دورية أكاديمية

Therapeutic potential of alkaloids in autoimmune diseases: Promising candidates for clinical trials.

التفاصيل البيبلوغرافية
العنوان: Therapeutic potential of alkaloids in autoimmune diseases: Promising candidates for clinical trials.
المؤلفون: Khan H; Abdul Wali khan university Mardan, Abdul Wali khan university Mardan, Department of Pharmacy, Abdul Wali Khan university Mardan, Pakistan, Mardan, Pakistan, 23200, Pakistan., Ullah H; Department of Pharmacy, University of Naples Federico II, Naples, Italy., Khattak S; Abdul Wali khan university Mardan, Abdul Wali khan university Mardan, Department of Pharmacy, Abdul Wali Khan university Mardan, Pakistan, Mardan, Pakistan, 23200, Pakistan., Aschner M; Department of Molecular Pharmacology, Albert Einstein College of Medicine, New York, New York, USA., Aguilar CN; School of Chemistry, Universidad Autónoma de Coahuila Saltillo, Saltillo, Mexico., Halimi SMA; Department of Pharmacy, University of Peshawar, Peshawar, Pakistan., Cauli O; Department of Nursing, University of Valencia, Valencia, Spain., Shah SMM; Department of Pharmacy, University of Swabi Pakistan, Swabi, Pakistan.
المصدر: Phytotherapy research : PTR [Phytother Res] 2021 Jan; Vol. 35 (1), pp. 50-62. Date of Electronic Publication: 2020 Jul 15.
نوع المنشور: Journal Article; Review
اللغة: English
بيانات الدورية: Publisher: Wiley Country of Publication: England NLM ID: 8904486 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1099-1573 (Electronic) Linking ISSN: 0951418X NLM ISO Abbreviation: Phytother Res Subsets: MEDLINE
أسماء مطبوعة: Publication: : Chichester : Wiley
Original Publication: London : Heyden & Son, c1987-
مواضيع طبية MeSH: Alkaloids/*therapeutic use , Autoimmune Diseases/*drug therapy, Alkaloids/pharmacology ; Animals ; Humans
مستخلص: Clinical investigations have characterized numerous disorders like autoimmune diseases, affecting the population at a rate of approximately 8-10%. These disorders are characterized by T-cell and auto-antibodies responses to self-molecules by immune system reactivity. Several therapeutic options have been adopted in clinics to combat such diseases, however, most of them are recurring. Thus, the discovery of new effective agents for the treatment of autoimmune diseases is paramount. In this context, natural products might be a useful alternative to the current therapies. Plant alkaloids with their substantial therapeutic history can be particularly interesting candidates for the alleviation of autoimmune ailments. This review encompasses various alkaloids with significant effects against autoimmune diseases in preclinical trials. These results suggest further clinical assessment with respect to autoimmune illnesses. Furthermore, the application of modern technologies such as nanoformulation could be also helpful in the design of more effective therapies and thus further studies are needed to decipher their therapeutic efficacy as well as potential limitations.
(© 2020 John Wiley & Sons, Ltd.)
References: Abdollahi, E., Momtazi, A. A., Johnston, T. P., & Sahebkar, A. (2018). Therapeutic effects of curcumin in inflammatory and immune-mediated diseases: A nature-made jack-of-all-trades? Journal of Cellular Physiology, 233, 830-848.
Ain, Q., Khan, H., Mubarak, M., & Pervaiz, A. (2016). Plant alkaloids as antiplatelet agent: Drugs of future in the light of recent development. Frontiers in Pharmacology, 7, 292.
Amirkia, V., & Heinrich, M. (2014). Alkaloids as drug leads - A predictive structural and biodiversity-based analysis. Phytochemistry Letters, 10, xlviii-liii.
Anderson, R. P., & Jabri, B. (2013). Vaccine against autoimmune disease: Antigen-specific immunotherapy. Current Opinion in Immunology, 25, 410-417.
Ayuso, C., Pagés, M., & Donoso, L. (2017). Imaging techniques in digestive diseases. In Handbook of systemic autoimmune diseases (Vol. 13, pp. 67-80). Amsterdam, Netherlands: Elsevier.
Azizi, G., Pouyani, M. R., Abolhassani, H., Sharifi, L., Zaki dizaji, M., Mohammadi, J., … Aghamohammadi, A. (2016). Cellular and molecular mechanisms of immune dysregulation and autoimmunity. Cellular Immunology, 310, 14-26.
Baccala, R., Hoebe, K., Kono, D. H., Beutler, B., & Theofilopoulos, A. N. (2007). TLR-dependent and TLR-independent pathways of type I interferon induction in systemic autoimmunity. Nature Medicine, 13, 543-551.
Bent, S. (2008). Herbal medicine in the United States: Review of efficacy, safety, and regulation. Journal of General Internal Medicine, 23, 854-859.
Betancourt, B. Y., Biehl, A., Katz, J. D., & Subedi, A. (2018). Pharmacotherapy pearls in rheumatology for the care of older adult patients: Focus on oral disease-modifying antirheumatic drugs and the newest small molecule inhibitors. Rheumatic Disease Clinics of North America, 44, 371-391.
Bettelli, E., Korn, T., Oukka, M., & Kuchroo, V. K. (2008). Induction and effector functions of T^ sub H^ 17 cells. Nature, 453, 1051-1057.
Brčić Karačonji, I. (2005). Facts about nicotine toxicity. Arhiv Za Higijenu Rada i Toksikologiju, 56, 363-371.
Canivet, C., Rostaing, L., Galvani, S., Böhler, T., Gandia, P., Mengelle, C., … Kamar, N. (2009). Polyoma BK virus-associated nephropathy in kidney-transplant patients: Effects of leflunomide on T-cell functions and disease outcome. International Immunopharmacology, 9, 1131-1136.
Cassim, S., Bilodeau, M., Vincent, C., & Lapierre, P. (2017). Novel immunotherapies for autoimmune hepatitis. Frontiers in Pediatrics, 5. https://doi.org/10.3389/fped.2017.00008.
Chang, C. (2014). Unmet needs in the treatment of autoimmunity: From aspirin to stem cells. Autoimmunity Reviews, 13, 331-346.
Chen, I.-S., Chen, H.-F., Cheng, M.-J., Chang, Y.-L., Teng, C.-M., Tsutomu, I., … Tsai, I.-L. (2001). Quinoline alkaloids and other constituents of Melicope semecarpifolia with antiplatelet aggregation activity. Journal of Natural Products, 64, 1143-1147.
Cui, G., Qin, X., Zhang, Y., Gong, Z., Ge, B., & Zang, Y. Q. (2009). Berberine differentially modulates the activities of Erk, p38 MAPK and JNK to suppress Th17 and Th1 T cell differentiation in type 1 diabetic mice. Journal of Biological Chemistry, M109, 012674.
de Körverstraat, W., 2002. Scientific Discussion.
DeBerardinis, R. J., & Thompson, C. B. (2012). Cellular metabolism and disease: What do metabolic outliers teach us? Cell, 148, 1132-1144.
Deng, Y., Huang, X., Wu, H., Zhao, M., Lu, Q., Israeli, E., … Shoenfeld, Y. (2016). Some like it hot: The emerging role of spicy food (capsaicin) in autoimmune diseases. Autoimmunity Reviews, 15, 451-456.
Dey, A., Bhattacharya, R., Mukherjee, A., & Pandey, D. K. (2017). Natural products against Alzheimer's disease: Pharmaco-therapeutics and biotechnological interventions. Biotechnology Advances, 35, 178-216.
Dolati, S., Sadreddini, S., Rostamzadeh, D., Ahmadi, M., Jadidi-Niaragh, F., & Yousefi, M. (2016). Utilization of nanoparticle technology in rheumatoid arthritis treatment. Biomedicine and Pharmacotherapy, 80, 30-41.
Doumtsis, P., Oikonomou, T., Goulis, I., Zachou, K., Dalekos, G., & Cholongitas, E. (2018). Type 1 autoimmune hepatitis presenting with severe autoimmune neutropenia. Annals of Gastroenterology, 31, 123-126.
Efthimiou, P., & Kukar, M. (2010). Complementary and alternative medicine use in rheumatoid arthritis: Proposed mechanism of action and efficacy of commonly used modalities. Rheumatology International, 30, 571-586.
Emery, P., Keystone, E., Tony, H., Cantagrel, A., Van Vollenhoven, R., Sanchez, A., … Kremer, J. (2008). IL-6 receptor inhibition with tocilizumab improves treatment outcomes in patients with rheumatoid arthritis refractory to anti-tumor necrosis factor biologicals: Results from a 24-week multicentre randomized placebo-controlled trial. Annals of the Rheumatic Diseases, 67, 1516-1523.
Encinas, J. A., & Kuchroo, V. K. (2000). Mapping and identification of autoimmunity genes. Current Opinion in Immunology, 12, 691-697.
Fan, X.-X., Pan, H.-D., Li, Y., Guo, R.-J., Leung, E. L.-H., & Liu, L. (2018). Novel therapeutic strategy for cancer and autoimmune conditions: Modulating cell metabolism and redox capacity. Pharmacology and Therapeutics, 191, 148-161.
Farinon, M., Clarimundo, V. S., Pedrazza, G. P., Gulko, P. S., Zuanazzi, J. A., Xavier, R. M., & de Oliveira, P. G. (2017). Disease modifying anti-rheumatic activity of the alkaloid montanine on experimental arthritis and fibroblast-like synoviocytes. European Journal of Pharmacology, 799, 180-187.
Farzaei, M. H., Farzaei, F., Abdollahi, M., Abbasabadi, Z., Abdolghaffari, A. H., & Mehraban, B. (2016). A mechanistic review on medicinal plants used for rheumatoid arthritis in traditional Persian medicine. Journal of Pharmacy and Pharmacology, 68, 1233-1248.
Fedi, P., Kimmelman, A., Aaronson, S.A., 2000. Growth factor signal transduction in cancer, NY: BC Decker Inc. https://www.ncbi.nlm.nih.gov/books/NBK20941/.
Filippini, P., Cesario, A., Fini, M., Locatelli, F., & Rutella, S. (2012). The Yin and Yang of non-neuronal α7-nicotinic receptors in inflammation and autoimmunity. Current Drug Targets, 13, 644-655.
Filler, G., Hansen, M., LeBlanc, C., Lepage, N., Franke, D., Mai, I., & Feber, J. (2003). Pharmacokinetics of mycophenolate mofetil for autoimmune disease in children. Pediatric Nephrology, 18, 445-449.
Fontana, A. C. (2015). Current approaches to enhance glutamate transporter function and expression. Journal of Neurochemistry, 134, 982-1007.
Fox, D. A. (1997). The role of T cells in the immunopathogenesis of rheumatoid arthritis. New perspectives. Arthritis and Rheumatism, 40, 598-609.
Fox, D. A., Gizinski, A., Morgan, R., & Lundy, S. K. (2010). Cell-cell interactions in rheumatoid arthritis Synovium. Rheumatic Diseases Clinics of North America, 36, 311-323.
Friedman, M. A., & Winthrop, K. L. (2017). Vaccines and disease-modifying antirheumatic drugs: Practical implications for the rheumatologist. Rheumatic Disease Clinics of North America, 43, 1-13.
Furst, D. E. (1995). Cyclosporin, leflunomide and nitrogen mustard. Baillière's Clinical Rheumatology, 9, 711-729.
Gabrilovich, D. I., & Nagaraj, S. (2009). Myeloid-derived-suppressor cells as regulators of the immune system. Nature Reviews Immunology, 9, 162-174.
Gebhardt, C., von Bohlen und Halbach, O., Hadler, M. D., Harteneck, C., & Albrecht, D. (2016). A novel form of capsaicin-modified amygdala LTD mediated by TRPM1. Neurobiology of Learning and Memory, 136, 1-12.
Geissmann, F., Manz, M. G., Jung, S., Sieweke, M. H., Merad, M., & Ley, K. (2010). Development of monocytes, macrophages, and dendritic cells. Science, 327, 656-661.
Grainger, J. D., Bolton-Maggs, P. H., Godeau, B., Bussel, J., Donato, H., Elalfy, M., … Rovó, A. (2010). Diagnosis and management of chronic ITP: Comments from an ICIS expert group. Annals of Hematology, 89, 11-17.
Greven, D., Leng, L., & Bucala, R. (2010). Autoimmune diseases: MIF as a therapeutic target. Expert Opinion on Therapeutic Targets, 14, 253-264.
Grynkiewicz, G., & Gadzikowska, M. (2008). Tropane alkaloids as medicinally useful natural products and their synthetic derivatives as new drugs. Pharmacological Reports, 60, 439-463.
Gupta, S. C., Sundaram, C., Reuter, S., & Aggarwal, B. B. (2010). Inhibiting NF-κB activation by small molecules as a therapeutic strategy. Biochimica et Biophysica Acta (BBA)-Gene Regulatory Mechanisms, 1799, 775-787.
Halevy, O., Nagler, A., Levi-Schaffer, F., Genina, O., & Pines, M. (1996). Inhibition of collagen type I synthesis by skin fibroblasts of graft versus host disease and scleroderma patients: Effect of halofuginone. Biochemical Pharmacology, 52, 1057-1063.
Han, G., Shao, H., Peng, Y., Zhang, P., Ke, Y., Kaplan, H. J., & Sun, D. (2007). Suppressor role of rat CD8+ CD45RC low T cells in experimental autoimmune uveitis (EAU). Journal of Neuroimmunology, 183, 81-88.
Hartwell, B. L., Pickens, C. J., Leon, M., Northrup, L., Christopher, M. A., Griffin, J. D., … Berkland, C. (2018). Soluble antigen arrays disarm antigen-specific B cells to promote lasting immune tolerance in experimental autoimmune encephalomyelitis. Journal of Autoimmunity, 93, 76-88.
Henderson, J., Bhattacharyya, S., Varga, J., & O'Reilly, S. (2018). Targeting TLRs and the inflammasome in systemic sclerosis. Pharmacology and Therapeutics, 192, 163-169.
Herrmann, M. L., Schleyerbach, R., & Kirschbaum, B. J. (2000). Leflunomide: An immunomodulatory drug for the treatment of rheumatoid arthritis and other autoimmune diseases. Immunopharmacology, 47, 273-289.
Hirsch, D. L., & Ponda, P. (2015). Antigen-based immunotherapy for autoimmune disease: Current status. Immunotargets and Therapy, 4, 1-11.
Hitchon, C. A., & El-Gabalawy, H. S. (2011). The Synovium in rheumatoid arthritis. The Open Rheumatology Journal, 5, 107-114.
Hunter, Z., McCarthy, D. P., Yap, W. T., Harp, C. T., Getts, D. R., Shea, L. D., & Miller, S. D. (2014). A biodegradable nanoparticle platform for the induction of antigen-specific immune tolerance for treatment of autoimmune disease. ACS Nano, 8, 2148-2160.
Javadi, B., & Sahebkar, A. (2017). Natural products with anti-inflammatory and immunomodulatory activities against autoimmune myocarditis. Pharmacological Research, 124, 34-42.
Jenn-Haung, L. (2002). Immunomodulatory effects and mechanisms of plant alkaloid tetrandrine in autoimmune diseases. Acta Pharmacologica Sinica, 23, 1093-1101.
Jin, H., Li, L., Zhong, D., Liu, J., Chen, X., & Zheng, J. (2011). Pulmonary toxicity and metabolic activation of tetrandrine in CD-1 mice. Chemical Research in Toxicology, 24, 2142-2152.
Jindal, A., Rao, R., & Bhogal, B. S. (2017). Advanced diagnostic techniques in autoimmune Bullous diseases. Indian Journal of Dermatology, 62, 268-278.
Kaleem, W. A., Muhammad, N., Qayum, M., Khan, H., Khan, A., Aliberti, L., & De Feo, V. (2013). Antinociceptive activity of cyclopeptide alkaloids isolated from Ziziphus oxyphylla Edgew (Rhamnaceae). Fitoterapia, 91, 154-158.
Khan, H. (2015). Alkaloids: Potential therapeuty modality in the management of asthma. Journal of Ayurvedic and Herbal Medicine, 1, 3-3.
Khan, H., Patel, S., & Kamal, M. (2017). Pharmacological and toxicological profile of harmane-β-Carboline alkaloid: Friend or foe. Current Drug Metabolism, 18, 853-857.
Khan, H., Sureda, A., Belwal, T., Çetinkaya, S., Süntar, İ., Tejada, S., … Aschner, M. (2019). Polyphenols in the treatment of autoimmune diseases. Autoimmunity Reviews., 18, 647-657.
Khan, H., Ullah, H., Martorell, M., Valdes, S. E., Belwal, T., Tejada, S., … Kamal, M. A. (2019). Flavonoids nanoparticles in cancer: Treatment, prevention and clinical prospects. seminars in cancer biology.
Khan, H., Ullah, H., & Nabavi, S. M. (2019). Mechanistic insights of hepatoprotective effects of curcumin: Therapeutic updates and future prospects. Food and Chemical Toxicology, 124, 182-191.
Khattak, S., & Khan, H. (2016). Anti-cancer potential of phyto-alkaloids: A prospective review. Current Cancer Therapy Reviews, 12, 66-75.
Klingel, R., Heibges, A., & Fassbender, C. (2009). Plasma exchange and immunoadsorption for autoimmune neurologic diseases-current guidelines and future perspectives. Atherosclerosis Supplements, 10, 129-132.
Kontos, S., Grimm, A. J., & Hubbell, J. A. (2015). Engineering antigen-specific immunological tolerance. Current Opinion in Immunology, 35, 80-88.
Kreiner, E., Waage, J., Standl, M., Brix, S., Pers, T. H., Alves, A. C., … Franke, L. (2017). Shared genetic variants suggest common pathways in allergy and autoimmune diseases. Journal of Allergy and Clinical Immunology, 140, 771-781.
Lambert, J.-F., & Nydegger, U. E. (2010). Geoepidemiology of autoimmune hemolytic anemia. Autoimmunity Reviews, 9, A350-A354.
Lee, D.-U., Kang, Y. J., Park, M. K., Lee, Y. S., Seo, H. G., Kim, T. S., … Chang, K. C. (2003). Effects of 13-alkyl-substituted berberine alkaloids on the expression of COX-II, TNF-α, iNOS, and IL-12 production in LPS-stimulated macrophages. Life Sciences, 73, 1401-1412.
Lee, S. T., Welch, K. D., Panter, K. E., Gardner, D. R., Garrossian, M., & Chang, C.-W. T. (2014). Cyclopamine: From cyclops lambs to cancer treatment. Journal of Agricultural and Food Chemistry, 62, 7355-7362.
Levy, D. T., Cummings, K. M., Villanti, A. C., Niaura, R., Abrams, D. B., Fong, G. T., & Borland, R. (2017). A framework for evaluating the public health impact of e-cigarettes and other vaporized nicotine products. Addiction, 112, 8-17.
Li, H., Li, X. L., Zhang, M., Xu, H., Wang, C., Wang, S., & Duan, R. (2014). Berberine ameliorates experimental autoimmune neuritis by suppressing both cellular and humoral immunity. Scandinavian Journal of Immunology, 79, 12-19.
Li, M., Chen, X., Liu, J., Wang, D., Gan, L., Lv, X., & Qiao, Y. (2016). Treatment of experimental autoimmune uveoretinitis with different natural compounds. Molecular Medicine Reports, 13, 4654-4658.
Li, R. W., Lin, G. D., Myers, S. P., & Leach, D. N. (2003). Anti-inflammatory activity of Chinese medicinal vine plants. Journal of Ethnopharmacology, 85, 61-67.
Li, Y., Sattler, R., Yang, E. J., Nunes, A., Ayukawa, Y., Akhtar, S., … Rothstein, J. D. (2011). Harmine, a natural beta-carboline alkaloid, Upregulates astroglial glutamate transporter expression. Neuropharmacology, 60, 1168-1175.
Ling-Jun, H., Deh-Ming, C., Ta-Chung, L., Mu-Lan, C., & Jenn-Haung, L. (1999). Plant alkaloid tetrandrine downregulates protein kinase C-dependent signaling pathway in T cells. European Journal of Pharmacology, 367, 389-398.
Ling-Jun, H., & Jenn-Haung, L. (2004). Chinese herbs as immunomodulators and potential disease-modifying antirheumatic drugs in autoimmune disorders. Current Drug Metabolism, 5, 181-192.
Liu, J., Zhang, X., Xue, D., Jiang, Z., Gu, Q., & Chen, J. (2006). Studies on chemical constituents from leaves of Isatis indigotica. Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China Journal of Chinese Materia Medica, 31, 1961-1965.
Liu, L., Resch, K., & Kaever, V. (1994). Inhibition of lymphocyte proliferation by the anti-arthritic drug sinomenine. International Journal of Immunopharmacology, 16, 685-691.
Liu, M., Su, X., Li, G., Zhao, G., & Zhao, L. (2015). Validated UPLC-MS/MS method for simultaneous determination of simvastatin, simvastatin hydroxy acid and berberine in rat plasma: Application to the drug-drug pharmacokinetic interaction study of simvastatin combined with berberine after oral administration in rats. Journal of Chromatography B, 1006, 8-15.
Liu, Q.-F., Shi, X.-J., Li, Z.-D., Zhong, M.-k., Jiao, Z., & Wang, B. (2014). Pharmacokinetic comparisons of berberine and palmatine in normal and metabolic syndrome rats. Journal of Ethnopharmacology, 151, 287-291.
Luo, S., Wang, Y., Zhao, M., & Lu, Q. (2016). The important roles of type I interferon and interferon-inducible genes in systemic lupus erythematosus. International Immunopharmacology, 40, 542-549.
Luo, Y., Liu, M., Xia, Y., Dai, Y., Chou, G., & Wang, Z. (2010). Therapeutic effect of norisoboldine, an alkaloid isolated from Radix Linderae, on collagen-induced arthritis in mice. Phytomedicine, 17, 726-731.
Maecker, H. T., Nolan, G. P., & Fathman, C. G. (2010). New technologies for autoimmune disease monitoring. Current Opinion in Endocrinology, Diabetes, and Obesity, 17, 322-328.
Mahler, M., Hanly, J. G., & Fritzler, M. J. (2012). Importance of the dense fine speckled pattern on HEp-2 cells and anti-DFS70 antibodies for the diagnosis of systemic autoimmune diseases. Autoimmunity Reviews, 11, 642-645.
Maini, R., Taylor, P., Szechinski, J., Pavelka, K., Bröll, J., Balint, G., … Smolen, J. (2006). Double-blind randomized controlled clinical trial of the interleukin-6 receptor antagonist, tocilizumab, in European patients with rheumatoid arthritis who had an incomplete response to methotrexate. Arthritis and Rheumatology, 54, 2817-2829.
Malik, K. (2018). Antitumor necrosis factor-α drugs and disease-modifying antirheumatic drugs for low back pain. In H. T. Benzon, S. N. Raja, S. S. Liu, S. M. Fishman, & S. P. Cohen (Eds.), Essentials of pain medicine (4th ed., 585-590.e581Canada: ). Elsevier. Chapter 64.
Mao, H., Yang, W., Latour, S., Yang, J., Winter, S., Zheng, J., … Lau, Y.-L. (2018). RASGRP1 mutation in autoimmune lymphoproliferative syndrome-like disease. Journal of Allergy and Clinical Immunology, 142, 595-604.e516.
Marya, & Khan, H. (2017). Anti-inflammatory potential of alkaloids as a promising therapeutic modality. Letters in Drug Design and Discovery, 14, 240-249.
McInnes, I. B., & Schett, G. (2011). The pathogenesis of rheumatoid arthritis. New England Journal of Medicine, 365, 2205-2219.
Mehta, P., Shah, R., Lohidasan, S., & Mahadik, K. R. (2015). Pharmacokinetic profile of phytoconstituent(s) isolated from medicinal plants-A comprehensive review. Journal of Traditional and Complementary Medicine, 5, 207-227.
Moudi, M., Go, R., Yien, C. Y. S., & Nazre, M. (2013). Vinca alkaloids. International Journal of Preventive Medicine, 4, 1231.
Navarro, G., Taroumian, S., Barroso, N., Duan, L., Furst, D., 2014. Tocilizumab in rheumatoid arthritis: A meta-analysis of efficacy and selected clinical conundrums, seminars in arthritis and rheumatism. Elsevier, pp. 458-469.
O'Donovan, S. M., Sullivan, C. R., & McCullumsmith, R. E. (2017). The role of glutamate transporters in the pathophysiology of neuropsychiatric disorders. NPJ Schizophrenia, 3, 32.
Paris, D., Beaulieu-Abdelahad, D., Mullan, M., Ait-Ghezala, G., Mathura, V., Bachmeier, C., … Mullan, M. J. (2013). Amelioration of experimental autoimmune encephalomyelitis by Anatabine. PLoS One, 8, e55392.
Park, G., Kim, S. Y., & Song, Y.-J. (2017). Ester alkaloids from Cephalotaxus interfere with the 2′3′-cGAMP-induced type I interferon pathway in vitro. PLoS One, 12, e0182701.
Paterna, A., Gomes, S. E., Borralho, P. M., Mulhovo, S., Rodrigues, C. M., & Ferreira, M.-J. U. (2016). Vobasinyl-Iboga alkaloids from Tabernaemontana elegans: Cell cycle arrest and apoptosis-inducing activity in HCT116 colon cancer cells. Journal of Natural Products, 79, 2624-2634.
Pervaiz, A., Khan, R., Anwar, F., Kamal, M. A., Mushtaq, G., & Khan, H. (2016). Alkaloids: An emerging antibacterial modality against methicillin resistant Staphylococcus aureus. Current Pharmaceutical Design, 22, 4420-4429.
Pervez, S., Khan, H., & Pervaiz, A. (2016). Plant alkaloids as an emerging therapeutic alternative for the treatment of depression. Frontiers in Pharmacology, 7, 28.
Petersen, F., Yue, X., Riemekasten, G., & Yu, X. (2017). Dysregulated homeostasis of target tissues or autoantigens - a novel principle in autoimmunity. Autoimmunity Reviews, 16, 602-611.
Pietra, D., Borghini, A., & Bianucci, A. M. (2015). In vitro studies of antifibrotic and cytoprotective effects elicited by proto-berberine alkaloids in human dermal fibroblasts. Pharmacological Reports, 67, 1081-1089.
Qiu, S., Sun, H., Zhang, A.-H., Xu, H.-Y., Yan, G.-L., Han, Y., & Wang, X.-J. (2014). Natural alkaloids: Basic aspects, biological roles, and future perspectives. Chinese Journal of Natural Medicines, 12, 401-406.
Rasmussen, A., Radfar, L., Lewis, D., Grundahl, K., Stone, D. U., Kaufman, C. E., … Weisman, M. H. (2016). Previous diagnosis of Sjögren's syndrome as rheumatoid arthritis or systemic lupus erythematosus. Rheumatology, 55, 1195-1201.
Rehman, S., & Khan, H. (2016). Advances in antioxidant potential of natural alkaloids. Current Bioactive Compounds, 13, 101-108.
Saint-Marcoux, F., Guigonis, V., Decramer, S., Gandia, P., Ranchin, B., Parant, F., … Marquet, P. (2011). Development of a Bayesian estimator for the therapeutic drug monitoring of mycophenolate mofetil in children with idiopathic nephrotic syndrome. Pharmacological Research, 63, 423-431.
Schmitz, K., Barthelmes, J., Stolz, L., Beyer, S., Diehl, O., & Tegeder, I. (2015). “Disease modifying nutricals” for multiple sclerosis. Pharmacology & Therapeutics, 148, 85-113.
Seifried, H. E., Anderson, D. E., Fisher, E. I., & Milner, J. A. (2007). A review of the interaction among dietary antioxidants and reactive oxygen species. The Journal of Nutritional Biochemistry, 18, 567-579.
Shakya, A. K., & Nandakumar, K. S. (2018). Antigen-specific tolerization and targeted delivery as therapeutic strategies for autoimmune diseases. Trends in Biotechnology, 36, 686-699.
Shi, J.-P., Li, S.-X., Ma, Z.-L., Gao, A.-L., Song, Y.-J., & Zhang, H. (2016). Acute and sub-chronic toxicity of tetrandrine in intravenously exposed female BALB/c mice. Chinese Journal of Integrative Medicine, 22, 925-931.
Sikorska, A., Slomkowski, M., Lanka, K. M., Konopka, L., & Górski, T. (2004). The use of vinca alkaloids in adult patients with refractory chronic idiopathic thrombocytopenia. Clinical & Laboratory Hematology, 26, 407-411.
Singh, R. P., Waldron, R. T., & Hahn, B. H. (2012). Genes, tolerance and systemic autoimmunity. Autoimmunity Reviews, 11, 664-669.
Song, J., Bi, H., Xie, X., Guo, J., Wang, X., & Liu, D. (2013). Preparation and evaluation of sinomenine hydrochloride in situ gel for uveitis treatment. International Immunopharmacology, 17, 99-107.
Stephen, H., Thompson, G., & Staines, N. A. (1990). Could specific oral tolerance be a therapy for autoimmune disease? Immunology Today, 11, 396-399.
Stummvoll, G., Aringer, M., Handisurya, A., & Derfler, K. (2017). Immunoadsorption in autoimmune diseases affecting the kidney. Seminars in Nephrology, 37, 478-487.
Sun, D., Zhuang, X., Xiang, X., Liu, Y., Zhang, S., Liu, C., … Zhang, H.-G. (2010). A novel nanoparticle drug delivery system: The anti-inflammatory activity of curcumin is enhanced when encapsulated in exosomes. Molecular Therapy, 18, 1606-1614.
Szentpétery, Á., Horváth, Á., Gulyás, K., Pethö, Z., Bhattoa, H. P., Szántó, S., … Szekanecz, Z. (2017). Effects of targeted therapies on the bone in arthritides. Autoimmunity Reviews, 16, 313-320.
Tong, B., Dou, Y., Wang, T., Yu, J., Wu, X., Lu, Q., … Xia, Y. (2015). Norisoboldine ameliorates collagen-induced arthritis through regulating the balance between Th17 and regulatory T cells in gut-associated lymphoid tissues. Toxicology and Applied Pharmacology, 282, 90-99.
Turvey, S. E., & Broide, D. H. (2010). Innate immunity. Journal of Allergy and Clinical Immunology, 125, S24-S32.
Vistica, B. P., Shi, G., Nugent, L., Tan, C., Altman, A., & Gery, I. (2012). SLAT/Def6 plays a critical role in the pathogenic process of experimental autoimmune uveitis (EAU). Molecular Vision, 18, 1858-1864.
Vivier, E., Tomasello, E., Baratin, M., Walzer, T., & Ugolini, S. (2008). Functions of natural killer cells. Nature Immunology, 9, 503-510.
Wagner, J., von Matt, P., Faller, B., Cooke, N. G., Albert, R., Sedrani, R., … Cottens, S. (2011). Structure-activity relationship and pharmacokinetic studies of sotrastaurin (AEB071), a promising novel medicine for prevention of graft rejection and treatment of psoriasis. Journal of Medicinal Chemistry, 54, 6028-6039.
Wahren-Herlenius, M., & Dörner, T. (2013). Immunopathogenic mechanisms of systemic autoimmune disease. The Lancet, 382, 819-831.
Wang, C., Dai, Y., Yang, J., Chou, G., Wang, C., & Wang, Z. (2007). Treatment with total alkaloids from radix Linderae reduces inflammation and joint destruction in type II collagen-induced model for rheumatoid arthritis. Journal of Ethnopharmacology, 111, 322-328.
Wang, W., Shen, Q., Liang, H., Hua, C., Liu, Y., Li, F., & Li, Q. (2016). Pharmacokinetic studies of novel berberine derivatives with ultra-performance liquid chromatography-tandem mass spectrometry. Journal of Chromatography B, 1031, 172-180.
Wang, Z., Jiang, W., Zhang, Z., Qian, M., & Dua, B. (2012). Nitidine chloride inhibits LPS-induced inflammatory cytokines production via MAPK and NF-kappaB pathway in RAW 264.7 cells. Journal of Ethnopharmacology, 144, 145-150.
Wang, Z., Yang, Z., Zhang, L., Wang, X., Peng, C., Meng, D., & Yan, D. (2017). Toxic effects of vinca alkaloids from Catharanthus roseus (L.) G. Don on Tetrahymena thermophila BF5 growth by microcalorimetry. Thermochimica Acta, 651, 53-57.
Watson, J. D. (2014). Type 2 diabetes as a redox disease. The Lancet, 383, 841-843.
Willemsen, M., & Schouten, H. C. (2017). Inappropriate costimulation and aberrant DNA methylation as therapeutic targets in angioimmunoblastic T-cell lymphoma. Biomarker Research, 5, 6.
Wraith, D. C., Goldman, M., & Lambert, P.-H. (2003). Vaccination and autoimmune disease: What is the evidence? The Lancet, 362, 1659-1666.
Wu, H., Liao, J., Li, Q., Yang, M., Zhao, M., & Lu, Q. (2018). Epigenetics as biomarkers in autoimmune diseases. Clinical Immunology, 196, 34-39.
Wu, X., Liu, Y., Sheng, W., Sun, J., & Qin, G. (1997). Chemical constituents of Isatis indigotica. Planta Medica, 63, 55-57.
Wu, Y.-J., Wang, C., & Wei, W. (2018). The effects of DMARDs on the expression and function of P-gp, MRPs, BCRP in the treatment of autoimmune diseases. Biomedicine and Pharmacotherapy, 105, 870-878.
Yadav, U. C., Shoeb, M., Srivastava, S. K., & Ramana, K. V. (2011). Aldose reductase deficiency protects from autoimmune-and endotoxin-induced uveitis in mice. Investigative Ophthalmology and Visual Science, 52, 8076-8085.
Yan, Z.-R., Wang, Z.-Y., Wang, B., Zhu, P.-F., Wei, X., Yu, H.-F., … Luo, X.-D. (2018). Immune-inhibitive phenyl-C1 substituent aporphine alkaloids from Thalictrum cirrhosum. Fitoterapia, 128, 247-252.
Yang, L., & Stöckigt, J. (2010). Trends for diverse production strategies of plant medicinal alkaloids. Natural Product Reports, 27, 1469-1479.
Yin, W., Deng, X.-K., Yin, F.-Z., Zhang, X.-C., & Cai, B.-C. (2007). The cytotoxicity induced by brucine from the seed of Strychnos nux-vomica proceeds via apoptosis and is mediated by cyclooxygenase 2 and caspase 3 in SMMC 7221 cells. Food and Chemical Toxicology, 45, 1700-1708.
Yuan, X., Tong, B., Dou, Y., Wu, X., Wei, Z., & Dai, Y. (2016). Tetrandrine ameliorates collagen-induced arthritis in mice by restoring the balance between Th17 and Treg cells via the aryl hydrocarbon receptor. Biochemical Pharmacology, 101, 87-99.
Zafar, M., Khan, H., Rauf, A., Khan, A., & Lodhi, M. A. (2016). In silico study of alkaloids as α-glucosidase inhibitors: Hope for the discovery of effective lead compounds. Frontiers in Endocrinology, 7.153-161.
Zhang, M., Wang, Y., Sun, X., Ren, L., Zhang, L., & Lu, H. (2016). Effects of 10-hydroxycamptothecin on differentiation of RAW264. 7 cells into osteoclasts. Journal of Biological Regulators and Homeostatic Agents, 30, 789-794.
Zhang, Y., Yang, S.-H., & Guo, X.-L. (2017). New insights into Vinca alkaloids resistance mechanism and circumvention in lung cancer. Biomedicine and Pharmacotherapy, 96, 659-666.
Zhou, H., Wong, Y. F., Wang, J., Cai, X., & Liu, L. (2008). Sinomenine ameliorates arthritis via MMPs, TIMPs, and cytokines in rats. Biochemical and Biophysical Research Communications, 376, 352-357.
Zhou, X.-J., & Rahmani, R. (1992). Preclinical and clinical pharmacology of vinca alkaloids. Drugs, 44, 1-16.
Zhuang, W.-J., Fong, C.-C., Cao, J., Ao, L., Leung, C.-H., Cheung, H.-Y., … Yang, M.-S. (2004). Involvement of NF-κB and c-myc signaling pathways in the apoptosis of HL-60 cells induced by alkaloids of Tripterygium hypoglaucum (levl.) Hutch. Phytomedicine, 11, 295-302.
Zolnik, B. S., González-Fernández, Á., Sadrieh, N., & Dobrovolskaia, M. A. (2010). Minireview: Nanoparticles and the immune system. Endocrinology, 151, 458-465.
معلومات مُعتمدة: R01ES020852 United States ES NIEHS NIH HHS; R01ES10563 United States ES NIEHS NIH HHS; R01ES07331 United States ES NIEHS NIH HHS; R01ES020852 United States ES NIEHS NIH HHS; R01ES10563 United States ES NIEHS NIH HHS; R01ES07331 United States ES NIEHS NIH HHS
فهرسة مساهمة: Keywords: alkaloids; autoimmune diseases; preclinical trials, clinical perspective; therapeutic limitations
المشرفين على المادة: 0 (Alkaloids)
تواريخ الأحداث: Date Created: 20200716 Date Completed: 20210226 Latest Revision: 20210226
رمز التحديث: 20221213
DOI: 10.1002/ptr.6763
PMID: 32667693
قاعدة البيانات: MEDLINE
الوصف
تدمد:1099-1573
DOI:10.1002/ptr.6763