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This enzyme helps metabolize fatty acids and isoleucine, and could be key in treating neurological diseases and certain cancers.

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

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

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

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

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

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

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

Finasteride treatment changes brain steroid levels and receptors, affecting brain function even after stopping treatment.

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

Neurotrophin-4 increases calcium current in specific mouse neurons through the PI3K pathway.

Neurosteroids regulate synaptic inhibition in the spinal cord and may help manage spinal pain.

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

Progesterone affects GABA_A receptor function by altering δ subunit levels.

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

Stress increases neurosteroids that help prevent seizures.

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

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

New treatments for prostate cancer and BPH show promise, including novel compounds that target hormone synthesis and response.

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

Meis2 is essential for touch sensation and nerve function in mice.

Certain steroids in the brain affect mood and symptoms of depression, and treatments targeting these steroids show promise for improving these symptoms.

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

Neuroimaging suggests that treatments targeting brain steroids could help control epilepsy, especially types linked to the menstrual cycle.

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

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

Glycine likely affects dendrites connected to hair follicle terminals in rats.

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

Progesterone's seizure-reducing effects are mainly due to allopregnanolone, not progesterone receptors.

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