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Chlorophyll Derivatives from Marine Cyanobacteria with Lipid-Reducing Activities
Marine organisms, particularly cyanobacteria, are important resources for the production of bioactive secondary metabolites for the treatment of human diseases. In this study, a bioassay-guided approach was used to discover metabolites with lipid-reducing activity. Two chlorophyll derivatives were s...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6520785/ https://www.ncbi.nlm.nih.gov/pubmed/30999602 http://dx.doi.org/10.3390/md17040229 |
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author | Freitas, Sara Silva, Natália Gonçalves Sousa, Maria Lígia Ribeiro, Tiago Rosa, Filipa Leão, Pedro N. Vasconcelos, Vitor Reis, Mariana Alves Urbatzka, Ralph |
author_facet | Freitas, Sara Silva, Natália Gonçalves Sousa, Maria Lígia Ribeiro, Tiago Rosa, Filipa Leão, Pedro N. Vasconcelos, Vitor Reis, Mariana Alves Urbatzka, Ralph |
author_sort | Freitas, Sara |
collection | PubMed |
description | Marine organisms, particularly cyanobacteria, are important resources for the production of bioactive secondary metabolites for the treatment of human diseases. In this study, a bioassay-guided approach was used to discover metabolites with lipid-reducing activity. Two chlorophyll derivatives were successfully isolated, the previously described 13(2)-hydroxy-pheophytin a (1) and the new compound 13(2)-hydroxy-pheofarnesin a (2). The structure elucidation of the new compound 2 was established based on one- and two-dimensional (1D and 2D) NMR spectroscopy and mass spectrometry. Compounds 1 and 2 showed significant neutral lipid-reducing activity in the zebrafish Nile red fat metabolism assay after 48 h of exposure with a half maximal effective concentration (EC(50)) of 8.9 ± 0.4 µM for 1 and 15.5 ± 1.3 µM for 2. Both compounds additionally reduced neutral lipid accumulation in 3T3-L1 multicellular spheroids of murine preadipocytes. Molecular profiling of mRNA expression of some target genes was evaluated for the higher potent compound 1, which indicated altered peroxisome proliferator activated receptor gamma (PPARγ) mRNA expression. Lipolysis was not affected. Different food materials (Spirulina, Chlorella, spinach, and cabbage) were evaluated for the presence of 1, and the cyanobacterium Spirulina, with GRAS (generally regarded as safe) status for human consumption, contained high amounts of 1. In summary, known and novel chlorophyll derivatives were discovered from marine cyanobacteria with relevant lipid-reducing activities, which in the future may be developed into nutraceuticals. |
format | Online Article Text |
id | pubmed-6520785 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-65207852019-06-03 Chlorophyll Derivatives from Marine Cyanobacteria with Lipid-Reducing Activities Freitas, Sara Silva, Natália Gonçalves Sousa, Maria Lígia Ribeiro, Tiago Rosa, Filipa Leão, Pedro N. Vasconcelos, Vitor Reis, Mariana Alves Urbatzka, Ralph Mar Drugs Article Marine organisms, particularly cyanobacteria, are important resources for the production of bioactive secondary metabolites for the treatment of human diseases. In this study, a bioassay-guided approach was used to discover metabolites with lipid-reducing activity. Two chlorophyll derivatives were successfully isolated, the previously described 13(2)-hydroxy-pheophytin a (1) and the new compound 13(2)-hydroxy-pheofarnesin a (2). The structure elucidation of the new compound 2 was established based on one- and two-dimensional (1D and 2D) NMR spectroscopy and mass spectrometry. Compounds 1 and 2 showed significant neutral lipid-reducing activity in the zebrafish Nile red fat metabolism assay after 48 h of exposure with a half maximal effective concentration (EC(50)) of 8.9 ± 0.4 µM for 1 and 15.5 ± 1.3 µM for 2. Both compounds additionally reduced neutral lipid accumulation in 3T3-L1 multicellular spheroids of murine preadipocytes. Molecular profiling of mRNA expression of some target genes was evaluated for the higher potent compound 1, which indicated altered peroxisome proliferator activated receptor gamma (PPARγ) mRNA expression. Lipolysis was not affected. Different food materials (Spirulina, Chlorella, spinach, and cabbage) were evaluated for the presence of 1, and the cyanobacterium Spirulina, with GRAS (generally regarded as safe) status for human consumption, contained high amounts of 1. In summary, known and novel chlorophyll derivatives were discovered from marine cyanobacteria with relevant lipid-reducing activities, which in the future may be developed into nutraceuticals. MDPI 2019-04-17 /pmc/articles/PMC6520785/ /pubmed/30999602 http://dx.doi.org/10.3390/md17040229 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Freitas, Sara Silva, Natália Gonçalves Sousa, Maria Lígia Ribeiro, Tiago Rosa, Filipa Leão, Pedro N. Vasconcelos, Vitor Reis, Mariana Alves Urbatzka, Ralph Chlorophyll Derivatives from Marine Cyanobacteria with Lipid-Reducing Activities |
title | Chlorophyll Derivatives from Marine Cyanobacteria with Lipid-Reducing Activities |
title_full | Chlorophyll Derivatives from Marine Cyanobacteria with Lipid-Reducing Activities |
title_fullStr | Chlorophyll Derivatives from Marine Cyanobacteria with Lipid-Reducing Activities |
title_full_unstemmed | Chlorophyll Derivatives from Marine Cyanobacteria with Lipid-Reducing Activities |
title_short | Chlorophyll Derivatives from Marine Cyanobacteria with Lipid-Reducing Activities |
title_sort | chlorophyll derivatives from marine cyanobacteria with lipid-reducing activities |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6520785/ https://www.ncbi.nlm.nih.gov/pubmed/30999602 http://dx.doi.org/10.3390/md17040229 |
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