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1.
Exp Parasitol ; 87(3): 171-84, 1997 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-9371082

RESUMO

Polyamines (PA) are essential for viability and replication of all cells; organisms either synthesize PA or acquire them from the environment. How nematodes that parasitize the gut satisfy their PA requirement has not been resolved. The primary regulatory enzyme in PA biosynthesis in most animals is ornithine decarboxylase (ODC). This enzyme has recently been characterized in free-living nematodes and in the parasitic species. Haemonchus contortus. Nematode and mammalian ODC are reported to differ in subcellular localization, kinetics, and sensitivity to inhibitors. We cloned an H. contortus cDNA that encodes a full-length ODC (sequence data from this article have been deposited with the GenBank Data Library under Accession Nos. AF016538 and AF016891). This cDNA was functionally expressed in strains of Escherichia coli and Saccharomyces cerevisiae that lack ODC and are dependent upon exogenous PA for survival. Expression of nematode ODC reversed the PA-dependence phenotype of both microorganisms. The complemented yeast strain was used to develop a nutrient-dependent viability screen for selective inhibitors of nematode ODC. The antiprotozoal drug stilbamidine isethionate was identified as active in this screen, but biochemical characterization revealed that this compound did not inhibit ODC. Instead, like other cationic diamidines, stilbamidine probably inhibits yeast S-adenosylmethionine decarboxylase. Nonetheless, the activity in the screen of the known ODC inhibitor difluoromethylornithine (DFMO) validates the concept that specific recombinant microorganisms can serve as the basis for extremely selective and facile screens.


Assuntos
Avaliação Pré-Clínica de Medicamentos/métodos , Haemonchus/enzimologia , Inibidores da Ornitina Descarboxilase , Estilbamidinas/farmacologia , Sequência de Aminoácidos , Animais , Sequência de Bases , Clonagem Molecular , DNA Complementar/genética , Inibidores Enzimáticos , Escherichia coli/genética , Teste de Complementação Genética , Haemonchus/genética , Proteínas de Helminto/efeitos dos fármacos , Dados de Sequência Molecular , Ornitina Descarboxilase/genética , Poliaminas/metabolismo , Proteínas Recombinantes/biossíntese , Saccharomyces cerevisiae/genética , Seleção Genética , Homologia de Sequência de Aminoácidos
2.
Exp Parasitol ; 77(1): 88-96, 1993 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-8344410

RESUMO

How the avermectins cause the elimination of gastrointestinal nematodes from host animals has not yet been clearly identified. Using visual and radiometric parameters to measure oral ingestion in Haemonchus contortus, we showed that ivermectin (IVM) rapidly inhibited ingestion at concentrations > or = 10(-10) M. Motility, monitored quantitatively with an automated motility meter, was unaffected by IVM at concentrations < or = 10(-8) M, while ATP levels were unaffected at concentrations < or = 10(-6) M. Since motility and ATP levels, independent measures of short-term viability, are unaffected by concentrations of IVM that effectively block oral ingestion, the drug can be used as a chemical ligature. Although H. contortus was shown to be dependent upon an exogenous supply of glucose for survival in culture, IVM (10(-9) and 10(-7) M) altered neither the uptake of 3-O-[3H]methylglucose nor the metabolism of [13C]glucose by the parasite. These data suggest that H. contortus depends upon the transcuticular uptake of glucose in culture. If oral ingestion of other nutrients is essential for long-term survival in vivo, disruption of this process may represent the primary mechanism of IVM action.


Assuntos
Haemonchus/efeitos dos fármacos , Ivermectina/farmacologia , 3-O-Metilglucose , Trifosfato de Adenosina/metabolismo , Animais , Carbonil Cianeto m-Clorofenil Hidrazona/farmacologia , Feminino , Glucose/metabolismo , Haemonchus/fisiologia , Metilglucosídeos/metabolismo , Mitocôndrias/efeitos dos fármacos , Mitocôndrias/metabolismo , Movimento/efeitos dos fármacos , Faringe/efeitos dos fármacos , Faringe/fisiologia
3.
J Parasitol ; 78(2): 215-30, 1992 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-1556638

RESUMO

Processes that critically differentiate parasitic helminths and their hosts are obvious candidates for chemotherapeutic intervention. The recognition that neurobiology distinguishes helminths from their vertebrate hosts is due in part to the fact that several efficacious anthelmintics, derived generally from empirical screening, have been found to act selectively on the neuromuscular system of these parasites. In addition, basic physiological and pharmacological research has revealed considerable differences in the ways in which helminths and their hosts transmit information in the nervous system and respond to it in innervated tissues. Unfortunately, most of these differences have yet to be exploited in chemotherapy. The topics for this review include an analysis of mechanistic aspects of the pharmacology of anthelmintics that act on neuromuscular systems and a consideration of the prospects for discovery of novel drugs that act on this system.


Assuntos
Anti-Helmínticos/farmacologia , Helmintíase/tratamento farmacológico , Helmintos/efeitos dos fármacos , Animais , Anti-Helmínticos/uso terapêutico , Cestoides/efeitos dos fármacos , Nematoides/efeitos dos fármacos , Sistema Nervoso/efeitos dos fármacos , Trematódeos/efeitos dos fármacos
4.
Biosystems ; 26(3): 155-8, 1992.
Artigo em Inglês | MEDLINE | ID: mdl-1567994

RESUMO

Neuromass, the mass of central nervous tissue per unit area, is suggested as a new parameter for studying ecosystems. Its use is demonstrated with a comparison of biomass and neuromass distributions for a stream riffle ecosystem in the Huron River, southeastern Michigan. Biomass and neuromass were estimated for three animal groups: small invertebrates, crayfish, and fish. For small invertebrates the mass of the longitudinal nerve cord was estimated with histological sectioning and volumetric calculation. For crayfish and fish the central nervous system was dissected out and weighed. Total biomass was about 12 g dry wt/m2 and was dominated by small invertebrates that made up 76% of the total. Total neuromass was about 0.2 g wet wt/m2. Fish neuromass made up 93% of the total neuromass even though their biomass contribution was only 18% of the total. These results are discussed in relation to the potential of this approach for developing a view of information processing at the ecosystem level of organization.


Assuntos
Sistema Nervoso Central/anatomia & histologia , Ecologia , Animais , Astacoidea/anatomia & histologia , Peixes/anatomia & histologia , Água Doce , Invertebrados/anatomia & histologia , Michigan , Neurobiologia
5.
Mol Biochem Parasitol ; 22(2-3): 241-8, 1987 Jan 15.
Artigo em Inglês | MEDLINE | ID: mdl-3033496

RESUMO

Ascaris suum L3 larvae isolated from rabbit lungs undergo the third ecdysis to L4 larvae after 3 days in culture under a gas phase of 85% N2/10% CO2/5% O2. The L3 larvae contain substantial malic enzyme activity and are capable of producing small amounts of the reduced organic acids characteristic of the fermentative pathways which operate in the adult. However, only a small portion of the total carbon utilized is accounted for by these reduced acids and their motility is cyanide-sensitive, suggesting that their energy-generating pathways are predominantly aerobic. In contrast, after ecdysis, the L4 larvae begin to utilize glucose at a greater rate and the proportion of total carbon utilized which is accounted for as propionate, 2-methylbutyrate and 2-methylvalerate also increases. In addition, motility becomes increasingly cyanide-insensitive, suggesting that these L4 larvae are able to utilize the anaerobic energy-generating pathways of the adult. Surprisingly, on day 10 in culture, these L4 larvae, although capable of producing reduced volatile acids, still retain substantial cyanide-sensitive cytochrome oxidase activity.


Assuntos
Ascaris/metabolismo , Ácidos Graxos Voláteis/biossíntese , Aerobiose , Anaerobiose , Animais , Ascaris/enzimologia , Ascaris/crescimento & desenvolvimento , Butiratos/biossíntese , Cianetos/farmacologia , Complexo IV da Cadeia de Transporte de Elétrons/metabolismo , Metabolismo Energético , Glucose/metabolismo , Larva/enzimologia , Larva/metabolismo , Malato Desidrogenase/metabolismo , Movimento/efeitos dos fármacos , Oxirredução , Ácidos Pentanoicos/biossíntese , Propionatos/biossíntese
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