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      Natural Withanolides in the Treatment of Chronic Diseases

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          Abstract

          Withanolides, and in particular extracts from Withania somnifera, have been used for over 3,000 years in traditional Ayurvedic and Unani Indian medical systems as well as within several other Asian countries. Traditionally, the extracts were ascribed a wide range of pharmacologic properties with corresponding medical uses, including adaptogenic, diuretic, anti-inflammatory, sedative/anxiolytic, cytotoxic, antitussive, and immunomodulatory. Since the discovery of the archetype withaferin A in 1965, approximately 900 of these naturally occurring, polyoxygenated steroidal lactones with 28-carbon ergostane skeletons have been discovered across 24 diverse structural types. Subsequently, extensive pharmacologic research has identified multiple mechanisms of action across key inflammatory pathways. In this chapter we identify and describe the major withanolides with anti-inflammatory properties, illustrate their role within essential and supportive inflammatory pathways (including NF-κB, JAK/STAT, AP-1, PPARγ, Hsp90 Nrf2, and HIF-1), and then discuss the clinical application of these withanolides in inflammation-mediated chronic diseases (including arthritis, autoimmune, cancer, neurodegenerative, and neurobehavioral). These naturally derived compounds exhibit remarkable biologic activity across these complex disease processes, while showing minimal adverse effects. As novel compounds and analogs continue to be discovered, characterized, and clinically evaluated, the interest in withanolides as a novel therapeutic only continues to grow.

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              A limited list of transcription factors are overactive in most human cancer cells, which makes them targets for the development of anticancer drugs. That they are the most direct and hopeful targets for treating cancer is proposed, and this is supported by the fact that there are many more human oncogenes in signalling pathways than there are oncogenic transcription factors. But how could specific transcription-factor activity be inhibited?
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                Author and article information

                Contributors
                subhashchandra@bhu.ac.in
                sprasad@mdanderson.org
                bbaggarwal@gmail.com
                (734) 615-4741 , cohenmar@med.umich.edu
                Journal
                978-3-319-41334-1
                10.1007/978-3-319-41334-1
                Anti-inflammatory Nutraceuticals and Chronic Diseases
                Anti-inflammatory Nutraceuticals and Chronic Diseases
                978-3-319-41332-7
                978-3-319-41334-1
                25 September 2016
                2016
                : 928
                : 329-373
                Affiliations
                [1 ]GRID grid.411507.6, ISNI 0000000122878816, Banaras Hindu University , ; Varanasi, Uttar Pradesh India
                [2 ]GRID grid.267308.8, ISNI 0000000092062401, MD Anderson Cancer Center, , University of Texas, ; Houston, Texas USA
                [3 ]Anti-Inflammation Research Institute, San Diego, California USA
                GRID grid.412590.b, ISNI 0000000090812336, Department of Surgery, , University of Michigan Hospital and Health Systems, ; 2920K Taubman Center, SPC 5331, 1500 East Medical Center Drive, Ann Arbor, MI 48109-5331 USA
                Article
                14
                10.1007/978-3-319-41334-1_14
                7121644
                27671823
                46d8e291-b7d8-4f93-9c62-d797aefb7a69
                © Springer International Publishing Switzerland 2016

                This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.

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                © Springer International Publishing Switzerland 2016

                autoimmune,cancer,inflammation,neurodegenerative,nf-κb,withaferin a,withanolide

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