Characterization of Pyrethroid Action on Ciliary Calcium Channels in Paramecium tetraurelia
Type-II pyrethroids, including deltamethrin, are highly toxic to Paramecium tetraurelia, an organism that does not possess a voltage-sensitive sodium channel. Previous research has established that deltamethrin is toxic to P. tetraurelia in mortality bioassays at concentrations as low as 10−10 and 1...
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Published in | Pesticide biochemistry and physiology Vol. 65; no. 3; pp. 181 - 193 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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San Diego, CA
Elsevier Inc
01.11.1999
Elsevier |
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Abstract | Type-II pyrethroids, including deltamethrin, are highly toxic to Paramecium tetraurelia, an organism that does not possess a voltage-sensitive sodium channel. Previous research has established that deltamethrin is toxic to P. tetraurelia in mortality bioassays at concentrations as low as 10−10 and 10−11 M under resting and depolarizing conditions, respectively. Deltamethrin, likewise, stimulated P. tetraurelia backward-swimming behavior, an avoidance behavioral response that is controlled exclusively by Ca2+ uptake via the voltage-sensitive calcium channels associated with the cilia. We have now characterized the action of various calcium channel agonists and antagonists on the avoidance behavior and Ca2+ influx in P. tetraurelia and have determined that the voltage-sensitive calcium channel associated with the cilia is blocked by the divalent cation Ni2+ but is insensitive to octanol and amiloride. Radioisotope tracer experiments, using whole cells under resting conditions, established that the toxic 1R isomer of deltamethrin resulted in increased Ca2+ influx, while the nontoxic 1S enantiomer produced no significant effect. Pawn mutants, which lack a functional voltage-sensitive calcium channel, were unaffected by deltamethrin. Fluorescent bioassays, under depolarizing conditions, corroborated behavioral and radioisotope experiments. Specifically, these experiments established that deltamethrin stimulated Ca2+ uptake in a stereospecfic manner and that this uptake was blocked by the phenethylamine-type calcium channel blocker D595 under physiological conditions. Deltamethrin treatment resulted in a dose-dependent increase in Ca2+ uptake and membrane depolarization with concentrations as low as 10−11 M. Electrophysiological recordings of whole cells showed that treatment of 10−9 M deltamethrin resulted in membrane destabilization, increased number of spontaneous action potentials, prolonged repetitive discharges following stimulation, membrane depolarization, and death by osmotic lysis. Our findings establish that the toxic effect of deltamethrin is structurally related, dose dependent, and enhanced by depolarization and provide substantial evidence that Type-II pyrethroids, specifically deltamethrin, act as potent calcium channel agonists on the ciliary voltage-sensitive calcium channel of P. tetraurelia. |
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AbstractList | Type-II pyrethroids, including deltamethrin, are highly toxic to Paramecium tetraurelia, an organism that does not possess a voltage-sensitive sodium channel. Previous research has established that deltamethrin is toxic to P. tetraurelia in mortality bioassays at concentrations as low as 10−10 and 10−11 M under resting and depolarizing conditions, respectively. Deltamethrin, likewise, stimulated P. tetraurelia backward-swimming behavior, an avoidance behavioral response that is controlled exclusively by Ca2+ uptake via the voltage-sensitive calcium channels associated with the cilia. We have now characterized the action of various calcium channel agonists and antagonists on the avoidance behavior and Ca2+ influx in P. tetraurelia and have determined that the voltage-sensitive calcium channel associated with the cilia is blocked by the divalent cation Ni2+ but is insensitive to octanol and amiloride. Radioisotope tracer experiments, using whole cells under resting conditions, established that the toxic 1R isomer of deltamethrin resulted in increased Ca2+ influx, while the nontoxic 1S enantiomer produced no significant effect. Pawn mutants, which lack a functional voltage-sensitive calcium channel, were unaffected by deltamethrin. Fluorescent bioassays, under depolarizing conditions, corroborated behavioral and radioisotope experiments. Specifically, these experiments established that deltamethrin stimulated Ca2+ uptake in a stereospecfic manner and that this uptake was blocked by the phenethylamine-type calcium channel blocker D595 under physiological conditions. Deltamethrin treatment resulted in a dose-dependent increase in Ca2+ uptake and membrane depolarization with concentrations as low as 10−11 M. Electrophysiological recordings of whole cells showed that treatment of 10−9 M deltamethrin resulted in membrane destabilization, increased number of spontaneous action potentials, prolonged repetitive discharges following stimulation, membrane depolarization, and death by osmotic lysis. Our findings establish that the toxic effect of deltamethrin is structurally related, dose dependent, and enhanced by depolarization and provide substantial evidence that Type-II pyrethroids, specifically deltamethrin, act as potent calcium channel agonists on the ciliary voltage-sensitive calcium channel of P. tetraurelia. Type-II pyrethroids, including deltamethrin, are highly toxic to Paramecium tetraurelia, an organism that does not possess a voltage-sensitive sodium channel. Previous research has established that deltamethrin is toxic to P. tetraurelia in mortality bioassays at concentrations as low as 10 super(-10) and 10 super(-11) M under resting and depolarizing conditions, respectively. Deltamethrin, likewise, stimulated P. tetraurelia backward-swimming behavior, an avoidance behavioral response that is controlled exclusively by Ca super(2+) uptake via the voltage-sensitive calcium channels associated with the cilia. We have now characterized the action of various calcium channel agonists and antagonists on the avoidance behavior and Ca super(2+) influx in P. tetraurelia and have determined that the voltage-sensitive calcium channel associated with the cilia is blocked by the divalent cation Ni super(2+) but is insensitive to octanol and amiloride. Radioisotope tracer experiments, using whole cells under resting conditions, established that the toxic 1R isomer of deltamethrin resulted in increased Ca super(2+) influx, while the nontoxic 1S enantiomer produced no significant effect. Pawn mutants, which lack a functional voltage-sensitive calcium channel, were unaffected by deltamethrin. Fluorescent bioassays, under depolarizing conditions, corroborated behavioral and radioisotope experiments. Specifically, these experiments established that deltamethrin stimulated Ca super(2+) uptake in a stereospecfic manner and that this uptake was blocked by the phenethylamine-type calcium channel blocker D595 under physiological conditions. Deltamethrin treatment resulted in a dose-dependent increase in Ca super(2+) uptake and membrane depolarization with concentrations as low as 10 super(-11) M. Electrophysiological recordings of whole cells showed that treatment of 10 super(-9) M deltamethrin resulted in membrane destabilization, increased number of spontaneous action potentials, prolonged repetitive discharges following stimulation, membrane depolarization, and death by osmotic lysis. Our findings establish that the toxic effect of deltamethrin is structurally related, dose dependent, and enhanced by depolarization and provide substantial evidence that Type-II pyrethroids, specifically deltamethrin, act as potent calcium channel agonists on the ciliary voltage-sensitive calcium channel of P. tetraurelia. |
Author | Karstens, William Zhang, Aiguo Van Houten, Judith Marshall Clark, J. Symington, Steven B. |
Author_xml | – sequence: 1 givenname: Steven B. surname: Symington fullname: Symington, Steven B. organization: Department of Entomology, University of Massachusetts, Amherst, Massachusetts, 01003 – sequence: 2 givenname: Aiguo surname: Zhang fullname: Zhang, Aiguo organization: Department of Entomology, University of Massachusetts, Amherst, Massachusetts, 01003 – sequence: 3 givenname: William surname: Karstens fullname: Karstens, William organization: Department of Zoology, University of Vermont, Burlington, Vermont, 05405 – sequence: 4 givenname: Judith surname: Van Houten fullname: Van Houten, Judith organization: Department of Zoology, University of Vermont, Burlington, Vermont, 05405 – sequence: 5 givenname: J. surname: Marshall Clark fullname: Marshall Clark, J. organization: Department of Entomology, University of Massachusetts, Amherst, Massachusetts, 01003 |
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Keywords | Protozoa Agonist Insecticide Calcium Paramecium tetraurelia Toxicity Mortality Pesticides Pyrethroids Electrophysiology Ionic channel Characterization Depolarization Ciliata Membrane potential Mechanism of action Deltamethrin |
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Snippet | Type-II pyrethroids, including deltamethrin, are highly toxic to Paramecium tetraurelia, an organism that does not possess a voltage-sensitive sodium channel.... |
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SubjectTerms | Animal, plant and microbial ecology Applied ecology Biological and medical sciences Ecotoxicology, biological effects of pollution Effects of pollution and side effects of pesticides on protozoa and invertebrates Freshwater Fundamental and applied biological sciences. Psychology Paramecium tetraurelia |
Title | Characterization of Pyrethroid Action on Ciliary Calcium Channels in Paramecium tetraurelia |
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