ABSTRACT
Organophosphates (OPs) can provoke toxicity by inhibiting acetylcholinesterase (AChE) in non-target organisms, like fish. In a previous pilot study, the anticholinesterase effects of paraoxon on the heart of Sparus aurata were examined [Tryfonos, M., Antonopoulou, E., Papaefthimiou, C., Chaleplis, G., Theophilidis, G., 2009. An in vitro assay for the assessment of the effects of an organophosphate, paraoxon, and a triazine, atrazine, on the heart of the gilthead sea bream (Sparus aurata). Pest. Biochem. Physiol. 93, 40-46]. The objective of the present study was to investigate the effects of the five protoxicant OPs, azinphos-methyl (MeAZP), parathion-methyl (MePS), chlorpyriphos-methyl (MeCCP), methamidophos (MET) and diazinon (DZ), on the spontaneously beating auricle of S. aurata. The results showed that: (1) MeAZP and MET induced exclusively cholinergic effects on auricle contractility. These effects were expressed as a significant decrease in the force and frequency of contractions and were fully reversible (140%) after the application of the muscarinic cholinergic receptor antagonist, atropine (15 microM). MeAZP was found to be the most effective anticholinesterase compound, with an IC(50) of 2.19+/-1.05 microM (n=6), while MET was less effective, with an IC(50) of 72.3+/-1.2 microM (n=6). (2) DZ and MePS, although classified as OPs, induced non-cholinergic effects. These effects were observed as an irreversible decrease in force and frequency of the auricle in all the concentrations examined; the depression is retained even after application of 15 microM atropine. (3) MeCCP was halfway between a typical OP and an OP lacking anticholinesterase properties, since there was a partial recovery in the force, but no recovery in the frequency of the auricle contractions. (4) The toxicity order, based on the IC(50), was as follows: MeAZP, 2.19+/-1.05 microM>paraoxon, 3.2+/-1.5 microM"MET, 72.3+/-1.2 microM>MePS, 80.3+/-1.03 microM>MeCPP, 93.7+/-1.01 microM>DZ, 164+/-1.01 microM. (5) There was a good correlation (r=0.779, p=0.04, n=5) between IC(50) and the previously determined logP (octanol:water partition coefficient) values for MeAZP, paraoxon, MeCCP, MePS and DZ. The results indicated that the increase in lipophilicity of MePS, MeCCP and DZ is accompanied by a decrease in their acute cardiotoxic properties in vitro. The non-cholinergic effects of these relatively high lipophilic OPs, might be caused by their tendency to distribute preferentially in the lipid bilayer of cardiac cells, affecting the proper functioning of the ionic channels which regulate the force (Ca(2+) channels) and the frequency (K(+) channels) of the spontaneous auricle contractions.
Subject(s)
Cholinesterase Inhibitors/toxicity , Insecticides/toxicity , Myocardial Contraction/drug effects , Organophosphates/toxicity , Sea Bream/physiology , Water Pollutants, Chemical/toxicity , Acetylcholinesterase/metabolism , Animals , Azinphosmethyl/chemistry , Azinphosmethyl/toxicity , Chlorpyrifos/analogs & derivatives , Chlorpyrifos/chemistry , Chlorpyrifos/toxicity , Cholinesterase Inhibitors/chemistry , Diazinon/chemistry , Diazinon/toxicity , Heart/drug effects , In Vitro Techniques , Insecticides/chemistry , Methyl Parathion/chemistry , Methyl Parathion/toxicity , Organophosphates/chemistry , Organothiophosphorus Compounds/chemistry , Organothiophosphorus Compounds/toxicity , Water Pollutants, Chemical/chemistryABSTRACT
To assess the relative toxicity of the herbicides acetochlor and 2,4,5-trichlorophenoxyacetic acid (2,4,5-T) on the nervous system, the sciatic nerve of the frog (Rana ridibunda) nerve was incubated in saline inside a specially designed recording chamber. This chamber permits monitoring of the evoked compound action potential (CAP) of the nerve, a parameter that could be used to quantify the vitality of the nerve in normal conditions as well as when the nerve was exposed to the compounds under investigation. Thus, when the nerve was exposed to acetochlor, the EC(50) was estimated to be 0.22mM, while for 2,4,5-T the EC(50) was 0.90mM. Using the identical nerve preparation, the EC(50) of 2,4-D was estimated to be 3.80mM [Kouri, G., Theophilidis, G., 2002. The action of the herbicide 2,4-dichlorophenoxyacetic acid on the isolated sciatic nerve of the frog (Rana ridibunda). Neurotoxicol. Res. 4, 25-32]. The ratio of the relative toxicity for acetochlor, 2,4,5-T and 2,4-D was found to be 1:4:17.2. However, because it is well-known that the action of 2,4-D is dependent on the pH, the relative toxicity of the three compounds was tested at pH 3.3, since it has been found that the sciatic nerve of the frog is tolerant of such a low pH. Under these conditions, the EC(50) was 0.77mM (from 0.22mM at pH 7.2) for acetochlor, 0.20mM (from 0.90mM) for 2,4,5-T and 0.24mM (from 3.80mM at pH 7.2) for 2,4-D. Thus, the relative toxicity of the three compounds changed drastically to 1:0.25:0.31. This change in the relative toxicity is due not only to the increase in the toxicity of 2,4,5-T and 2,4-D at low pH levels, but also to the decrease in the toxicity of acetochlor at pH 3.3.
