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[Anticholinesterase agents and axial teratogenesis in quail embryos]
1Laboratoire de Biologie animale, Université Clermont-Ferrand II E.R.A. au C.N.R.S. no 408, B.P. 45, F-63170, Aubière, France.
Abstract:
The results of an investigation made with organo-phosphorous compounds (OP), carbamates (C), and a compound including oxamide groups (GO), indicate that spine anomalies in Japanese quail embryos are linked with cholinesterase inhibition. The blocking effect of these various compounds on cholinesterases has been examined both in vitro and in vivo.In vitro, the embryonic cholinesterases are particularly sensitive to carbamates, whereas high concentrations of organo-phosphorous compounds-and especially those which need to be activated at the level of metabolism-block only part of the relevant activities of the enzyme.In vivo, among the products examined, only malathion (OP) and ambenonium (GO) were found to be inactive (or having little effect) so far as cholinesterases are concerned. Although they appeared rather strongly embryotoxic, these two poisons did not prove teratogenic. A strong inhibition of cholinesterase activities was noticed in all cases, when applying the other compounds at teratogenic doses.The close relationship between the inhibition of cholinesterases and the appearance of axial abnormalities is confirmed by using increasing doses of parathion (OP) and neostigmine (C).Beak and leg malformations were brought about only by dicrotophos and eserine, and did not prove to be linked with cholinesterase inhibition, since they were not observed with compounds having a high activity towards these enzymes, such as parathion (OP), neostigmine (C) and demecarium (C).
Insights
Cholinesterase inhibition in Japanese quail embryos by organophosphates and carbamates is linked to spine anomalies. However, specific malformations like beak and leg defects were not associated with this enzyme inhibition.
Area of Science:
- Toxicology
- Developmental Biology
- Neuroscience
Context:
- Investigating the teratogenic effects of chemical compounds on embryonic development.
- Examining the mechanism of action of organophosphorous (OP) and carbamate (C) compounds on enzyme activity.
Purpose:
- To determine the relationship between cholinesterase inhibition and the induction of spinal anomalies in Japanese quail embryos.
- To differentiate between teratogenic effects directly linked to cholinesterase inhibition and those caused by other mechanisms.
Summary:
- Organophosphorous (OP) and carbamate (C) compounds were tested for their effects on Japanese quail embryos and cholinesterase activity.
- In vitro studies showed embryonic cholinesterases are sensitive to carbamates; in vivo, spine anomalies correlated with cholinesterase inhibition by most tested compounds.
- Malathion (OP) and ambenonium (GO) were embryotoxic but not teratogenic, and showed little cholinesterase inhibition. Beak/leg malformations were not linked to cholinesterase inhibition.
Impact:
- Confirms a strong link between cholinesterase inhibition and axial abnormalities in developing quail embryos.
- Highlights that not all chemical-induced embryotoxicity or teratogenicity is mediated by cholinesterase inhibition.
- Provides insights into the specific mechanisms of teratogenesis for different classes of chemical agents.
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