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      Chemical Characterization and Wound Healing Property of Jacaranda decurrens Cham. (Bignoniaceae): An Experimental Study Based on Molecular Mechanisms

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          Abstract

          Background

          Jacaranda decurrens Cham., known as carobinha, is prevalent in the Cerrado biome and presents popular use in treatment of dermatological diseases. The present study aimed to investigate the healing action of topical formulation of Jacaranda decurrens Cham. (FtEHJ) in mice cutaneous lesions.

          Methods

          Phytochemical analysis of J. decurrens hydroalcoholic extract was carried out by using HPLC-PDA-ESI-MS and FIA-ESI-IT-MSn. Swiss mice were treated topically with formulation base (FtB) or Fibrinase® or ointment FtEHJ (15 mg/g; 50 mg/Kg). At the end of treatment periods, the inflammatory cytokines (TNF- α, IL-1 β, and IL-6) in the lesions were measured by using ELISA and gene expression of TGF- β, Collagen I, and Collagen III was demonstrated by RTqPCR method and histological evaluation.

          Results

          Ten compounds were identified in the extract, distributed among the classes of flavonoids and triterpenes. Treatment with FtEHJ increased the wound contraction in 24 hours, such as reduction of TNF- α, IL-1 β, and IL-6 (pg/mL) cytokines in the lesion. The TGF- β and collagen gene expression was increased and the wound closure accelerated to nine days, with discrete inflammation, collagenization, and accented reepithelialization. Conclusions. The results obtained suggest chemical compounds present in the FtEHJ accelerates wound healing by being a gene expression modulator, and protein content of different molecules are involved in tissue repair.

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          Most cited references43

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          Angiogenesis in wound healing.

          During wound healing, angiogenic capillary sprouts invade the fibrin/fibronectin-rich wound clot and within a few days organize into a microvascular network throughout the granulation tissue. As collagen accumulates in the granulation tissue to produce scar, the density of blood vessels diminishes. A dynamic interaction occurs among endothelial cells, angiogenic cytokines, such as FGF, VEGF, TGF-beta, angiopoietin, and mast cell tryptase, and the extracellular matrix (ECM) environment. Specific endothelial cell ECM receptors are critical for these morphogenetic changes in blood vessels during wound repair. In particular, alpha(v)beta3, the integrin receptor for fibrin and fibronectin, appears to be required for wound angiogenesis: alpha(v)beta3 is expressed on the tips of angiogenic capillary sprouts invading the wound clot, and functional inhibitors of alpha(v)beta3 transiently inhibit granulation tissue formation. Recent investigations have shown that the wound ECM can regulate angiogenesis in part by modulating integrin receptor expression. mRNA levels of alpha(v)beta3 in human dermal microvascular endothelial cells either plated on fibronectin or overlaid by fibrin gel were higher than in cells plated on collagen or overlaid by collagen gel. Wound angiogenesis also appears to be regulated by endothelial cell interaction with the specific three-dimensional ECM environment in the wound space. In an in vitro model of human sprout angiogenesis, three-dimensional fibrin gel, simulating early wound clot, but not collagen gel, simulating late granulation tissue, supported capillary sprout formation. Understanding the molecular mechanisms that regulate wound angiogenesis, particularly how ECM modulates ECM receptor and angiogenic factor requirements, may provide new approaches for treating chronic wounds.
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            Pharmacology of oleanolic acid and ursolic acid.

            Jie Liu (1995)
            Oleanolic acid and ursolic acid are triterpenoid compounds that exist widely in food, medicinal herbs and other plants. This review summarizes the pharmacological studies on these two triterpenoids. Both oleanolic acid and ursolic acid are effective in protecting against chemically induced liver injury in laboratory animals. Oleanolic acid has been marketed in China as an oral drug for human liver disorders. The mechanism of hepatoprotection by these two compounds may involve the inhibition of toxicant activation and the enhancement of the body defense systems. Oleanolic acid and ursolic acid have also been long-recognized to have antiinflammatory and antihyperlipidemic properties in laboratory animals, and more research is warranted to develop a therapy for patients. Recently, both compounds have been noted for their antitumor-promotion effects, which are stimulating additional research in this field. Oleanolic acid and ursolic acid are relatively non-toxic, and have been used in cosmetics and health products. The possible mechanisms for the pharmacological effects and the prospects for these two compounds are discussed.
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              The Potential of Plant Phenolics in Prevention and Therapy of Skin Disorders

              Phenolic compounds constitute a group of secondary metabolites which have important functions in plants. Besides the beneficial effects on the plant host, phenolic metabolites (polyphenols) exhibit a series of biological properties that influence the human in a health-promoting manner. Evidence suggests that people can benefit from plant phenolics obtained either by the diet or through skin application, because they can alleviate symptoms and inhibit the development of various skin disorders. Due to their natural origin and low toxicity, phenolic compounds are a promising tool in eliminating the causes and effects of skin aging, skin diseases, and skin damage, including wounds and burns. Polyphenols also act protectively and help prevent or attenuate the progression of certain skin disorders, both embarrassing minor problems (e.g., wrinkles, acne) or serious, potentially life-threatening diseases such as cancer. This paper reviews the latest reports on the potential therapy of skin disorders through treatment with phenolic compounds, considering mostly a single specific compound or a combination of compounds in a plant extract.
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                Author and article information

                Contributors
                Journal
                Evid Based Complement Alternat Med
                Evid Based Complement Alternat Med
                ECAM
                Evidence-based Complementary and Alternative Medicine : eCAM
                Hindawi
                1741-427X
                1741-4288
                2020
                20 April 2020
                20 April 2020
                : 2020
                : 4749712
                Affiliations
                1Physiological Sciences Department, Federal University of Maranhão, São Luís, Maranhão 65080-805, Brazil
                2Clinical Medicine Department, University of São Paulo, São Paulo 01246-903, Brazil
                3Department of Chemistry, Federal University of Maranhão, São Luís, Maranhão 65080-805, Brazil
                4DNA Medical Diagnóstics, Rio Branco, Acre 69900-622, Brazil
                5Institute of Biosciences, Paulista State University (UNESP), São Paulo 11330-900, Brazil
                6Pharmacy Department, Federal University of Maranhão, São Luís, Maranhão 65080-805, Brazil
                Author notes

                Guest Editor: Reggiani Vilela Gonçalves

                Author information
                https://orcid.org/0000-0002-1407-3505
                https://orcid.org/0000-0002-1411-4266
                https://orcid.org/0000-0002-3578-1869
                https://orcid.org/0000-0002-5498-6499
                https://orcid.org/0000-0002-2896-4990
                https://orcid.org/0000-0003-1539-5888
                Article
                10.1155/2020/4749712
                7191437
                b1da1481-820f-4d61-b2d2-dafe0fd63ee4
                Copyright © 2020 Mariana B. Serra et al.

                This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 19 February 2020
                : 14 March 2020
                Funding
                Funded by: Health Science of Federal University of Maranhão (UFMA)
                Funded by: Conselho Nacional de Desenvolvimento Científico e Tecnológico
                Award ID: 02677/17
                Funded by: Fundação de Amparo à Pesquisa e ao Desenvolvimento Científico e Tecnológico do Maranhão
                Funded by: Federal University of Maranhão (UFMA)
                Funded by: Luís Magno Viana dos Santos
                Categories
                Research Article

                Complementary & Alternative medicine
                Complementary & Alternative medicine

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