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      Tannin-rich extracts from Lannea stuhlmannii and Lannea humilis (Anacardiaceae) exhibit hepatoprotective activities in vivo via enhancement of the anti-apoptotic protein Bcl-2

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          Abstract

          The potential hepatoprotective activities of two Lannea species were explored in vivo. Furthermore, the binding activities of their main polyphenols to the antiapoptotic protein Bcl-2 were investigated. Based on HPLC-MS/MS results, 22 secondary metabolites were characterized in L. stuhlmannii (mainly tannins), while 20 secondary metabolites (mainly sulphated tannins) were identified in L. humilis. Both extracts exhibited substantial antioxidant activities in vitro and counteracted D-galactosamine induced intoxication in rats in vivo and increased the total antioxidant capacity (TAC) of liver tissues. In addition to reducing the elevated levels of AST and total bilirubin, both extracts significantly attenuated the deleterious histopathologic changes in liver after D-galactosamine-intoxication. Also, both extracts protected hepatocytes from apoptotic cell death and increased the expression of the anti-apoptotic protein Bcl-2. The identified compounds from both extracts can bind to the Bcl-2: Bim (BH3) interface with an appreciable binding free energy. Hydrogen and ionic bonds and hydrophobic interactions with amino acid residues in the hydrophobic face of Bim (BH3) domain were discovered. To sum up, L. humilis and L. stuhlmanni exhibited promising hepatoprotective activities in vivo against D-GalN-induced liver injury and their hepatoprotection is due to the antioxidant and anti-apoptotic effects of tannins and proanthocyanidins.

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          Most cited references33

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          Mechanisms of apoptosis.

          J Reed (2000)
          Programmed cell death plays critical roles in a wide variety of physiological processes during fetal development and in adult tissues. In most cases, physiological cell death occurs by apoptosis as opposed to necrosis. Defects in apoptotic cell death regulation contribute to many diseases, including disorders where cell accumulation occurs (cancer, restenosis) or where cell loss ensues (stroke, heart failure, neurodegeneration, AIDS). In recent years, the molecular machinery responsible for apoptosis has been elucidated, revealing a family of intracellular proteases, the caspases, which are responsible directly or indirectly for the morphological and biochemical changes that characterize the phenomenon of apoptosis. Diverse regulators of the caspases have also been discovered, including activators and inhibitors of these cell death proteases. Inputs from signal transduction pathways into the core of the cell death machinery have also been identified, demonstrating ways of linking environmental stimuli to cell death responses or cell survival maintenance. Knowledge of the molecular mechanisms of apoptosis is providing insights into the causes of multiple pathologies where aberrant cell death regulation occurs and is beginning to provide new approaches to the treatment of human diseases.
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            Modes of Action of Herbal Medicines and Plant Secondary Metabolites

            Plants produce a wide diversity of secondary metabolites (SM) which serve them as defense compounds against herbivores, and other plants and microbes, but also as signal compounds. In general, SM exhibit a wide array of biological and pharmacological properties. Because of this, some plants or products isolated from them have been and are still used to treat infections, health disorders or diseases. This review provides evidence that many SM have a broad spectrum of bioactivities. They often interact with the main targets in cells, such as proteins, biomembranes or nucleic acids. Whereas some SM appear to have been optimized on a few molecular targets, such as alkaloids on receptors of neurotransmitters, others (such as phenolics and terpenoids) are less specific and attack a multitude of proteins by building hydrogen, hydrophobic and ionic bonds, thus modulating their 3D structures and in consequence their bioactivities. The main modes of action are described for the major groups of common plant secondary metabolites. The multitarget activities of many SM can explain the medical application of complex extracts from medicinal plants for more health disorders which involve several targets. Herbal medicine is not a placebo medicine but a rational medicine, and for several of them clinical trials have shown efficacy.
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              Structure of Bcl-xL-Bak peptide complex: recognition between regulators of apoptosis.

              Heterodimerization between members of the Bcl-2 family of proteins is a key event in the regulation of programmed cell death. The molecular basis for heterodimer formation was investigated by determination of the solution structure of a complex between the survival protein Bcl-xL and the death-promoting region of the Bcl-2-related protein Bak. The structure and binding affinities of mutant Bak peptides indicate that the Bak peptide adopts an amphipathic alpha helix that interacts with Bcl-xL through hydrophobic and electrostatic interactions. Mutations in full-length Bak that disrupt either type of interaction inhibit the ability of Bak to heterodimerize with Bcl-xL.
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                Author and article information

                Contributors
                sobeh@uni-heidelberg.de
                wink@uni-heidelberg.de
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                19 June 2018
                19 June 2018
                2018
                : 8
                : 9343
                Affiliations
                [1 ]ISNI 0000 0001 2190 4373, GRID grid.7700.0, Institute of Pharmacy and Molecular Biotechnology, , Heidelberg University, ; Im Neuenheimer Feld 364, 69120 Heidelberg, Germany
                [2 ]ISNI 0000 0001 2158 2757, GRID grid.31451.32, Department of Pharmacology and Toxicology, Faculty of Pharmacy, , Zagazig University, ; Zagazig, 44519 Egypt
                [3 ]ISNI 0000 0001 2155 6022, GRID grid.411303.4, Department of Histology, Faculty of Medicine for Girls, , Al-Azhar University, ; Cairo, 11651 Egypt
                [4 ]ISNI 0000 0004 0418 1945, GRID grid.472279.d, Department of Chemistry, , American University of the Middle East, ; Egaila, 54200 Kuwait
                [5 ]ISNI 0000 0004 0639 9286, GRID grid.7776.1, Department of Pharmacognosy, College of Pharmacy, Cairo University, ; Cairo, 11562 Egypt
                [6 ]ISNI 0000 0001 0165 571X, GRID grid.420091.e, Medicinal Chemistry Department, , Theodor Bilharz Research Institute, ; Kornish El-Nile, Warrak El-Hadar 12411, Imbaba, Giza, Egypt
                [7 ]ISNI 0000 0001 2158 2757, GRID grid.31451.32, Department of Pharmacognosy, , Faculty of Pharmacy, Zagazig University, ; Zagazig, 44519 Egypt
                Article
                27452
                10.1038/s41598-018-27452-8
                6008440
                29921841
                6ab4ede8-a196-4353-9e90-3ee40ca9163b
                © The Author(s) 2018

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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                : 27 March 2018
                : 25 May 2018
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