"We've known for some time that ovarian hormones, and particularly estradiol - a type of estrogen - have important consequences for neurons' structure and function," said UCSB neuroscientist Michael Goard, senior author of a paper published in the journal Neuron. In the 1990s, ex vivo experiments examined female rodent brain tissue taken at different stages of the estrous cycle. They found that during the "proestrus" stage - when estradiol levels peak - neurons in the hippocampus tend to form more dendritic spines, small protuberances that extend from dendrites of neurons, and serve as the primary site of connections between neurons.
"To date, there was little understanding of how the estrous cycle affects neurons in living mice," said Nora Wolcott, the paper's lead author. Now, thanks to advanced microscopy techniques, Goard's team was able to measure the structure and activity of neurons across multiple estrous cycles, thereby gaining insight into sex hormones' role in brain plasticity and memory. Other authors on the paper include William Redman, Marie Karpinska, and Emily Jacobs.
Taking up where previous studies left off, the researchers deployed two-photon laser scanning microscopy,tracking the formation and pruning of these dendritic spines in mice over several four-day estrous cycles. They observed many new spines during proestrus, which were then pruned as the cycle advanced through ovulation. These were not subtle changes - the density of spines differed by 20-30% across the cycle, representing thousands of synaptic connections for each neuron.
"How does the ebb and flow of spines influence the function of brain cells? Perhaps this influences how neurons integrate signals from other neurons," Goard said. "You can imagine if they're suddenly adding more synaptic connections, the neurons are going to get a lot more input and this is going to affect how they respond."
To investigate, the scientists examined the action potential - the 'firing' of the neuron - and how the impulse propagates through the neuron. Typically, the dendrites receive the signal, which travels to the cell body and out to the axon. "But the signal also travels backward back through the dendrite, which is usually where the neuron receives information," Goard said. This backpropagating signal is thought to play a role in learning and memory consolidation. They found that during peak estradiol, the backpropagating signal traveled farther back into the dendrites, which the researchers suspect may have implications for plasticity - the brain's ability to form new neural connections.
So what are the functional consequences of the increased dendritic spine density and backpropagation? One answer lay in the "place cells," or neurons in the hippocampus that fire when the animal is in a particular location in its environment - they help build mental maps and aid with spatial learning and navigation. To test the animals' ability to learn and remember new places, the researchers let them explore different environments while measuring the activity of neurons in the hippocampus.
The researchers found that place cells responded to familiar locations most reliably during proestrus - the high estradiol phase - and were most variable when the estradiol was lowest. "This is the first time that these microscopic differences in neural structure and function have been tracked across time in the same animal," Wolcott pointed out.
These findings in mice have strong implications for humans as well. Indeed, work from co-author Emily Jacobs' lab found that endocrine rhythms across the menstrual cycle are tied to structural changes in the human hippocampus. While hormone cycles are typically associated with female mammals, males also experience hormone fluctuations, many of which act on similar receptors. For example, testosterone can be converted to estrogen via aromatization, where it acts on estrogen receptors in the hippocampus. This indicates that hormone-driven plasticity is a widespread phenomenon, and underscores the importance of considering endocrine factors in neuroscience research.
"We suspect that there is some adaptive evolutionary purpose," Goard said, "and the reason I suspect that's true is because receptors for ovarian hormones don't have to be in the hippocampus, which is not thought to be directly involved in reproductive functions. But for some reason they're being expressed in the hippocampus - probably for some learning and memory related purpose. We don't know exactly what it is, but we think it's important."
Understanding the relationship between hormonal cycle fluctuations and the brain not only furthers our fundamental understanding of brain biology, it also opens up new possibilities for medicine personalized not just to individuals, but with respect to hormone cycle phase. "The finding that the brain physically changes in response to naturally cycling hormones challenges our understanding of mammalian cognition," Wolcott said.
Research Report:The estrous cycle modulates hippocampal spine dynamics, dendritic processing, and spatial coding
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