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δ-GABAA receptors affect alcohol consumption based on the estrous cycle and influence movement regardless of the cycle.

Removing certain brain receptors in mice worsens seizure severity and response to treatment during hormone withdrawal.

2-DG reduces seizures by enhancing brain inhibition through specific receptor activation.

During late pregnancy in rats, hormonal changes increased certain GABAA receptors in specific brain cells.

Three drugs change mice's alcohol drinking patterns by affecting GABAA receptors.

Midazolam's antiseizure effects are mainly due to synaptic GABA-A receptors, not neurosteroids or extrasynaptic receptors.

Neurosteroids change how GABA_A receptors work in the brain, which could be important for treating temporal lobe epilepsy.

Pregnancy increases certain GABA_A receptors in rat brains, influenced by steroid levels.

Neuroactive steroids show promise for treating mental and neurological disorders by targeting GABA_A receptors.

Progesterone and its byproducts control a specific receptor in the brain independently of progesterone receptors, affecting conditions related to the menstrual cycle.

Neurosteroids can influence behavior by modulating brain inhibition, with potential for treating psychiatric disorders.

Chronic ethanol increases certain brain receptor levels, influenced by steroids and protein changes.

Hormones during puberty increase certain receptors in the brain, and this change is influenced by estrogen levels.

A brain-produced steroid causes increased scratching in mice with a skin condition similar to eczema.

Neurosteroids are crucial for stress response, and targeting specific receptors may help treat certain disorders.

Ovarian and stress hormones can change GABA A receptors through neurosteroids.

Stress and hormones like progesterone can affect absence seizures, but their effects change with different life stages.

Neurosteroids may help metyrapone reduce cocaine addiction.

Progesterone affects GABA_A receptor function by altering δ subunit levels.

14,15-EET may help reduce poststroke pain by affecting certain brain proteins.

Finasteride treatment can decrease certain steroids and increase others, possibly leading to depression symptoms in some cases.

Stress increases neurosteroids that help prevent seizures.

Neurosteroids in the brain can increase or decrease seizure risk in mice.

Pregnancy affects fear memory and brain activity in female rats.

A brain-made hormone can protect against memory-related brain damage caused by harmful proteins.

Neurosteroids show promise for treating epilepsy and more research is needed.

Blocking neurosteroid production can lead to more seizures and faster epilepsy onset in rats.

Midazolam impairs learning and memory by increasing neurosteroids through specific receptor activation.

Midazolam reduces PTSD-like behavior in rats by acting on specific brain receptors.

New targets for making and using brain-synthesized steroids could lead to better treatments for brain disorders and alcoholism.