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Identification of Cyanobacterial Strains with Potential for the Treatment of Obesity-Related Co-Morbidities by Bioactivity, Toxicity Evaluation and Metabolite Profiling
Obesity is a complex disease resulting in several metabolic co-morbidities and is increasing at epidemic rates. The marine environment is an interesting resource of novel compounds and in particular cyanobacteria are well known for their capacity to produce novel secondary metabolites. In this work,...
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Published in: | Marine drugs 2019-05, Vol.17 (5), p.280 |
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creator | Costa, Margarida Rosa, Filipa Ribeiro, Tiago Hernandez-Bautista, Rene Bonaldo, Marco Gonçalves Silva, Natália Eiríksson, Finnur Thorsteinsdóttir, Margrét Ussar, Siegfried Urbatzka, Ralph |
description | Obesity is a complex disease resulting in several metabolic co-morbidities and is increasing at epidemic rates. The marine environment is an interesting resource of novel compounds and in particular cyanobacteria are well known for their capacity to produce novel secondary metabolites. In this work, we explored the potential of cyanobacteria for the production of compounds with relevant activities towards metabolic diseases using a blend of target-based, phenotypic and zebrafish assays as whole small animal models. A total of 46 cyanobacterial strains were grown and biomass fractionated, yielding in total 263 fractions. Bioactivities related to metabolic function were tested in different
and
models. Studying adipogenic and thermogenic gene expression in brown adipocytes, lipid metabolism and glucose uptake in hepatocytes, as well as lipid metabolism in zebrafish larvae, we identified 66 (25%) active fractions. This together with metabolite profiling and the evaluation of toxicity allowed the identification of 18 (7%) fractions with promising bioactivity towards different aspects of metabolic disease. Among those, we identified several known compounds, such as eryloside T, leptosin F, pheophorbide A, phaeophytin A, chlorophyll A, present as minor peaks. Those compounds were previously not described to have bioactivities in metabolic regulation, and both known or unknown compounds could be responsible for such effects. In summary, we find that cyanobacteria hold a huge repertoire of molecules with specific bioactivities towards metabolic diseases, which needs to be explored in the future. |
doi_str_mv | 10.3390/md17050280 |
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and
models. Studying adipogenic and thermogenic gene expression in brown adipocytes, lipid metabolism and glucose uptake in hepatocytes, as well as lipid metabolism in zebrafish larvae, we identified 66 (25%) active fractions. This together with metabolite profiling and the evaluation of toxicity allowed the identification of 18 (7%) fractions with promising bioactivity towards different aspects of metabolic disease. Among those, we identified several known compounds, such as eryloside T, leptosin F, pheophorbide A, phaeophytin A, chlorophyll A, present as minor peaks. Those compounds were previously not described to have bioactivities in metabolic regulation, and both known or unknown compounds could be responsible for such effects. In summary, we find that cyanobacteria hold a huge repertoire of molecules with specific bioactivities towards metabolic diseases, which needs to be explored in the future.</description><identifier>ISSN: 1660-3397</identifier><identifier>EISSN: 1660-3397</identifier><identifier>DOI: 10.3390/md17050280</identifier><identifier>PMID: 31083362</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Adipocytes ; Animal models ; anti-obesity drugs ; bioactivity screening ; Biocompatibility ; Biological activity ; Chlorophyll ; Chlorophyll a ; Cyanobacteria ; Cytotoxicity ; Danio rerio ; diabetes ; Diseases ; Ecosystems ; Evaluation ; fatty liver disease ; Freshwater fishes ; Gastrointestinal surgery ; Gene expression ; Glucose ; Glucose metabolism ; Hepatocytes ; Homeostasis ; Identification ; Larvae ; Lipid metabolism ; Lipids ; Marine environment ; Metabolic disorders ; Metabolism ; metabolite profiling ; Metabolites ; Morbidity ; Natural products ; Obesity ; Phaeophytin ; Principal components analysis ; Profiling ; Secondary metabolites ; Toxicity ; uncoupling protein 1 ; Uptake ; Weight control ; Zebrafish ; zebrafish Nile red fat metabolism assay</subject><ispartof>Marine drugs, 2019-05, Vol.17 (5), p.280</ispartof><rights>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/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2019 by the authors. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c472t-27f2ad0a1e4ec6ef605d207bf05b87ab73bf1796eaa3f85a8d41b47cf785084c3</citedby><cites>FETCH-LOGICAL-c472t-27f2ad0a1e4ec6ef605d207bf05b87ab73bf1796eaa3f85a8d41b47cf785084c3</cites><orcidid>0000-0001-9147-8621 ; 0000-0001-7476-9195</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2548612267/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2548612267?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,74998</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31083362$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Costa, Margarida</creatorcontrib><creatorcontrib>Rosa, Filipa</creatorcontrib><creatorcontrib>Ribeiro, Tiago</creatorcontrib><creatorcontrib>Hernandez-Bautista, Rene</creatorcontrib><creatorcontrib>Bonaldo, Marco</creatorcontrib><creatorcontrib>Gonçalves Silva, Natália</creatorcontrib><creatorcontrib>Eiríksson, Finnur</creatorcontrib><creatorcontrib>Thorsteinsdóttir, Margrét</creatorcontrib><creatorcontrib>Ussar, Siegfried</creatorcontrib><creatorcontrib>Urbatzka, Ralph</creatorcontrib><title>Identification of Cyanobacterial Strains with Potential for the Treatment of Obesity-Related Co-Morbidities by Bioactivity, Toxicity Evaluation and Metabolite Profiling</title><title>Marine drugs</title><addtitle>Mar Drugs</addtitle><description>Obesity is a complex disease resulting in several metabolic co-morbidities and is increasing at epidemic rates. The marine environment is an interesting resource of novel compounds and in particular cyanobacteria are well known for their capacity to produce novel secondary metabolites. In this work, we explored the potential of cyanobacteria for the production of compounds with relevant activities towards metabolic diseases using a blend of target-based, phenotypic and zebrafish assays as whole small animal models. A total of 46 cyanobacterial strains were grown and biomass fractionated, yielding in total 263 fractions. Bioactivities related to metabolic function were tested in different
and
models. Studying adipogenic and thermogenic gene expression in brown adipocytes, lipid metabolism and glucose uptake in hepatocytes, as well as lipid metabolism in zebrafish larvae, we identified 66 (25%) active fractions. This together with metabolite profiling and the evaluation of toxicity allowed the identification of 18 (7%) fractions with promising bioactivity towards different aspects of metabolic disease. Among those, we identified several known compounds, such as eryloside T, leptosin F, pheophorbide A, phaeophytin A, chlorophyll A, present as minor peaks. Those compounds were previously not described to have bioactivities in metabolic regulation, and both known or unknown compounds could be responsible for such effects. 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Ralph</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of Cyanobacterial Strains with Potential for the Treatment of Obesity-Related Co-Morbidities by Bioactivity, Toxicity Evaluation and Metabolite Profiling</atitle><jtitle>Marine drugs</jtitle><addtitle>Mar Drugs</addtitle><date>2019-05-10</date><risdate>2019</risdate><volume>17</volume><issue>5</issue><spage>280</spage><pages>280-</pages><issn>1660-3397</issn><eissn>1660-3397</eissn><abstract>Obesity is a complex disease resulting in several metabolic co-morbidities and is increasing at epidemic rates. The marine environment is an interesting resource of novel compounds and in particular cyanobacteria are well known for their capacity to produce novel secondary metabolites. In this work, we explored the potential of cyanobacteria for the production of compounds with relevant activities towards metabolic diseases using a blend of target-based, phenotypic and zebrafish assays as whole small animal models. A total of 46 cyanobacterial strains were grown and biomass fractionated, yielding in total 263 fractions. Bioactivities related to metabolic function were tested in different
and
models. Studying adipogenic and thermogenic gene expression in brown adipocytes, lipid metabolism and glucose uptake in hepatocytes, as well as lipid metabolism in zebrafish larvae, we identified 66 (25%) active fractions. This together with metabolite profiling and the evaluation of toxicity allowed the identification of 18 (7%) fractions with promising bioactivity towards different aspects of metabolic disease. Among those, we identified several known compounds, such as eryloside T, leptosin F, pheophorbide A, phaeophytin A, chlorophyll A, present as minor peaks. Those compounds were previously not described to have bioactivities in metabolic regulation, and both known or unknown compounds could be responsible for such effects. In summary, we find that cyanobacteria hold a huge repertoire of molecules with specific bioactivities towards metabolic diseases, which needs to be explored in the future.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>31083362</pmid><doi>10.3390/md17050280</doi><orcidid>https://orcid.org/0000-0001-9147-8621</orcidid><orcidid>https://orcid.org/0000-0001-7476-9195</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adipocytes Animal models anti-obesity drugs bioactivity screening Biocompatibility Biological activity Chlorophyll Chlorophyll a Cyanobacteria Cytotoxicity Danio rerio diabetes Diseases Ecosystems Evaluation fatty liver disease Freshwater fishes Gastrointestinal surgery Gene expression Glucose Glucose metabolism Hepatocytes Homeostasis Identification Larvae Lipid metabolism Lipids Marine environment Metabolic disorders Metabolism metabolite profiling Metabolites Morbidity Natural products Obesity Phaeophytin Principal components analysis Profiling Secondary metabolites Toxicity uncoupling protein 1 Uptake Weight control Zebrafish zebrafish Nile red fat metabolism assay |
title | Identification of Cyanobacterial Strains with Potential for the Treatment of Obesity-Related Co-Morbidities by Bioactivity, Toxicity Evaluation and Metabolite Profiling |
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