Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Review Article
  • Published:

Oestradiol as a neuromodulator of learning and memory

Abstract

Although hormones such as glucocorticoids have been broadly accepted in recent decades as general neuromodulators of memory processes, sex steroid hormones such as the potent oestrogen 17β-oestradiol have been less well recognized by the scientific community in this capacity. The predominance of females in studies of oestradiol and memory and the general (but erroneous) perception that oestrogens are ‘female’ hormones have probably prevented oestradiol from being more widely considered as a key memory modulator in both sexes. Indeed, although considerable evidence supports a crucial role for oestradiol in regulating learning and memory in females, a growing body of literature indicates a similar role in males. This Review discusses the mechanisms of oestradiol signalling and provides an overview of the effects of oestradiol on spatial, object recognition, social and fear memories. Although the primary focus is on data collected in females, effects of oestradiol on memory in males will be discussed, as will sex differences in the molecular mechanisms that regulate oestrogenic modulation of memory, which may have important implications for the development of future cognitive therapeutics.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Fig. 1: Membrane-initiated oestrogen signalling and downstream intracellular events.
Fig. 2: Behavioural approaches to studying oestrogenic effects on memory.
Fig. 3: Summary of oestrogenic actions on memory processes.

Similar content being viewed by others

References

  1. Gould, E., Woolley, C. S., Frankfurt, M. & McEwen, B. S. Gonadal steroids regulate dendritic spine density in hippocampal pyramidal cells in adulthood. J. Neurosci. 10, 1286–1291 (1990).

    CAS  PubMed  PubMed Central  Google Scholar 

  2. Woolley, C. & McEwen, B. Estradiol mediates fluctuation in hippocampal synapse density during the estrous cycle in the adult rat. J. Neurosci. 12, 2549–2554 (1992). This foundational study links dynamic changes in hippocampal spine density to oestrous cyclicity, such that elevated spine density is correlated with higher levels of E2.

    CAS  PubMed  PubMed Central  Google Scholar 

  3. Woolley, C. S. & McEwen, B. S. Roles of estradiol and progesterone in regulation of hippocampal dendritic spine density during the estrous cycle in the rat. J. Comp. Neurol. 336, 293–306 (1993).

    CAS  PubMed  Google Scholar 

  4. Woolley, C. S. & McEwen, B. S. Estradiol regulates hippocampal dendritic spine density via an N-methyl-D-aspartate receptor-dependent mechanism. J. Neurosci. 14, 7680–7687 (1994).

    CAS  PubMed  PubMed Central  Google Scholar 

  5. Woolley, C. S., Weiland, N. G., McEwen, B. S. & Schwartzkroin, P. A. Estradiol increases the sensitivity of hippocampal CA1 pyramidal cells to NMDA receptor-mediated synaptic input: correlation with dendritic spine density. J. Neurosci. 17, 1848–1859 (1997).

    CAS  PubMed  PubMed Central  Google Scholar 

  6. Wong, M. & Moss, R. Long-term and short-term electrophysiological effects of estrogen on the synaptic properties of hippocampal CA1 neurons. J. Neurosci. 12, 3217–3225 (1992).

    CAS  PubMed  PubMed Central  Google Scholar 

  7. Gu, Q. & Moss, R. L. 17β-Estradiol potentiates kainate-induced currents via activation of the cAMP cascade. J. Neurosci. 16, 3620–3629 (1996).

    CAS  PubMed  PubMed Central  Google Scholar 

  8. Azcoitia, I., Sierra, A. & Garcia-Segura, L. M. Estradiol prevents kainic acid-induced neuronal loss in the rat dentate gyrus. Neuroreport 9, 3075–3079 (1998).

    CAS  PubMed  Google Scholar 

  9. Frick, K. M., Tuscher, J. J., Koss, W. A., Kim, J. & Taxier, L. R. Estrogenic regulation of memory consolidation: a look beyond the hippocampus, ovaries, and females. Physiol. Behav. 187, 57–66 (2018).

    CAS  PubMed  Google Scholar 

  10. Rossetti, M. F., Cambiasso, M. J., Holschbach, M. A. & Cabrera, R. Oestrogens and progestagens: synthesis and action in the brain. J. Neuroendocrinol. https://doi.org/10.1111/jne.12402 (2016).

    Article  PubMed  Google Scholar 

  11. Hara, Y., Waters, E. M., McEwen, B. S. & Morrison, J. H. Estrogen effects on cognitive and synaptic health over the lifecourse. Physiol. Rev. 95, 785–807 (2015).

    CAS  PubMed  PubMed Central  Google Scholar 

  12. Morrison, J. H. & Baxter, M. G. The aging cortical synapse: hallmarks and implications for cognitive decline. Nat. Rev. Neurosci. 13, 240–250 (2012).

    CAS  PubMed  PubMed Central  Google Scholar 

  13. Dumitriu, D., Rapp, P. R., McEwen, B. S. & Morrison, J. H. Estrogen and the aging brain: an elixir for the weary cortical network. Ann. N. Y. Acad. Sci. 1204, 104–112 (2010).

    CAS  PubMed  PubMed Central  Google Scholar 

  14. Miller, W. L. & Auchus, R. J. The molecular biology, biochemistry, and physiology of human steroidogenesis and its disorders. Endocr. Rev. 32, 81–151 (2011).

    CAS  PubMed  Google Scholar 

  15. Compagnone, N. A. & Mellon, S. H. Neurosteroids: biosynthesis and function of these novel neuromodulators. Front. Neuroendocrinol. 21, 1–56 (2000).

    CAS  PubMed  Google Scholar 

  16. Österlund, M., Kuiper, G. G. J. M., Gustafsson, J.-Å. & Hurd, Y. L. Differential distribution and regulation of estrogen receptor-α and -β mRNA within the female rat brain. Mol. Brain Res. 54, 175–180 (1998).

    PubMed  Google Scholar 

  17. Prange-Kiel, J., Wehrenberg, U., Jarry, H. & Rune, G. M. Para/autocrine regulation of estrogen receptors in hippocampal neurons. Hippocampus 13, 226–234 (2003).

    PubMed  Google Scholar 

  18. Stanic´, D. et al. Characterization of aromatase expression in the adult male and female mouse brain. I. Coexistence with oestrogen receptors α and β, and androgen receptors. PLoS ONE 9, e90451 (2014).

    PubMed  PubMed Central  Google Scholar 

  19. Kretz, O. et al. Hippocampal synapses depend on hippocampal estrogen synthesis. J. Neurosci. 24, 5913–5921 (2004). This study provides early evidence that locally synthesized oestrogens are critical for maintenance of hippocampal synapses.

    CAS  PubMed  PubMed Central  Google Scholar 

  20. Balthazart, J. & Ball, G. F. Is brain estradiol a hormone or a neurotransmitter? Trends Neurosci. 29, 241–249 (2006).

    CAS  PubMed  Google Scholar 

  21. Remage-Healey, L., Saldanha, C. J. & Schlinger, B. A. Estradiol synthesis and action at the synapse: evidence for “synaptocrine” signaling. Front. Endocrinol. 2, 28 (2011).

    Google Scholar 

  22. Allen, E. The oestrous cycle in the mouse. Am. J. Anat. 30, 297–371 (1922).

    Google Scholar 

  23. Long, J. A. & Evans, H. M. The Oestrous Cycle in the Rat and Its Associated Phenomena. (University of California Press, 1922).

  24. Kato, A. et al. Female hippocampal estrogens have a significant correlation with cyclic fluctuation of hippocampal spines. Front. Neural. Circuits https://doi.org/10.3389/fncir.2013.00149 (2013).

  25. Pawluski, J. L., Brummelte, S., Barha, C. K., Crozier, T. M. & Galea, L. A. M. Effects of steroid hormones on neurogenesis in the hippocampus of the adult female rodent during the estrous cycle, pregnancy, lactation and aging. Front. Neuroendocrinol. 30, 343–357 (2009).

    CAS  PubMed  Google Scholar 

  26. Mendoza-Garcés, L. et al. Differential expression of estrogen receptors in two hippocampal regions during the estrous cycle of the rat. Anat. Rec. 294, 1913–1919 (2011).

    Google Scholar 

  27. Balthazart, J., Choleris, E. & Remage-Healey, L. Steroid and the brain: 50 years of research, conceptual shifts and the ascent of non-classical and membrane-initiated actions. Horm. Behav. 99, 1–8 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  28. Vasudevan, N. & Pfaff, D. W. Non-genomic actions of estrogens and their interaction with genomic actions in the brain. Front. Neuroendocrinol. 29, 238–257 (2008).

    CAS  PubMed  Google Scholar 

  29. Szego, C. M. & Davis, J. S. Adenosine 3′,5′-monophosphate in rat uterus: acute elevation by estrogen. Proc. Natl Acad. Sci. USA 58, 1711–1718 (1967).

    CAS  PubMed  Google Scholar 

  30. Kelly, M. J., Moss, R. L. & Dudley, C. A. Differential sensitivity of preoptic-septal neurons to microelectrophoressed estrogen during the estrous cycle. Brain Res. 114, 152–157 (1976).

    CAS  PubMed  Google Scholar 

  31. Zhao, Z., Fan, L. & Frick, K. M. Epigenetic alterations regulate estradiol-induced enhancement of memory consolidation. Proc. Natl Acad. Sci. USA 107, 5605–5610 (2010).

    CAS  PubMed  Google Scholar 

  32. Akama, K. T. & McEwen, B. S. Estrogen stimulates postsynaptic density-95 rapid protein synthesis via the Akt/protein kinase B pathway. J. Neurosci. 23, 2333–2339 (2003).

    CAS  PubMed  PubMed Central  Google Scholar 

  33. Phan, A. et al. Low doses of 17β-estradiol rapidly improve learning and increase hippocampal dendritic spines. Neuropsychopharmacology 37, 2299–2309 (2012).

    CAS  PubMed  PubMed Central  Google Scholar 

  34. Woolley, C. S. Acute effects of estrogen on neuronal physiology. Annu. Rev. Pharmacol. Toxicol. 47, 657–680 (2007).

    CAS  PubMed  Google Scholar 

  35. Kramár, E. A. et al. Cytoskeletal changes underlie estrogen’s acute effects on synaptic transmission and plasticity. J. Neurosci. 29, 12982–12993 (2009).

    PubMed  PubMed Central  Google Scholar 

  36. Pappas, T. C., Gametchu, B. & Watson, C. S. Membrane estrogen receptors identified by multiple antibody labeling and impeded-ligand binding. FASEB J. 9, 404–410 (1995).

    CAS  PubMed  Google Scholar 

  37. Watsona, C. S., Norfleet, A. M., Pappas, T. C. & Gametchu, B. Rapid actions of estrogens in GH3/B6 pituitary tumor cells via a plasma membrane version of estrogen receptor-α. Steroids 64, 5–13 (1999).

    Google Scholar 

  38. Razandi, M., Pedram, A., Greene, G. L. & Levin, E. R. Cell membrane and nuclear estrogen receptors (ERs) originate from a single transcript: studies of ERα and ERβ expressed in Chinese hamster ovary cells. Mol. Endocrinol. 13, 307–319 (1999).

    CAS  PubMed  Google Scholar 

  39. Clarke, C. H. et al. Perimembrane localization of the estrogen receptor α protein in neuronal processes of cultured hippocampal neurons. Neuroendocrinology 71, 34–42 (2000).

    CAS  PubMed  Google Scholar 

  40. Gorosito, S. V., Lorenzo, A. G. & Cambiasso, M. J. Estrogen receptor α is expressed on the cell-surface of embryonic hypothalamic neurons. Neuroscience 154, 1173–1177 (2008).

    CAS  PubMed  Google Scholar 

  41. Razandi, M., Pedram, A., Park, S. T. & Levin, E. R. Proximal events in signaling by plasma membrane estrogen receptors. J. Biol. Chem. 278, 2701–2712 (2003).

    CAS  PubMed  Google Scholar 

  42. Ábrahám, I. M., Todman, M. G., Korach, K. S. & Herbison, A. E. Critical in vivo roles for classical estrogen receptors in rapid estrogen actions on intracellular signaling in mouse brain. Endocrinology 145, 3055–3061 (2004).

    PubMed  Google Scholar 

  43. Blaustein, J. D. Cytoplasmic estrogen receptors in rat brain: immunocytochemical evidence using three antibodies with distinct epitopes. Endocrinology 131, 1336–1342 (1992).

    CAS  PubMed  Google Scholar 

  44. Milner, T. A. et al. Ultrastructural evidence that hippocampal alpha estrogen receptors are located at extranuclear sites. J. Comp. Neurol. 429, 355–371 (2001).

    CAS  PubMed  Google Scholar 

  45. Milner, T. A. et al. Ultrastructural localization of estrogen receptor β immunoreactivity in the rat hippocampal formation. J. Comp. Neurol. 491, 81–95 (2005).

    CAS  PubMed  Google Scholar 

  46. Andersson, S. et al. Insufficient antibody validation challenges oestrogen receptor beta research. Nat. Commun. 8, 15840 (2017).

    CAS  PubMed  PubMed Central  Google Scholar 

  47. Zhang, Z., Kumar, R., Santen, R. J. & Song, R. X.-D. The role of adapter protein Shc in estrogen non-genomic action. Steroids 69, 523–529 (2004).

    CAS  PubMed  Google Scholar 

  48. Russell, K. S., Haynes, M. P., Sinha, D., Clerisme, E. & Bender, J. R. Human vascular endothelial cells contain membrane binding sites for estradiol, which mediate rapid intracellular signaling. Proc. Natl Acad. Sci. USA 97, 5930–5935 (2000).

    CAS  PubMed  Google Scholar 

  49. Acconcia, F., Ascenzi, P., Fabozzi, G., Visca, P. & Marino, M. S-palmitoylation modulates human estrogen receptor-α functions. Biochem. Biophys. Res. Commun. 316, 878–883 (2004).

    CAS  PubMed  Google Scholar 

  50. Pedram, A. et al. A conserved mechanism for steroid receptor translocation to the plasma membrane. J. Biol. Chem. 282, 22278–22288 (2007).

    CAS  PubMed  Google Scholar 

  51. Meitzen, J. et al. Palmitoylation of estrogen receptors is essential for neuronal membrane signaling. Endocrinology 154, 4293–4304 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  52. Schlegel, A., Wang, C., Katzenellenbogen, B. S., Pestell, R. G. & Lisanti, M. P. Caveolin-1 potentiates estrogen receptor α (ERα) signaling. J. Biol. Chem. 274, 33551–33556 (1999).

    CAS  PubMed  Google Scholar 

  53. Razandi, M., Oh, P., Pedram, A., Schnitzer, J. & Levin, E. R. ERs associate with and regulate the production of caveolin: implications for signaling and cellular actions. Mol. Endocrinol. 16, 100–115 (2002).

    CAS  PubMed  Google Scholar 

  54. Acconcia, F. et al. Palmitoylation-dependent estrogen receptor α membrane localization: regulation by 17β-estradiol. Mol. Biol. Cell 16, 231–237 (2004).

    PubMed  Google Scholar 

  55. Boulware, M. I., Kordasiewicz, H. & Mermelstein, P. G. Caveolin proteins are essential for distinct effects of membrane estrogen receptors in neurons. J. Neurosci. 27, 9941–9950 (2007).

    CAS  PubMed  PubMed Central  Google Scholar 

  56. Boulware, M. I. et al. Estradiol activates group I and II metabotropic glutamate receptor signaling, leading to opposing influences on cAMP response element-binding protein. J. Neurosci. 25, 5066–5078 (2005).

    CAS  PubMed  PubMed Central  Google Scholar 

  57. Boulware, M. I., Heisler, J. D. & Frick, K. M. The memory-enhancing effects of hippocampal estrogen receptor activation involve metabotropic glutamate receptor signaling. J. Neurosci. 33, 15184–15194 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  58. Martinez, L. A. et al. Estradiol facilitation of cocaine self-administration in female rats requires activation of mGluR5. eNeuro https://doi.org/10.1523/ENEURO.0140-16.2016 (2016).

    Article  PubMed  PubMed Central  Google Scholar 

  59. Dewing, P. et al. Membrane estrogen receptor-α interactions with metabotropic glutamate receptor 1a modulate female sexual receptivity in rats. J. Neurosci. 27, 9294–9300 (2007).

    CAS  PubMed  PubMed Central  Google Scholar 

  60. Kahlert, S. et al. Estrogen receptor α rapidly activates the IGF-1 receptor pathway. J. Biol. Chem. 275, 18447–18453 (2000).

    CAS  PubMed  Google Scholar 

  61. Mendez, P., Azcoitia, I. & Garcia-Segura, L. M. Estrogen receptor alpha forms estrogen-dependent multimolecular complexes with insulin-like growth factor receptor and phosphatidylinositol 3-kinase in the adult rat brain. Mol. Brain. Res. 112, 170–176 (2003).

    CAS  PubMed  Google Scholar 

  62. Spencer-Segal, J. L. et al. Estradiol acts via estrogen receptors alpha and beta on pathways important for synaptic plasticity in the mouse hippocampal formation. Neuroscience 202, 131–146 (2012).

    CAS  PubMed  Google Scholar 

  63. Kramár, E. A., Babayan, A. H., Gall, C. M. & Lynch, G. Estrogen promotes learning-related plasticity by modifying the synaptic cytoskeleton. Neuroscience 239, 3–16 (2013).

    PubMed  Google Scholar 

  64. Quesada, A. & Micevych, P. E. Estrogen interacts with the IGF-1 system to protect nigrostriatal dopamine and maintain motoric behavior after 6-hydroxdopamine lesions. J. Neurosci. Res. 75, 107–116 (2004).

    CAS  PubMed  Google Scholar 

  65. Selvamani, A. & Sohrabji, F. The neurotoxic effects of estrogen on ischemic stroke in older female rats is associated with age-dependent loss of insulin-like growth factor-1. J. Neurosci. 30, 6852–6861 (2010).

    CAS  PubMed  PubMed Central  Google Scholar 

  66. Witty, C. F., Gardella, L. P., Perez, M. C. & Daniel, J. M. Short-term estradiol administration in aging ovariectomized rats provides lasting benefits for memory and the hippocampus: a role for insulin-like growth factor-I. Endocrinology 154, 842–852 (2013).

    CAS  PubMed  Google Scholar 

  67. Cabodi, S. et al. p130Cas interacts with estrogen receptor α and modulates non-genomic estrogen signaling in breast cancer cells. J. Cell Sci. 117, 1603–1611 (2004).

    CAS  PubMed  Google Scholar 

  68. Lu, Q. et al. Striatin assembles a membrane signaling complex necessary for rapid, nongenomic activation of endothelial NO synthase by estrogen receptor α. Proc. Natl Acad. Sci. USA 101, 17126–17131 (2004).

    CAS  PubMed  Google Scholar 

  69. Filardo, E. J., Quinn, J. A., Bland, K. I. & Frackelton, A. R. Estrogen-induced activation of Erk-1 and Erk-2 requires the G protein-coupled receptor homolog, GPR30, and occurs via trans-activation of the epidermal growth factor receptor through release of HB-EGF. Mol. Endocrinol. 14, 1649–1660 (2000).

    CAS  PubMed  Google Scholar 

  70. Thomas, P., Pang, Y., Filardo, E. J. & Dong, J. Identity of an estrogen membrane receptor coupled to a G protein in human breast cancer cells. Endocrinology 146, 624–632 (2005). This study describes GPER as a membrane-tethered receptor that binds oestrogens, thereby establishing the existence of a novel, non-nuclear ER.

    CAS  PubMed  Google Scholar 

  71. Filardo, E. J., Quinn, J. A., Frackelton, A. R. & Bland, K. I. Estrogen action via the G protein-coupled receptor, GPR30: stimulation of adenylyl cyclase and cAMP-mediated attenuation of the epidermal growth factor receptor-to-MAPK signaling axis. Mol. Endocrinol. 16, 70–84 (2002).

    CAS  PubMed  Google Scholar 

  72. Revankar, C. M., Cimino, D. F., Sklar, L. A., Arterburn, J. B. & Prossnitz, E. R. A transmembrane intracellular estrogen receptor mediates rapid cell signaling. Science 307, 1625–1630 (2005).

    CAS  PubMed  Google Scholar 

  73. Hazell, G. G. J. et al. Localisation of GPR30, a novel G protein-coupled oestrogen receptor, suggests multiple functions in rodent brain and peripheral tissues. J. Endocrinol. 202, 223–236 (2009).

    CAS  PubMed  PubMed Central  Google Scholar 

  74. Brailoiu, E. et al. Distribution and characterization of estrogen receptor G protein-coupled receptor 30 in the rat central nervous system. J. Endocrinol. 193, 311–321 (2019).

    Google Scholar 

  75. Hammond, R., Nelson, D., Kline, E. & Gibbs, R. B. Chronic treatment with a GPR30 antagonist impairs acquisition of a spatial learning task in young female rats. Horm. Behav. 62, 367–374 (2012).

    CAS  PubMed  PubMed Central  Google Scholar 

  76. Hawley, W. R., Grissom, E. M., Moody, N. M., Dohanich, G. P. & Vasudevan, N. Activation of G-protein-coupled receptor 30 is sufficient to enhance spatial recognition memory in ovariectomized rats. Behav. Brain Res. 262, 68–73 (2014).

    CAS  PubMed  Google Scholar 

  77. Gabor, C., Lymer, J., Phan, A. & Choleris, E. Rapid effects of the G-protein coupled oestrogen receptor (GPER) on learning and dorsal hippocampus dendritic spines in female mice. Physiol. Behav. 149, 53–60 (2015).

    CAS  PubMed  Google Scholar 

  78. Kim, J., Szinte, J. S., Boulware, M. I. & Frick, K. M. 17β-Estradiol and agonism of G-protein-coupled estrogen receptor enhance hippocampal memory via different cell-signaling mechanisms. J. Neurosci. 36, 3309–3321 (2016).

    CAS  PubMed  PubMed Central  Google Scholar 

  79. Ervin, K. S. J., Mulvale, E., Gallagher, N., Roussel, V. & Choleris, E. Activation of the G protein-coupled estrogen receptor, but not estrogen receptor α or β, rapidly enhances social learning. Psychoneuroendocrinology 58, 51–66 (2015).

    CAS  PubMed  Google Scholar 

  80. Anchan, D., Gafur, A., Sano, K., Ogawa, S. & Vasudevan, N. Activation of the GPR30 receptor promotes lordosis in female mice. Neuroendocrinology 100, 71–80 (2014).

    CAS  PubMed  Google Scholar 

  81. Long, N., Serey, C. & Sinchak, K. 17β-estradiol rapidly facilitates lordosis through G protein-coupled estrogen receptor 1 (GPER) via deactivation of medial preoptic nucleus μ-opioid receptors in estradiol primed female rats. Horm. Behav. 66, 663–666 (2014).

    CAS  PubMed  PubMed Central  Google Scholar 

  82. Briz, V. & Baudry, M. Estrogen regulates protein synthesis and actin polymerization in hippocampal neurons through different molecular mechanisms. Neuroendocr. Sci. 5, 22 (2014).

    Google Scholar 

  83. Zhao, L., Chen, S., Ming Wang, J. & Brinton, R. D. 17β-Estradiol induces Ca2+ influx, dendritic and nuclear Ca2+ rise and subsequent cyclic AMP response element-binding protein activation in hippocampal neurons: a potential initiation mechanism for estrogen neurotrophism. Neuroscience 132, 299–311 (2005).

    CAS  PubMed  Google Scholar 

  84. Wu, T.-W., Chen, S. & Brinton, R. D. Membrane estrogen receptors mediate calcium signaling and MAP kinase activation in individual hippocampal neurons. Brain Res. 1379, 34–43 (2011).

    CAS  PubMed  PubMed Central  Google Scholar 

  85. Moss, R. L. & Gu, Q. Estrogen: mechanisms for a rapid action in CA1 hippocampal neurons. Steroids 64, 14–21 (1999).

    CAS  PubMed  Google Scholar 

  86. Kuroki, Y., Fukushima, K., Kanda, Y., Mizuno, K. & Watanabe, Y. Putative membrane-bound estrogen receptors possibly stimulate mitogen-activated protein kinase in the rat hippocampus. Eur. J. Pharmacol. 400, 205–209 (2000).

    CAS  PubMed  Google Scholar 

  87. Fernandez, S. M. et al. Oestradiol-induced enhancement of object memory consolidation involves hippocampal extracellular signal-regulated kinase activation and membrane-bound oestrogen receptors. J. Neurosci. 28, 8660–8667 (2008). This study reveals a crucial role for rapidly activated cell signalling activity in the memory-enhancing effects of E2.

  88. Lee, S. J. et al. Estrogen induces phosphorylation of cyclic AMP response element binding (pCREB) in primary hippocampal cells in a time-dependent manner. Neuroscience 124, 549–560 (2004).

    CAS  PubMed  Google Scholar 

  89. Yokomaku, D. et al. Estrogen enhances depolarization-induced glutamate release through activation of phosphatidylinositol 3-kinase and mitogen-activated protein kinase in cultured hippocampal neurons. Mol. Endocrinol. 17, 831–844 (2003).

    CAS  PubMed  Google Scholar 

  90. Spencer, J. L., Waters, E. M., Milner, T. A. & McEwen, B. S. Estrous cycle regulates activation of hippocampal Akt, LIMK, and neurotrophin receptors in C57BL6 mice. Neuroscience 155, 1106–1119 (2008).

    CAS  PubMed  PubMed Central  Google Scholar 

  91. Fan, L. et al. Estradiol-induced object memory consolidation in middle-aged female mice requires dorsal hippocampal extracellular signal-regulated kinase and phosphatidylinositol 3-kinase activation. J. Neurosci. 30, 4390–4400 (2010).

    CAS  PubMed  PubMed Central  Google Scholar 

  92. Ruiz-Palmero, I., Hernando, M., Garcia-Segura, L. M. & Arevalo, M.-A. G protein-coupled estrogen receptor is required for the neuritogenic mechanism of 17β-estradiol in developing hippocampal neurons. Mol. Cell. Endocrinol. 372, 105–115 (2013).

    CAS  PubMed  Google Scholar 

  93. Lewis, M. C., Kerr, K. M., Orr, P. T. & Frick, K. M. Estradiol-induced enhancement of object memory consolidation involves NMDA receptors and protein kinase A in the dorsal hippocampus of female C57BL/6 mice. Behav. Neurosci. 122, 716–721 (2008).

    CAS  PubMed  PubMed Central  Google Scholar 

  94. Sato, K., Akaishi, T., Matsuki, N., Ohno, Y. & Nakazawa, K. β-Estradiol induces synaptogenesis in the hippocampus by enhancing brain-derived neurotrophic factor release from dentate gyrus granule cells. Brain Res. 1150, 108–120 (2007).

    CAS  PubMed  Google Scholar 

  95. Gu, Q., Korach, K. S. & Moss, R. L. Rapid action of 17β-estradiol on kainate-induced currents in hippocampal neurons lacking intracellular estrogen receptors. Endocrinology 140, 660–666 (1999).

    CAS  PubMed  Google Scholar 

  96. Hasegawa, Y. et al. Estradiol rapidly modulates synaptic plasticity of hippocampal neurons: Involvement of kinase networks. Brain Res. 1621, 147–161 (2015).

    CAS  PubMed  Google Scholar 

  97. Fortress, A. M., Fan, L., Orr, P. T., Zhao, Z. & Frick, K. M. Estradiol-induced object recognition memory consolidation is dependent on activation of mTOR signaling in the dorsal hippocampus. Learn. Mem. 20, 147–155 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  98. Sarkar, S. N., Smith, L. T., Logan, S. M. & Simpkins, J. W. Estrogen-induced activation of extracellular signal-regulated kinase signaling triggers dendritic resident mRNA translation. Neuroscience 170, 1080–1085 (2010).

    CAS  PubMed  PubMed Central  Google Scholar 

  99. Tuscher, J. J., Luine, V., Frankfurt, M. & Frick, K. M. Estradiol-mediated spine changes in the dorsal hippocampus and medial prefrontal cortex of ovariectomized female mice depend on ERK and mTOR activation in the dorsal hippocampus. J. Neurosci. 36, 1483–1489 (2016).

    CAS  PubMed  PubMed Central  Google Scholar 

  100. Yuen, G. S., McEwen, B. S. & Akama, K. T. LIM kinase mediates estrogen action on the actin depolymerization factor cofilin. Brain Res. 1379, 44–52 (2011).

    CAS  PubMed  Google Scholar 

  101. Zhao, Y. et al. Estrogen receptor alpha and beta regulate actin polymerization and spatial memory through an SRC-1/mTORC2-dependent pathway in the hippocampus of female mice. J. Steroid Biochem. Mol. Biol. 174, 96–113 (2017).

    CAS  PubMed  Google Scholar 

  102. Yildirim, M. et al. Estrogen and aging affect synaptic distribution of phosphorylated LIM Kinase (LIMK) in CA1 region of female rat hippocampus. Neuroscience 152, 360–370 (2008).

    CAS  PubMed  PubMed Central  Google Scholar 

  103. Kim, J. et al. Dorsal hippocampal actin polymerization is necessary for activation of G-protein-coupled estrogen receptor (GPER) to increase CA1 dendritic spine density and enhance memory consolidation. J. Neurosci. 39, 9598–9610 (2019).

    PubMed  PubMed Central  Google Scholar 

  104. Zhou, Y., Watters, J. J. & Dorsa, D. M. Estrogen rapidly induces the phosphorylation of the cAMP response element binding protein in rat brain. Endocrinology 137, 2163–2166 (1996).

    CAS  PubMed  Google Scholar 

  105. Zhao, Z., Fan, L., Fortress, A. M., Boulware, M. I. & Frick, K. M. Hippocampal histone acetylation regulates object recognition and the estradiol-induced enhancement of object recognition. J. Neurosci. 32, 2344–2351 (2012).

    CAS  PubMed  PubMed Central  Google Scholar 

  106. Fortress, A. M., Kim, J., Poole, R. L., Gould, T. J. & Frick, K. M. 17β-Estradiol regulates histone alterations associated with memory consolidation and increases Bdnf promoter acetylation in middle-aged female mice. Learn. Mem. 21, 457–467 (2014).

    CAS  PubMed  PubMed Central  Google Scholar 

  107. Carrer, H. F., Araque, A. & Buño, W. Estradiol regulates the slow Ca2+-activated K+ current in hippocampal pyramidal neurons. J. Neurosci. 23, 6338–6344 (2003).

    CAS  PubMed  PubMed Central  Google Scholar 

  108. Kumar, A. & Foster, T. C. 17β-estradiol benzoate decreases the AHP amplitude in CA1 pyramidal neurons. J. Neurophysiol. 88, 621–626 (2002).

    CAS  PubMed  Google Scholar 

  109. Foy, M. R. et al. 17β-estradiol enhances NMDA receptor-mediated EPSPs and long-term potentiation. J. Neurophysiol. 81, 925–929 (1999).

    CAS  PubMed  Google Scholar 

  110. Pozzo-Miller, L. D., Inoue, T. & Murphy, D. D. Estradiol increases spine density and NMDA-dependent Ca2+ transients in spines of CA1 pyramidal neurons from hippocampal slices. J. Neurophysiol. 81, 1404–1411 (1999).

    CAS  PubMed  Google Scholar 

  111. Oberlander, J. G. & Woolley, C. S. 17β-estradiol acutely potentiates glutamatergic synaptic transmission in the hippocampus through distinct mechanisms in males and females. J. Neurosci. 37, 12314–12327 (2017). This article provides a detailed example of how E2 can work through sex-specific molecular mechanisms to produce the same functional outcomes in both males and females.

    CAS  PubMed Central  Google Scholar 

  112. Bi, R., Broutman, G., Foy, M. R., Thompson, R. F. & Baudry, M. The tyrosine kinase and mitogen-activated protein kinase pathways mediate multiple effects of estrogen in hippocampus. Proc. Natl Acad. Sci. USA 97, 3602–3607 (2000).

    CAS  PubMed  Google Scholar 

  113. Smith, C. C. & McMahon, L. L. Estrogen-induced increase in the magnitude of long-term potentiation occurs only when the ratio of NMDA transmission to AMPA transmission is increased. J. Neurosci. 25, 7780–7791 (2005).

    CAS  PubMed  PubMed Central  Google Scholar 

  114. Liu, F. et al. Activation of estrogen receptor-β regulates hippocampal synaptic plasticity and improves memory. Nat. Neurosci. 11, 334–343 (2008).

    CAS  PubMed  Google Scholar 

  115. Xu, X. et al. Bisphenol-A rapidly promotes dynamic changes in hippocampal dendritic morphology through estrogen receptor-mediated pathway by concomitant phosphorylation of NMDA receptor subunit NR2B. Toxicol. Appl. Pharmacol. 249, 188–196 (2010).

    CAS  PubMed  Google Scholar 

  116. Avila, J. A. et al. Estradiol rapidly increases GluA2-mushroom spines and decreases GluA2-filopodia spines in hippocampus CA1. Hippocampus 27, 1224–1229 (2017).

    CAS  PubMed  PubMed Central  Google Scholar 

  117. Waters, E. M. et al. Effects of estrogen and aging on synaptic morphology and distribution of phosphorylated Tyr1472 NR2B in the female rat hippocampus. Neurobiol. Aging 73, 200–210 (2019).

    CAS  PubMed  Google Scholar 

  118. Potier, M. et al. Temporal memory and its enhancement by estradiol requires surface dynamics of hippocampal CA1 N-methyl-D-aspartate receptors. Biol. Psychiatry 79, 735–745 (2016).

    CAS  PubMed  Google Scholar 

  119. Phan, A. et al. Rapid increases in immature synapses parallel estrogen-induced hippocampal learning enhancements. Proc. Natl Acad. Sci. USA 112, 16018–16023 (2015). This comprehensive study links rapid oestrogen-induced hippocampal spine formation with modulation of glutamatergic synapses and enhancement of spatial and recognition memory.

    CAS  PubMed  Google Scholar 

  120. Vedder, L. C., Smith, C. C., Flannigan, A. E. & McMahon, L. L. Estradiol-induced increase in novel object recognition requires hippocampal NR2B-containing NMDA receptors. Hippocampus 23, 108–115 (2013).

    CAS  PubMed  Google Scholar 

  121. Smith, C. C. & McMahon, L. L. Estradiol-induced increase in the magnitude of long-term potentiation is prevented by blocking NR2B-containing receptors. J. Neurosci. 26, 8517–8522 (2006).

    CAS  PubMed  PubMed Central  Google Scholar 

  122. Huang, G. Z. & Woolley, C. S. Estradiol acutely suppresses inhibition in the hippocampus through a sex-specific endocannabinoid and mGluR-dependent mechanism. Neuron 74, 801–808 (2012).

    CAS  PubMed  PubMed Central  Google Scholar 

  123. Tabatadze, N., Huang, G., May, R. M., Jain, A. & Woolley, C. S. Sex differences in molecular signaling at inhibitory synapses in the hippocampus. J. Neurosci. 35, 11252–11265 (2015).

    CAS  PubMed  PubMed Central  Google Scholar 

  124. Fugger, H. N., Foster, T. C., Gustafsson, J. & Rissman, E. F. Novel effects of estradiol and estrogen receptor alpha and beta on cognitive function. Brain Res. 883, 258–264 (2000).

    CAS  PubMed  Google Scholar 

  125. Walf, A. A., Koonce, C. J. & Frye, C. A. Estradiol or diarylpropionitrile administration to wild type, but not estrogen receptor beta knockout, mice enhances performance in the object recognition and object placement tasks. Neurobiol. Learn. Mem. 89, 513–521 (2008).

    CAS  PubMed  PubMed Central  Google Scholar 

  126. Rissman, E. F., Heck, A. L., Leonard, J. E., Shupnik, M. A. & Gustafsson, J.-A. Disruption of estrogen receptor beta gene impairs spatial learning in female mice. Proc. Natl Acad. Sci. USA 99, 3996–4001 (2002).

    CAS  PubMed  Google Scholar 

  127. Witty, C. F., Foster, T. C., Semple-Rowland, S. L. & Daniel, J. M. Increasing hippocampal estrogen receptor alpha levels via viral vectors increases MAP kinase activation and enhances memory in aging rats in the absence of ovarian estrogens. PLoS ONE 7, e51385 (2012).

    CAS  PubMed  PubMed Central  Google Scholar 

  128. Hanson, A. M. et al. A-C estrogens as potent and selective estrogen receptor-beta agonists (SERBAs) to enhance memory consolidation under low-estrogen conditions. J. Med. Chem. 61, 4720–4738 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  129. Frick, K. M. Estrogens and age-related memory decline in rodents: what have we learned and where do we go from here? Horm. Behav. 55, 2–23 (2009).

    CAS  PubMed  Google Scholar 

  130. Boulware, M. I., Kent, B. A. & Frick, K. M. The impact of age-related ovarian hormone loss on cognitive and neural function. Curr. Top. Behav. Neurosci. 10, 165–184 (2012).

    PubMed  Google Scholar 

  131. Mehra, R. D., Sharma, K., Nyakas, C. & Vij, U. Estrogen receptor α and β immunoreactive neurons in normal adult and aged female rat hippocampus: a qualitative and quantitative study. Brain Res. 1056, 22–35 (2005).

    CAS  PubMed  Google Scholar 

  132. Zhang, Q.-G. et al. Estrogen attenuates ischemic oxidative damage via an estrogen receptor α-mediated inhibition of NADPH oxidase activation. J. Neurosci. 29, 13823–13836 (2009).

    CAS  PubMed  PubMed Central  Google Scholar 

  133. Daniel, J. M. Estrogens, estrogen receptors, and female cognitive aging: the impact of timing. Horm. Behav. 63, 231–237 (2013).

    CAS  PubMed  Google Scholar 

  134. Luine, V. & Frankfurt, M. Estrogenic regulation of memory: the first 50 years. Horm. Behav. 121, 104711 (2020).

    CAS  PubMed  Google Scholar 

  135. Foster, T. C. Role of estrogen receptor alpha and beta expression and signaling on cognitive function during aging. Hippocampus 22, 656–669 (2012).

    CAS  PubMed  Google Scholar 

  136. Warren, S. G. & Juraska, J. M. Spatial and nonspatial learning across the rat estrous cycle. Behav. Neurosci. 111, 259–266 (1997).

    CAS  PubMed  Google Scholar 

  137. Daniel, J. M., Roberts, S. L. & Dohanich, G. P. Effects of ovarian hormones and environment on radial maze and water maze performance of female rats. Physiol. Behav. 66, 11–20 (1999).

    CAS  PubMed  Google Scholar 

  138. Chesler, E. J. & Juraska, J. M. Acute administration of estrogen and progesterone impairs the acquisition of the spatial Morris water maze in ovariectomized rats. Horm. Behav. 38, 234–242 (2000).

    CAS  PubMed  Google Scholar 

  139. Frick, K. M. & Berger-Sweeney, J. Spatial reference memory and neocortical neurochemistry vary with the estrous cycle in C57BL/6 mice. Behav. Neurosci. 115, 229–237 (2001).

    CAS  PubMed  Google Scholar 

  140. Sandstrom, N. J. & Williams, C. L. Memory retention is modulated by acute estradiol and progesterone replacement. Behav. Neurosci. 115, 384–393 (2001).

    CAS  PubMed  Google Scholar 

  141. Galea, L. A., Kavaliers, M., Ossenkopp, K. P. & Hampson, E. Gonadal hormone levels and spatial learning performance in the Morris water maze in male and female meadow voles, Microtus pennsylvanicus. Horm. Behav. 29, 106–125 (1995).

    CAS  PubMed  Google Scholar 

  142. Packard, M. G. & Teather, L. A. Intra-hippocampal estradiol infusion enhances memory in ovariectomized rats. Neuroreport 8, 3009–3013 (1997). This pioneering study demonstrates that intrahippocampally administered E2 rapidly enhances spatial memory consolidation within just 2 h after training.

    CAS  PubMed  Google Scholar 

  143. Daniel, J. M., Fader, A. J., Spencer, A. L. & Dohanich, G. P. Estrogen enhances performance of female rats during acquisition of a radial arm maze. Horm. Behav. 32, 217–225 (1997).

    CAS  PubMed  Google Scholar 

  144. Bimonte, H. A. & Denenberg, V. H. Estradiol facilitates performance as working memory load increases. Psychoneuroendocrinology 24, 161–173 (1999).

    CAS  PubMed  Google Scholar 

  145. Luine, V. N., Richards, S. T., Wu, V. Y. & Beck, K. D. Estradiol enhances learning and memory in a spatial memory task and effects levels of monoaminergic neurotransmitters. Horm. Behav. 34, 149–162 (1998).

    CAS  PubMed  Google Scholar 

  146. Gibbs, R. B. & Johnson, D. A. Sex-specific effects of gonadectomy and hormone treatment on acquisition of a 12-arm radial maze task by Sprague Dawley rats. Endocrinology 149, 3176–3183 (2008).

    CAS  PubMed  PubMed Central  Google Scholar 

  147. Nelson, B. S., Springer, R. C. & Daniel, J. M. Antagonism of brain insulin-like growth factor-1 receptors blocks estradiol effects on memory and levels of hippocampal synaptic proteins in ovariectomized rats. Psychopharmacology 231, 899–907 (2014).

    CAS  PubMed  Google Scholar 

  148. Sinopoli, K. J., Floresco, S. B. & Galea, L. A. M. Systemic and local administration of estradiol into the prefrontal cortex or hippocampus differentially alters working memory. Neurobiol. Learn. Mem. 86, 293–304 (2006).

    CAS  PubMed  Google Scholar 

  149. Wallace, M., Luine, V., Arellanos, A. & Frankfurt, M. Ovariectomized rats show decreased recognition memory and spine density in the hippocampus and prefrontal cortex. Brain Res. 1126, 176–182 (2006).

    CAS  PubMed  Google Scholar 

  150. Fonseca, C. S. et al. Object recognition memory and temporal lobe activation after delayed estrogen replacement therapy. Neurobiol. Learn. Mem. 101, 19–25 (2013).

    CAS  PubMed  Google Scholar 

  151. Inagaki, T., Gautreaux, C. & Luine, V. Acute estrogen treatment facilitates recognition memory consolidation and alters monoamine levels in memory-related brain areas. Horm. Behav. 58, 415–426 (2010).

    CAS  PubMed  PubMed Central  Google Scholar 

  152. Luine, V. N., Jacome, L. F. & MacLusky, N. J. Rapid enhancement of visual and place memory by estrogens in rats. Endocrinology 144, 2836–2844 (2003).

    CAS  PubMed  Google Scholar 

  153. Gresack, J. E. & Frick, K. M. Post-training estrogen enhances spatial and object memory consolidation in female mice. Pharmacol. Biochem. Behav. 84, 112–119 (2006).

    CAS  PubMed  Google Scholar 

  154. Pereira, L. M., Bastos, C. P., de Souza, J. M., Ribeiro, F. M. & Pereira, G. S. Estradiol enhances object recognition memory in Swiss female mice by activating hippocampal estrogen receptor α. Neurobiol. Learn. Mem. 114, 1–9 (2014).

    CAS  PubMed  Google Scholar 

  155. Tuscher, J. J., Taxier, L. R., Schalk, J. C., Haertel, J. M. & Frick, K. M. Chemogenetic suppression of medial prefrontal-dorsal hippocampal interactions prevents estrogenic enhancement of memory consolidation in female mice. eNeuro https://doi.org/10.1523/ENEURO.0451-18.2019 (2019). This study leverages novel chemogenetic tools to demonstrate that activity of multiple brain regions in concert is required for oestrogenic enhancement of memory consolidation.

    Article  PubMed  PubMed Central  Google Scholar 

  156. Gervais, N. J., Jacob, S., Brake, W. G. & Mumby, D. G. Systemic and intra-rhinal-cortical 17-β estradiol administration modulate object-recognition memory in ovariectomized female rats. Horm. Behav. 64, 642–652 (2013).

    CAS  PubMed  Google Scholar 

  157. Gervais, N. J., Hamel, L. M., Brake, W. G. & Mumby, D. G. Intra-perirhinal cortex administration of estradiol, but not an ERβ agonist, modulates object-recognition memory in ovariectomized rats. Neurobiol. Learn. Mem. 133, 89–99 (2016).

    CAS  PubMed  Google Scholar 

  158. Taxier, L. R., Philippi, S. M., Fortress, A. M. & Frick, K. M. Dickkopf-1 blocks 17β-estradiol-enhanced object memory consolidation in ovariectomized female mice. Horm. Behav. 114, 104545 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  159. Luine, V. & Frankfurt, M. Interactions between estradiol, BDNF and dendritic spines in promoting memory. Neuroscience 239, 34–45 (2013).

    CAS  PubMed  Google Scholar 

  160. Warren, S. G., Humphreys, A. G., Juraska, J. M. & Greenough, W. T. LTP varies across the estrous cycle: enhanced synaptic plasticity in proestrus rats. Brain Res. 703, 26–30 (1995).

    CAS  PubMed  Google Scholar 

  161. Good, M., Day, M. & Muir, J. L. Cyclical changes in endogenous levels of oestrogen modulate the induction of LTD and LTP in the hippocampal CA1 region. Eur. J. Neurosci. 11, 4476–4480 (1999).

    CAS  PubMed  Google Scholar 

  162. Vedder, L. C., Bredemann, T. M. & McMahon, L. L. Estradiol replacement extends the window of opportunity for hippocampal function. Neurobiol. Aging 35, 2183–2192 (2014).

    CAS  PubMed  PubMed Central  Google Scholar 

  163. Ferguson, J. N., Young, L. J. & Insel, T. R. The neuroendocrine basis of social recognition. Front. Neuroendocrinol. 23, 200–224 (2002).

    CAS  PubMed  Google Scholar 

  164. Gabor, C. S., Phan, A., Clipperton-Allen, A. E., Kavaliers, M. & Choleris, E. Interplay of oxytocin, vasopressin, and sex hormones in the regulation of social recognition. Behav. Neurosci. 126, 97–109 (2012).

    CAS  PubMed  Google Scholar 

  165. Sánchez-Andrade, G. & Kendrick, K. M. Roles of α- and β-estrogen receptors in mouse social recognition memory: effects of gender and the estrous cycle. Horm. Behav. 59, 114–122 (2011).

    PubMed  Google Scholar 

  166. Hlinˇáck, Z. Social recognition in ovariectomized and estradiol-treated female rats. Horm. Behav. 27, 159–166 (1993).

    Google Scholar 

  167. Tang, A. C. et al. Effects of long-term estrogen replacement on social investigation and social memory in ovariectomized C57BL/6 mice. Horm. Behav. 47, 350–357 (2005).

    CAS  PubMed  Google Scholar 

  168. Spiteri, T. & Ågmo, A. Ovarian hormones modulate social recognition in female rats. Physiol. Behav. 98, 247–250 (2009).

    CAS  PubMed  Google Scholar 

  169. Choleris, E. et al. An estrogen-dependent four-gene micronet regulating social recognition: a study with oxytocin and estrogen receptor-α and -β knockout mice. Proc. Natl Acad. Sci. USA 100, 6192–6197 (2003).

    CAS  PubMed  Google Scholar 

  170. Ferguson, J. N., Aldag, J. M., Insel, T. R. & Young, L. J. Oxytocin in the medial amygdala is essential for social recognition in the mouse. J. Neurosci. 21, 8278–8285 (2001).

    CAS  PubMed  PubMed Central  Google Scholar 

  171. Choleris, E. et al. Involvement of estrogen receptor α, β and oxytocin in social discrimination: a detailed behavioral analysis with knockout female mice. Genes Brain Behav. 5, 528–539 (2006).

    CAS  PubMed  Google Scholar 

  172. Spiteri, T. et al. The role of the estrogen receptor α in the medial amygdala and ventromedial nucleus of the hypothalamus in social recognition, anxiety and aggression. Behav. Brain Res. 210, 211–220 (2010).

    CAS  PubMed  Google Scholar 

  173. Phan, A., Lancaster, K. E., Armstrong, J. N., MacLusky, N. J. & Choleris, E. Rapid effects of estrogen receptor α and β selective agonists on learning and dendritic spines in female mice. Endocrinology 152, 1492–1502 (2011).

    CAS  PubMed  Google Scholar 

  174. Lymer, J., Robinson, A., Winters, B. D. & Choleris, E. Rapid effects of dorsal hippocampal G-protein coupled estrogen receptor on learning in female mice. Psychoneuroendocrinology 77, 131–140 (2017).

    CAS  PubMed  Google Scholar 

  175. Lymer, J. M. et al. Estrogens and their receptors in the medial amygdala rapidly facilitate social recognition in female mice. Psychoneuroendocrinology 89, 30–38 (2018).

    CAS  PubMed  Google Scholar 

  176. Morgan, M. A. & Pfaff, D. W. Effects of estrogen on activity and fear-related behaviors in mice. Horm. Behav. 40, 472–482 (2001).

    CAS  PubMed  Google Scholar 

  177. Jasnow, A. M., Schulkin, J. & Pfaff, D. W. Estrogen facilitates fear conditioning and increases corticotropin-releasing hormone mRNA expression in the central amygdala in female mice. Horm. Behav. 49, 197–205 (2006).

    CAS  PubMed  Google Scholar 

  178. Hiroi, R. & Neumaier, J. F. Differential effects of ovarian steroids on anxiety versus fear as measured by open field test and fear-potentiated startle. Behav. Brain Res. 166, 93–100 (2006).

    CAS  PubMed  Google Scholar 

  179. Markus, E. J. & Zecevic, M. Sex differences and estrous cycle changes in hippocampus-dependent fear conditioning. Psychobiology 25, 246–252 (1997).

    Google Scholar 

  180. Gupta, R. R., Sen, S., Diepenhorst, L. L., Rudick, C. N. & Maren, S. Estrogen modulates sexually dimorphic contextual fear conditioning and hippocampal long-term potentiation (LTP) in rats. Brain Res. 888, 356–365 (2001).

    CAS  PubMed  Google Scholar 

  181. McDermott, C. M., Liu, D., Ade, C. & Schrader, L. A. Estradiol replacement enhances fear memory formation, impairs extinction and reduces COMT expression levels in the hippocampus of ovariectomized female mice. Neurobiol. Learn. Mem. 118, 167–177 (2015).

    CAS  PubMed  Google Scholar 

  182. Matsumoto, Y. K., Kasai, M. & Tomihara, K. The enhancement effect of estradiol on contextual fear conditioning in female mice. PLoS ONE 13, e0197441 (2018).

    PubMed  PubMed Central  Google Scholar 

  183. Barha, C. K., Dalton, G. L. & Galea, L. A. Low doses of 17α -estradiol and 17β-estradiol facilitate, whereas higher doses of estrone and 17α- and 17β-estradiol impair, contextual fear conditioning in adult female rats. Neuropsychopharmacology 35, 547–559 (2010).

    CAS  PubMed  Google Scholar 

  184. Rivas-Arancibia, S. & Vazquez-Pereyra, F. Hormonal modulation of extinction responses induced by sexual steroid hormones in rats. Life Sci. 54, PL363–PL367 (1994).

    CAS  PubMed  Google Scholar 

  185. Yuan, D. L. & Chambers, K. C. Estradiol accelerates extinction of a conditioned taste aversion in female and male rats. Horm. Behav. 36, 1–16 (1999).

    CAS  PubMed  Google Scholar 

  186. Chang, Y.-J. et al. Estrogen modulates sexually dimorphic contextual fear extinction in rats through estrogen receptor β. Hippocampus 19, 1142–1150 (2009).

    CAS  PubMed  Google Scholar 

  187. Milad, M. R., Igoe, S. A., Lebron-Milad, K. & Novales, J. E. Estrous cycle phase and gonadal hormones influence conditioned fear extinction. Neuroscience 164, 887–895 (2009). This article defines E2 as an important modulator of fear extinction learning.

    CAS  PubMed  PubMed Central  Google Scholar 

  188. Zeidan, M. A. et al. Estradiol modulates medial prefrontal cortex and amygdala activity during fear extinction in women and female rats. Biol. Psychiatry 70, 920–927 (2011).

    CAS  PubMed  PubMed Central  Google Scholar 

  189. Graham, B. M. & Milad, M. R. Blockade of estrogen by hormonal contraceptives impairs fear extinction in female rats and women. Biol. Psychiatry 73, 371–378 (2013).

    CAS  PubMed  Google Scholar 

  190. Graham, B. M. & Scott, E. Effects of systemic estradiol on fear extinction in female rats are dependent on interactions between dose, estrous phase, and endogenous estradiol levels. Horm. Behav. 97, 67–74 (2018).

    CAS  PubMed  Google Scholar 

  191. de Castilhos, J., Forti, C. D., Achaval, M. & Rasia-Filho, A. A. Dendritic spine density of posterodorsal medial amygdala neurons can be affected by gonadectomy and sex steroid manipulations in adult rats: a Golgi study. Brain Res. 1240, 73–81 (2008).

    PubMed  Google Scholar 

  192. Ferri, S. L., Hildebrand, P. F., Way, S. E. & Flanagan-Cato, L. M. Estradiol regulates markers of synaptic plasticity in the hypothalamic ventromedial nucleus and amygdala of female rats. Horm. Behav. 66, 409–420 (2014).

    CAS  PubMed  Google Scholar 

  193. Amano, T., Unal, C. T. & Paré, D. Synaptic correlates of fear extinction in the amygdala. Nat. Neurosci. 13, 489–494 (2010).

    CAS  PubMed  PubMed Central  Google Scholar 

  194. Shansky, R. M. et al. Estrogen promotes stress sensitivity in a prefrontal cortex–amygdala pathway. Cereb. Cortex 20, 2560–2567 (2010).

    PubMed  PubMed Central  Google Scholar 

  195. Maeng, L. Y. et al. Estradiol shifts interactions between the infralimbic cortex and central amygdala to enhance fear extinction memory in female rats. J. Neurosci. Res. 95, 163–175 (2017).

    CAS  PubMed  PubMed Central  Google Scholar 

  196. Rey, C. D., Lipps, J. & Shansky, R. M. Dopamine D1 receptor activation rescues extinction impairments in low-estrogen female rats and induces cortical layer-specific activation changes in prefrontal–amygdala circuits. Neuropsychopharmacology 39, 1282–1289 (2014).

    CAS  PubMed  PubMed Central  Google Scholar 

  197. Lynch, J., Cullen, P. K., Jasnow, A. M. & Riccio, D. C. Sex differences in the generalization of fear as a function of retention intervals. Learn. Mem. 20, 628–632 (2013).

    PubMed  Google Scholar 

  198. Lynch, J. F., Winiecki, P., Vanderhoof, T., Riccio, D. C. & Jasnow, A. M. Hippocampal cytosolic estrogen receptors regulate fear generalization in females. Neurobiol. Learn. Mem. 130, 83–92 (2016).

    CAS  PubMed  Google Scholar 

  199. Ooishi, Y. et al. Modulation of synaptic plasticity in the hippocampus by hippocampus-derived estrogen and androgen. J. Steroid Biochem. Mol. Biol. 131, 37–51 (2012).

    CAS  PubMed  Google Scholar 

  200. Hojo, Y. et al. Adult male rat hippocampus synthesizes estradiol from pregnenolone by cytochromes P45017α and P450 aromatase localized in neurons. Proc. Natl Acad. Sci. USA 101, 865–870 (2004).

    CAS  PubMed  Google Scholar 

  201. Wang, W. et al. Memory-related synaptic plasticity is sexually dimorphic in rodent hippocampus. J. Neurosci. 38, 7935–7951 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  202. Jain, A., Huang, G. Z. & Woolley, C. S. Latent sex differences in molecular signaling that underlies excitatory synaptic potentiation in the hippocampus. J. Neurosci. 39, 1552–1565 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  203. Fester, L. et al. Control of aromatase in hippocampal neurons. J. Steroid Biochem. Mol. Biol. 160, 9–14 (2016).

    CAS  PubMed  Google Scholar 

  204. Vierk, R. et al. Aromatase inhibition abolishes LTP generation in female but not in male mice. J. Neurosci. 32, 8116–8126 (2012).

    CAS  PubMed  PubMed Central  Google Scholar 

  205. Zhou, L. et al. Oestradiol-induced synapse formation in the female hippocampus: roles of oestrogen receptor subtypes. J. Neuroendocrinol. 26, 439–447 (2014).

    CAS  PubMed  Google Scholar 

  206. Lu, Y. et al. Neuron-derived estrogen regulates synaptic plasticity and memory. J. Neurosci. 39, 2792–2809 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  207. Brandt, N. & Rune, G. M. Sex-dependency of oestrogen-induced structural synaptic plasticity: inhibition of aromatase versus application of estradiol in rodents. Eur. J. Neurosci. https://doi.org/10.1111/ejn.14541 (2019).

    Article  PubMed  Google Scholar 

  208. Jacome, L. F. et al. Gonadal hormones rapidly enhance spatial memory and increase hippocampal spine density in male rats. Endocrinology 157, 1357–1362 (2016). This study shows that rapid E2 signalling produces parallel effects on hippocampal structure and function in males comparable to historical findings in females.

    CAS  PubMed  PubMed Central  Google Scholar 

  209. Koss, W. A., Haertel, J. M., Philippi, S. M. & Frick, K. M. Sex differences in the rapid cell signaling mechanisms underlying the memory-enhancing effects of 17β-estradiol. eNeuro https://doi.org/10.1523/ENEURO.0267-18.2018 (2018).

  210. Frye, C. A., Rhodes, M. E. & Dudek, B. Estradiol to aged female or male mice improves learning in inhibitory avoidance and water maze tasks. Brain Res. 1036, 101–108 (2005).

    CAS  PubMed  PubMed Central  Google Scholar 

  211. Packard, M. G. Posttraining estrogen and memory modulation. Horm. Behav. 34, 126–139 (1998).

    CAS  PubMed  Google Scholar 

  212. Heikkinen, T., Puoliväli, J., Liu, L., Rissanen, A. & Tanila, H. Effects of ovariectomy and estrogen treatment on learning and hippocampal neurotransmitters in mice. Horm. Behav. 41, 22–32 (2002).

    CAS  PubMed  Google Scholar 

  213. Pierman, S. et al. Activational effects of estradiol and dihydrotestosterone on social recognition and the arginine-vasopressin immunoreactive system in male mice lacking a functional aromatase gene. Horm. Behav. 54, 98–106 (2008).

    CAS  PubMed  PubMed Central  Google Scholar 

  214. Alejandre-Gomez, M., Garcia-Segura, L. M. & Gonzalez-Burgos, I. Administration of an inhibitor of estrogen biosynthesis facilitates working memory acquisition in male rats. Neurosci. Res. 58, 272–277 (2007).

    CAS  PubMed  Google Scholar 

  215. Koss, W. A. & Frick, K. M. Activation of androgen receptors protects intact male mice from memory impairments caused by aromatase inhibition. Horm. Behav. 111, 96–104 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  216. Koss, W. A. & Frick, K. M. Sex differences in hippocampal function. J. Neurosci. Res. 95, 539–562 (2017).

    CAS  PubMed  Google Scholar 

  217. Frick, K. M., Kim, J., Tuscher, J. J. & Fortress, A. M. Sex steroid hormones matter for learning and memory: estrogenic regulation of hippocampal function in male and female rodents. Learn. Mem. 22, 472–493 (2015).

    CAS  PubMed  PubMed Central  Google Scholar 

  218. Prendergast, B. J., Onishi, K. G. & Zucker, I. Female mice liberated for inclusion in neuroscience and biomedical research. Neurosci. Biobehav. Rev. 40, 1–5 (2014).

    PubMed  Google Scholar 

  219. Clayton, J. A. Studying both sexes: a guiding principle for biomedicine. FASEB J. 30, 519–524 (2016).

    CAS  PubMed  Google Scholar 

  220. Clayton, J. A. Applying the new SABV (sex as a biological variable) policy to research and clinical care. Physiol. Behav. 187, 2–5 (2018).

    CAS  PubMed  Google Scholar 

  221. Brooks, C. E. & Clayton, J. A. Sex/gender influences on the nervous system: basic steps toward clinical progress. J. Neurosci. Res. 95, 14–16 (2017).

    CAS  PubMed  PubMed Central  Google Scholar 

  222. Woitowich, N. C. & Woodruff, T. K. Implementation of the NIH sex-inclusion policy: Attitudes and opinions of study section members. J. Womens Health 28, 9–16 (2018).

    Google Scholar 

  223. Sandoval, A., Elahi, H. & Ploski, J. E. Genetically engineering the nervous system with CRISPR-Cas. eNeuro https://doi.org/10.1523/ENEURO.0419-19.2020 (2020).

  224. Mitchnick, K. A. et al. Dissociable involvement of estrogen receptors in perirhinal cortex-mediated object-place memory in male rats. Psychoneuroendocrinology 107, 98–108 (2019).

    CAS  PubMed  Google Scholar 

  225. Kim, J. & Frick, K. M. Distinct effects of estrogen receptor antagonism on object recognition and spatial memory consolidation in ovariectomized mice. Psychoneuroendocrinology 85, 110–114 (2017).

    CAS  PubMed  Google Scholar 

  226. Tuscher, J. J. et al. Inhibition of local estrogen synthesis in the hippocampus impairs hippocampal memory consolidation in ovariectomized female mice. Horm. Behav. 83, 60–67 (2016).

    CAS  PubMed  PubMed Central  Google Scholar 

  227. Bayer, J. et al. The effect of estrogen synthesis inhibition on hippocampal memory. Psychoneuroendocrinology 56, 213–225 (2015).

    CAS  PubMed  Google Scholar 

  228. Gervais, N. J. et al. Adverse effects of aromatase inhibition on the brain and behavior in a nonhuman primate. J. Neurosci. 39, 918–928 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  229. Morris, R. Developments of a water-maze procedure for studying spatial learning in the rat. J. Neurosci. Methods 11, 47–60 (1984).

    CAS  PubMed  Google Scholar 

  230. Vorhees, C. V. & Williams, M. T. Morris water maze: procedures for assessing spatial and related forms of learning and memory. Nat. Protoc. 1, 848–858 (2006).

    PubMed  PubMed Central  Google Scholar 

  231. Olton, D. S. The radial arm maze as a tool in behavioral pharmacology. Physiol. Behav. 40, 793–797 (1987).

    CAS  PubMed  Google Scholar 

  232. Olton, D. S. & Papas, B. C. Spatial memory and hippocampal function. Neuropsychologia 17, 669–682 (1979).

    CAS  PubMed  Google Scholar 

  233. Ennaceur, A. & Delacour, J. A new one-trial test for neurobiological studies of memory in rats. 1: behavioral data. Behav. Brain Res. 31, 47–59 (1988).

    CAS  PubMed  Google Scholar 

  234. Ennaceur, A. & Aggleton, J. P. Spontaneous recognition of object configurations in rats: effects of fornix lesions. Exp. Brain Res. 100, 85–92 (1994).

    CAS  PubMed  Google Scholar 

  235. Phillips, R. G. & LeDoux, J. E. Differential contribution of amygdala and hippocampus to cued and contextual fear conditioning. Behav. Neurosci. 106, 274–285 (1992).

    CAS  PubMed  Google Scholar 

  236. Frick, K. M., Fortress, A. M. in The Maze Book: Theories, Practice, and Protocols for Testing Rodent Cognition (ed Bimonte-Nelson, H.) 165–210 (Springer, 2015).

  237. Naftolin, F., Ryan, K. J. & Petro, Z. Aromatization of androstenedione by the anterior hypothalamus of adult male and female rats. Endocrinology 90, 295–298 (1972).

    CAS  PubMed  Google Scholar 

  238. Sato, S. M. & Woolley, C. S. Acute inhibition of neurosteroid estrogen synthesis suppresses status epilepticus in an animal model. eLife 5, e12917 (2016).

    PubMed  PubMed Central  Google Scholar 

  239. Prange-Kiel, J. et al. Inhibition of hippocampal estrogen synthesis causes region-specific downregulation of synaptic protein expression in hippocampal neurons. Hippocampus 16, 464–471 (2006).

    PubMed  Google Scholar 

  240. Zhou, L. et al. Aromatase inhibitors induce spine synapse loss in the hippocampus of ovariectomized mice. Endocrinology 151, 1153–1160 (2010).

    CAS  PubMed  Google Scholar 

  241. Bailey, D. J., Ma, C., Soma, K. K. & Saldanha, C. J. Inhibition of hippocampal aromatization impairs spatial memory performance in a male songbird. Endocrinology 154, 4707–4714 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  242. Blaustein, J. D. Treatments for breast cancer that affect cognitive function in postmenopausal women. Policy Insights Behav. Brain Sci. 4, 170–177 (2017).

    Google Scholar 

  243. Bimonte-Nelson, H. A., Acosta, J. I. & Talboom, J. S. Neuroscientists as cartographers: mapping the crossroads of gonadal hormones, memory and age using animal models. Molecules 15, 6050–6105 (2010).

    CAS  PubMed  PubMed Central  Google Scholar 

  244. Wise, P. M. Alterations in the proestrous pattern of median eminence LHRH, serum LH, FSH, estradiol and progesterone concentrations in middle-aged rats. Life Sci. 31, 165–173 (1982).

    CAS  PubMed  Google Scholar 

  245. Richardson, S. J. & Nelson, J. F. Follicular depletion during the menopausal transition. Ann. N. Y. Acad. Sci. 592, 13–20 (1990).

    CAS  PubMed  Google Scholar 

  246. Talboom, J. S., Williams, B. J., Baxley, E. R., West, S. G. & Bimonte-Nelson, H. A. Higher levels of estradiol replacement correlate with better spatial memory in surgically menopausal young and middle-aged rats. Neurobiol. Learn. Mem. 90, 155–163 (2008).

    CAS  PubMed  PubMed Central  Google Scholar 

  247. Markham, J. A., Pych, J. C. & Juraska, J. M. Ovarian hormone replacement to aged ovariectomized female rats benefits acquisition of the Morris water maze. Horm. Behav. 42, 284–293 (2002).

    CAS  PubMed  Google Scholar 

  248. Gresack, J. E., Kerr, K. M. & Frick, K. M. Life-long environmental enrichment differentially affects the mnemonic response to estrogen in young, middle-aged, and aged female mice. Neurobiol. Learn. Mem. 88, 393–408 (2007).

    PubMed  PubMed Central  Google Scholar 

  249. Singh, M., Meyer, E. M., Millard, W. J. & Simpkins, J. W. Ovarian steroid deprivation results in a reversible learning impairment and compromised cholinergic function in female Sprague-Dawley rats. Brain Res. 644, 305–312 (1994).

    CAS  PubMed  Google Scholar 

  250. Foster, T. C., Sharrow, K. M., Kumar, A. & Masse, J. Interaction of age and chronic estradiol replacement on memory and markers of brain aging. Neurobiol. Aging 24, 839–852 (2003).

    CAS  PubMed  Google Scholar 

  251. Frick, K. M., Fernandez, S. M. & Bulinski, S. C. Estrogen replacement improves spatial reference memory and increases hippocampal synaptophysin in aged female mice. Neuroscience 115, 547–558 (2002).

    CAS  PubMed  Google Scholar 

  252. Vaucher, E. et al. Estrogen effects on object memory and cholinergic receptors in young and old female mice. Neurobiol. Aging 23, 87–95 (2002).

    CAS  PubMed  Google Scholar 

  253. Prakapenka, A. V. et al. Contrasting effects of individual versus combined estrogen and progestogen regimens as working memory load increases in middle-aged ovariectomized rats: one plus one does not equal two. Neurobiol. Aging 64, 1–14 (2018).

    CAS  PubMed  Google Scholar 

  254. Gresack, J. E. & Frick, K. M. Effects of continuous and intermittent estrogen treatments on memory in aging female mice. Brain Res. 1115, 135–147 (2006).

    CAS  PubMed  Google Scholar 

  255. Markowska, A. L. & Savonenko, A. V. Effectiveness of estrogen replacement in restoration of cognitive function after long-term estrogen withdrawal in aging rats. J. Neurosci. 22, 10985–10995 (2002).

    CAS  PubMed  PubMed Central  Google Scholar 

  256. Daniel, J. M., Hulst, J. L. & Berbling, J. L. Estradiol replacement enhances working memory in middle-aged rats when initiated immediately after ovariectomy but not after a long-term period of ovarian hormone deprivation. Endocrinology 147, 607–614 (2006).

    CAS  PubMed  Google Scholar 

  257. Gresack, J. E., Kerr, K. M. & Frick, K. M. Short-term environmental enrichment decreases the mnemonic response to estrogen in young, but not aged, female mice. Brain Res. 1160, 91–101 (2007).

    CAS  PubMed  Google Scholar 

  258. Aenlle, K. K. & Foster, T. C. Aging alters the expression of genes for neuroprotection and synaptic function following acute estradiol treatment. Hippocampus 20, 1047–1060 (2010).

    CAS  PubMed  PubMed Central  Google Scholar 

  259. Adams, M. M. et al. Estrogen and aging affect the subcellular distribution of estrogen receptor-α in the hippocampus of female rats. J. Neurosci. 22, 3608–3614 (2002).

    CAS  PubMed  PubMed Central  Google Scholar 

  260. Waters, E. M. et al. Estrogen and aging affect the synaptic distribution of estrogen receptor beta-immunoreactivity in the CA1 region of female rat hippocampus. Brain Res. 1379, 86–97 (2011).

    CAS  PubMed  Google Scholar 

Download references

Acknowledgements

The Frick laboratory is supported by the US National Institutes of Health (R01MH107886, 2R15GM118304-02, F31MH118822 and F32MH118782), the Alzheimer’s Association (SAGA-17-419092), the University of Wisconsin System, the University of Wisconsin-Milwaukee Research Foundation, the University of Wisconsin-Milwaukee Office of Undergraduate Research and the University of Wisconsin-Milwaukee College of Letters and Science.

Author information

Authors and Affiliations

Authors

Contributions

The authors contributed equally to all aspects of the article.

Corresponding author

Correspondence to Karyn M. Frick.

Additional information

Competing interests

K.M.F. is a co-founder and Chief Scientific Officer of Estrigenix Therapeutics Inc., and is listed as an inventor of a pending patent held by the University of Wisconsin-Milwaukee, Marquette University and Concordia University Wisconsin entitled “Substituted (4′-hydroxyphenyl)cycloalkane and (4′-hydroxyphenyl)cycloalkene compounds and uses thereof as selective agonists of the estrogen receptor beta isoform for enhanced memory consolidation”, inventors W. A. Donaldson, D. S. Sem and K.M.F. (WO2018183800A1). The other authors declare no competing interests.

Peer review information

Nature Reviews Neuroscience thanks H. Bimonte-Nelson, who co-reviewed with V. Bernaud, and the other, anonymous, reviewer(s) for their contribution to the peer review of this work.

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Glossary

Retention

Storage of acquired and consolidated information that enables subsequent recall or retrieval of the information.

Ovariectomized

Ovariectomy involves surgical removal of the ovaries to eliminate ovarian hormone cycling. Subjects that have undergone ovariectomy are considered ovariectomized.

Consolidation

Process through which learned information is encoded and stored to form a memory that can be recalled at a later time.

Hormone response elements

Short DNA sequence within the promoter region of a gene that binds a hormone receptor complex to enable gene transcription.

Caveolins

Integral membrane proteins that form functional microdomains of receptors and their associated signalling proteins at the plasma membrane.

Sexual receptivity

A positive state of responsivity towards the initiation of sexual behaviour by another individual. Often indicated by a species-specific mating posture.

Gonadectomy

Surgical removal of the gonads (ovaries or testes); because ‘ovariectomy’ is the preferred term for females, ‘gonadectomy’ is most commonly used for males.

Acquisition

A process through which information is learned through physical or sensory interaction with environmental stimuli.

Spatial reference memory

Memory for locations that do not change over time (for example, the layout of buildings on a college campus). Used for navigating through an environment.

Spatial working memory

Memory for locations that change over time (for example, the locations of your keys or your car in your campus car park).

Delayed non-match-to-sample task

Test of memory for items that differ from an initial stimulus array, assessed at some delay after the original stimulus presentation.

Silent synapses

Immature synapses containing few AMPA receptors, which could allow greater synaptic potentiation and learning facilitation on interaction with a training stimulus.

Extinction

Process whereby a learned association between two stimuli (for example, shock occurs in context A) becomes unlearned through repetitive exposure to one stimulus (context A) without the other (shock).

Contextual fear conditioning

Model of fear learning in which repeated exposure to foot shocks in one context eventually elicits fear (freezing) of the context in the absence of shock.

FOS

A transcription factor encoded by an immediate early gene that is activated rapidly and transiently in response to neuronal activity, leading to expression of memory-related genes.

Generalization

Process whereby a stimulus–response association learned in one context (for example, a stimulus induces fear) becomes transferred to another, similar context.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Taxier, L.R., Gross, K.S. & Frick, K.M. Oestradiol as a neuromodulator of learning and memory. Nat Rev Neurosci 21, 535–550 (2020). https://doi.org/10.1038/s41583-020-0362-7

Download citation

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/s41583-020-0362-7

This article is cited by

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing