Adams Michelle M, Morrison John H
Kastor Neurobiology of Aging Laboratory, Fishberg Research Center for Neurobiology, and Henry L. Schwartz Department of Geriatrics and Adult Development, Mount Sinai School of Medicine, New York, NY 10029, USA.
Cereb Cortex. 2003 Dec;13(12):1271-5. doi: 10.1093/cercor/bhg078.
The ramifications of endocrine and neural senescence converge in the hippocampus, particularly with respect to glutamatergic synapses. In this review, we will focus on current literature suggesting that potential synaptic alterations induced by estrogen in the hippocampus are mediated through interactions between ER-alpha and NMDA receptors. In addition, we will examine the data suggesting that these interactions may be uncoupled with aging. These studies demonstrate that while estrogen helps retain a youthful synaptic phenotype by some measures, the aged synapse may differ from the young synapse in several key respects that impact plasticity in general, and endocrine influences on the synapse, in particular.
内分泌衰老和神经衰老的影响在海马体中交织在一起,尤其是在谷氨酸能突触方面。在本综述中,我们将聚焦于当前的文献,这些文献表明雌激素在海马体中诱导的潜在突触改变是通过雌激素受体α(ER-α)和N-甲基-D-天冬氨酸(NMDA)受体之间的相互作用介导的。此外,我们将审视那些表明这些相互作用可能会随着衰老而解偶联的数据。这些研究表明,虽然从某些指标来看雌激素有助于维持年轻的突触表型,但衰老的突触在几个关键方面可能与年轻突触不同,这些方面总体上会影响可塑性,尤其是对突触的内分泌影响。