author_facet Wu, Wendy W.
Bryant, Damani N.
Dorsa, Daniel M.
Adelman, John P.
Maylie, James
Wu, Wendy W.
Bryant, Damani N.
Dorsa, Daniel M.
Adelman, John P.
Maylie, James
author Wu, Wendy W.
Bryant, Damani N.
Dorsa, Daniel M.
Adelman, John P.
Maylie, James
spellingShingle Wu, Wendy W.
Bryant, Damani N.
Dorsa, Daniel M.
Adelman, John P.
Maylie, James
The Journal of Neuroscience
Ovarian Hormone Loss Impairs Excitatory Synaptic Transmission at Hippocampal CA3–CA1 Synapses
General Neuroscience
author_sort wu, wendy w.
spelling Wu, Wendy W. Bryant, Damani N. Dorsa, Daniel M. Adelman, John P. Maylie, James 0270-6474 1529-2401 Society for Neuroscience General Neuroscience http://dx.doi.org/10.1523/jneurosci.2001-13.2013 <jats:p>Premature and long-term ovarian hormone loss following ovariectomy (OVX) is associated with cognitive impairment. This condition is prevented by estradiol (E<jats:sub>2</jats:sub>) therapy when initiated shortly following OVX but not after substantial delay. To determine whether these clinical findings are correlated with changes in synaptic functions, we used adult OVX rats to evaluate the consequences of short-term (7–10 d, OVX<jats:sub>Control</jats:sub>) and long-term (∼5 months, OVX<jats:sub>LT</jats:sub>) ovarian hormone loss, as well as subsequent<jats:italic>in vivo</jats:italic>E<jats:sub>2</jats:sub>treatment, on excitatory synaptic transmission at the hippocampal CA3–CA1 synapses important for learning and memory. The results show that ovarian hormone loss was associated with a marked decrease in synaptic strength. E<jats:sub>2</jats:sub>treatment increased synaptic strength in OVX<jats:sub>Control</jats:sub>but not OVX<jats:sub>LT</jats:sub>rats, demonstrating a change in the efficacy for E<jats:sub>2</jats:sub>5 months following OVX. E<jats:sub>2</jats:sub>also had a more rapid effect: within minutes of bath application, E<jats:sub>2</jats:sub>acutely increased synaptic strength in all groups except OVX<jats:sub>LT</jats:sub>rats that did not receive<jats:italic>in vivo</jats:italic>E<jats:sub>2</jats:sub>treatment. E<jats:sub>2</jats:sub>'s acute effect was mediated postsynaptically, and required Ca<jats:sup>2+</jats:sup>influx through the voltage-gated Ca<jats:sup>2+</jats:sup>channels. Despite E<jats:sub>2</jats:sub>'s acute effect, synaptic strength of OVX<jats:sub>LT</jats:sub>rats remained significantly lower than that of OVX<jats:sub>Control</jats:sub>rats. Thus, changes in CA3–CA1 synaptic transmission associated with ovarian hormone loss cannot be fully reversed with delayed E<jats:sub>2</jats:sub>treatment. Given that synaptic strength at CA3–CA1 synapses is related to the ability to learn hippocampus-dependent tasks, these findings provide additional insights for understanding cognitive impairment-associated long-term ovarian hormone loss and ineffectiveness for delayed E<jats:sub>2</jats:sub>treatment to maintain cognitive functions.</jats:p> Ovarian Hormone Loss Impairs Excitatory Synaptic Transmission at Hippocampal CA3–CA1 Synapses The Journal of Neuroscience
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series The Journal of Neuroscience
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title Ovarian Hormone Loss Impairs Excitatory Synaptic Transmission at Hippocampal CA3–CA1 Synapses
title_unstemmed Ovarian Hormone Loss Impairs Excitatory Synaptic Transmission at Hippocampal CA3–CA1 Synapses
title_full Ovarian Hormone Loss Impairs Excitatory Synaptic Transmission at Hippocampal CA3–CA1 Synapses
title_fullStr Ovarian Hormone Loss Impairs Excitatory Synaptic Transmission at Hippocampal CA3–CA1 Synapses
title_full_unstemmed Ovarian Hormone Loss Impairs Excitatory Synaptic Transmission at Hippocampal CA3–CA1 Synapses
title_short Ovarian Hormone Loss Impairs Excitatory Synaptic Transmission at Hippocampal CA3–CA1 Synapses
title_sort ovarian hormone loss impairs excitatory synaptic transmission at hippocampal ca3–ca1 synapses
topic General Neuroscience
url http://dx.doi.org/10.1523/jneurosci.2001-13.2013
publishDate 2013
physical 16158-16169
description <jats:p>Premature and long-term ovarian hormone loss following ovariectomy (OVX) is associated with cognitive impairment. This condition is prevented by estradiol (E<jats:sub>2</jats:sub>) therapy when initiated shortly following OVX but not after substantial delay. To determine whether these clinical findings are correlated with changes in synaptic functions, we used adult OVX rats to evaluate the consequences of short-term (7–10 d, OVX<jats:sub>Control</jats:sub>) and long-term (∼5 months, OVX<jats:sub>LT</jats:sub>) ovarian hormone loss, as well as subsequent<jats:italic>in vivo</jats:italic>E<jats:sub>2</jats:sub>treatment, on excitatory synaptic transmission at the hippocampal CA3–CA1 synapses important for learning and memory. The results show that ovarian hormone loss was associated with a marked decrease in synaptic strength. E<jats:sub>2</jats:sub>treatment increased synaptic strength in OVX<jats:sub>Control</jats:sub>but not OVX<jats:sub>LT</jats:sub>rats, demonstrating a change in the efficacy for E<jats:sub>2</jats:sub>5 months following OVX. E<jats:sub>2</jats:sub>also had a more rapid effect: within minutes of bath application, E<jats:sub>2</jats:sub>acutely increased synaptic strength in all groups except OVX<jats:sub>LT</jats:sub>rats that did not receive<jats:italic>in vivo</jats:italic>E<jats:sub>2</jats:sub>treatment. E<jats:sub>2</jats:sub>'s acute effect was mediated postsynaptically, and required Ca<jats:sup>2+</jats:sup>influx through the voltage-gated Ca<jats:sup>2+</jats:sup>channels. Despite E<jats:sub>2</jats:sub>'s acute effect, synaptic strength of OVX<jats:sub>LT</jats:sub>rats remained significantly lower than that of OVX<jats:sub>Control</jats:sub>rats. Thus, changes in CA3–CA1 synaptic transmission associated with ovarian hormone loss cannot be fully reversed with delayed E<jats:sub>2</jats:sub>treatment. Given that synaptic strength at CA3–CA1 synapses is related to the ability to learn hippocampus-dependent tasks, these findings provide additional insights for understanding cognitive impairment-associated long-term ovarian hormone loss and ineffectiveness for delayed E<jats:sub>2</jats:sub>treatment to maintain cognitive functions.</jats:p>
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author Wu, Wendy W., Bryant, Damani N., Dorsa, Daniel M., Adelman, John P., Maylie, James
author_facet Wu, Wendy W., Bryant, Damani N., Dorsa, Daniel M., Adelman, John P., Maylie, James, Wu, Wendy W., Bryant, Damani N., Dorsa, Daniel M., Adelman, John P., Maylie, James
author_sort wu, wendy w.
container_issue 41
container_start_page 16158
container_title The Journal of Neuroscience
container_volume 33
description <jats:p>Premature and long-term ovarian hormone loss following ovariectomy (OVX) is associated with cognitive impairment. This condition is prevented by estradiol (E<jats:sub>2</jats:sub>) therapy when initiated shortly following OVX but not after substantial delay. To determine whether these clinical findings are correlated with changes in synaptic functions, we used adult OVX rats to evaluate the consequences of short-term (7–10 d, OVX<jats:sub>Control</jats:sub>) and long-term (∼5 months, OVX<jats:sub>LT</jats:sub>) ovarian hormone loss, as well as subsequent<jats:italic>in vivo</jats:italic>E<jats:sub>2</jats:sub>treatment, on excitatory synaptic transmission at the hippocampal CA3–CA1 synapses important for learning and memory. The results show that ovarian hormone loss was associated with a marked decrease in synaptic strength. E<jats:sub>2</jats:sub>treatment increased synaptic strength in OVX<jats:sub>Control</jats:sub>but not OVX<jats:sub>LT</jats:sub>rats, demonstrating a change in the efficacy for E<jats:sub>2</jats:sub>5 months following OVX. E<jats:sub>2</jats:sub>also had a more rapid effect: within minutes of bath application, E<jats:sub>2</jats:sub>acutely increased synaptic strength in all groups except OVX<jats:sub>LT</jats:sub>rats that did not receive<jats:italic>in vivo</jats:italic>E<jats:sub>2</jats:sub>treatment. E<jats:sub>2</jats:sub>'s acute effect was mediated postsynaptically, and required Ca<jats:sup>2+</jats:sup>influx through the voltage-gated Ca<jats:sup>2+</jats:sup>channels. Despite E<jats:sub>2</jats:sub>'s acute effect, synaptic strength of OVX<jats:sub>LT</jats:sub>rats remained significantly lower than that of OVX<jats:sub>Control</jats:sub>rats. Thus, changes in CA3–CA1 synaptic transmission associated with ovarian hormone loss cannot be fully reversed with delayed E<jats:sub>2</jats:sub>treatment. Given that synaptic strength at CA3–CA1 synapses is related to the ability to learn hippocampus-dependent tasks, these findings provide additional insights for understanding cognitive impairment-associated long-term ovarian hormone loss and ineffectiveness for delayed E<jats:sub>2</jats:sub>treatment to maintain cognitive functions.</jats:p>
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spelling Wu, Wendy W. Bryant, Damani N. Dorsa, Daniel M. Adelman, John P. Maylie, James 0270-6474 1529-2401 Society for Neuroscience General Neuroscience http://dx.doi.org/10.1523/jneurosci.2001-13.2013 <jats:p>Premature and long-term ovarian hormone loss following ovariectomy (OVX) is associated with cognitive impairment. This condition is prevented by estradiol (E<jats:sub>2</jats:sub>) therapy when initiated shortly following OVX but not after substantial delay. To determine whether these clinical findings are correlated with changes in synaptic functions, we used adult OVX rats to evaluate the consequences of short-term (7–10 d, OVX<jats:sub>Control</jats:sub>) and long-term (∼5 months, OVX<jats:sub>LT</jats:sub>) ovarian hormone loss, as well as subsequent<jats:italic>in vivo</jats:italic>E<jats:sub>2</jats:sub>treatment, on excitatory synaptic transmission at the hippocampal CA3–CA1 synapses important for learning and memory. The results show that ovarian hormone loss was associated with a marked decrease in synaptic strength. E<jats:sub>2</jats:sub>treatment increased synaptic strength in OVX<jats:sub>Control</jats:sub>but not OVX<jats:sub>LT</jats:sub>rats, demonstrating a change in the efficacy for E<jats:sub>2</jats:sub>5 months following OVX. E<jats:sub>2</jats:sub>also had a more rapid effect: within minutes of bath application, E<jats:sub>2</jats:sub>acutely increased synaptic strength in all groups except OVX<jats:sub>LT</jats:sub>rats that did not receive<jats:italic>in vivo</jats:italic>E<jats:sub>2</jats:sub>treatment. E<jats:sub>2</jats:sub>'s acute effect was mediated postsynaptically, and required Ca<jats:sup>2+</jats:sup>influx through the voltage-gated Ca<jats:sup>2+</jats:sup>channels. Despite E<jats:sub>2</jats:sub>'s acute effect, synaptic strength of OVX<jats:sub>LT</jats:sub>rats remained significantly lower than that of OVX<jats:sub>Control</jats:sub>rats. Thus, changes in CA3–CA1 synaptic transmission associated with ovarian hormone loss cannot be fully reversed with delayed E<jats:sub>2</jats:sub>treatment. Given that synaptic strength at CA3–CA1 synapses is related to the ability to learn hippocampus-dependent tasks, these findings provide additional insights for understanding cognitive impairment-associated long-term ovarian hormone loss and ineffectiveness for delayed E<jats:sub>2</jats:sub>treatment to maintain cognitive functions.</jats:p> Ovarian Hormone Loss Impairs Excitatory Synaptic Transmission at Hippocampal CA3–CA1 Synapses The Journal of Neuroscience
spellingShingle Wu, Wendy W., Bryant, Damani N., Dorsa, Daniel M., Adelman, John P., Maylie, James, The Journal of Neuroscience, Ovarian Hormone Loss Impairs Excitatory Synaptic Transmission at Hippocampal CA3–CA1 Synapses, General Neuroscience
title Ovarian Hormone Loss Impairs Excitatory Synaptic Transmission at Hippocampal CA3–CA1 Synapses
title_full Ovarian Hormone Loss Impairs Excitatory Synaptic Transmission at Hippocampal CA3–CA1 Synapses
title_fullStr Ovarian Hormone Loss Impairs Excitatory Synaptic Transmission at Hippocampal CA3–CA1 Synapses
title_full_unstemmed Ovarian Hormone Loss Impairs Excitatory Synaptic Transmission at Hippocampal CA3–CA1 Synapses
title_short Ovarian Hormone Loss Impairs Excitatory Synaptic Transmission at Hippocampal CA3–CA1 Synapses
title_sort ovarian hormone loss impairs excitatory synaptic transmission at hippocampal ca3–ca1 synapses
title_unstemmed Ovarian Hormone Loss Impairs Excitatory Synaptic Transmission at Hippocampal CA3–CA1 Synapses
topic General Neuroscience
url http://dx.doi.org/10.1523/jneurosci.2001-13.2013