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1.
Toxicon ; 57(2): 266-74, 2011 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-21145338

RESUMO

Nigriventrine was isolated from the "armed" spider Phoneutria nigriventer, in which it constitutes about 0.4% of the total venom content. Its structure was determined to be [1,1'-(1-hydroxyhydrazine-1,2-diyl)bis(oxy)bis(4-hydroxy-2,6-dioxopiperidine-4 carboxylic acid)] by NMR, HR-ES/IMS and MS/MS methods. The intracerebroventricular application of nigriventrine in rat brain, followed by the detection of c-Fos protein expression, indicated that the compound was neuroactive in the motor cortex, sensory cortex, piriform cortex, median preoptic nucleus, dorsal endopiriform nucleus, lateral septal nucleus and hippocampus of rat brain. Nigriventrine causes convulsions in rats, even when peripherally applied.


Assuntos
Neurotoxinas/farmacologia , Ácidos Pipecólicos/farmacologia , Venenos de Aranha/química , Aranhas/química , Animais , Encéfalo/efeitos dos fármacos , Fracionamento Químico , Masculino , Neurônios/efeitos dos fármacos , Neurônios/metabolismo , Neurotoxinas/química , Neurotoxinas/isolamento & purificação , Ressonância Magnética Nuclear Biomolecular , Ácidos Pipecólicos/química , Ácidos Pipecólicos/isolamento & purificação , Proteínas Proto-Oncogênicas c-fos/metabolismo , Ratos , Ratos Wistar , Espectrometria de Massas por Ionização por Electrospray , Venenos de Aranha/isolamento & purificação , Venenos de Aranha/farmacologia
2.
J Nat Prod ; 73(4): 527-31, 2010 Apr 23.
Artigo em Inglês | MEDLINE | ID: mdl-20158240

RESUMO

Polybioside (1) was isolated from the venom of the social wasp Polybia paulista, and its structure was assigned as 3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl 3-(1H-imidazol-4-yl)propanimidate by NMR and MS protocols. The application of polybioside in rat brain, followed by the detection of c-Fos protein expression in some brain regions, indicated the compound is neuroactive in a number of brain areas. Polybioside causes convulsions in rats, even when peripherally applied.


Assuntos
Fármacos do Sistema Nervoso Central/isolamento & purificação , Fármacos do Sistema Nervoso Central/farmacologia , Glucosídeos/isolamento & purificação , Glucosídeos/farmacologia , Imidazóis/isolamento & purificação , Imidazóis/farmacologia , Venenos de Vespas/química , Vespas/química , Animais , Encéfalo/citologia , Encéfalo/efeitos dos fármacos , Brasil , Fármacos do Sistema Nervoso Central/química , Glucosídeos/química , Imidazóis/química , Masculino , Estrutura Molecular , Neurônios/efeitos dos fármacos , Ressonância Magnética Nuclear Biomolecular , Proteínas Proto-Oncogênicas c-fos/efeitos dos fármacos , Proteínas Proto-Oncogênicas c-fos/metabolismo , Ratos , Ratos Wistar , Convulsões/induzido quimicamente
3.
Toxicon ; 54(6): 717-24, 2009 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-19501115

RESUMO

Colonial spiders evolved a differential prey-capture behaviour in concert with their venom chemistry, which may be a source of novel drugs. Some highly active tetrahydro-beta-carboline (THbetaC) toxins were recently isolated from the venom of the colonial spider Parawixia bistriata; the spiders use these toxins as part of their chemical arsenal to kill and/or paralyze preys. The major THbetaC compound isolated from this venom was identified as 6-hydroxytrypargine, also known as PwTX-I. Most natural compounds of animal origin occur in low abundance, and the natural abundance of PwTX-I is insufficient for complete functional characterization. Thus, PwTx-I was synthesized using a Pictet-Spengler condensation strategy, and the stereoisomers of the synthetic toxin were separated by chiral chromatography. The fraction of venom containing a mixture of three natural THbetaC toxins and enantiomers of PwTx-I were analyzed for inhibition of monoamine oxidase (MAO)-A and -B and for toxicity to insects. We reveal that the mixture of the natural THbetaC toxins, as well as the enantiomers of PwTx-I, were non-competitive inhibitors of MAO-A and MAO-B and caused potent paralysis of honeybees. The (-)-PwTX-I enantiomer is 2-fold more potent than the (+)-PwTX-I enantiomer in the assays performed.


Assuntos
Alcaloides Indólicos/toxicidade , Inibidores da Monoaminoxidase/farmacologia , Venenos de Aranha/química , Animais , Alcaloides Indólicos/isolamento & purificação , Cinética , Espectroscopia de Ressonância Magnética , Espectrometria de Massas , Monoaminoxidase/efeitos dos fármacos , Monoaminoxidase/metabolismo , Espectrometria de Fluorescência , Aranhas , Estereoisomerismo
4.
J Environ Manage ; 90(2): 1060-8, 2009 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-18550265

RESUMO

In recent years, growing interest has focused on determining the performance of materials and evaluating the service life of structures exposed to various environmental forces. In this context, the determination of the aggressive potential of marine salts on mortars used as external renders is critical. The present study aimed to evaluate the spatial distribution of marine salts relative to distance from the sea. This was done by monitoring the deposition rate of chlorides and sulfates in wet candle sensors, located at nine stations scattered around the Metropolitan Region of Salvador, state of Bahia, Brazil. The study also determined the effectiveness of water-soluble salts at penetrating three different types of mortars of varying cement content via deposition and diffusion. The methodology employed enabled an evaluation of the efficiency of the monitoring sensors' measurement of the aggressiveness potential of local marine aerosol, and determination of the comparative performance of the three mortars tested, from the standpoint of resistance to salt penetration. The type and amount of salts captured both in solution and in powder samples extracted from the mortars were determined by ion chromatography. The analysis of the various types of mortars tested indicated which types are more resistant to the aggressive potential of the region's marine aerosol and the distance from the shore where local buildings are liable to be most strongly affected.


Assuntos
Cloretos/química , Materiais de Construção , Água Doce , Sulfatos/química , Brasil
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