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Changing neuroactive steroids in baby male rats affects their memory and learning differently as they grow up.

Finasteride may cause long-lasting sexual side effects.

Some common medications can harm male fertility, but many effects can be reversed.

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

5-alpha reductase inhibitors slightly increase the risk of sexual and mood side effects, and breast growth in men.

Finasteride use can cause depression-like behavior in male rats.

Finasteride helps protect brain in old male rats.

The steroids allopregnanolone and allotetrahydrodeoxycorticosteron worsened absence seizures in rats.

Finasteride might affect memory by impacting cholinergic system.

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

Androgens like testosterone may help treat traumatic brain injury by reducing mitochondrial stress and inflammation.

Some people experience lasting sexual, psychological, and sleep problems after using finasteride or SSRI antidepressants, possibly due to similar underlying causes.

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

Finasteride affects SRD5A2 gene pattern, possibly causing lasting side effects.

Researchers created a new method to measure brain steroids, finding higher levels of certain steroids and changes due to a drug.

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

Estazolam reduces anxiety-like behavior in PTSD by increasing allopregnanolone levels.

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

Dutasteride makes alcohol less sedating and may lead to less drinking in men.

Finasteride for hair loss may cause lasting sexual, genitourinary, mental, and anti-androgenic side effects in young men.

5-alpha reductase inhibitors may help protect the brain and gut in Parkinson's disease.

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

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

DHEA improved brain function and behavior in old monkeys and had additional health benefits.

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

Diabetic neuropathy in mice is linked to poor mitochondria function and lower brain hormone production.

Mitochondrial problems in diabetic nerve damage might cause pain by lowering the production of certain nerve-related steroids.

Finasteride reduces inflammation and improves immune response after trauma by altering hormone levels.