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Changing Allopregnanolone levels in newborns affects adult behavior and anxiety.

Early-life neurosteroid changes affect adolescent exploration and adult behavior.

A drug improved schizophrenia-like symptoms in stressed rats by changing brain steroid levels.

Changing allopregnanolone levels in baby rats affects their adult behavior and alcohol use.

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

Neurosteroid withdrawal increases α4 subunit expression in the hippocampus, which may relate to catamenial epilepsy in women.

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

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

Post-finasteride syndrome causes lasting sexual, neurological, and physical side effects in some people after taking finasteride.

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

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

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

Finasteride given to baby rats causes anxiety-like behavior and worsens learning from punishment in adult rats.

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

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

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

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

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

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

Finasteride can have lasting negative effects on brain function and behavior by disrupting neurosteroid production.

Ketogenic diet, neurosteroids, and HMGB1-TLR4 signaling pathway are potential targets for new epilepsy treatments.

Neurosteroids help protect the brain and improve behavior after a stroke in mice.

Finasteride affects alcohol intake in male mice, possibly due to neurosteroids.

Early NAS level changes affect alcohol consumption vulnerability.

In late pregnancy, allopregnanolone reduces stress responses in rats by affecting brain chemicals.

Neonatal neurosteroid levels affect adult brain function and behavior.

Early neurosteroid changes can alter adult brain function and behavior.

Progesterone-derived neurosteroids affect GABA-A receptor expression, influencing epilepsy during menstrual cycles.

Adjusting neurosteroid levels may help reduce alcohol withdrawal symptoms.

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