Effects of chronic lead exposure on short-term and long-term depression in area CA1 of the rat hippocampus in vivo

Chemosphere

Volumn 41, Issue 1-2, 2000, Pages 165-171

  Ruan, D Y ^a   Yan, K F ^a   Ge, S Y ^a   Xu, Y Z ^a   Chen, J T ^a   Wang, M ^a  

^a UNIVERSITY OF SCIENCE AND TECHNOLOGY OF CHINA   (China)

Author keywords

[No Author keywords available]

Indexed keywords

LEAD;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BRAIN CORTEX; CONTROLLED STUDY; ENVIRONMENTAL EXPOSURE; HIPPOCAMPUS; IN VIVO STUDY; LEAD POISONING; LONG TERM EXPOSURE; LONG TERM POTENTIATION; NEWBORN; NONHUMAN; PRENATAL EXPOSURE; RAT;

ANIMALS; ANIMALS, NEWBORN; ELECTRIC STIMULATION; ELECTROENCEPHALOGRAPHY; EVOKED POTENTIALS; FEMALE; HIPPOCAMPUS; LEAD; MALE; RATS; RATS, WISTAR; SYNAPTIC TRANSMISSION;

ANIMALIA; RATTUS NORVEGICUS;

EID: 0034008076     PISSN: 00456535     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0045-6535(99)00406-3     Document Type: Article

References (59)

1. Alkondon M., Costa A.C.S., Radhakrishnan V., Aronstam R.S., Albuquerque E.X. Selective blockade of NMDA-activated channel currents may be implicated in learning deficits caused by lead. FEBS Lett. 261:1990;124-130.
2. Altmann L., Lohman H. Acute lead exposure transiently inhibits hippocampal neuronal activities in vitro. Brain Res. 455:1988;254-261.
3. Altmann L., Sveinsson K., Wiegand H. Long-term potentiation in rat hippocampal slices is impaired following acute lead perfusion. Neurosci. Lett. 128:1991;109-120.
4. Altmann L., Weinsberg F., Sveinsson K., Lilienthal H., Wiegand H., Winneke G. Impairment of long-term potentiation and learning following chronic lead exposure. Toxicol. Lett. 66:1993;105-112.
5. Amaral D.G., Witter M.P. The three-dimensional organization of the hippocampal formation: a review of anatomical data. Neuroscience. 31:1989;571-591.
6. Andersen P., Sundberg S., Sveen O., Wigstrom H. Specific long-lasting potentiation of synaptic transmission in hippocampal slices. Nature. 266:1977;736-737.
7. Artola A., Singer W. Long-term depression of excitatory synaptic transmission and its relationship to long-term potentiation. Trends Neurosci. 16:1993;480-487.
8. Audesirk G., Audesirk T. The effects of inorganic lead on voltage-sensitive calcium channels differs among cell types and among channel subtypes. Neurotoxicology. 14:1993;259-266.
9. Barbour B., Szatkowski M., Ingledew N., Attwell D. Arachidonic acid induces a prolonged inhibition of glutamate uptake into glial cells. Nature. 342:1989;918-920.
10. Barrionuevo G., Shottler F., Lynch G. The effects of repetitive low-frequency stimulation on control and "potentiated" synaptic responses in the hippocampus. Life Sci. 27:1980;2385-2391.
11. Bekkers J.M., Stevens C.F. Presynaptic mechanism for long-term potentiation in the hippocampus. Nature. 346:1990;724-729.
12. Bellinger D., Sloman J., Leviton A., Rabinowitz M., Needlemen H., Waternaux C. Low-level lead exposure and children's cognitive function in the preschool years. Pediatrics. 87:1991;219-227.
13. Berger T.W. Long-term potentiation of hippocampal synaptic transmission affects rate of behavioral learning. Science. 224:1984;627-630.
14. Bliss T.V.P., Collingridge G.L. A synaptic model of memory: long-term potentiation in the hippocampus. Nature. 361:1993;31-39.
15. Bliss T.V.P., Lomo L. Long-lasting potentiation of synaptic transmission in the dentate area of the anaesthetized rabbit following stimulation of the perforant path. J. Physiol. 232:1973;331-356.
16. Bramham C.R., Srebro B. Induction of long-term depression and potentiation by low-and high-frequency stimulation in the dentate area of the anesthetized rat: magnitude, time course and EEG. Brain Res. 405:1987;100-107.
17. Brooks W.J., Petit T.L., Leboutillier J.C., Nobrega J.N., Jarvis M.F. Differential effects of early chronic lead exposure on postnatal rat brain NMDA, PCP, and Adenosine A1 receptors: an autoradiographic study. Drug Dev. Res. 29:1993;40-47.
18. Brown T.H., Chapman P.F., Kairiss E.W., Keenan C.L. Long-term synaptic potentiation. Science. 242:1988;724-728.
19. Byrne J. Cellular analysis of associative learning. Physiol. Rev. 67:1987;329-423.
20. Calabresi P., Maj R., Pisani A., Mercuri N.B., Bernardi G. Long-term synaptic depression in the striatum: physiological and pharmacological characterization. J. Neurosci. 12:1992;4224-4233.
21. Collingridge G. The role of NMDA receptors in learning and memory. Nature. 330:1987;604-605.
22. Collingridge G.L., Bliss T.V.P. NMDA receptors-their role in long-term potentiation. Trends Neurosci. 10:1987;288-293.
23. Creager R., Dunwiddie T., Lynch G. Paired-pulse and frequency facilitation in the CA1 region of the invitro rat hippocampus. J. Physiol. 299:1980;409-424.
24. Davis J.M., Svendsgaard D.J. Lead and child development. Nature. 329:1987;297-300.
25. Dingledine R., Langmoen I.A. Conductance changes and inhibitory actions of hippocampal recurrent IPSPs. Brain Res. 185:1980;277-287.
26. Dudek, S.M., Bear, M.F., 1992. Homosynaptic long-term depression in area CA1 of hippocampus and effects of N-methyl-D-aspartate receptor blockade. In: Proceedings of National Academic Science USA 89, pp. 4363-4367.
27. Dunwiddie T., Lynch G.S. Long-term potentiation and depression of synaptic responses in the rat hippocampus: localization and frequency dependency. J. Physiol. 276:1978;353-367.
28. Errington M.L., Bliss T.V.P., Richter-Levin G., Yenk K., Doyère V., Laroche S. Stimulation at 1-5 Hz does not produce long-term depression or depotentiation in the hippocampus of the adult rat in vivo. J. Neurophysiol. 74:1995;1793-1799.
29. 2+-dependent protein kinase and immunocytochemical localization of the enzyme in rat brain. In: Proceedings of National Academic Science USA 82, pp. 3030-3034.
30. Hebb D.O. The Organization of Behavior: A Neuropsychological Theory. 1949;Wiley, New York.
31. Heynen A.J., Abraham W.C., Bear M.F. Bidirectional modification of CA1 synapses in the adult hippocampus in vivo. Nature. 381:1996;163-166.
32. Hopfield, J.J., 1982. Neural networks and physical systems with emergent collective computational abilities. In: Proceedings of the National Academic Science USA 79, pp. 2554-2558.
33. Hori N., Büsselberg D., Matthews M.R., Parsons P.J., Carpenter D.O. Lead blocks LTP by an action not at NMDA receptors. Exp. Neurol. 119:1993;192-197.
34. Ito M., Sakurai M., Tongroach P. Climbing fiber induced depression of both mossy fiber responsiveness and glutamate sensitivity of cerebellar Purkinje cells. J. Physiol. 324:1982;113-134.
35. Kim, J.J., Foy, M.R., Thompson, R.F., 1996. Behavioral stress modifies hippocampal plasticity through N-methyl-D-aspartate receptor activation. In: Proceedings of the National Academic Science USA 93, pp. 4750-4753.
36. Lasley S.M., Polan-Curtain J., Armstrong D.L. Chronic exposure to environmental levels of lead impairs in vivo induction of long-term potentiation in rat hippocampal dentate. Brain Res. 614:1993;347-351.
37. Linden D.J., Connor J.A. Long-term synaptic depression. Annu. Rev. Neurosci. 18:1995;319-357.
38. Lynch G.S., Dunwiddie T., Gribkoff V. Heterosynaptic depression: a postsynaptic correlate of long-term potentiation. Nature. 266:1977;737-739.
39. Lynch G., Larson J., Kelso S., Barrionuevo G., Schottler F. Intracellular injections of EGTA block induction of hippocampal long-term potentiation. Nature. 305:1983;719-721.
40. MacDermott A.B., Mayer M.L., Westbrook G.L., Smith S.J., Barker J.L. NMDA-receptor activation increases cytoplasmic calcium concentration in cultured spinal cord neurons. Nature. 321:1986;519-522.
41. Malenka R.C., Kauer J.A., Perkel D.G., Mauk M.D., Kelly P.T., Nicoll R.A., Waxham M.N. An essential role for postsynaptic calmodulin and protein kinase activity in long-term potentiation. Nature. 340:1989;554-557.
42. Malinow R., Schulman H., Tsien R.W. Inhibition of postsynaptic PKC or CaMKII blocks induction but not expression of LTP. Science. 245:1989;862-866.
43. Markovac J., Goldstein G.W. Picomolar concentrations of lead stimulate brain protein kinase C. Nature. 334:1988;71-73.
44. McNaughton B.L. Long-term synaptic enhancement and short-term potentiation in rat fascia act through different mechanisms. J. Physiol. 324:1982;249-262.
45. Mulkey R.M., Herron C.E., Malenka R.C. An essential role for protein phosphatases in hippocampal long-term depression. Science. 261:1993;1051-1055.
46. Mulkey R.M., Malenka R.C. Mechanisms underlying induction of homosynaptic long-term depression in area CA1 of the hippocampus. Neuron. 9:1992;967-975.
47. 2+ influx by multivalent mental cations. J. Gen. Physiol. 83:1984;941-967.
48. Needleman H.L., Gatsonis C.A. Low-level lead exposure and the IQ of children. JAMA. 263:1990;673-678.
49. 2+-stimulated nitric oxide synthase activity from rat cerebellum. Neurosci. Lett. 196:1995;65-68.
50. Robinson G.B. Enhanced long-term potentiation induced in rat dentate gyrus by coactivation of septal and entorhinal inputs: temporal constraints. Brain Res. 379:1986;56-57.
51. Ruan D.Y., Chen J.T., Zhao C., Xu Y.Z., Wang M., Zhao W.F. Impairment of long-term potentiation and paired-pulse facilitation in rat hippocampal dentate gyrus following developmental lead exposure in vivo. Brain Res. 806:1998;196-201.
52. Stanton P.K., Sejnowski T.J. Associative long-term depression in the hippocampus induced by Hebbian covariance. Nature. 339:1989;215-218.
53. Staubli U., Lynch G. Stable depression of potentiated synaptic responses in the hippocampus with 1-5 Hz stimulation. Brain Res. 513:1990;113-118.
54. 2+ movements in synaptosomes and subcellular fractions from rat brain and Torpedo electric organ. Brain Res. 323:1984;31-46.
55. Thiels E., Barrionuevo G., Berger T.W. Excitatory stimulation during postsynaptic inhibition induces long-term depression in hippocampus in vivo. J. Neurophysiol. 72:1994;3009-3016.
56. Williams J.H., Errington M.L., Lynch M.A., Bliss T.V.P. Arachidonic acid induces a long-term activity-dependent enhancement of synaptic transmission in the hippocampus. Nature. 341:1989;739-742.
57. Xu L., Anwyl R., Rowan M.J. Behavioural stress facilitates the induction of long-term depression in the hippocampus. Nature. 387:1995;497-500.
58. Xu Y.Z., Ruan D.Y., Wu Y., Jiang Y.B., Chen S.Y. Nitric oxide affects LPT in area CA1 and CA3 of hippocampus in low-level lead-exposed rat. Neurotoxicology and Teratology. 20:1998;69-73.
59. Zucker R.S. Short-term synaptic plasticity. Ann. Rev. Neurosci. 12:1989;13-31.