Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Freitas, Sara, Silva, Natália Gonçalves, Sousa, Maria Lígia, Ribeiro, Tiago, Rosa, Filipa, Leão, Pedro N., Vasconcelos, Vitor, Reis, Mariana Alves, Urbatzka, Ralph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
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
_version_ 1783418811240677376
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
work_keys_str_mv AT freitassara chlorophyllderivativesfrommarinecyanobacteriawithlipidreducingactivities
AT silvanataliagoncalves chlorophyllderivativesfrommarinecyanobacteriawithlipidreducingactivities
AT sousamarialigia chlorophyllderivativesfrommarinecyanobacteriawithlipidreducingactivities
AT ribeirotiago chlorophyllderivativesfrommarinecyanobacteriawithlipidreducingactivities
AT rosafilipa chlorophyllderivativesfrommarinecyanobacteriawithlipidreducingactivities
AT leaopedron chlorophyllderivativesfrommarinecyanobacteriawithlipidreducingactivities
AT vasconcelosvitor chlorophyllderivativesfrommarinecyanobacteriawithlipidreducingactivities
AT reismarianaalves chlorophyllderivativesfrommarinecyanobacteriawithlipidreducingactivities
AT urbatzkaralph chlorophyllderivativesfrommarinecyanobacteriawithlipidreducingactivities