Effects of serum response factor (SRF) deletion on conditioned reinforcement

Behavioural Brain Research

Volumn 220, Issue 2, 2011, Pages 312-318

  Johnson, A W ^a   Crombag, H S ^a   Smith, D R ^a   Ramanan, N ^b  

^a JOHNS HOPKINS UNIVERSITY   (United States)

^b WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Conditioned reinforcement; IEG; Mice; Pavlovian conditioning; SRF; Transcription factor

Indexed keywords

SERUM RESPONSE FACTOR;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; ASSOCIATION; BRAIN CORTEX; CONTROLLED STUDY; CORPUS STRIATUM; FOREBRAIN; GENE DELETION; HIPPOCAMPUS; MOUSE; MUTANT; NEWBORN; NONHUMAN; PERINATAL PERIOD; PRIORITY JOURNAL; REINFORCEMENT; REWARD; SPATIAL DISCRIMINATION; STRAIN DIFFERENCE; WILD TYPE;

ANALYSIS OF VARIANCE; ANIMALS; BEHAVIOR, ANIMAL; BRAIN; CALCIUM-CALMODULIN-DEPENDENT PROTEIN KINASE TYPE 2; CONDITIONING, CLASSICAL; CONDITIONING, OPERANT; FOOD DEPRIVATION; MICE; MICE, KNOCKOUT; NEURONS; REINFORCEMENT (PSYCHOLOGY); SERUM RESPONSE FACTOR; SYNAPSINS;

EID: 79953280900     PISSN: 01664328     EISSN: 18727549     Source Type: Journal    
DOI: 10.1016/j.bbr.2011.02.015     Document Type: Article

References (34)

1. Lanahan A., Worley P. Immediate-early genes and synaptic function. Neurobiol Learn Mem 1998, 70:37-43.
2. Dash P.K., Hochner B., Kandel E.R. Injection of the cAMP-responsive element into the nucleus of Aplysia sensory neurons blocks long-term facilitation. Nature 1990, 345:718-721.
3. Yin J.C., Wallach J.S., Del Vecchio M., Wilder E.L., Zhou H., Quinn W.G., et al. Induction of a dominant negative CREB transgene specifically blocks long-term memory in Drosophila. Cell 1994, 79:49-58.
4. Meffert M.K., Chang J.M., Wiltgen B.J., Fanselow M.S., Baltimore D. NF-kappa B functions in synaptic signaling and behavior. Nat Neurosci 2003, 6:1072-1078.
5. Romano A., Freugenthal R., Merio E., Routtenberg A. Evolutionarily-conserved role of the NF-kappa B transcription factor in neural plasticity and memory. Eur J Neurosci 2006, 24:1507-1516.
6. 2+ channel-regulated neuronal gene expression. J Neurobiol 1998, 37:171-189.
7. Bading H., Ginty D.D., Greenberg M.E. Regulation of gene expression in hippocampal neurons by distinct calcium signaling pathways. Science 1993, 260:181-186.
8. Treisman R. The SRE: a growth factor responsive transcriptional regulator. Semin Cancer Biol 1990, 1:47-58.
9. Ramanan N., Shen Y., Sarsfield S., Lemberger T., Schutz G., Linden D.J., et al. SRF mediates activity-induced gene expression and synaptic plasticity but not neuronal viability. Nat Neurosci 2005, 8:759-767.
10. Etkin A., Alarcon J.M., Weisberg S.P., Touzani K., Huang Y.Y., Nordheim A., et al. A role in learning for SRF: deletion in the adult forebrain disrupts LTD and the formation of an immediate memory of a novel context. Neuron 2006, 50:127-143.
11. Lindecke A., Korte M., Zagrebelsky M., Horejschi V., Elvers M., Widera D., et al. Long-term depression activates transcription of immediate early transcription factor genes: involvement of serum response factor/Elk-1. Eur J Neurosci 2006, 24:555-563.
12. Nicoll R.A., Malenka R.C. Expression mechanisms underlying NMDA receptor-dependent long-term potentiation. Ann N Y Acad Sci 1999, 868:515-525.
13. Cador M., Robbins T.W., Everitt B.J. Involvement of the amygdala in stimulus-reward associations: interaction with the ventral striatum. Neuroscience 1989, 30:77-86.
14. Parkinson J.A., Olmstead M.C., Burns L.H., Robbins T.W., Everitt B.J. Dissociation in effects of lesions of the nucleus accumbens core and shell on appetitive Pavlovian approach behavior and the potentiation of conditioned reinforcement and locomotor activity by d-amphetamine. J Neurosci 1999, 19:2401-2411.
15. Pears A., Parkinson J.A., Hopewell L., Everitt B.J., Roberts A.C. Lesions of the orbitofrontal but not medial prefrontal cortex disrupt conditioned reinforcement in primates. J Neurosci 2003, 23:11189-11201.
16. Burns L.H., Robbins T.W., Everitt B.J. Differential effects of excitotoxic lesions of the basolateral amygdala, ventral subiculum and medial prefrontal cortex on responding with conditioned reinforcement and locomotor activity potentiated by intra-accumbens infusions of d-amphetamine. Behav Brain Res 1993, 55:167-183.
17. Wyckoff L.B., Sidowski J., Chambliss D.J. An experimental study of the relationship between secondary reinforcing and cue effects of a stimulus. J Comp Physiol Psychol 1958, 51:103-109.
18. de Wit H., Stewart J. Reinstatement of cocaine-reinforced responding in the rat. Psychopharmacology (Berl) 1981, 75:134-143.
19. Taylor J.R., Robbins T.W. 6-Hydroxydopamine lesions of the nucleus accumbens, but not of the caudate nucleus, attenuate enhanced responding with reward-related stimuli produced by intra-accumbens d-amphetamine. Psychopharmacology (Berl) 1986, 90:390-397.
20. Setlow B., Gallagher M., Holland P.C. The basolateral complex of the amygdala is necessary for acquisition but not expression of CS motivational value in appetitive Pavlovian second-order conditioning. Eur J Neurosci 2002, 15:1841-1853.
21. Baxter M.G., Murray E.A. The amygdala and reward. Nat Rev Neurosci 2002, 3:563-573.
22. Rossiarnaud C., Ammassariteule M. Modifications of open-field and novelty behaviors by hippocampal and amygdaloid-lesions in 2 inbred strains of mice-lack of strain×lesion interactions. Behav Pro 1992, 27:155-164.
23. Parktina J.R., Bilbao A., Rieker C., Engblom D., Piechota M., Nordheim A., et al. Loss of the serum response factor in the dopamine system leads to hyperactivity. Fed Am Soc Exp Biol 2010, 24:2427-2435.
24. Biedenkapp J.C., Rudy J.W. Context preexposure prevents forgetting of a contextual fear memory: implication for regional changes in brain activation patterns associated with recent and remote memory tests. Learn Mem 2007, 14:200-203.
25. Chan K.H., Morell J.R., Jarrard L.E., Davidson T.L. Reconsideration of the role of the hippocampus in learned inhibition. Behav Brain Res 2001, 119:111-130.
26. Ito R., Everitt B.J., Robbins T.W. The hippocampus and appetitive Pavlovian conditioning: effects of excitotoxic hippocampal lesions on conditioned locomotor activity and autoshaping. Hippocampus 2005, 15:713-721.
27. Cenquizca L.A., Swanson L.W. Analysis of direct hippocampal cortical field CA1 axonal projections to diencephalon in the rat. J Comp Neurol 2006, 497:101-114.
28. Zhong Y.M., Yukie M., Rockland K.S. Distinctive morphology of hippocampal CA1 terminations in orbital and medial frontal cortex in macaque monkeys. Exp Brain Res 2006, 169:549-553.
29. Lindgren J.L., Gallagher M., Holland P.C. Lesions of basolateral amygdala impair extinction of CS motivational value, but not of explicit conditioned responses, in Pavlovian appetitive second-order conditioning. Eur J Neurosci 2003, 17:160-166.
30. Everitt B.J., Robbins T.W. Neural systems of reinforcement for drug addiction: from actions to habits to compulsion. Nature Neurosci 2005, 11:1481-1489.
31. Johnson A.W., Chen X., Crombag H.S., Zhang C., Smith D.R., Shokat K.M., et al. The brain-derived neurotrophic factor receptor TrkB is critical for the acquisition but not expression of conditioned incentive value. Eur J Neurosci 2008, 28:997-1002.
32. Miano J Mol Cell 2003, 35(6):577-593.
33. Knoll, Nordheim Trends Neurosci 2009, 32(8):432-442.
34. Smith-Hicks, et al. Nature Neurosci 2010, 13(9). 1082-U73.