Skip to main content
Cellular and Molecular Neurobiology logoLink to Cellular and Molecular Neurobiology
. 2002 Dec;22(5-6):663–674. doi: 10.1023/A:1021848706159

Signaling Mechanisms Mediating BDNF Modulation of Memory Formation In Vivo in the Hippocampus

Mariana Alonso 1, Monica R M Vianna 2, Ivan Izquierdo 2, Jorge H Medina 1
PMCID: PMC11533773  PMID: 12585686

Abstract

Given that brain-derived neutrophic factor (BDNF) modulates both short-term synaptic function and activity-dependent synaptic plasticity in the adult hippocampus, here we examined signaling mechanisms in vivo in the hippocampus mediating BDNF modulation of long-term memory (LTM) formation of a one-trial fear-motivated learning task in rats. Bilateral infusions of function-blocking anti-BDNF antibody into the CA1 region of the dorsal hippocampus decreased extracellular-signal regulated kinase 2 (ERK2) and CREB activation and impaired LTM retention scores. Inhibition of ERK1/2 activation by PD098059 produced similar effects and also reduced CREB phosphorylation. In contrast, intrahippocampal administration of recombinant human BDNF increased ERK1/2 and CREB activation and facilitated LTM. Activated-p38, activated-PKC isoforms, and activated-AKT were unaltered after BDNF or anti-BDNF infusion. In addition, no changes were found on αPKA and βPKA catalytic subunits in nuclear samples. Thus, our results suggest that BDNF exerts its role in LTM formation in vivo in CA1 region of the hippocampus, at least in part, via CREB activation. Moreover, BDNF-induced CREB activation appears to be mediated mainly through the activation of ERK1/2 signaling pathway.

Keywords: endogenous BDNF, anti-BDNF antibody, memory consolidation, inhibitory avoidance learning, signaling pathways, ERK1/2, CREB

REFERENCES

  1. Alonso, M., Vianna, M. R. M., Depino, A. M., Mello e Souza, T., Pereira, P., Szapiro, G., Viola, H., Pitossi, F., Izquierdo, I., and Medina, J. H. (2002). BNDF-triggered events in the rat hippocampus are required for both short-and long-term memory formation. Hippocampus12:551–560. [DOI] [PubMed] [Google Scholar]
  2. Atkins, C. M., Selcher, J. C., Petraitis, J. J., Trzaskos, J. M., and Sweatt, J. D. (1998). The MAPK cascade is required for mammalian associative learning. Nat. Neurosci.1:602–609. [DOI] [PubMed] [Google Scholar]
  3. Bernabeu, R., Bevilaqua, L., Ardenghi, P., Bromberg, E., Schmitz, P., Bianchin, M., Izquierdo, I., and Medina, J. H. (1997). Involvement of hippocampal cAMP/cAMP-dependent protein kinase signaling pathways in a late memory consolidation phase of aversively motivated learning in rats. Proc. Natl. Acad. Sci. U.S.A.94,7041–7046. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Bevilaqua, L., Ardenghi, P., Schroder, N., Bromberg, E., Schmitz, P. K., Schaeffer, E., Quevedo, J., Bianchin, M., Walz, R., Medina, J. H., and Izquierdo, I. (1997). Drug acting upon the protein kinase A/CREB pathways modulate memory consolidation when given late after training into rat hippocampus but not amygdala. Behav. Pharmacol.8:331–338. [DOI] [PubMed] [Google Scholar]
  5. Blanquet, P. R. (2000). Identification of two persistently activated neurotrophin-regulated pathways in rat hippocampus. Neuroscience95:705–719. [DOI] [PubMed] [Google Scholar]
  6. Blanquet, P. R., and Lamour, Y. (1997). Brain-derived neurotrophic factor increases Ca2C/calmodulindependent protein kinase 2 activity in hippocampus. J. Biol. Chem. 272:24133–24136. [DOI] [PubMed] [Google Scholar]
  7. Bourtchuladze, R., Frenguelli, B., Blendy, J., Schutz,G., and Silva, A. (1994). Deficient long-term memory in mice with a targeted mutation of the cAMP-responsive element binding protein. Cell79:59–68. [DOI] [PubMed] [Google Scholar]
  8. Burgering, B. M., and Coffer, P. J. (1995). Protein kinase B (c-AKT) in phosphatidylinositol-3-OH kinase signal transduction. Nature376:599–602. [DOI] [PubMed] [Google Scholar]
  9. Cammarota, M., Bevilaqua, L. R. M., Ardenghi, P., Paratcha, G., Levi de Stein, M., Izquierdo, I., and Medina, J. H. (2000). Learning-associated activation of nuclear MAPK, CREB and Elk-1, along with Fos production, in the rat hippocampus after a one-trial avoidance learning: Abolition by NMDA receptor blockade. Mol. Brain Res.76:36–46. [DOI] [PubMed] [Google Scholar]
  10. Cavanaugh, J. E., Ham, J., Hetman, M., Poser, S., Yan, C., and Xia, Z. (2001). Differential regulation of mitogen-activated protein kinases ERK1/2 and ERK5 by neurotrophins, neural activity, and cAMP in neurons. J. Neurosci. 21:434–443. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Chen, G., Kolbeck, R., Barde, Y.-A., Bonhoeffer, T., and Kossel, A. (1999). Relative contribution of endogenous neurotrophins in hippocampal long-term potentiation. J. Neurosci.19(18):7983–7990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Cirulli, F., Berry, A., and Alleva, E. (2000) Intracerebroventricular administration of brain-derived neurotrophic factor in adult rats affects analgesia and spontanous behavior but not memory retention in a Morris water maze task. Neurosci. Lett. 287:207–210. [DOI] [PubMed] [Google Scholar]
  13. Croll, S. D., Suri, C., Compton, D. L., Simmons, M. V., Yancopoulos, G. D., Lindsay, R. M., Wiegand, S. J., Rudge, J. S., and Scharfman, H. E. (1999). Brain-derived neurotrophic factor transgenic mice exhibit passive avoidance deficits, increased seizure severity and in vitro hyperexcitability in the hippocampus and entorhinal cortex. Neuroscience93:1491–1506. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Davis, H. P., and Squire, L. R. (2000). Protein synthesis and memory: A review. Psychol. Bull.96:518–559. [PubMed] [Google Scholar]
  15. Figurov, A., Pozzo-Miller, L., Olafsson, P., Wang, T., and Lu, B. (1996). Regulation of synaptic responses to high-frequency stimulation and LTP by neurotrophins in the hippocampus. Nature381:706–709. [DOI] [PubMed] [Google Scholar]
  16. Finkbeiner, S., Tavazoie, S., Maloratsky, A., Jacobs, K., Harris, K., and Greenberg, M. (1997). CREB: A major mediator of neuronal neurotrophin responses. Neuron19:1031–1047. [DOI] [PubMed] [Google Scholar]
  17. Fischer, W., Strevaag, A., Wiegand, S. J., Lindsay, R. M., and Björklund, A. (1994). Reversal of spatial memory impairments in aged rats by nerve growth factor and neurotrophins 3 and 4/5 but not by brain-derived neurotrophic factor. Proc. Natl. Acad. Sci. U.S.A.91:8607–8611. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Franke, T. F., Yang, S. I., Chan, T.O., Datta, K., Kazlauskas, A., Morrison, D. K., Kaplan, D. R., and Tsichlis, P. N. (1995). The protein kinase encoded by akt proto-oncogene is a target of the PDGF-activated phosphatidylinositol 3-kinase. Cell81:727–736. [DOI] [PubMed] [Google Scholar]
  19. Gottschalk, W. A., Jiang, H., Tartaglia, N., Feng, L., Figurov, A., and Lu, B. (1999). Signaling mechanisms mediating BDNF modulation of synaptic plasticity in the hippocampus. Learn. Mem. 6:243–256. [PMC free article] [PubMed] [Google Scholar]
  20. Han, B. H., and Holtzman, D. M. (2000). BDNF protects the neonatal brain from hypoxic-ischemic injury in vivo via the ERK pathway. J. Neurosci. 20:5775–5781. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Impey, S., Smith, D. M., Obrietan, K., Donahue, R., Wade, C., and Storm, D. R. (1998). Stimulation of cAMP response element (CRE)-mediated transcription during contextual learning. Nat. Neurosci.1:595–601. [DOI] [PubMed] [Google Scholar]
  22. Izquierdo, I., Barros, D. M., Izquierdo, L., Mello e Souza, T., Souza, M., and Medina, J. H. (1998). Mechanisms for memory types differ. Nature393:635–636. [DOI] [PubMed] [Google Scholar]
  23. Johnston, A. N. B., Clements, M. P., and Rose, S. P. R. (1999). Role of brain-derived neurotrophic factor and presynaptic proteins in passive avoidance learning in day-old domestic chicks. Neuroscience88:1033–1042. [DOI] [PubMed] [Google Scholar]
  24. Johnston, A. N. B., and Rose, S. P. R. (2001). Memory consolidation in day-old chicks requires BDNF but not NGF or NT-3: An antisense study. Mol. Brain Res.88:26–36. [DOI] [PubMed] [Google Scholar]
  25. Kafitz, K.W., Rose, C. R., Thoenen, H., and Konnerth, A. (1999). Neurotrophin-evoked rapid excitation through TrkB receptors. Nature401:918–921. [DOI] [PubMed] [Google Scholar]
  26. Kang, H., Welcher, A. A., Shelton, D., and Schuman, E. M. (1997). Neurotrophins and time: Differents roles for TrkB signaling in hippocampal long-term potentiation. Neuron19:653–664. [DOI] [PubMed] [Google Scholar]
  27. Kaplan, D. R., and Stephens, R.M. (1994). Neurotrophin signal transduction by trk receptor. J. Neurobiol. 25:1404–1417. [DOI] [PubMed] [Google Scholar]
  28. Korte, M., Kang, H. B., Bonhoeffer, T., and Schuman, E. (1998). A role for BDNF in the late-phase of hippocampal long-term potentiation. Neuropharmacol.37:553–559. [DOI] [PubMed] [Google Scholar]
  29. Kossel, A. H., Cambridge, S. B., Wagner, U., and Bonhoeffer, T. (2001). A caged Ab reveals an immediate/ instructive effect of BDNF during hippocampal synaptic potentiation. Proc. Natl. Acad. Sci. U.S.A.98:14702–14707. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Li, Y. X., Zhang, Y., Lester, H. A., Schuman, E. M., and Davidson, N. (1998). Enhancement of neurotransmitter release induced by brain-derived neurotrophic factor in cultured hippocampal neurons. J. Neurosci.18:10231–10240. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. Linnarsson, S., Björklund, A., and Ernfors, P. (1997). Learning deficit in BDNF mutant mice. Eur. J. Neurosci.9:2581–2587. [DOI] [PubMed] [Google Scholar]
  32. Lu, B., and Chow, A. (1999). Neurotrophins and hippocampal synaptic transmission and plasticity. J. Neurosci. Res.58:76–87. [PubMed] [Google Scholar]
  33. Ma, Y. L., Wang, H. L., Wu, H. C., Wei, C. L., and Lee, E. H. (1998). Brain-derived neurotrophic factor antisense oligonucleotide impairs memory retention and inhibits long-term potentiation in rats. Neuroscience82:957–967. [DOI] [PubMed] [Google Scholar]
  34. McAllister, A. K., Katz, L. C., and Lo, D. C. (1999). Neurotrophins and synaptic plasticity. Annu. Rev. Neurosci.22:295–318. [DOI] [PubMed] [Google Scholar]
  35. Mizuno, M., Yamada, K., Olariu, A., Nawa, H., and Nabeshima, T. (2000). Involvement of brain-derived neurotrophic factor in spatial memory formation and maintenance in a radial arm maze test in rats. J. Neurosci.20:7116–7121. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Mu, J. S., Li, W. P., Yao, Z. B., and Zhou, X. F. (1999). Deprivation of endogenous brain-derived neurotrophic factor results in impairment of spatial learning and memory in adult rats. Brain Res.835:259–265. [DOI] [PubMed] [Google Scholar]
  37. Patterson, S. L., Pittenger, C., Morozov, A., Martin, K. C., Scanlin, H., Drake, C., and Kandel, E. (2001). Some forms of cAMP-mediated long-lasting potentiation are associated with release of BDNF and nuclear translocation of phospho-MAP kinase. Neuron32:123–140. [DOI] [PubMed] [Google Scholar]
  38. Paxinos, G., and Watson, C. (1986). The Rat Brain in Stereotaxic Coordinates, Academic Press, San Diego, CA. [Google Scholar]
  39. Pelleymounter, M. A., Cullen, M. J., Baker, M. B., Gollub, M., and Wellman, C. (1996). The effects of intrahippocampal BDNF and NGF on spatial learning in aged Long Evans rats. Mol. Chem. Neuropathol.29:211–226. [DOI] [PubMed] [Google Scholar]
  40. Pizzorusso,T., Ratto, G. M., Putignano, E., and Maffei, L. (2000). Brain-derived neurotrophic factor causes cAMP response element-binding protein phosphorylation in absence of calcium increase in slices and cultured neurons from rat visual cortex. J. Neurosci.20:2809–2816. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Poo, M. (2001). Neurotrophins as synaptic modulators. Nat. Rev. Neurosci.2:24–32. [DOI] [PubMed] [Google Scholar]
  42. Roberson, E. D., English, J. D., Adams, J. P., Selcher, J. C., Kondratick, C., and Sweatt, J. D. (1999). The mitogen-activated protein kinase cascade couples PKA and PKC to cAMP response element binding protein phosphorylation in area CA1 of hippocampus. J. Neurosci. 19:4337–4348. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Rutherford, L. C., Nelson, S. B., and Turrigiano, G. G. (1998). BDNF has opposite effects on the quantal amplitude of pyramidal neuron and interneuron excitatory synapses. Neuron21:521–530. [DOI] [PubMed] [Google Scholar]
  44. Schinder, A. F., and Poo, M. (2000). The neurotrophin hypothesis for synaptic plasticity. TINS23:639–645. [DOI] [PubMed] [Google Scholar]
  45. Segal, R. A., and Greenberg, M. E. (1996). Intracellular signaling pathways activated by neurotrophic factor. Annu. Rev. Neurosci.19:463–489. [DOI] [PubMed] [Google Scholar]
  46. Silva, A. J., Kogan, J. H., Frankland, P.W., and Kida, S. (1998). CREB and memory. Annu. Rev. Neurosci.21:127–148. [DOI] [PubMed] [Google Scholar]
  47. Soppet, D. E., Escandon, E., Maragos, J., Middlemas, D. S., Reid, S. W., Blair, J., Burton, L. E., Stanton, B. R., Kaplan, T., Hunter, T., and Kaptan, D. R. (1991). The neurotrophic factors, brain-derived neurotrophic factor, and neurotrophin-3 are ligands for the trkB tyrosine receptor. Cell65:895–903. [DOI] [PubMed] [Google Scholar]
  48. Stephens, R. M., Loeb, D. M., Copeland, T. D., Pawson, T., Greene, L. A., and Kaplan, D. R. (1994). Trk receptors use redundant signal transduction pathways involving SHC and PLC-gamma1 to mediate NGF responses. Neuron12:691–705. [DOI] [PubMed] [Google Scholar]
  49. Sweatt, J. D. (2001). The neuronal MAP kinase cascade: A biochemical signal integration system subserving synaptic plasticity and memory. J. Neurochem.76:1–10. [DOI] [PubMed] [Google Scholar]
  50. Taubenfeld, S. M., Wiig, K. A., Bear, M. F., and Alberini, C. M. (1999). A molecular correlate of memory and amnesia in the hippocampus. Nat. Neurosci.2:309–310. [DOI] [PubMed] [Google Scholar]
  51. Tyler, W. J., and Pozzo-Miller, L.D. (2001).BDNFenhances quantal neurotransmitter release and increases the number of docked vesicles at the active zones of hippocampal excitatory synapses. J. Neurosci.21:4249–4258. [DOI] [PMC free article] [PubMed] [Google Scholar]
  52. Vianna, M. R. M., Izquierdo, L. A., Barros, D. M., Medina, J. H., and Izquierdo, I. (1999). Intrahippocampal infusion of inhibitor of protein kinaseAseparates short-from long-term memory. Behav. Pharmacol.10:223–227. [DOI] [PubMed] [Google Scholar]
  53. Viola, H., Furman, M., Izquierdo, L. A., Alonso, M., Barros, D. M., de Souza, M. M., Izquierdo, I., and Medina, J. H. (2000). PhosphorylatedcAMPresponse element-binding protein as a molecular marker of memory processing in rat hippocampus: Effect of novelty. J. Neurosci.20:RC112 (1–5). [DOI] [PMC free article] [PubMed] [Google Scholar]
  54. Walz, R., Roesler, R., Quevedo, J., Sant'Anna, M. K., Madruga, M., Rodrigues, C., Gottfried, C., Medina, J. H., and Izquierdo, I. (1999). Time-dependent impairment of inhibitory avoidance retention in rats by posttraining infusion of a mitogen-activated protein kinase inhibitor into cortical and limbic structures. Neurobiol. Learn. Mem.73:11–20. [DOI] [PubMed] [Google Scholar]
  55. Xing, J., Ginty, D. D., and Greenberg, M. E. (1996). Coupling of the RAS-MAPK pathway to gene activation by RSK2, a growth factor-regulated CREB kinase. Science273:959–963. [DOI] [PubMed] [Google Scholar]
  56. Yamada, K., Mizuno, M., and Nabeshina, T. (2002). Role for brain-derived neurotrophic factor in learning and memory. Life Sci.70:735–744. [DOI] [PubMed] [Google Scholar]
  57. Ying, S.-W., Futter, M., Rosenblum, K., Webber, M. J., Hunt, S. R., Bliss, T.V.P., and Bramham, C. R. (2002). Brain-derived neurotrophic factor induced long-term potentiation in intact adult hippocampus: Requirement for ERK activation coupled to CREB and upregulation of Arc synthesis. J. Neurosci. 22: 1532–1540. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Cellular and Molecular Neurobiology are provided here courtesy of Springer

RESOURCES