Researchers from Northwestern University, Evanston, Illinois, have discovered a new factor in the escalation of seizures: the synthesis, or generation, of estrogens in the brain.
Their study in rats, published in the journal eLife, also suggests that using a drug that inhibits estrogen synthesis, called an aromatase inhibitor, may be an effective approach to controlling seizures.
Seizures occur when connected groups of cells in the brain become over-active and fire together. Current treatments work by dampening brain activity generally, which is often effective in controlling seizures, but can also lead to negative side-effects such as drowsiness, dizziness, or difficulty concentrating. As a result, there is a need for new and effective therapies.
“One alternative to current treatments may be to target a factor that promotes activity more selectively during seizures,” says corresponding author Catherine Woolley.
“Estrogens could play such a role. While most people think of estrogens as being female sex hormones, they are also synthesized in the brains of both males and females where they could influence seizure activity.”
To test this idea, the team injected both male and female rats with kainic acid to induce a severe form of seizures known as status epilepticus. This common, life-threatening condition occurs when epileptic fits last too long or follow one another so closely that patients are unable to recover consciousness between them. The researchers found that, in both sexes, seizures stimulate the synthesis of estrogens in the hippocampus, a part of the brain that is often involved in these episodes.
Each rat was then randomly administered with either a substance without therapeutic action, known as a vehicle, or an aromatase inhibitor, fadrozole or letrozole, the latter of which is already in clinical use for breast cancer. The vehicle-treated rats displayed the expected progression of seizure activity, while the fadrozole and letrozole-treated rats showed much lower activity. This demonstrated that aromatase inhibitors strongly suppressed the escalation of seizures in both sexes, without the need for anti-seizure drugs.
“As estrogens are known to increase the activity of cells in the hippocampus, estrogen synthesis during seizures could contribute to this activity, making the episodes worse,” Woolley explains.
“Our findings show that breaking this cycle with aromatase inhibitor therapy may be a novel approach to clinically controlling seizures.”
Stephen M. Smith, Professor of Medicine at Oregon Health & Science University, and Director of Medical Critical Care at the VA Portland Health Care System, adds: “Building on past work that shows how estrogen increases neuronal activity in a number of ways, this study clearly demonstrates that inhibiting estrogen production suppresses seizures quickly and effectively in a rat model of status epilepticus.
“Given the unacceptably high mortality rate of status epilepticus in humans, these findings are likely to elicit great interest by physicians in the field. They will hopefully also trigger clinical trials to determine the efficacy and safety of currently available aromatase inhibitors in patients with this condition.”
One concern over this approach is that aromatase inhibition would eliminate the ability of estrogens to protect neuronal structures and function, which could worsen seizure-related damage in the brain. The team investigated this, however, and found no negative effects of fadrozole or letrozole within the hippocampus.
“Further experiments with more detailed analyses of seizure-related neuronal damage are needed to investigate how aromatase inhibition during seizures affects the consequences of these episodes for the brain,” says Woolley.
“It is also important to understand how exactly seizure activity leads to estrogen synthesis in the brain, how estrogen levels go back down after a seizure, and what other circumstances stimulate brain estrogen synthesis. Answers to these questions will provide context for future drug development.”
About this neurology research
Funding: The research was supported by NIH/National Institute of Neurological Disorders and Stroke, Office of Research on Women’s Health.
Source: Emily Packer – eLife Image Source: The image is credited to Sato and Woolley. Original Research: Full open access research for “Acute inhibition of neurosteroid estrogen synthesis suppresses status epilepticus in an animal model” by Satoru M Sato and Catherine S Woolley in eLife. Published online April 15 2016 doi:10.7554/eLife.12917
Acute inhibition of neurosteroid estrogen synthesis suppresses status epilepticus in an animal model
Status epilepticus (SE) is a common neurological emergency for which new treatments are needed. In vitro studies suggest a novel approach to controlling seizures in SE: acute inhibition of estrogen synthesis in the brain. Here, we show in rats that systemic administration of an aromatase (estrogen synthase) inhibitor after seizure onset strongly suppresses both electrographic and behavioral seizures induced by kainic acid (KA). We found that KA-induced SE stimulates synthesis of estradiol (E2) in the hippocampus, a brain region commonly involved in seizures and where E2 is known to acutely promote neural activity. Hippocampal E2 levels were higher in rats experiencing more severe seizures. Consistent with a seizure-promoting effect of hippocampal estrogen synthesis, intra-hippocampal aromatase inhibition also suppressed seizures. These results reveal neurosteroid estrogen synthesis as a previously unknown factor in the escalation of seizures and suggest that acute administration of aromatase inhibitors may be an effective treatment for SE.
“Acute inhibition of neurosteroid estrogen synthesis suppresses status epilepticus in an animal model” by Satoru M Sato and Catherine S Woolley in eLife. Published online April 15 2016 doi:10.7554/eLife.12917