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      Anti-inflammatory activities of flavonoid derivates

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          Abstract

          Background and purpose

          Flavonoids are a group of phytochemicals found abundantly in various plants. Scientific evidence has revealed that flavonoids display potential biological activities, including their ability to alleviate inflammation. This activity is closely related to their action in blocking the inflammatory cascade and inhibiting the production of pro-inflammatory factors. However, as flavonoids typically have poor bioavailability and pharmacokinetic profile, it is quite challenging to establish these compounds as a drug. Nevertheless, progressive advancements in drug delivery systems, particularly in nanotechnology, have shown promising approaches to overcome such challenges.

          Review approach

          This narrative review provides an overview of scientific knowledge about the mechanism of action of flavonoids in the mitigation of inflammatory reaction prior to delivering a comprehensive discussion about the opportunity of the nanotechnology-based delivery system in the preparation of the flavonoid-based drug.

          Key results

          Various studies conducted in silico, in vitro, in vivo, and clinical trials have deciphered that the anti-inflammatory activities of flavonoids are closely linked to their ability to modulate various biochemical mediators, enzymes, and signalling pathways involved in the inflammatory processes. This compound could be encapsulated in nanotechnology platforms to increase the solubility, bioavailability, and pharmacological activity of flavonoids as well as reduce the toxic effects of these compounds.

          Conclusion

          In Summary, we conclude that flavonoids and their derivates have given promising results in their development as new anti-inflammatory drug candidates, especially if they formulate in nanoparticles.

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          Most cited references213

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          Pattern recognition receptors and inflammation.

          Infection of cells by microorganisms activates the inflammatory response. The initial sensing of infection is mediated by innate pattern recognition receptors (PRRs), which include Toll-like receptors, RIG-I-like receptors, NOD-like receptors, and C-type lectin receptors. The intracellular signaling cascades triggered by these PRRs lead to transcriptional expression of inflammatory mediators that coordinate the elimination of pathogens and infected cells. However, aberrant activation of this system leads to immunodeficiency, septic shock, or induction of autoimmunity. In this Review, we discuss the role of PRRs, their signaling pathways, and how they control inflammatory responses. 2010 Elsevier Inc. All rights reserved.
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            Inflammatory responses and inflammation-associated diseases in organs

            Inflammation is a biological response of the immune system that can be triggered by a variety of factors, including pathogens, damaged cells and toxic compounds. These factors may induce acute and/or chronic inflammatory responses in the heart, pancreas, liver, kidney, lung, brain, intestinal tract and reproductive system, potentially leading to tissue damage or disease. Both infectious and non-infectious agents and cell damage activate inflammatory cells and trigger inflammatory signaling pathways, most commonly the NF-κB, MAPK, and JAK-STAT pathways. Here, we review inflammatory responses within organs, focusing on the etiology of inflammation, inflammatory response mechanisms, resolution of inflammation, and organ-specific inflammatory responses.
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              Toll-Like Receptor Signaling Pathways

              Toll-like receptors (TLRs) play crucial roles in the innate immune system by recognizing pathogen-associated molecular patterns derived from various microbes. TLRs signal through the recruitment of specific adaptor molecules, leading to activation of the transcription factors NF-κB and IRFs, which dictate the outcome of innate immune responses. During the past decade, the precise mechanisms underlying TLR signaling have been clarified by various approaches involving genetic, biochemical, structural, cell biological, and bioinformatics studies. TLR signaling appears to be divergent and to play important roles in many aspects of the innate immune responses to given pathogens. In this review, we describe recent progress in our understanding of TLR signaling regulation and its contributions to host defense.
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                Author and article information

                Journal
                ADMET DMPK
                ADMET DMPK
                ADMET
                ADMET & DMPK
                International Association of Physical Chemists
                1848-7718
                26 July 2023
                2023
                : 11
                : 3
                : 331-359
                Affiliations
                [1 ]Department of Pharmacotherapy, Faculty of Medicine, Universitas Palangka Raya , Palangka Raya 73111, Indonesia
                [2 ]Department of Pharmacy, Politeknik Kesehatan Kementerian Kesehatan Gorontalo , Gorontalo 96135, Indonesia
                [3 ]Department of Midwivery, Politeknik Kesehatan Kementerian Kesehatan Palangka Raya 73111 , Palangka Raya, Indonesia
                [4 ]Faculty of mathematics and natural sciences, Universitas Palangka Raya , Palangka Raya 73111, Indonesia
                [5 ]Department of Internal Medicine, Faculty of Medicine and Health Sciences, Universitas Warmadewa , Denpasar, Bali 80235, Indonesia
                [6 ]Department of Internal Medicine, Sanjiwani Hospital , Denpasar, Bali 80235, Indonesia
                [7 ]Medical Research Unit, School of Medicine, Universitas Syiah Kuala , Banda Aceh 23111, Indonesia
                [8 ]Tropical Disease Centre, School of Medicine, Universitas Syiah Kuala , Banda Aceh 23111, Indonesia
                [9 ]Department of Microbiology, School of Medicine, Universitas Syiah Kuala , Banda Aceh 23111, Indonesia
                [10 ]Department of Pharmacy, Faculty of Pharmacy, Hasanuddin University , Makassar 90245, Indonesia
                [11 ]Department of Pathology and Laboratory Medicine, Warren Alpert Medical School & Legorreta Cancer Center, Brown University , Providence, RI 02912, USA
                [12 ]Department of Pharmacy, Faculty of Allied Health Sciences, Daffodil International University , Dhaka 1207, Bangladesh
                Author notes
                *Corresponding Author: E-mail: ysrafil0155@ 123456gmail.com
                Article
                10.5599/admet.1918
                10567070
                37829324
                3f615818-36e7-4b97-95c1-d8e0a53696d7
                Copyright © 2023 by the authors.

                This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 16 May 2023
                : 29 June 2023
                Page count
                Figures: 9, Tables: 3, Equations: 0, References: 214, Pages: 29
                Categories
                Review

                inflammation treatment,bioactive compounds,plants-base drug,nanotechnology

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