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Penetration of diazoxon and acetyl choline into the thoracic ganglia in susceptible and resistant houseflies and the effects of fixatives

Published online by Cambridge University Press:  10 July 2009

K. A. Lord
Affiliation:
Department of Insecticides and Fungicides, Rothamsted Experimental Station.
Frances M. Molloy
Affiliation:
Department of Insecticides and Fungicides, Rothamsted Experimental Station.
C. Potter
Affiliation:
Department of Insecticides and Fungicides, Rothamsted Experimental Station.

Extract

The nerve sheath of the thoracic ganglion of the house-fly (Musca domestica L.) is readily permeable to diazoxon but is impermeable to acetyl choline and acetyl thiocholine. Acetone and other lipoidal solvents, but not formaldehyde, were found to destroy the barrier to entry of the substrates, acetyl choline and acetyl thiocholine, and it is inferred that the barrier is lipoidal. At − 16°C., acetone does not destroy the cholinesterase of the ganglion.

Cholinesterase associated with the ganglion could be divided into three regions which showed different inhibition characteristics: (a) ‘ superficial ’ enzyme outside the nerve sheath, inhibited by 3·3 × 10−8M diazoxon; (b) ‘ peripheral ’ enzyme in the cellular region of the ganglion, inhibited by 3·3 × 10−8M and 3·3 × 10−9M diazoxon; (c) ‘ central ’ enzyme in the synaptic area, inhibited by not less than 3·3 × 10−7M diazoxon. Using inhibition of cholinesterase as an indicator of penetration, no difference in permeability was found between the ganglia of the susceptible and resistant strains. No difference was found in the inhibition of cholinesterase by diazoxon in the ganglia of susceptible and resistant strains.

It is concluded from this and previous work that if inhibition of cholinesterase of the nervous system is the cause of death there are no differences between the ganglia of the susceptible and resistant strains which affect resistance; and, furthermore, that inhibition of cholinesterase in the thoracic ganglion is unlikely to be the cause of death.

Type
Research Paper
Copyright
Copyright © Cambridge University Press 1963

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References

Ashurst, D. E. (1959). The connective tissue sheath of the locust nervous system: a histochemical study.—Quart. J. micr. Sci. 100 pp. 401412.Google Scholar
Asperen, K. Van & Oppenoorth, F. J. (1959). Organophosphate resistance and esterase activity in houseflies.—Ent. exp. appl. 2 pp. 4857.CrossRefGoogle Scholar
Dettbarn, W. D. & Hoskin, F. C. G. (1962). Electrical and esterase activity in axons.—Biochim. biophys. Acta 62 pp. 566573.CrossRefGoogle ScholarPubMed
Gomori, G. (1952). Microscopic histochemistry.—273 pp. Chicago, Univ. Pr.Google Scholar
Koelle, G. B. & Friedenwald, J. S. (1949). A histochemical method for localising cholinesterase activity.—Proc. Soc. exp. Biol., N.Y. 70 pp. 617622.CrossRefGoogle ScholarPubMed
Krueger, H. R., O'brien, R. D. & Dauterman, W. C. (1960). Relationship between metabolism and differential toxicity in insects and mice of diazinon, dimethoate, parathion, and acethion.—J. econ. Ent. 53 pp. 2531.CrossRefGoogle Scholar
Lord, K. A. & Solly, S. R. B. (1956). The rate of disappearance of para-oxon from two strains of houseflies.—Chem. & Ind. 1956 pp. 13521353.Google Scholar
Mengle, D. C. & O'Brien, R. D. (1960). The spontaneous and induced recovery of fly brain cholinesterase after inhibition by organophosphates.—Biochem. J. 75 pp. 201207.CrossRefGoogle ScholarPubMed
Molloy, F. M. (1961). The histochemistry of the cholinesterases in the central nervous system of susceptible and resistant strains of the house-fly, Musca domestica L., in relation to diazinon poisoning.—Bull. ent. Res. 52 pp. 667681.CrossRefGoogle Scholar
O'Brien, R. D. (1957). Esterases in the semi-intact cockroach.—Ann. ent. Soc. Amer. 50 pp. 223229.CrossRefGoogle Scholar
Twarog, B. M. & Roeder, K. D. (1956). Properties of the connective tissue sheath of the cockroach abdominal nerve cord.—Biol. Bull. 111 pp. 278286.CrossRefGoogle Scholar
Wilson, I. B. & Cohen, M. (1953). The essentiality of acetylcholinesterase in conduction.—Biochim. biophys. Acta 11 pp. 147156.CrossRefGoogle ScholarPubMed
Winton, M. Y., Metcalf, R. L. & Fukuto, T. R. (1958). The use of acetyl thiocholine in the histochemical study of the action of organophosphorus insecticides.—Ann. ent. Soc. Amer. 51 pp. 436441.CrossRefGoogle Scholar