Behavioral responses to ethanol in rats perinatally exposed to low lead levels

Neurotoxicology and Teratology

Volumn 21, Issue 5, 1999, Pages 551-557

  Cancela, Liliana M ^a   Fulginiti, Susana ^a  

^a UNIVERSIDAD NACIONAL DE CÓRDOBA   (Argentina)

Author keywords

Anxiety; Corticosterone; Developmental neurotoxicity; Ethanol consumption; Lead; Rats

Indexed keywords

ALCOHOL; CORTICOSTERONE; LEAD;

ALCOHOL CONSUMPTION; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BRAIN DEVELOPMENT; CONTROLLED STUDY; DRUG SENSITIVITY; NEUROTOXICITY; NEWBORN; NONHUMAN; PERINATAL PERIOD; PRIORITY JOURNAL; RAT; TRANQUILIZING ACTIVITY;

ALCOHOL DRINKING; ANALYSIS OF VARIANCE; ANIMALS; ANTI-ANXIETY AGENTS; BEHAVIOR, ANIMAL; CENTRAL NERVOUS SYSTEM DEPRESSANTS; CORTICOSTERONE; DOSE-RESPONSE RELATIONSHIP, DRUG; ETHANOL; FEMALE; LEAD; MALE; MAZE LEARNING; PREGNANCY; PRENATAL EXPOSURE DELAYED EFFECTS; RATS; RATS, WISTAR;

EID: 0033199279     PISSN: 08920362     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0892-0362(99)00020-3     Document Type: Article

References (48)

1. Altman J., Everitt B.J., Glautier S., Markou A., Nutt D., Oretti R., Phillips G.D., Robbins T.W. The biological, social and clinical bases of drug addiction. Commentary and debate Psychopharmacology. 125:1996;285-345.
2. Bailey C.C., Kitchen I. Ontogeny of catecholamine and GABA levels in rat brain. Lack of effect of perinatal lead exposure Toxicol. Lett. 30:1986;97-102.
3. Baraldi M., Zanoli P., Rossi T., Borella P., Caselgrandi E., Petraglia F. Neurobehavioral and neurochemical abnormalities of pre- and postnatally lead-exposed rats. Zinc, copper and calcium status Neurobehav. Toxicol. Teratol. 7:1985;499-509.
4. Bellinger D., Leviton A., Needleman H.L., Waternaux C., Rabinowitz M. Low-level lead exposure and infant development in the first year. Neurobehav. Toxicol. Teratol. 8:1986;151-161.
5. Bisaga A., Kostowski W. Individual behavioral differences and ethanol consumption in Wistar rats. Physiol. Behav. 54:1993;1125-1131.
6. Cloninger C.R. Neurogenetic adaptive mechanisms in alcoholism. Science. 236:1987;410-416.
7. Cory-Slechta D.A. Relationships between lead-induced learning impairments and changes in dopaminergic, cholinergic, and glutamatergic neurotransmitter system functions. Annu. Rev. Pharmacol. Toxicol. 35:1995;391-415.
8. Cory-Slechta D.A., Widzowski D.V., Pokora M.J. Functional alterations in dopamine systems assessed using drug discrimination procedures. Neurotoxicology. 14:1993;105-114.
9. Crofton K.M., Taylor D.H., Bull R.J., Sivulka D.J., Lutbenhoff S.D. Developmental delays in exploration and locomotor activity in male rats exposed to low level lead. Life Sci. 26:1980;823-831.
10. Davis J.M., Otto D.A., Weil D.E., Grant L.D. The comparative developmental neurotoxicity of lead in humans and animals. Neurotoxicol. Teratol. 12:1990;215-229.
11. Dubas T.C., Hrdina P.D. Behavioural and neurochemical consequences of neonatal exposure to lead in rats. J. Environ. Pathol. Toxicol. 2:1978;471-484.
12. Fahlke C., Engel J.A., Eriksson C.P., Hård E., Söderpalm B. Involvement of corticosterone in the modulation of ethanol consumption in the rat. Alcohol. 11:1994;195-202.
13. Fahlke C., Hård E., Thomasson R., Engel J.A., Hansen S. Metyrapone-induced suppression of corticosterone synthesis reduces ethanol consumption in high-preferring rats. Pharmacol. Biochem. Behav. 48:1994;977-981.
14. Grant K.A. Emerging neurochemical concepts in the actions of ethanol al ligand-gated ion channels. Behav. Pharmacol. 5:1994;383-404.
15. Kishi R., Ikeda T., Miyake H., Uchino E., Tsuzuki T., Inoue K. Effects of low lead exposure on neuro-behavioral function in the rat. Arch. Environ. Health. 38:1983;25-33.
16. Kitchen I. Lead toxicity and alterations in opioid systems. Neurotoxicology. 14:1993;115-124.
17. Kitchen I., Kelly M. Effect of perinatal lead treatment on morphine dependence in the adult rat. Neurotoxicology. 14:1993;125-130.
18. A receptors in the actions of alcohol and in alcoholism. Recent advances Alcohol Alcohol. 29:1994;115-129.
19. Levin E.D., Bowman R.E. Long term lead effects on the Hamilton search task and delayed alternation in monkeys. Neurobehav. Toxicol. Teratol. 8:1986;219-224.
20. Lister R.G. the use of a plus-maze to measure anxiety in the mouse. Psychopharmacology. 92:1987;180-185.
21. Malec T.S., Malec E.A., Dongier M. Efficacy of buspirone in alcohol dependence. A review Alcohol. Clin. Exp. Res. 20:1996;853-858.
22. Memo M., Lucchi L., Spano P.F., Trabucchi M. Dose-dependent and reversible effects of lead on rat dopaminergic system. Life Sci. 28:1981;795-799.
23. Moresco R.M., Dall'Olio R., Gandolfi O., Govoni S., Di Giovine S., Trabucchi M. Lead neurotoxicity. A role for dopamine receptors Toxicology. 53:1988;315-322.
24. Murphy B.E.P. Some studies of the protein-binding steroids and their application to the routine micro- and ultramicro measurement of various steroids in body fluids by competitive protein-binding radio assay. J. Clin. Endocrinol. Metab. 27:1967;973-983.
25. Nation J.R., Baker D.M., Taylor B., Clark D.E. Dietary lead increases ethanol consumption in the rat. Behav. Neurosci. 100:1986;525-530.
26. Nation J.R., Baker D.M., Fantasia M.A., Ruscher A.E., Clark D.E. Ethanol consumption and free operant avoidance performance following exposure to dietary lead. Neurotoxicology. 8:1987;561-568.
27. Needleman H.L., Bellinger D. The health effects of low level exposure to lead. Annu. Rev. Public Health. 12:1991;111-140.
28. Newland M.C., Yezhou S., Lögdberg B., Berlin M. In utero lead exposure in squirrel monkeys. Motor effects seen with schedule-controlled behavior Neurotoxicol. Teratol. 18:1996;33-40.
29. Overstreet D.H., Rezvani A.H., Janowsky D.S. Genetic animal models of depression and ethanol preference provide support for cholinergic and serotonergic involvement in depression and alcoholism. Biol. Psychiatry. 31:1992;919-936.
30. Pellow S., Chopin P., File S., Briley M. Validation of open-closed arm entries in an elevated plus-maze as a measure of anxiety in the rat. J. Neurosci. Methods. 14:1985;149-167.
31. Piazza P.V., Deminière J.M., Le Moal M., Simon H. Factors that predict individual vulnerability to amphetamine self-administration. Science. 245:1989;1511-1513.
32. Piazza P.V., Maccari S., Deminière J.M., Le Moal M., Mormède P., Simon H. Corticosterone levels determine individual vulnerability to amphetamine self-administration. Proc. Natl. Acad. Sci. USA. 88:1991;2088-2092.
33. Piazza P.V., Le Moal M. Pathophysiological basis of vulnerability to drug abuse. Role of an interaction between stress, glucocorticoids and dopaminergic neurons Annu. Rev. Pharmacol. Toxicol. 36:1996;359-378.
34. Pohorecky L.A. The interaction of alcohol and stress. A review. Neurosci. Biobehav. Rev. 5:1981;209-229.
35. Prasad C., Prasad A. A relationship between increased voluntary alcohol preference and basal hypercorticosteronemia associated with an attenuated rise in corticosterone output during stress. Alcohol. 12:1995;59-63.
36. Roske I., Baeger I., Frenzel R., Oehme P. Does a relationship exist between the quality of stress and the motivation to ingest alcohol? Alcohol. 11:1994;113-124.
37. Sauerhoff M.V., Michaelson I.A. Hyperactivity and brain catecholamines in lead-exposed developing rats. Science. 182:1973;1022-1024.
38. Silbergeld E.K., Goldberg A.M. Lead-induced behavioural dysfunction. An animal model of hyperactivity Exp. Neurol. 42:1974;146-157.
39. Spanagel R., Montkowski A., Allingham K., Stöhr T., Shoaib M., Holsboer F., Landgraf R. Anxiety. A potential predictor of vulnerability to the initiation of ethanol self-administration in rats Psychopharmacology. 122:1995;369-373.
40. Subramedian K.S., Meranger C. A rapid electrothermal atomic absorption spectrophotometric method for cadmium and lead in human. Clin. Chem. 27:1981;1866-1871.
41. Tomkins D.M. Strategies for revealing the multiple determinants of drinking. Pharmacological and environmental manipulations Alcohol. Clin. Exp. Res. 20(Suppl. A):1996;125-127.
42. Ujiwara H., Sasa M., Ban T. Selective blockade of P-type calcium channels by lead in cultured hippocampal neurons. Jpn. J. Pharmacol. 67:1995;267-269.
43. Virgolini M.B., Fulginiti A.S. Exposición perinatal a bajas dosis de plomo en ratas. Respuestas conductuales a etanol. X Congreso Argentino de Toxicología, XVI Jornadas Interdisciplinarias de Toxicología:1996;Toxicología y Medio Ambiente, Buenos Aires, Argentina.
44. Widmer H.R., Bütikofer E.E., Schlumpf M., Lichtensteiger W. Pre- and postnatal lead exposure affects the serotonergic system in the immature rat brain. Experientia. 47:1991;463-466.
45. 3 exposure. J. Pharmacol. Exp. Ther. 214:1980;642-650.
46. Winder C. Lead, reproduction and development. Neurotoxicology. 14:1993;303-318.
47. Wolffgram J. Free choice ethanol intake of laboratory rats under different social conditions. Psychopharmacology. 101:1990;233-239.
48. Zhou F.C., Pu C.F., Murphy J., Lumeng L., Li T.K. Serotonergic neurons in the alcohol preferring rats. Alcohol. 11:1994;397-403.