10 results on '"Maria, Harizani"'
Search Results
2. New C15 Acetogenins from Two Species of Laurencia from the Aegean Sea
- Author
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Maria Harizani, Dafni-Ioanna Diakaki, Stamatios Perdikaris, Vassilios Roussis, and Efstathia Ioannou
- Subjects
Laurencia microcladia ,Laurencia obtusa ,red algae ,C15 acetogenins ,isolation ,structure elucidation ,Organic chemistry ,QD241-441 - Abstract
The chemical diversity of the approximately 1,200 natural products isolated from red algae of the genus Laurencia, in combination with the wide range of their biological activities, have placed species of Laurencia in the spotlight of marine chemists’ attention for over 60 years. The chemical investigation of the organic (CH2Cl2/MeOH) extracts of Laurencia microcladia and Laurencia obtusa, both collected off the coasts of Tinos island in the Aegean Sea, resulted in the isolation of 32 secondary metabolites, including 23 C15 acetogenins (1–23), 7 sesquiterpenes (24–30) and 2 diterpenes (31 and 32). Among them, six new C15 acetogenins, namely 10-acetyl-sagonenyne (2), cis-sagonenyne (3), trans-thuwalenyne C (4), tinosallene A (11), tinosallene B (12) and obtusallene XI (17), were identified and their structures were elucidated by extensive analysis of their spectroscopic data. Compounds 1–3, 5–11, 13 and 15–32 were evaluated for their antibacterial activity against Staphylococcus aureus and Escherichia coli.
- Published
- 2022
- Full Text
- View/download PDF
3. In Vivo Evaluation of the Wound Healing Activity of Extracts and Bioactive Constituents of the Marine Isopod Ceratothoa oestroides
- Author
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Evgenia Sofrona, Leto-Aikaterini Tziveleka, Maria Harizani, Panagiota Koroli, Ioannis Sfiniadakis, Vassilios Roussis, Michail Rallis, and Efstathia Ioannou
- Subjects
Ceratothoa oestroides ,marine isopod ,wound healing ,SKH-hr1 hairless mice ,eicosapentaenoic acid ,Biology (General) ,QH301-705.5 - Abstract
Wound healing is a fundamental response to tissue injury and a number of natural products has been found to accelerate the healing process. Herein, we report the preparation of a series of different polarity (organic and aqueous) extracts of the marine isopod Ceratothoa oestroides and the in vivo evaluation of their wound healing activity after topical administration of ointments incorporating the various extracts on wounds inflicted on SKH-hr1 hairless mice. The most active extract was fractionated for enrichment in the bioactive constituents and the fractions were further evaluated for their wound healing activity, while their chemical profiles were analyzed. Wound healing was evaluated by clinical assessment, photo-documentation, histopathological analysis and measurement of biophysical skin parameters, such as transepidermal water loss (TEWL), hydration, elasticity, and skin thickness. The highest levels of activity were exerted by treatment of the wounds with a fraction rich in eicosapentaenoic acid (EPA), as well as myristic and palmitoleic acids. Topical application of the bioactive fraction on the wounds of mice resulted in complete wound closure with a skin of almost normal architecture without any inflammatory elements.
- Published
- 2020
- Full Text
- View/download PDF
4. New Chlorinated 2,5-Diketopiperazines from Marine-Derived Bacteria Isolated from Sediments of the Eastern Mediterranean Sea
- Author
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Maria Harizani, Eleni Katsini, Panagiota Georgantea, Vassilios Roussis, and Efstathia Ioannou
- Subjects
2,5-diketopiperazine ,marine bacteria ,sediment ,natural products ,structure elucidation ,antifungal activity evaluation ,Organic chemistry ,QD241-441 - Abstract
From the organic extracts of five bacterial strains isolated from marine sediments collected in the East Mediterranean Sea, three new (15, 16, 31) and twenty-nine previously reported (1−14, 17−30, 32) metabolites bearing the 2,5-diketopiperazine skeleton were isolated. The structures of the chlorinated compounds 15, 16, and 31 were elucidated by extensive analysis of their spectroscopic data (NMR, MS, UV, IR). Compounds 15 and 16 were evaluated for their antifungal activity against Candida albicans and Aspergillus niger but were proven inactive. The relevant literature is supplemented with complete NMR assignments and revisions for the 29 previously reported compounds.
- Published
- 2020
- Full Text
- View/download PDF
5. Neorogioltriol and Related Diterpenes from the Red Alga Laurencia Inhibit Inflammatory Bowel Disease in Mice by Suppressing M1 and Promoting M2-Like Macrophage Responses
- Author
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Maria G. Daskalaki, Dimitra Vyrla, Maria Harizani, Christina Doxaki, Aristides G. Eliopoulos, Vassilios Roussis, Efstathia Ioannou, Christos Tsatsanis, and Sotirios C. Kampranis
- Subjects
Laurencia ,halogenated diterpenes ,neorogioltriol ,cytokine ,nitric oxide ,TNF-alpha ,colitis ,Biology (General) ,QH301-705.5 - Abstract
Macrophages are central mediators of inflammation, orchestrating the inflammatory response through the production of cytokines and nitric oxide. Macrophages obtain pro-inflammatory (M1) and anti-inflammatory (M2) phenotypes, which can be modulated by soluble factors, including natural products. Despite the crucial protective role of inflammation, chronic or deregulated inflammation can lead to pathological states, such as autoimmune diseases, metabolic disorders, cardiovascular diseases, and cancer. In this case, we studied the anti-inflammatory activity of neorogioltriol (1) in depth and identified two structurally related diterpenes, neorogioldiol (2), and O11,15-cyclo-14-bromo-14,15-dihydrorogiol-3,11-diol (3), with equally potent activity. We investigated the mechanism of action of metabolites 1⁻3 and found that all three suppressed macrophage activation and promoted an M2-like anti-inflammatory phenotype by inducing expression of Arginase1, MRC1, IRAK-M, the transcription factor C/EBPβ, and the miRNA miR-146a. In addition, they suppressed iNOS induction and nitric oxide production. Importantly, treatment of mice with 2 or 3 suppressed DSS-induced colitis by reducing tissue damage and pro-inflammatory cytokine production. Thus, all these three diterpenes are promising lead molecules for the development of anti-inflammatory agents targeting macrophage polarization mechanisms.
- Published
- 2019
- Full Text
- View/download PDF
6. New C
- Author
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Maria, Harizani, Dafni-Ioanna, Diakaki, Stamatios, Perdikaris, Vassilios, Roussis, and Efstathia, Ioannou
- Subjects
Biological Products ,Acetogenins ,Rhodophyta ,Laurencia ,Sesquiterpenes - Abstract
The chemical diversity of the approximately 1,200 natural products isolated from red algae of the genus
- Published
- 2022
7. In Vivo Evaluation of the Wound Healing Activity of Extracts and Bioactive Constituents of the Marine Isopod Ceratothoa oestroides
- Author
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Efstathia Ioannou, Michail Rallis, Maria Harizani, Vassilios Roussis, Evgenia Sofrona, Panagiota Koroli, Ioannis Sfiniadakis, and Leto-Aikaterini Tziveleka
- Subjects
Male ,eicosapentaenoic acid ,Administration, Topical ,Pharmaceutical Science ,Pharmacology ,Ceratothoa oestroides ,SKH-hr1 hairless mice ,01 natural sciences ,Skin thickness ,Myristic Acid ,Article ,Fatty Acids, Monounsaturated ,Ointments ,03 medical and health sciences ,Mice ,In vivo ,Drug Discovery ,Animals ,Pharmacology, Toxicology and Pharmaceutics (miscellaneous) ,lcsh:QH301-705.5 ,030304 developmental biology ,marine isopod ,Skin ,0303 health sciences ,Transepidermal water loss ,Mice, Hairless ,Wound Healing ,integumentary system ,010405 organic chemistry ,Chemistry ,Tissue Extracts ,Histopathological analysis ,Eicosapentaenoic acid ,0104 chemical sciences ,Hairless ,lcsh:Biology (General) ,Wound healing ,Isopoda - Abstract
Wound healing is a fundamental response to tissue injury and a number of natural products has been found to accelerate the healing process. Herein, we report the preparation of a series of different polarity (organic and aqueous) extracts of the marine isopod Ceratothoa oestroides and the in vivo evaluation of their wound healing activity after topical administration of ointments incorporating the various extracts on wounds inflicted on SKH-hr1 hairless mice. The most active extract was fractionated for enrichment in the bioactive constituents and the fractions were further evaluated for their wound healing activity, while their chemical profiles were analyzed. Wound healing was evaluated by clinical assessment, photo-documentation, histopathological analysis and measurement of biophysical skin parameters, such as transepidermal water loss (TEWL), hydration, elasticity, and skin thickness. The highest levels of activity were exerted by treatment of the wounds with a fraction rich in eicosapentaenoic acid (EPA), as well as myristic and palmitoleic acids. Topical application of the bioactive fraction on the wounds of mice resulted in complete wound closure with a skin of almost normal architecture without any inflammatory elements.
- Published
- 2020
8. Neorogioltriol and Related Diterpenes from the Red Alga
- Author
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Maria G, Daskalaki, Dimitra, Vyrla, Maria, Harizani, Christina, Doxaki, Aristides G, Eliopoulos, Vassilios, Roussis, Efstathia, Ioannou, Christos, Tsatsanis, and Sotirios C, Kampranis
- Subjects
Molecular Structure ,colitis ,Macrophages ,Dextran Sulfate ,Inflammatory Bowel Diseases ,Laurencia ,Article ,Mice, Inbred C57BL ,Mice ,RAW 264.7 Cells ,halogenated diterpenes ,nitric oxide ,cytokine ,Animals ,Diterpenes ,neorogioltriol ,Cell Proliferation ,TNF-alpha - Abstract
Macrophages are central mediators of inflammation, orchestrating the inflammatory response through the production of cytokines and nitric oxide. Macrophages obtain pro-inflammatory (M1) and anti-inflammatory (M2) phenotypes, which can be modulated by soluble factors, including natural products. Despite the crucial protective role of inflammation, chronic or deregulated inflammation can lead to pathological states, such as autoimmune diseases, metabolic disorders, cardiovascular diseases, and cancer. In this case, we studied the anti-inflammatory activity of neorogioltriol (1) in depth and identified two structurally related diterpenes, neorogioldiol (2), and O11,15-cyclo-14-bromo-14,15-dihydrorogiol-3,11-diol (3), with equally potent activity. We investigated the mechanism of action of metabolites 1–3 and found that all three suppressed macrophage activation and promoted an M2-like anti-inflammatory phenotype by inducing expression of Arginase1, MRC1, IRAK-M, the transcription factor C/EBPβ, and the miRNA miR-146a. In addition, they suppressed iNOS induction and nitric oxide production. Importantly, treatment of mice with 2 or 3 suppressed DSS-induced colitis by reducing tissue damage and pro-inflammatory cytokine production. Thus, all these three diterpenes are promising lead molecules for the development of anti-inflammatory agents targeting macrophage polarization mechanisms.
- Published
- 2018
9. The Laurencia Paradox: An Endless Source of Chemodiversity
- Author
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Maria, Harizani, Efstathia, Ioannou, and Vassilios, Roussis
- Subjects
Biological Products ,Animals ,Humans ,Biodiversity ,Laurencia - Abstract
Nature, the most prolific source of biological and chemical diversity, has provided mankind with treatments for health problems since ancient times and continues to be the most promising reservoir of bioactive chemicals for the development of modern drugs. In addition to the terrestrial organisms that still remain a promising source of new bioactive metabolites, the marine environment, covering approximately 70% of the Earth's surface and containing a largely unexplored biodiversity, offers an enormous resource for the discovery of novel compounds. According to the MarinLit database, more than 27,000 metabolites from marine macro- and microorganisms have been isolated to date providing material and key structures for the development of new products in the pharmaceutical, food, cosmeceutical, chemical, and agrochemical sectors. Algae, which thrive in the euphotic zone, were among the first marine organisms that were investigated as sources of food, nutritional supplements, soil fertilizers, and bioactive metabolites.Red algae of the genus Laurencia are accepted unanimously as one of the richest sources of new secondary metabolites. Their cosmopolitan distribution, along with the chemical variation influenced to a significant degree by environmental and genetic factors, have resulted in an endless parade of metabolites, often featuring multiple halogenation sites.The present contribution, covering the literature until August 2015, offers a comprehensive view of the chemical wealth and the taxonomic problems currently impeding chemical and biological investigations of the genus Laurencia. Since mollusks feeding on Laurencia are, in many cases, bioaccumulating, and utilize algal metabolites as chemical weaponry against natural enemies, metabolites of postulated dietary origin of sea hares that feed on Laurencia species are also included in the present review. Altogether, 1047 secondary metabolites, often featuring new carbocyclic skeletons, have been included.The chapter addresses: (1) the "Laurencia complex", the botanical description and the growth and population dynamics of the genus, as well as its chemical diversity and ecological relations; (2) the secondary metabolites, which are organized according to their chemical structures and are classified into sesquiterpenes, diterpenes, triterpenes, acetogenins, indoles, aromatic compounds, steroids, and miscellaneous compounds, as well as their sources of isolation which are depicted in tabulated form, and (3) the biological activity organized according to the biological target and the ecological functions of Laurencia metabolites.
- Published
- 2016
10. The Laurencia Paradox: An Endless Source of Chemodiversity
- Author
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Efstathia Ioannou, Vassilios Roussis, and Maria Harizani
- Subjects
Resource (biology) ,biology ,010405 organic chemistry ,Agrochemical ,business.industry ,Ecology ,Biodiversity ,Laurencia ,010402 general chemistry ,biology.organism_classification ,01 natural sciences ,0104 chemical sciences ,Providing material ,Health problems ,Algae ,Chemical diversity ,business - Abstract
Nature, the most prolific source of biological and chemical diversity, has provided mankind with treatments for health problems since ancient times and continues to be the most promising reservoir of bioactive chemicals for the development of modern drugs. In addition to the terrestrial organisms that still remain a promising source of new bioactive metabolites, the marine environment, covering approximately 70% of the Earth’s surface and containing a largely unexplored biodiversity, offers an enormous resource for the discovery of novel compounds. According to the MarinLit database, more than 27,000 metabolites from marine macro- and microorganisms have been isolated to date providing material and key structures for the development of new products in the pharmaceutical, food, cosmeceutical, chemical, and agrochemical sectors. Algae, which thrive in the euphotic zone, were among the first marine organisms that were investigated as sources of food, nutritional supplements, soil fertilizers, and bioactive metabolites.
- Published
- 2016
- Full Text
- View/download PDF
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