Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 2 de 2
Filtrar
Mais filtros

Base de dados
País/Região como assunto
Ano de publicação
Tipo de documento
País de afiliação
Intervalo de ano de publicação
1.
J Ind Microbiol Biotechnol ; 42(1): 57-72, 2015 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-25371290

RESUMO

Marine sediments from Newfoundland, Canada were explored for biotechnologically promising Actinobacteria using culture-independent and culture-dependent approaches. Culture-independent pyrosequencing analyses uncovered significant actinobacterial diversity (H'-2.45 to 3.76), although the taxonomic diversity of biotechnologically important actinomycetes could not be fully elucidated due to limited sampling depth. Assessment of culturable actinomycete diversity resulted in the isolation of 360 actinomycetes representing 59 operational taxonomic units, the majority of which (94 %) were Streptomyces. The biotechnological potential of actinomycetes from NL sediments was assessed by bioactivity and metabolomics-based screening of 32 representative isolates. Bioactivity was exhibited by 41 % of isolates, while 11 % exhibited unique chemical signatures in metabolomics screening. Chemical analysis of two isolates resulted in the isolation of the cytotoxic metabolite 1-isopentadecanoyl-3ß-D-glucopyranosyl-X-glycerol from Actinoalloteichus sp. 2L868 and sungsanpin from Streptomyces sp. 8LB7. These results demonstrate the potential for the discovery of novel bioactive metabolites from actinomycetes isolated from Atlantic Canadian marine sediments.


Assuntos
Actinobacteria/química , Actinobacteria/isolamento & purificação , Sedimentos Geológicos/microbiologia , Streptomyces/química , Actinobacteria/genética , Actinomycetales/química , Actinomycetales/genética , Actinomycetales/isolamento & purificação , Anti-Infecciosos/farmacologia , Antineoplásicos/farmacologia , Linhagem Celular Tumoral , Meios de Cultura/química , DNA Bacteriano/genética , Resistência Microbiana a Medicamentos , Fermentação , Humanos , Metabolômica , Terra Nova e Labrador , Peptídeos/farmacologia , Filogenia , RNA Ribossômico 16S/genética , Análise de Sequência de DNA , Streptomyces/genética , Streptomyces/isolamento & purificação
2.
Behav Brain Res ; 337: 151-159, 2018 Jan 30.
Artigo em Inglês | MEDLINE | ID: mdl-28935439

RESUMO

It has been established that both adult and larval zebrafish are capable of showing nociceptive responses to noxious stimuli; however, the use of larvae to test novel analgesics has not been fully explored. Zebrafish larvae represent a low-cost, high-throughput alternative to traditional mammalian models for the assessment of product efficacy during the initial stages of drug development. In the current study, a novel model of nociception using zebrafish larvae is described. During the recovery from an acute exposure to low levels of acetic acid, larvae display innate changes in behaviour that may be indicative of nociception. To assess the usefulness of this model for testing potential analgesics, three known synthetic pain medications were assessed (ibuprofen, acetaminophen and tramadol) along with three naturally occurring products (honokiol, tetrahydrocannabinol and cannabidiol). When the effect of each compound on both the acetic acid recovery and control activity was compared there appeared to be both similarities and differences between the compounds. One of the most interesting effects was found for cannabidiol which appeared to oppose the activity change during the recovery period of AA exposed larvae while having a nominal effect on control activity. This would appear to be in line with current research that has demonstrated the nociceptive properties of cannabidiol. Here we have provided a novel model that will complement existing zebrafish models and will expand on the potential use of zebrafish larvae for studying both nociception and new analgesics.


Assuntos
Analgésicos/uso terapêutico , Canabinoides/metabolismo , Canabinoides/uso terapêutico , Nociceptividade/fisiologia , Dor/tratamento farmacológico , Acetaminofen , Ácido Acético/toxicidade , Animais , Agonistas de Receptores de Canabinoides/uso terapêutico , Modelos Animais de Doenças , Relação Dose-Resposta a Droga , Dronabinol/uso terapêutico , Ibuprofeno , Larva , Locomoção/efeitos dos fármacos , Nociceptividade/efeitos dos fármacos , Dor/induzido quimicamente , Análise de Componente Principal , Fatores de Tempo , Tramadol , Peixe-Zebra
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA