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avr-15 encodes a chloride channel subunit that mediates inhibitory glutamatergic neurotransmission and ivermectin sensitivity in Caenorhabditis elegans
- Source :
- The EMBO journal. 16(19)
- Publication Year :
- 1997
-
Abstract
- Ivermectin is a widely used anthelmintic drug whose nematocidal mechanism is incompletely understood. We have used Caenorhabditis elegans as a model system to understand ivermectin9s effects. We found that the M3 neurons of the C.elegans pharynx form fast inhibitory glutamatergic neuromuscular synapses. avr‐15 , a gene that confers ivermectin sensitivity on worms, is necessary postsynaptically for a functional M3 synapse and for the hyperpolarizing effect of glutamate on pharyngeal muscle. avr‐15 encodes two alternatively spliced channel subunits that share ligand binding and transmembrane domains and are members of the family of glutamate‐gated chloride channel subunits. An avr‐15 ‐encoded subunit forms a homomeric channel that is ivermectin‐sensitive and glutamate‐gated. These results indicate that: (i) an ivermectin‐sensitive chloride channel mediates fast inhibitory glutamatergic neuromuscular transmission; and (ii) a nematocidal property of ivermectin derives from its activity as an agonist of glutamate‐gated chloride channels in essential excitable cells such as those of the pharynx.
- Subjects :
- Protein subunit
Muscle Relaxation
Molecular Sequence Data
Neuromuscular transmission
Glutamic Acid
Biology
Neurotransmission
Inhibitory postsynaptic potential
Synaptic Transmission
General Biochemistry, Genetics and Molecular Biology
Glutamatergic
Chloride Channels
parasitic diseases
Homomeric
Animals
Caenorhabditis elegans
Molecular Biology
Ivermectin
General Immunology and Microbiology
General Neuroscience
Antinematodal Agents
Iontophoresis
biology.organism_classification
Cell biology
Alternative Splicing
Biochemistry
Chloride channel
Pharynx
Research Article
Subjects
Details
- ISSN :
- 02614189
- Volume :
- 16
- Issue :
- 19
- Database :
- OpenAIRE
- Journal :
- The EMBO journal
- Accession number :
- edsair.doi.dedup.....82d9ea5cde02c024c1b6f4f6d3171b82