Toxicity of cypermethrin and fenitrothion on the hemolymph carbohydrates, head acetylcholinesterase, and thoracic muscle Na+, K+ - ATPase of emerging honeybees (Apis mellifera mellifera. L)

Ecotoxicology and Environmental Safety

Volumn 44, Issue 2, 1999, Pages 139-146

  Bendahou, Najib ^a   Bounias, Michel ^b   Fleche, Cecile ^a  

^a Healthy Pigs Production and Experimentation Section   (France)

^b UNIVERSITY OF AVIGNON   (France)

Author keywords

Acetylcholinesterase; Carbohydrates; Cypermethrin; Fenitrothion; Honeybees; Na+, K+ ATPase; Toxicity

Indexed keywords

ACETYLCHOLINESTERASE; ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); CARBOHYDRATE; CIPERMETHRIN; FENITROTHION;

ANIMAL TISSUE; ARTICLE; ENZYME ACTIVITY; ENZYME INHIBITION; HEMOLYMPH; HONEYBEE; NEUROTOXICITY; NONHUMAN;

ANIMALIA; APIS; APIS MELLIFERA; APIS MELLIFERA MELLIFERA; APOIDEA; HEXAPODA;

EID: 0032701531     PISSN: 01476513     EISSN: None     Source Type: Journal    
DOI: 10.1006/eesa.1999.1811     Document Type: Article

References (45)

1. 2+) ATPase in sorgum (Sorgum bicolor L.). Pestic. Biochem. Physiol. 34:1989;118-125.
2. Belzunces L. P., Toutant J. P., Bounias M. Acetylcholinesterase from Apis mellifera head. Biochem. J. 255:1988;463-470.
3. Bounias M. In vivo control of haemolymph a-glucosidase kinetics by glycemia components, according to development stages of Apis mellifera (Hymenoptera, Insecta). Comp. Biochem. Physiol. B. 66:1980;335-341.
4. Bounias M. Masson. L'analyse biochimique quantitative par nanochromatographie sur couche mince. 1983.
5. Bounias M. Analogie de deux affecteurs hyperglycémiants: I'AMPc et le glucagon injectés chez l'abeille in vivo. C.R. Acad. Sci. Serie III. 302:1986;141-144.
6. Bounias M. Propranolol and somatostatin interactions with the hyperglycemic effects of glucagon, octopamine, noradrenaline and cAMP in worker honeybees in vivo. Biochimie. 69:1987;655-660.
7. Bounias M. Algebraic potential of the Hill equation as an alternative tool for plotting dose (or time)/effects relationships in toxicology: A theoretical study. Fundam. Clin. Pharmacol. 3:1989;1-9.
8. Bounias M., Dujin N., Popeskovic D. S. Sublethal effects of synthetic pyrethroid, deltamethrin, on the glycemia, lipemia, and the gut alkaline phosphatase of honeybees. Pestic. Biochem. Physiol. 24:1985a;149-160.
9. Bounias M., Dujin N., Popeskovic D. S. A comparison of haemolymph lipid classes at different stages of the honeybee development. Acta Veterinaria. 35:1985b;273-282.
10. Bounias M., Morgan R. J. The yearly honey productivity of hives as correlated to the glycemia of emerging working bee. Indian J. Agric. Chem. 19:1987;156-160.
11. Bounias M., Pacheco H. Sensibilité de la glyucémie de l'abeille à l'action de l'insuline et du glucagon injectés in vivo. C.R. Soc. Biol. 182:1979a;37-43.
12. Bounias M., Pacheco H. Effect hyperglycémiant de l'adrénaline injectée chez l'abeille in vivo. C.R. Acad. Sci. D. 289:1979b;33-36.
13. Bratstten P. Resistance to carbamates and organophosphorus. Am. Chem. Soc. 3:1990;42-57.
14. Cascino P., Nectoux M. G., Guiraud, Bounias M. The formamidine Amitraz as a hyperglycemic agonist in worker honeybees (Apis mellifera L.) in vivo. Biomed. Environ. Sci. 2:1989;106-114.
15. Cheng E. Y., Cutkomp L. K. Agency in honeybee, Apis mellifera, as related to brain ATPase and DDT sensitivity. J. Insect. Physiol. 18:1972;2285-2291.
16. Clark J. M., Matsumura F. Two types of inhibitor effects of pyrethroids on nerve calcium ATPase and calcium and magnesium activity in the squid Loligo paelei. Pestic. Biochem. Physiol. 2:1982;180-190.
17. Cox R. L., Wilson T. W. Effect of permethrin on the behaviour of individualy targeted honeybees (Apis mellifera). Environ. Entomol. 2:1984;375-378.
18. Dagnelie P. Théorie et méthodes statistiques. 1984;Presses Agronomiques de Gembloux, Belgique.
19. Downer R. G. H. Effect of lindane (hexachlorocyclohexane) on carbohydrate and lipid reserves in the American cockroach, Periplaneta america L. Pestic. Biochem. Physiol. 17:1982;89-94.
20. Elliot M., Janes F. Development of pyrethroids in agriculture. Fitopath. 34:1984;11-14.
21. Ellman G. L., Courtney K. D., Andres V., Featherstone R. M. A new and rapid method for colorimetric determination of acetylcholinesterase activity. Biochem. Pharmacol. 7:1961;88-95.
22. Fleche, C, and, Faucon, J. P. 1985, Enquête Ecopathologique. Rapport interne, LPPRA-CNEVA, Sophia-Antipolis.
23. Ibrahim N., Archer T. E., Norman E., Marson J. Honeybee pesticide mortality, intoxication versus acetycholinesterase concentration. J. Apic. Res. 13:1974;55-60.
24. 2+) ATPase. Pestic. Biochem. Physiol. 25:1986;420-426.
25. Kasturi A. R., Chandrashkhar R. Inhibition of acetylcholinesterase as a criterion to determine the degree of insecticide poisoning in Apis cerana. J. Apic. Res. 16:1977;112-114.
26. Mary M. Fluvalinate, le respect de l'abeille. Rev. Fr. Apic. 455:1986;423-430.
27. M'diaye K., Bounias M. Time- and dose-related effects of the pyrethroid fluvalinate on haemolymph carbohydrates and gut lipids of honeybees following in vivo injection of very low doses. Biochem. Environ. Sci. 6:1993;145-153.
28. Metkalf L. R., March B. Properties of acetylcholinesterase from the fly and mouse and their relation to insecticide action. J. Environ. Entomol. 43:1990;670-676.
29. Myamoto J., Sato Y. Metabolic fate of sumithion in rice plant applied at the preheaving stage. Agric. Biol. Chem. 28:1968;422-440.
30. Narahashi T. Sites and types of action of pyrethroids on nerve membrane. Pyrethroids Insecticides, Chemistry and Action. 3:1980;Roussel uclaf, Paris. p. 15-17.
31. Orchard I. The effect of pyrethroids on the electrical activity of neurosecretory cells from the brain of Rhodnius prolixus. Pestic. Biochem. Physiol. 13:1980;220-227.
32. Osborne M. P. Site of action of pyrethroids in neuronal membrance as revelated by the resistances factors. Pestic. Sci. 10:1982;407-413.
33. Pain J. Nouveau modele de cagettes experimentales pour le maintien d'abeilles en captivité Ann. Abeille. 9:1969;71-76.
34. Pham Huu Chanh, Navarro-Delamasure C., Pham Huu Chanh A., Cheau S. L., Ziad F., Samaha F. Pharmacological effects of deltamethrin on the central nervous system. Arzneim. Forsuh. 34:1984a;175-181.
35. Pham Huu Chanh, Navarro-Delamasure C., Pham Huu Chanh A., Cheau S. L., Ziad F., Samaha F. Toxicological studies of deltamethrin. Int. J. Rea. 6:1984b;127-133.
36. Pullman M. E., Penefsky H. S., Datta A., Racker E. Partial resolution of the enzyme catalysing oxidative phosphorylation. I. Purification and properties of soluble dinitrophenol-stimulated adenosine triphosphatese. J. Biol. Chem. 235:1960;3322-3329.
37. Samaranayaka M. Insecticide-induced release of hyperglycemic and adipokinetic hormones of Schistoverca gregaria. Gen. Comp. Endocrinol. 24:1974;424-430.
38. Shires S. W., Bennet D., Debary P., Le Blanc J. The effects of large scale aerial applications of the pyrethroid insecticides on foraging bees. Proc. V. Int. Synth. Bull. 1983;27-30.
39. Singh G. J. P. Bioresmethin-induced alteration in the ultrastructure of neurosecretory cells of insects in the corpora allata. Pestic. Biochem. Physiol. 18:1982;1958-1968.
40. Singh G. J. P., Orchard I. Is insecticide-induced release of insect neurohormones a secondary effect of hyperactivity of the central nervous system? Pestic. Biochem. Physiol. 17:1982;232-240.
41. Singh G. J. P., Orchard I. Action of bioresmethrin on the corpus cardiacum of Locusta migratoria. Pestic. Sci. 229:1983;14-20.
42. Tripathi R. K., Obrien R. D. Effect of organophosphorus in vivo upon acetyl cholinesterase isoenzymes from housefly head and thorax. Pestic. Biochem. Physiol. 2:1973;418-424.
43. Vaissiere B. E. Honeybee stocking rate pollinator visitation, and pollination effectiveness in upland cotton grown for hybrid seed production. Acta Hort. 288:1991;359-363.
44. Washio H. Effect of uncoupling agent of oxidative phosphorylation on the spontaneous release of transmitter from insect motor nerve terminals. Comp. Biochem. Physiol. 72:1982;369-373.
45. Yap H., Cutkomp L. K. Activity and rhythm of ATPase in larvae of the mosquito, Aedes aegepti L. Life Sci. 9:1970;1419-1425.