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

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

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

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

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

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

RY-023, a specific drug, can improve early stage memory learning without affecting general activity in rats, but it's less effective for later learning stages and doesn't impact memory recall.

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

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

Finasteride may affect fetal brain development and increase arousal, but more research is needed for safety confirmation.

Benzothiazepines like diltiazem reduce anxiety in mice by making neurosteroids.

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

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

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

Lactium, a milk protein, can help reduce symptoms of skin disorders linked to stress and anxiety without side effects.

Asiasari radix extract may relieve certain types of pain by affecting GABA and NMDA receptors.

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

Allopregnanolone is needed for certain brain processing issues caused by D1 dopamine receptor activation.

Postpartum depression is linked to changes in brain chemicals, inflammation, stress, and certain genes, and can potentially be identified by markers like specific steroids, serotonin levels, and vitamin D levels.

Late pregnancy helps repair brain damage in rats due to the GABAergic system.

Early NAS level changes affect alcohol consumption vulnerability.

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

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

Progesterone initially worsens but later reduces neuropathic pain in mice, through different mechanisms.

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

Anabolic steroids can build muscle and strength but have risks and need more research on their clinical benefits and side effects.

Androgen self-administration might be controlled by membrane receptors, not nuclear ones.

Fluoxetine's effectiveness as an antidepressant in mice depends on a specific protein activity and a 5-minute pretest.

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

DHEA affects multiple receptors and may help with metabolic issues, but its safety and effectiveness in humans are unclear.