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      Efficacy of ursolic acid against Echinococcus granulosus in vitro and in a murine infection model

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          Abstract

          Background

          Cystic echinococcosis is a global public health problem; however, the drugs (albendazole and mebendazole) currently recommended by WHO for its treatment, have limited efficacy. Therefore, novel drugs are required to provide more choices for the treatment of this disease.

          Methods

          The anthelmintic effects of ursolic acid (UA) were tested on Echinococcus granulosus protoscoleces, germinal cells and metacestodes in vitro. The in vivo efficacy of UA was investigated in mice following secondary infection with E. granulosus. Furthermore, the corresponding ultrastructural damage induced by UA was evaluated by electron microscopy.

          Results

          In vitro, 45.95 ± 5.30% of protoscoleces were killed by UA at 40 μg/ml, while the growth of more than 90% of germinal cells was inhibited by UA at 10 to 40 μg/ml. The same effect was observed in metacestodes 7 days after treatment with UA at 10, 20 and 40 μg/ml, and more than 50% of metacestodes showed loss of integrity at the end of the experiment. In vivo, metacestode weight was significantly reduced following oral administration of UA at 200 and 100 mg/kg (39.5 and 38.3%, respectively). Additionally, ultrastructural damage, such as alternations in germinal cell morphology and formation of vacuoles and lipid granules were observed in parasites treated with UA in vitro, while detachment of the germinal layer from the laminated layer was also seen in metacestodes in vivo.

          Conclusions

          UA was demonstrated to exert parasiticidal activity against E. granulosus in vitro and in vivo, thus implicating UA as a potential anti-echinococcosis agent.

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          Most cited references33

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          Ursolic Acid—A Pentacyclic Triterpenoid with a Wide Spectrum of Pharmacological Activities

          Ursolic acid (UA) is a natural terpene compound exhibiting many pharmaceutical properties. In this review the current state of knowledge about the health-promoting properties of this widespread, biologically active compound, as well as information about its occurrence and biosynthesis are presented. Particular attention has been paid to the application of ursolic acid as an anti-cancer agent; it is worth noticing that clinical tests suggesting the possibility of practical use of UA have already been conducted. Amongst other pharmacological properties of UA one can mention protective effect on lungs, kidneys, liver and brain, anti-inflammatory properties, anabolic effects on skeletal muscles and the ability to suppress bone density loss leading to osteoporosis. Ursolic acid also exhibits anti-microbial features against numerous strains of bacteria, HIV and HCV viruses and Plasmodium protozoa causing malaria.
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            Ursolic acid in cancer prevention and treatment: molecular targets, pharmacokinetics and clinical studies.

            Discovery of bioactive molecules and elucidation of their molecular mechanisms open up an enormous opportunity for the development of improved therapy for different inflammatory diseases, including cancer. Triterpenoids isolated several decades ago from various medicinal plants now seem to have a prominent role in the prevention and therapy of a variety of ailments and some have already entered Phase I clinical trials. One such important and highly investigated pentacyclic triterpenoid, ursolic acid has attracted great attention of late for its potential as a chemopreventive and chemotherapeutic agent in various types of cancer. Ursolic acid has been shown to target multiple proinflammatory transcription factors, cell cycle proteins, growth factors, kinases, cytokines, chemokines, adhesion molecules, and inflammatory enzymes. These targets can potentially mediate the chemopreventive and therapeutic effects of ursolic acid by inhibiting the initiation, promotion and metastasis of cancer. This review not only summarizes the diverse molecular targets of ursolic acid, but also provides an insight into the various preclinical and clinical studies that have been performed in the last decade with this promising triterpenoid.
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              The taxonomy, phylogeny and transmission of Echinococcus.

              The application of molecular tools to the characterisation of the aetiological agents of echinococcosis has revealed a series of largely host-adapted species and genotypes that are maintained in distinct cycles of transmission. They can be defined on both genetic and phenotypic characteristics which complement previous observations made by descriptive parasitologists many years ago. A revised taxonomy for species in the genus Echinococcus has been proposed and widely accepted, particularly with respect to forms maintained in transmission cycles involving sheep, horses and cattle. However, molecular epidemiological studies are required in a number of endemic areas in order to determine cycles of transmission responsible for maintaining the parasite. The taxonomic status of forms in cervids, pigs and camels has still to be resolved, and the status and epidemiological significance of newly described species in China requires further research.
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                Author and article information

                Contributors
                chart2543@163.com
                lcs_hxy@hotmail.com
                amyshyj12@163.com
                zhang_haobing@163.com
                caojp@yahoo.com
                Journal
                Parasit Vectors
                Parasit Vectors
                Parasites & Vectors
                BioMed Central (London )
                1756-3305
                24 January 2018
                24 January 2018
                2018
                : 11
                : 58
                Affiliations
                [1 ]ISNI 0000 0000 8803 2373, GRID grid.198530.6, National Institute of Parasitic Diseases, Chinese Center for Disease Control and Prevention, ; Shanghai, 200025 China
                [2 ]Key Laboratory of Parasite and Vector Biology, MOH, Shanghai, 200025 China
                [3 ]National Center for International Research on Tropical Diseases, Shanghai, 200025 China
                [4 ]WHO Collaborating Centre for Tropical Diseases, Shanghai, 200025 China
                Article
                2628
                10.1186/s13071-018-2628-8
                5784668
                29368624
                7e232666-db51-497a-bab1-7f37ff3bebb0
                © The Author(s). 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 17 September 2017
                : 8 January 2018
                Funding
                Funded by: the National Natural Science Foundation of China
                Award ID: 81371842
                Award Recipient :
                Funded by: the National Natural Science Foundation of China
                Award ID: 81401691
                Award ID: 81371841
                Award Recipient :
                Funded by: the General Program of Shanghai Municipal Health Bureau
                Award ID: 201540170
                Award Recipient :
                Funded by: the Fourth Round of Three-Year Public Health Action Plan of Shanghai, China
                Award ID: 15GWZK0101
                Award Recipient :
                Categories
                Research
                Custom metadata
                © The Author(s) 2018

                Parasitology
                echinococcus granulosus,ursolic acid,protoscoleces,germinal cells,metacestodes,ultrastructural damage

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