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      The predictive utility of the plant phylogeny in identifying sources of cardiovascular drugs

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          Abstract

          Context: Cardiovascular disease (CVD) is the number one cause of death globally, responsible for over 17 million (31%) deaths in the world. Novel pharmacological interventions may be needed given the high prevalence of CVD.

          Objective: In this study, we aimed to find potential new sources of cardiovascular (CV) drugs from phylogenetic and pharmacological analyses of plant species that have experimental and traditional CV applications in the literature.

          Materials and methods: We reconstructed the molecular phylogeny of these plant species and mapped their pharmacological mechanisms of action on the phylogeny.

          Results: Out of 139 plant species in 71 plant families, seven plant families with 45 species emerged as phylogenetically important exhibiting common CV mechanisms of action within the family, as would be expected given their common ancestry: Apiaceae, Brassicaceae, Fabaceae, Lamiaceae, Malvaceae, Rosaceae and Zingiberaceae. Apiaceae and Brassicaceae promoted diuresis and hypotension; Fabaceae and Lamiaceae had anticoagulant/thrombolytic effects; Apiaceae and Zingiberaceae were calcium channel blockers. Moreover, Apiaceae, Lamiaceae, Malvaceae, Rosaceae and Zingiberaceae species were found to possess anti-atherosclerotic properties.

          Discussion and conclusions: The phylogeny identified certain plant families with disproportionately more species, highlighting their importance as sources of natural products for CV drug discovery. Though there were some species that did not show the same mechanism within the family, the phylogeny predicts that these species may contain undiscovered phytochemistry, and potentially, the same bioactivity. Evolutionary pharmacology, as applied here, may guide and expedite our efforts in discovering sources of new CV drugs.

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          A systematic screening of total antioxidants in dietary plants.

          A predominantly plant-based diet reduces the risk for development of several chronic diseases. It is often assumed that antioxidants contribute to this protection, but results from intervention trials with single antioxidants administered as supplements quite consistently do not support any benefit. Because dietary plants contain several hundred different antioxidants, it would be useful to know the total concentration of electron-donating antioxidants (i.e., reductants) in individual items. Such data might be useful in the identification of the most beneficial dietary plants. We have assessed systematically total antioxidants in a variety of dietary plants used worldwide, including various fruits, berries, vegetables, cereals, nuts and pulses. When possible, we analyzed three or more samples of dietary plants from three different geographic regions in the world. Total antioxidants was assessed by the reduction of Fe(3+) to Fe(2+) (i.e., the FRAP assay), which occurred rapidly with all reductants with half-reaction reduction potentials above that of Fe(3+)/Fe(2+). The values, therefore, expressed the corresponding concentration of electron-donating antioxidants. Our results demonstrated that there is more than a 1000-fold difference among total antioxidants in various dietary plants. Plants that contain most antioxidants included members of several families, such as Rosaceae (dog rose, sour cherry, blackberry, strawberry, raspberry), Empetraceae (crowberry), Ericaceae (blueberry), Grossulariaceae (black currant), Juglandaceae (walnut), Asteraceae (sunflower seed), Punicaceae (pomegranate) and Zingiberaceae (ginger). In a Norwegian diet, fruits, berries and cereals contributed 43.6%, 27.1% and 11.7%, respectively, of the total intake of plant antioxidants. Vegetables contributed only 8.9%. The systematic analysis presented here will facilitate research into the nutritional role of the combined effect of antioxidants in dietary plants.
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            Arthropod steroid hormone (20-Hydroxyecdysone) suppresses IL-1β- induced catabolic gene expression in cartilage

            Background In osteoarthritis (OA), the imbalance of chondrocytes’ anabolic and catabolic factors can induce cartilage destruction. Interleukin-1 beta (IL-1β) is a potent pro-inflammatory cytokine that is capable of inducing chondrocytes and synovial cells to synthesize MMPs. The hypoxia-inducible factor-2alpha (HIF-2alpha, encoded by Epas1) is the catabolic transcription factor in the osteoarthritic process. The purpose of this study is to validate the effects of ecdysteroids (Ecd) on IL-1β- induced cartilage catabolism and the possible role of Ecd in treatment or prevention of early OA. Methods Chondrocytes and articular cartilage was harvested from newborn ICR mice. Ecd effect on chondrocytes viability was tested and the optimal concentration was determined by MTT assay. The effect of HIF-2α (EPAS1) in cartilage catabolism simulated by IL-1β (5 ng/ml) was evaluated by articular cartilage explants culture. The effects of Ecd on IL-1β-induced inflammatory conditions and their related catabolic genes expression were analyzed. Results Interleukin-1β (IL-1β) treatment on primary mouse articular cartilage explants enhanced their Epas1, matrix metalloproteinases (MMP-3, MMP-13) and ADAMTS-5 genes expression and down-regulated collagen type II (Col2a1) gene expression. With the pre-treatment of 10−8M Ecd, the catabolic effects of IL-1β on articular cartilage were scavenged. Conclusion In conclusions, Ecd can reduce the IL-1β-induced inflammatory effect of the cartilage. Ecd may suppress IL-1β- induced cartilage catabolism via HIF-2α pathway.
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              Inflammation, Atherosclerosis and Coronary Artery Disease

              Supplement Aims and Scope Research into inflammation, atherosclerosis and coronary artery disease, including observational studies, clinical trials, epidemiology, and advances in applied (translational) research. The supplement is intended to include overviews of new concepts in pathophysiology, natural history, diagnostic strategies, and treatment approaches. Articles should focus on vascular disease may include: ■ Diagnosis ■ Prognosis ■ Treatment ■ Screening ■ Prevention ■ Risk factor modification ■ Systematic reviews ■ Risk and safety of medical interventions ■ Epidemiology and statistical methods ■ Evidence-based medicine ■ Evaluation of guidelines ■ Translational medicine Article types include original clinical and basic research articles, case reports, commentaries, meeting reports, methodology, perspectives. Inflammation has been well recognized to play an important role in the development of atherosclerosis.1,2 Since chronic infection may lead to chronic systemic inflammation, many studies have investigated the associations between atherosclerotic diseases, such as coronary artery disease (CAD) and chronic infections by various microorganisms, including Chlamydia pneumoniae, cytomegalovirus, herpes simplex virus, and hepatitis C virus (HCV). However, these associations and precise mechanisms remain controversial. Several studies have suggested that more infectious pathogens, referred to as the infectious burden, rather than any single pathogen, may be involved in the development of atherosclerosis.3 In this supplementary issue of Clinical Medicine Insights: Cardiology, Ishizaka et al.4, reviewed the possible association between atherosclerosis and chronic HCV infection. In 2002, Ishizaka et al.5, first reported the higher prevalence of carotid artery plaques in HCV-positive patients than in control subjects, however, the findings of subsequent studies remain controversial, with some studies showing positive results and others negative. Regarding the associations between inflammatory biomarkers and atherosclerotic diseases, many studies have demonstrated that elevated high sensitivity C-reactive protein (hsCRP) levels, which are one of the biomarkers of systemic inflammation, are a powerful predictor of future cardiovascular events, such as myocardial infarction (MI) and cardiac death.6 However, hsCRP levels vary remarkably among different ethnic populations, and hsCRP levels in East Asian populations are much lower in comparison to those in Western populations.7 In this supplementary issue of Clinical Medicine Insights: Cardiology, Saito et al.8, reported a meta-analysis of 8 prospective studies regarding the association between hsCRP levels and atherosclerotic diseases in East Asians. They demonstrated that East Asians had low hsCRP levels and that, even in East Asians, elevated hsCRP levels were associated with an increased risk of stroke, especially ischemic stroke. Enomoto et al.9, also showed hsCRP levels to be associated with all-cause death in 1920 healthy Japanese subjects. In addition to hsCRP levels, some new inflammatory biomarkers related to both metabolic and atherosclerotic diseases have been reported. In this supplementary issue, Furuhashi et al.10, reviewed the association between atherosclerosis and fatty acid-binding protein 4 (FABP4), one of adipokines, that is mainly expressed in adipocytes and macrophages and may play an important role in the development of insulin resistance and atherosclerosis. Elevated FABP4 levels were reported to be associated with obesity, diabetes mellitus and atherosclerotic diseases.11,12 Notably, there is a male preponderance of death due to atherosclerotic diseases, especially CAD, at a younger age than women, thus suggesting that sex hormones may play a major role in the process of atherosclerotic diseases.13,14 Estrogen has anti-inflammatory effects, and such hormones may alter the immune response during the development of atherosclerosis, thereby leading to different disease processes between men and women. In this supplementary issue, Fairweather et al.15, reviewed sex differences in the inflammatory immune response during atherosclerosis. Moreover, sex hormones are suggested to affect the process of myocardial inflammation and remodeling during myocarditis. Systemic inflammatory responses are considered to play a major role in the destabilization of atherosclerotic plaques. The presence of inflammation in one artery is highly predictive of inflammation in other arteries.16 Imaging modalities are expected to noninvasively evaluate atherosclerotic plaques and inflammation within vessel walls. The glucose analogue 18F-FDG is taken up by metabolically active cells, especially macrophages, thus allowing the detection of inflammatory activity. Using this 18F-FDG tracer, positron emission tomography (PET) has become recognized as a reliable imaging technique for the detection of metabolic activity of atherosclerosis.17 Because the most important disadvantage is its limited spatial resolution, PET/computed tomography (CT) combines the excellent spatial resolution of CT with the high sensitivity of PET for the detection of inflammation. In this supplementary issue, Alie et al.18, reviewed the clinical usefulness of 18F-FDG-PET/CT for the noninvasive evaluation of atherosclerosis and inflammation in the carotid, coronary arteries and aortas. A modern lifestyle with high fat diet and lack of physical activity promotes atherosclerosis. Obesity and high fat diet have been shown to be associated with chronic inflammation in human adipose tissues and arteries.19 Oxidative modification of LDL is an essential mechanism that increases their inflammatory potential, and dietary antioxidants, such as vitamins C and E and polyphenols, are the potential nutrients leading to the prevention of LDL oxidation and atherosclerosis progression. The inverse associations between the consumption of vegetables, fruits and fish and atherosclerotic diseases have been reported in many epidemiological studies, showing a reduced risk of such diseases. However, there are still many unclear points regarding the contribution of these foods to the prevention of atherosclerosis. In this supplementary issue, Saita et al.20, reviewed the preventative effects of antioxidant foods on atherosclerosis and CAD. In addition to vegetables and fruits, antioxidant polyphenols are rich in beverages, such as wine and black and green tea. Recently, a meta-analysis showed green tea consumption to be associated with a reduced risk of CAD.21 Green tea, which is very rich in catechins, is the most popular beverage in Japan. In this supplementary issue, Ohmori et al.22, reported the association between green tea consumption and MI in 725 Japanese patients. Moreover, they demonstrated the inhibitory effect of LDL oxidation and the anti-inflammatory effect of green tea in 22 healthy volunteers. Inflammation is recognized to play an important role in both the initiation and progression of atherosclerotic diseases, such as CAD, however, the aim to prevent or treat atherosclerosis via modulating inflammation remains challenging. The articles in this supplementary issue of Clinical Medicine Insights: Cardiology encompass new research or timely reviews regarding inflammation, atherosclerosis and coronary artery disease. Lead Guest Editor Dr Yukihiko Momiyama Dr Yukihiko Momiyama is the Director of the Department of Cardiology at NHO Tokyo Medical Center in Tokyo. He received his MD from Keio University school of Medicine. He has previously worked at St. George’s Hospital Medical school in London and at the National Defense Medical College in Saitama. His research interests have focused on biomarkers, coronary artery disease, epidemiology, and MRI, especially plaque imaging. His previous studies have been published in a variety of peer-reviewed journals including Journal of the American College of Cardiology; Arteriosclerosis, Thrombosis, and Vascular Biology; Atherosclerosis, American Heart Journal, and American Journal of Cardiology. ymomiyamajp@yahoo.co.jp https://www.researchgate.net/profile/Yukihiko_Momiyama Guest Editors HISASHI ADACHI Dr. Hisashi Adachi is a Professor in the Department of Community Medicine, Kurume University, School of Medicine. He received his MD from Kurume University School of Medicine. He has previously worked at the University of Minnesota in the USA as a research fellow. His research interests have focused on novel risk factors, coronary artery disease, and epidemiology, and he is also interested in trends in nutritional intake shown in the Tanushimaru Study, one of the original cohorts of the Seven Countries Study. His previous studies have been published in a variety of peer-reviewed journals including Hypertension, Journal of Hypertension, American Journal of Hypertension, Atherosclerosis and others. hadac@med.kurume-u.ac.jp https://www.researchgate.net/profile/Hisashi_Adach DELISA FAIRWEATHER Dr. DeLisa Fairweather is an Associate Professor of Cardiovascular Diseases and Director of Translational Research at Mayo Clinic in Jacksonville, Florida. She also has an Adjunct appointment in the Department of Environmental Health Sciences at the Johns Hopkins Bloomberg School of Public Health in Baltimore, Maryland. Dr. Fairweather was responsible for papers on inflammation, atherosclerosis and coronary artery disease. She completed her PhD at the University of Western Australia and conducted her Postdoctoral Fellowship with Dr. Noel R. Rose at Johns Hopkins University School of Medicine before joining the faculty at the Johns Hopkins Bloomberg School of Public Health. She now works primarily to understand how sex hormones and environmental co-exposures like infections and chemicals increase chronic inflammatory diseases like cardiovascular and autoimmune diseases. Dr. Fairweather has received funding from the national Institutes of Health, the American Heart Association, and industry. She has authored 70 manuscripts and book chapters and has given over 80 national and international presentations. Fairweather.DeLisa@mayo.edu http://mayoweb.mayo.edu/ NOBUKAZU ISHIZAKA Dr. Nobukazu Ishizaka is the Professor of the Faculty of Medicine at the Department of Cardiology, Osaka Medical College in Osaka. He received his MD from University Tokyo. He had previously worked at the Faculty of Medicine of University Tokyo in Tokyo. His previous studies have been published in a variety of peer-reviewed journals including Lancet, Circulation, Arterioscler Thromb Vasc Biol, Hypertension, Atherosclerosis, FEBS Lett, and Am Heart J. ishizaka@poh.osaka-med.ac.jp EMI SAITA Dr Emi Saita is a lecturer of Endowed Research Department “Food for Health” at Ochanomizu University, and was responsible for papers on Anti-inflammatory Diet for Atherosclerosis and Coronary Artery Disease: Antioxidant Foods. She completed her PhD at Ochanomizu University. She now works primarily in developing understanding of inhibitory effects of nutritional factors on atherosclerosis. Her previous studies have been published in a variety of peer-reviewed journals including J Oleo Sci, J Clin Biochem Nutr, and Eur J Nutr. saita.emi@ocha.ac.jp http://www.cf.ocha.ac.jp/food-health/index.html
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                Author and article information

                Journal
                Pharm Biol
                Pharm Biol
                IPHB
                iphb20
                Pharmaceutical Biology
                Taylor & Francis
                1388-0209
                1744-5116
                2018
                27 February 2018
                : 56
                : 1
                : 154-164
                Affiliations
                Department of Biology, Long Island University , Brooklyn, NY, USA
                Author notes
                CONTACT Jeanmaire Molina jeanmaire.molina@ 123456liu.edu Department of Biology, Long Island University , Brooklyn, NY, 11201, USA
                Author information
                http://orcid.org/0000-0001-5250-2684
                Article
                1444642
                10.1080/13880209.2018.1444642
                6130559
                29486635
                103ebf98-f322-4bd8-9130-e7f686c3251c
                © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 31 December 2017
                : 10 February 2018
                : 14 February 2018
                Page count
                Pages: 11, Words: 10041
                Categories
                Invited Article

                drug discovery,ethnobotany,ethnomedicine,evolutionary pharmacology,natural products

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