Activation and modulation of the caenorhabditis elegans serotonin-gated chloride channel

Serotonin-gated ion channels (5-HT3) belong to the family of Cys-loop receptors, which are pentameric proteins that mediate fast synaptic transmission. In mammals, 5- HT3 are non-selective cationic channels that can be found as homomers (5-HT3A) or heteromers. The free-leaving nematode Caenorhabditis elegans is a model for the study of the nervous system and for antiparasitic drug discovery. As parasitic nematodes, C. elegans contains a homomeric serotonin-gated chloride channel, MOD-1, that modulates locomotory behavior. The absence of this receptor in vertebrates, converts MOD-1 into a potential antiparasitic drug target. We expressed MOD-1 in mammalian cells and explored by patch-clamp recordings its activation and modulation properties. Dose-response curves revealed an EC50 for 5-HT activation of about 1 µM, which is in the same range as that of human 5-HT3A receptors. The analysis of whole-cell currents determined that MOD-1 channels do not show rectification, desensitize slowly in the presence of 5-HT, and recover from desensitization with a time constant of about 1 s. In contrast to their actions at mammalian 5-HT3 receptors, 5- hydroxyindol and thymol do not potentiate MOD-1 currents. The antiparasitic drug ivermectin (IVM), which acts as activator or potentiator of different Cys-loop receptors, neither activates nor potentiates MOD-1 but pre-exposure to IVM inhibits MOD-1 currents. To gain further insights into the molecular function of the native MOD-1, we sought to identify serotonin-activated chloride channels from C. elegans neurons expressing MOD-1 and compared to MOD-1 channels heterologously expressed in mammalian cells. The understanding of the molecular pharmacology of MOD-1 contributes to our knowledge of the Cys-loop receptor family and to its potential as a novel drug target for anthelmintic therapy.Fil: Rodriguez Araujo, Noelia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; ArgentinaFil: Corradi, Jeremias. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; ArgentinaFil: Bouzat, Cecilia Beatriz. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Investigaciones Bioquímicas de Bahía Blanca. Universidad Nacional del Sur. Instituto de Investigaciones Bioquímicas de Bahía Blanca; ArgentinaLXIV Reunión Anual de la Sociedad Argentina de Investigación Clínica; LI Reunión Anual de la Asociación Argentina de Farmacología Experimental; XXI Reunión Anual de la Sociedad Argentina de Biología; XXXI Reunión Anual de la Sociedad Argentina de Protozoología; IX Reunión Anual de la Asociación Argentina de Nanomedicinas y VI Reunión Científica Regional de la Asociación Argentina de Ciencia y Tecnología de Animales de LaboratorioBuenos AiresArgentinaSociedad Argentina de Investigación ClínicaAsociación Argentina de Farmacología ExperimentalSociedad Argentina de BiologíaSociedad Argentina de ProtozoologíaAsociación Argentina de NanomedicinasAsociación Argentina de Ciencia y Tecnología de Animales de LaboratorioThe Histochemical Societ