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

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

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

Testosterone increases 3α-androstanediol levels, which can be blocked by finasteride.

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

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

5α-reductase inhibitors can cause sexual problems, higher risk of aggressive prostate cancer, and depression.

PEA reduces pain by increasing neurosteroid synthesis in the spinal cord.

EETs can delay seizures by affecting GABA activity, offering potential new treatments for seizures.

Blocking progesterone metabolism can cause depression-like behavior in mice.

Social isolation makes rats more sensitive to alcohol's effects on the brain.

PEA boosts allopregnanolone production and reduces oxidative stress in brain cells.

The protein StAR is found in 17 different organs and can affect hair loss and brain functions, but its full role is not yet fully understood.

Isolation stress in rats reduces brain enzyme levels, affecting dopamine function.

Progesterone reduces spinal reflex activity by increasing certain GABA(A) receptor subtypes.

Men and women have different levels and production of brain steroids, which may affect their risk for certain brain disorders.

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

Neurosteroids help protect fetal brains from asphyxia damage.

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

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

Progesterone increases alcohol tolerance and withdrawal anxiety, while DHEAS prevents them.

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

Stress worsens Tourette symptoms by increasing allopregnanolone levels.

Estrogen and androgen signals control synaptic changes in rat brains.

Blocking 5α-reductase can harm memory and brain structure, and increase harmful brain changes in male mice used for Alzheimer's disease research.

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

Finasteride raises suicide-linked aggression and stops clozapine's positive effects in schizophrenia animals.

Testosterone significantly affects sexual desire in both men and women, but its impact on women is more complex and influenced by psychological factors.