61.9.804
Van den Berg, B. and Miossec, P. (2009) IL-17 as a Future Therapeutic Target for Rheumatoid Arthritis. Nature Reviews Rheumatology, 10, 549-553. http://dx.doi.org/10.1038/nrrheum.2009.179