» Articles » PMID: 25131507

Regulation of Object Recognition and Object Placement by Ovarian Sex Steroid Hormones

Overview
Journal Behav Brain Res
Date 2014 Aug 19
PMID 25131507
Citations 54
Authors
Affiliations
Soon will be listed here.
Abstract

The ovarian hormones 17β-estradiol (E2) and progesterone (P4) are potent modulators of hippocampal memory formation. Both hormones have been demonstrated to enhance hippocampal memory by regulating the cellular and molecular mechanisms thought to underlie memory formation. Behavioral neuroendocrinologists have increasingly used the object recognition and object placement (object location) tasks to investigate the role of E2 and P4 in regulating hippocampal memory formation in rodents. These one-trial learning tasks are ideal for studying acute effects of hormone treatments on different phases of memory because they can be administered during acquisition (pre-training), consolidation (post-training), or retrieval (pre-testing). This review synthesizes the rodent literature testing the effects of E2 and P4 on object recognition (OR) and object placement (OP), and the molecular mechanisms in the hippocampus supporting memory formation in these tasks. Some general trends emerge from the data. Among gonadally intact females, object memory tends to be best when E2 and P4 levels are elevated during the estrous cycle, pregnancy, and in middle age. In ovariectomized females, E2 given before or immediately after testing generally enhances OR and OP in young and middle-aged rats and mice, although effects are mixed in aged rodents. Effects of E2 treatment on OR and OP memory consolidation can be mediated by both classical estrogen receptors (ERα and ERβ), and depend on glutamate receptors (NMDA, mGluR1) and activation of numerous cell signaling cascades (e.g., ERK, PI3K/Akt, mTOR) and epigenetic processes (e.g., histone acetylation, DNA methylation). Acute P4 treatment given immediately after training also enhances OR and OP in young and middle-aged ovariectomized females by activating similar cell signaling pathways as E2 (e.g., ERK, mTOR). The few studies that have administered both hormones in combination suggest that treatment can enhance OR and OP, but that effects are highly dependent on factors such as dose and timing of administration. In addition to providing more detail on these general conclusions, this review will discuss directions for future avenues of research into the hormonal regulation of object memory.

Citing Articles

Medial entorhinal-hippocampal desynchronization parallels the emergence of memory impairment in a mouse model of Alzheimer's disease pathology.

Vetere L, Galas A, Vaughan N, Feng Y, Christenson Wick Z, Philipsberg P bioRxiv. 2025; .

PMID: 39868201 PMC: 11761809. DOI: 10.1101/2025.01.15.633171.


Syngap1 promotes cognitive function through regulation of cortical sensorimotor dynamics.

Vaissiere T, Michaelson S, Creson T, Goins J, Furth D, Balazsfi D Nat Commun. 2025; 16(1):812.

PMID: 39827187 PMC: 11743135. DOI: 10.1038/s41467-025-56125-0.


The novel estrogen receptor beta agonist EGX358 and genotype influence memory, vasomotor, and anxiety outcomes in an Alzheimer's mouse model.

Schwabe M, Fleischer A, Kuehn R, Chaudhury S, York J, Sem D Front Aging Neurosci. 2024; 16:1477045.

PMID: 39629477 PMC: 11613887. DOI: 10.3389/fnagi.2024.1477045.


Metabotropic NMDAR Signaling Contributes to Sex Differences in Synaptic Plasticity and Episodic Memory.

Le A, Lauterborn J, Jia Y, Cox C, Lynch G, Gall C J Neurosci. 2024; 44(50).

PMID: 39424366 PMC: 11638816. DOI: 10.1523/JNEUROSCI.0438-24.2024.


Treatment with brain specific estrogen prodrug ameliorates cognitive effects of surgical menopause in mice.

Salinero A, Abi-Ghanem C, Venkataganesh H, Sura A, Smith R, Thrasher C Horm Behav. 2024; 164:105594.

PMID: 38917776 PMC: 11330726. DOI: 10.1016/j.yhbeh.2024.105594.


References
1.
McGaugh J . Dissociating learning and performance: drug and hormone enhancement of memory storage. Brain Res Bull. 1989; 23(4-5):339-45. DOI: 10.1016/0361-9230(89)90220-7. View

2.
Smith C, McMahon L . Estradiol-induced increase in the magnitude of long-term potentiation is prevented by blocking NR2B-containing receptors. J Neurosci. 2006; 26(33):8517-22. PMC: 6674362. DOI: 10.1523/JNEUROSCI.5279-05.2006. View

3.
Singh M . Ovarian hormones elicit phosphorylation of Akt and extracellular-signal regulated kinase in explants of the cerebral cortex. Endocrine. 2001; 14(3):407-15. DOI: 10.1385/ENDO:14:3:407. View

4.
Singh M, Meyer E, Millard W, Simpkins J . Ovarian steroid deprivation results in a reversible learning impairment and compromised cholinergic function in female Sprague-Dawley rats. Brain Res. 1994; 644(2):305-12. DOI: 10.1016/0006-8993(94)91694-2. View

5.
Maki P . Minireview: effects of different HT formulations on cognition. Endocrinology. 2012; 153(8):3564-70. DOI: 10.1210/en.2012-1175. View