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1.
Nature ; 452(7184): 176-80, 2008 Mar 13.
Artículo en Inglés | MEDLINE | ID: mdl-18337814

RESUMEN

Anthelmintic resistance in human and animal pathogenic helminths has been spreading in prevalence and severity to a point where multidrug resistance against the three major classes of anthelmintics--the benzimidazoles, imidazothiazoles and macrocyclic lactones--has become a global phenomenon in gastrointestinal nematodes of farm animals. Hence, there is an urgent need for an anthelmintic with a new mode of action. Here we report the discovery of the amino-acetonitrile derivatives (AADs) as a new chemical class of synthetic anthelmintics and describe the development of drug candidates that are efficacious against various species of livestock-pathogenic nematodes. These drug candidates seem to have a novel mode of action involving a unique, nematode-specific clade of acetylcholine receptor subunits. The AADs are well tolerated and of low toxicity to mammals, and overcome existing resistances to the currently available anthelmintics.


Asunto(s)
Aminoacetonitrilo/análogos & derivados , Aminoacetonitrilo/farmacología , Antihelmínticos/clasificación , Antihelmínticos/farmacología , Resistencia a Medicamentos , Nematodos/efectos de los fármacos , Enfermedades Parasitarias en Animales/parasitología , Envejecimiento , Secuencia de Aminoácidos , Aminoacetonitrilo/efectos adversos , Aminoacetonitrilo/farmacocinética , Animales , Antihelmínticos/química , Antihelmínticos/farmacocinética , Caenorhabditis elegans/efectos de los fármacos , Caenorhabditis elegans/genética , Caenorhabditis elegans/metabolismo , Proteínas de Caenorhabditis elegans/química , Proteínas de Caenorhabditis elegans/genética , Proteínas de Caenorhabditis elegans/metabolismo , Bovinos , Enfermedades de los Bovinos/tratamiento farmacológico , Enfermedades de los Bovinos/parasitología , Resistencia a Medicamentos/genética , Larva/efectos de los fármacos , Larva/genética , Datos de Secuencia Molecular , Nematodos/genética , Nematodos/fisiología , Enfermedades Parasitarias en Animales/tratamiento farmacológico , Receptores Nicotínicos/química , Receptores Nicotínicos/genética , Receptores Nicotínicos/metabolismo , Ovinos/parasitología , Enfermedades de las Ovejas/tratamiento farmacológico , Enfermedades de las Ovejas/parasitología
2.
PLoS One ; 7(5): e34712, 2012.
Artículo en Inglés | MEDLINE | ID: mdl-22563457

RESUMEN

The efficacy of all major insecticide classes continues to be eroded by the development of resistance mediated, in part, by selection of alleles encoding insecticide insensitive target proteins. The discovery of new insecticide classes acting at novel protein binding sites is therefore important for the continued protection of the food supply from insect predators, and of human and animal health from insect borne disease. Here we describe a novel class of insecticides (Spiroindolines) encompassing molecules that combine excellent activity against major agricultural pest species with low mammalian toxicity. We confidently assign the vesicular acetylcholine transporter as the molecular target of Spiroindolines through the combination of molecular genetics in model organisms with a pharmacological approach in insect tissues. The vesicular acetylcholine transporter can now be added to the list of validated insecticide targets in the acetylcholine signalling pathway and we anticipate that this will lead to the discovery of novel molecules useful in sustaining agriculture. In addition to their potential as insecticides and nematocides, Spiroindolines represent the only other class of chemical ligands for the vesicular acetylcholine transporter since those based on the discovery of vesamicol over 40 years ago, and as such, have potential to provide more selective tools for PET imaging in the diagnosis of neurodegenerative disease. They also provide novel biochemical tools for studies of the function of this protein family.


Asunto(s)
Acetilcolina/metabolismo , Compuestos Heterocíclicos de 4 o más Anillos/metabolismo , Insectos/metabolismo , Insecticidas/metabolismo , Compuestos de Espiro/metabolismo , Proteínas de Transporte Vesicular de Acetilcolina/metabolismo , Acetilcolina/farmacocinética , Secuencia de Aminoácidos , Animales , Antinematodos/química , Antinematodos/metabolismo , Antinematodos/farmacología , Transporte Biológico/efectos de los fármacos , Caenorhabditis elegans/efectos de los fármacos , Caenorhabditis elegans/genética , Caenorhabditis elegans/metabolismo , Proteínas de Caenorhabditis elegans/genética , Proteínas de Caenorhabditis elegans/metabolismo , Células Cultivadas , Drosophila melanogaster/genética , Drosophila melanogaster/metabolismo , Compuestos Heterocíclicos de 4 o más Anillos/química , Compuestos Heterocíclicos de 4 o más Anillos/farmacología , Insectos/crecimiento & desarrollo , Insecticidas/química , Insecticidas/farmacología , Larva/efectos de los fármacos , Larva/crecimiento & desarrollo , Larva/metabolismo , Datos de Secuencia Molecular , Estructura Molecular , Células PC12 , Unión Proteica , Isoformas de Proteínas/genética , Isoformas de Proteínas/metabolismo , Ratas , Homología de Secuencia de Aminoácido , Compuestos de Espiro/química , Compuestos de Espiro/farmacología , Proteínas de Transporte Vesicular de Acetilcolina/genética
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