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Flutamide and a new synthetic steroid affected brain and prostate chemicals and showed potential for treating androgen-related conditions and epilepsy.

Finasteride reduces alcohol withdrawal severity and anxiety in mice, but may increase withdrawal severity in some cases.

Finasteride affects brain processes related to neurotransmission and metabolism, potentially helping with neuropsychiatric conditions.

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

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

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

Lower levels of certain brain chemicals are linked to worse PTSD symptoms in men.

Stress and alcohol affect brain chemicals differently in rats, mice, and humans, influenced by genetic differences.

Finasteride reduces alcohol withdrawal severity in male mice but increases it in female mice.

Using rodents for research shows that health problems in the womb can cause diseases later in life.

Excess androgens may cause PCOS, not just be a symptom.

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

Using anabolic androgenic steroids can cause serious, lasting health problems in many parts of the body.

Testosterone and its metabolites affect brain functions and could help treat neurological disorders.

GABA contributes to stress-related hair loss, and ginkgolide A may help treat it.

Disrupting natural body clocks increases the risk of developing type 2 diabetes.

Exposure to too much androgen before birth might cause polycystic ovary syndrome later in life.

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

Finasteride treats enlarged prostate and hair loss, but may cause side effects in some patients.

The circadian clock influences the behavior and regeneration of stem cells in the body.

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

The enzymes 5α-reductase and 3α/β-hydroxysteroid oxidoreductase help create brain-active substances from progesterone and testosterone, which could be used for treatment, but more research is needed to ensure their safety and effectiveness.

Low dose finasteride decreases certain steroids, possibly increasing depression risk.

Finasteride may protect brain and improve behavior in rats with liver failure.

5α-reductase inhibitors can cause serious and possibly lasting sexual and psychological side effects.

S5αR inhibitors might help treat schizophrenia and other mental disorders but need more research.

Finasteride affects brain and blood steroids, causing lasting sexual and emotional side effects.

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

Finasteride reduces new brain cells in male mice, possibly causing depression.