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Stimulation of diamondback moth (Plutella xylostella) adenylate cyclase activity by a carbodiimide
Affiliation:1. UMR BIPAR 956 INRA-ANSES-ENVA, Maisons-Alfort, France;2. Université de Strasbourg, Strasbourg, France;3. Centre National de Référence Borrelia, Strasbourg, France
Abstract:
1. DFCD or 3-(2,6-diisopropyl-4-phenoxyphenyl)-1-tert-butylcarbodiimide, a toxic metabolite of the thiourea acaricide/insecticide diafenthiuron, stimulated adenylate cyclase activity in preparations from heads of adult diamondback moths, Ptutella xylostella (L.).2. Depending upon assay conditions, DFCD gave a biphasic response with Ka, values of 0.025 and 1.25 μM for high and low affinity components, respectively, or a monophasic response with a Ka of 0.4 μM.3. Studies with potential agonists and antagonists suggested that octopamine-sensitive (Ka 7.5 μM) and dopamine-sensitive (Ka, 1.0μM) adenylate cyclases were present.4. At maximally effective concentrations, the activity of DFCD was nonadditive to that of octopamine or dopamine.5. It appeared that DFCD was binding to octopamine- and dopamine-sensitive adenylate cyclases and that affinity of the carbodiimide was higher for the former than for the latter.6. These actions on biogenic amine-sensitive adenylate cyclases likely are involved in the toxicity of diafenthiuron to diamondback moths.
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