Repeated third trimester-equivalent ethanol exposure inhibits long-term potentiation in the hippocampal CA1 region of neonatal rats

Alcohol

Volumn 44, Issue 3, 2010, Pages 283-290

  Puglia, Michael P ^a   Valenzuela, C Fernando ^a  

^a UNIVERSITY OF NEW MEXICO HEALTH SCIENCES CENTER   (United States)

Author keywords

Development; Fetal alcohol syndrome; Glutamate; Neurotransmission; Plasticity; Synaptic

Indexed keywords

ALCOHOL; AMPA RECEPTOR; GLUTAMIC ACID; N METHYL DEXTRO ASPARTIC ACID RECEPTOR;

ALCOHOL BLOOD LEVEL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BRAIN DEVELOPMENT; BRAIN SLICE; COGNITIVE DEFECT; CONTROLLED STUDY; FEMALE; FETAL ALCOHOL SYNDROME; HIPPOCAMPUS; IN VIVO STUDY; LONG TERM POTENTIATION; NERVE CELL PLASTICITY; NEUROTOXICITY; NEWBORN; NONHUMAN; PRENATAL EXPOSURE; PROTEIN FUNCTION; RAT; THIRD TRIMESTER PREGNANCY;

ANIMALS; ANIMALS, NEWBORN; CA1 REGION, HIPPOCAMPAL; CENTRAL NERVOUS SYSTEM DEPRESSANTS; ETHANOL; FEMALE; LONG-TERM POTENTIATION; MALE; MODELS, ANIMAL; PREGNANCY; RATS;

EID: 77953541887     PISSN: 07418329     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.alcohol.2010.03.001     Document Type: Article

References (36)

1. Bellinger F.P., Bedi K.S., Wilson P., Wilce P.A. Ethanol exposure during the third trimester equivalent results in long-lasting decreased synaptic efficacy but not plasticity in the CA1 region of the rat hippocampus. Synapse 1999, 31:51-58.
2. Bellinger F.P., Davidson M.S., Bedi K.S., Wilce P.A. Neonatal ethanol exposure reduces AMPA but not NMDA receptor levels in the rat neocortex. Brain Res. Dev. Brain Res. 2002, 136:77-84.
3. Ben-Ari Y., Gaiarsa J.L., Tyzio R., Khazipov R. GABA: a pioneer transmitter that excites immature neurons and generates primitive oscillations. Physiol. Rev. 2007, 87:1215-1284.
4. Berman R.F., Hannigan J.H. Effects of prenatal alcohol exposure on the hippocampus: spatial behavior, electrophysiology, and neuroanatomy. Hippocampus 2000, 10:94-110.
5. Byrnes M.L., Richardson D.P., Brien J.F., Reynolds J.N., Dringenberg H.C. Spatial acquisition in the Morris water maze and hippocampal long-term potentiation in the adult guinea pig following brain growth spurt-prenatal ethanol exposure. Neurotoxicol. Teratol. 2004, 26:543-551.
6. Carpenter-Hyland E.P., Chandler L.J. Homeostatic plasticity during alcohol exposure promotes enlargement of dendritic spines. Eur. J. Neurosci. 2006, 24:3496-3506.
7. Constantine-Paton M., Cline H.T. LTP and activity-dependent synaptogenesis: the more alike they are, the more different they become. Curr. Opin. Neurobiol. 1998, 8:139-148.
8. Durand G.M., Kovalchuk Y., Konnerth A. Long-term potentiation and functional synapse induction in developing hippocampus. Nature 1996, 381:71-75.
9. Elias G.M., Elias L.A., Apostolides P.F., Kriegstein A.R., Nicoll R.A. Differential trafficking of AMPA and NMDA receptors by SAP102 and PSD-95 underlies synapse development. Proc. Natl. Acad. Sci. U.S.A. 2008, 105:20953-20958.
10. Fang Z., Ionescu P., Gong D., Kendig J., Harris A., Eger E.I. Maturation decreases ethanol minimum alveolar anesthetic concentration in mice as previously demonstrated in rats: there is no species difference. Anesth. Analg. 1997, 85:160-163.
11. Galindo R., Valenzuela C.F. Immature hippocampal neuronal networks do not develop tolerance to the excitatory actions of ethanol. Alcohol 2006, 40:111-118.
12. Goodlett C.R., Johnson T.B. Neonatal binge ethanol exposure using intubation: timing and dose effects on place learning. Neurotoxicol. Teratol. 1997, 19:435-446.
13. Grosshans D.R., Clayton D.A., Coultrap S.J., Browning M.D. LTP leads to rapid surface expression of NMDA but not AMPA receptors in adult rat CA1. Nat. Neurosci. 2002, 5:27-33.
14. Hamilton D.A., Kodituwakku P., Sutherland R.J., Savage D.D. Children with fetal alcohol syndrome are impaired at place learning but not cued-navigation in a virtual Morris water task. Behav. Brain Res. 2003, 143:85-94.
15. Hollstedt C., Olsson O., Rydberg U. Effects of ethanol on the developing rat. II. Coordination as measured by the tilting-plane test. Med. Biol. 1980, 58:164-168.
16. Hou Q., Zhang D., Jarzylo L., Huganir R.L., Man H.Y. Homeostatic regulation of AMPA receptor expression at single hippocampal synapses. Proc. Natl. Acad. Sci. U. S. A. 2008, 105:775-780.
17. Kerchner G.A., Nicoll R.A. Silent synapses and the emergence of a postsynaptic mechanism for LTP. Nat. Rev. Neurosci. 2008, 9:813-825.
18. Lauri S.E., Palmer M., Segerstrale M., Vesikansa A., Taira T., Collingridge G.L. Presynaptic mechanisms involved in the expression of STP and LTP at CA1 synapses in the hippocampus. Neuropharmacology 2007, 52:1-11.
19. Leinekugel X. Developmental patterns and plasticities: the hippocampal model. J. Physiol. (Paris) 2003, 97:27-37.
20. Livy D.J., Miller E.K., Maier S.E., West J.R. Fetal alcohol exposure and temporal vulnerability: effects of binge-like alcohol exposure on the developing rat hippocampus. Neurotoxicol. Teratol. 2003, 25:447-458.
21. Mameli M., Zamudio P.A., Carta M., Valenzuela C.F. Developmentally regulated actions of alcohol on hippocampal glutamatergic transmission. J. Neurosci. 2005, 25:8027-8036.
22. O'Leary-Moore S.K., McMechan A.P., Mathison S.N., Berman R.F., Hannigan J.H. Reversal learning after prenatal or early postnatal alcohol exposure in juvenile and adult rats. Alcohol 2006, 38:99-110.
23. Puglia M.P., Valenzuela C.F. AMPAR-mediated synaptic transmission in the CA1 hippocampal region of neonatal rats: unexpected resistance to repeated ethanol exposure. Alcohol 2009, 43:619-625.
24. Puglia M.P., Valenzuela C.F. Ethanol acutely inhibits ionotropic glutamate receptor-mediated responses and long-term potentiation in the developing CA1 hippocampus. Alcohol. Clin. Exp. Res. 2010, 34:594-606.
25. Schummers J., Browning M.D. Evidence for a role for GABA(A) and NMDA receptors in ethanol inhibition of long-term potentiation. Brain Res. Mol. Brain Res. 2001, 94:9-14.
26. Silveri M.M., Spear L.P. Decreased sensitivity to the hypnotic effects of ethanol early in ontogeny. Alcohol. Clin. Exp. Res. 1998, 22:670-676.
27. Swann J.W. The effects of seizures on the connectivity and circuitry of the developing brain. Ment. Retard. Dev. Disabil. Res. Rev. 2004, 10:96-100.
28. Swartzwelder H.S., Wilson W.A., Tayyeb M.I. Age-dependent inhibition of long-term potentiation by ethanol in immature versus mature hippocampus. Alcohol. Clin. Exp. Res. 1995, 19:1480-1485.
29. Thomas J.D., Fleming S.L., Riley E.P. Administration of low doses of MK-801 during ethanol withdrawal in the developing rat pup attenuates alcohol's teratogenic effects. Alcohol. Clin. Exp. Res. 2002, 26:1307-1313.
30. Thomas J.D., Garcia G.G., Dominguez H.D., Riley E.P. Administration of eliprodil during ethanol withdrawal in the neonatal rat attenuates ethanol-induced learning deficits. Psychopharmacology (Berl.) 2004, 175:189-195.
31. Turrigiano G.G., Nelson S.B. Homeostatic plasticity in the developing nervous system. Nat. Rev. Neurosci. 2004, 5:97-107.
32. Uecker A., Nadel L. Spatial but not object memory impairments in children with fetal alcohol syndrome. Am. J. Ment. Retard. 1998, 103:12-18.
33. Valenzuela C.F., Partridge L.D., Mameli M., Meyer D.A. Modulation of glutamatergic transmission by sulfated steroids: role in fetal alcohol spectrum disorder. Brain Res. Rev. 2008, 57:506-519.
34. Yao L., Arolfo M.P., Dohrman D.P., Jiang Z., Fan P., Fuchs S., et al. betagamma Dimers mediate synergy of dopamine D2 and adenosine A2 receptor-stimulated PKA signaling and regulate ethanol consumption. Cell 2002, 109:733-743.
35. Yasuda H., Barth A.L., Stellwagen D., Malenka R.C. A developmental switch in the signaling cascades for LTP induction. Nat. Neurosci. 2003, 6:15-16.
36. Zhu J.J., Esteban J.A., Hayashi Y., Malinow R. Postnatal synaptic potentiation: delivery of GluR4-containing AMPA receptors by spontaneous activity. Nat. Neurosci. 2000, 3:1098-1106.