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Finasteride almost fully depletes allopregnanolone in rat brains and enhances 20α-DHP, but doesn't change 3α-DHP levels.

The availability of certain hormones and specific stimulation patterns affect long-term synaptic changes in the male rat brain.

Seeing trauma causes fear in mice by lowering their natural fear-reducing hormones.

Finasteride and dutasteride reduce neurosteroid production, possibly helping treat glioblastoma.

High-dose dutasteride reduces PMDD symptoms by stabilizing neurosteroid levels.

Progesterone and related compounds may help control seizures linked to the menstrual cycle but have limitations that need addressing.

The enzyme 5α-reductase is key in causing psychotic-like effects from sleep deprivation.

Finasteride use may lead to less alcohol consumption in men with lasting sexual side effects.

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

Medications for enlarged prostate can cause sexual side effects like reduced libido, erectile dysfunction, and ejaculatory problems.

Allopregnanolone increases KCC2 expression in baby male rats' brains, while finasteride doesn't affect it.

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

Finasteride worsens stress effects on sensory processes, possibly linking to anxiety/depression.

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

Finasteride given to baby rats reduces dopamine release and increases alcohol consumption in adult males.

Pregnancy and nursing increase certain brain activities in rats, but these changes disappear when the babies are taken away.

Finasteride treats hair loss but may cause low libido, erectile issues, and depression.

Agmatine may help reduce seizures linked to hormone changes in female rats.

A natural steroid in the body may protect against eye damage in glaucoma.

Progesterone treatment improved seizures in a woman with menstrual cycle-related epilepsy, but a wrong medication worsened her condition.

Neuroimaging suggests that treatments targeting brain steroids could help control epilepsy, especially types linked to the menstrual cycle.

Finasteride worsens seizures in epilepsy rats and speeds up epileptogenesis in mice.

Gene expression differences in PFS patients suggest a potential organic cause for symptoms.

Ferulic acid can reduce seizures and depression-like behaviors in catamenial epilepsy by balancing hormones and brain enzyme activity.

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

Increasing TSPO in the brain reduces anxiety and depression.

Neurosteroids play a key role in controlling the brain-adrenal gland activity in pregnant sheep, both in normal and stressful situations.

Sex hormones affect brain cells differently in males and females.

Altered metabolism can help control seizures by changing brain signaling and energy use, suggesting new treatments for epilepsy.

Short-term finasteride use in male rats caused anxiety, depression, and memory problems.