Search

everythinglearnresearchcommunity

for

Search:↓

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

Sodium valproate helps skin healing by affecting GABA and histone deacetylase.

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

Blocking GABA(A) receptors increases neuron sensitivity, showing GABA and glycine have different roles in pain.

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

Toluene lowers body temperature through different mechanisms depending on the concentration.

5α-reduced neurosteroids may help regulate glial cell differentiation.

Progesterone protects brain cells by converting to allopregnanolone and involving GABAA receptors.

Deoxycorticosterone and its metabolites help prevent seizures by interacting with specific receptors.

14,15-EET may help reduce poststroke pain by affecting certain brain proteins.

Progesterone protects neurons from damage by converting to allopregnanolone, which works through GABAA receptors.

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

Blocking CRF-R1 can reduce alcohol intake in stressed mice.

Progesterone boosts alcohol's effect on brain, finasteride counters it.

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

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

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

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

Activating TSPO helps protect the retina from damage caused by high eye pressure in glaucoma.

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

Benzothiazepines like diltiazem reduce anxiety in mice by making neurosteroids.

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

Progesterone can reduce seizures without relying on the GABAA receptor pathway.

Early changes in brain chemicals affect how a drug reduces alcohol intake in rats.

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

Diazepam's effects on anxiety and memory differ between male and female rats due to hormonal influences.

Brain-made chemicals can control nerve cell function differently in various parts of a mouse's brain, which may help us understand neurological conditions.

AC-5216 reduces anxiety in mice through neurosteroids affecting GABAA receptors.

Midazolam's seizure prevention is partly due to increased neurosteroid production.

Androgens improve memory in adolescent male rats by acting on brain receptors.